Dimitri Kullmann | Academic Influence

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Dimitri Kullmann

Medical

#729

World Rank

#964

Historical Rank

Neurology

#80

World Rank

#129

Historical Rank

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Why Is Dimitri Kullmann Influential?

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According to Wikipedia, Dimitri Michael Kullmann is a professor of neurology at the UCL Institute of Neurology, University College London , and leads the synaptopathies initiative funded by the Wellcome Trust. Kullmann is a member of the Queen Square Institute of Neurology Department of Clinical and Experimental Epilepsy and a consultant neurologist at the National Hospital for Neurology and Neurosurgery.

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Dimitri Kullmann's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

N-methyl-d-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes (2010) (921)
Tonically active GABAA receptors: modulating gain and maintaining the tone (2004) (753)
Extrasynaptic Glutamate Diffusion in the Hippocampus: Ultrastructural Constraints, Uptake, and Receptor Activation (1998) (442)
Extrasynaptic Glutamate Spillover in the Hippocampus: Dependence on Temperature and the Role of Active Glutamate Uptake (1997) (426)
GABA uptake regulates cortical excitability via cell type–specific tonic inhibition (2003) (425)
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel (2001) (379)
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy. (1999) (333)
Extrasynaptic glutamate spillover in the hippocampus: evidence and implications (1998) (324)
Long-term synaptic plasticity in hippocampal interneurons (2007) (302)
LTP of AMPA and NMDA Receptor–Mediated Signals: Evidence for Presynaptic Expression and Extrasynaptic Glutamate Spill-Over (1996) (293)
Oscillatory multiplexing of population codes for selective communication in the mammalian brain (2014) (286)
Amplitude fluctuations of (1994) (273)
Long-term potentiation is associated with increases in quantal content and quantal amplitude (1992) (270)
Anti-Hebbian Long-Term Potentiation in the Hippocampal Feedback Inhibitory Circuit (2007) (250)
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability (2000) (244)
Oscillations and Filtering Networks Support Flexible Routing of Information (2010) (240)
Multiple and Plastic Receptors Mediate Tonic GABAA Receptor Currents in the Hippocampus (2005) (233)
Presynaptic, extrasynaptic and axonal GABAA receptors in the CNS: where and why? (2005) (232)
Optogenetic and Potassium Channel Gene Therapy in a Rodent Model of Focal Neocortical Epilepsy (2012) (230)
Ca2+ Entry via postsynaptic voltage-sensitive Ca2+ channels can transiently potentiate excitatory synaptic transmission in the hippocampus (1992) (219)
Activation of AMPA, Kainate, and Metabotropic Receptors at Hippocampal Mossy Fiber Synapses Role of Glutamate Diffusion (1998) (211)
NR2B-Containing Receptors Mediate Cross Talk among Hippocampal Synapses (2004) (203)
Modulation of GABAergic Signaling among Interneurons by Metabotropic Glutamate Receptors (2000) (198)
Plasticity of Inhibition (2012) (196)
A genetically encoded fluorescent sensor for in vivo imaging of GABA (2018) (186)
Monosynaptic GABAergic Signaling from Dentate to CA3 with a Pharmacological and Physiological Profile Typical of Mossy Fiber Synapses (2001) (175)
Geometric and viscous components of the tortuosity of the extracellular space in the brain. (1998) (174)
Hebbian LTP in feed-forward inhibitory interneurons and the temporal fidelity of input discrimination (2005) (173)
The neuronal channelopathies. (2002) (165)
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia (2004) (163)
GABAA Receptors at Hippocampal Mossy Fibers (2003) (161)
The site of expression of NMDA receptor-dependent LTP: New fuel for an old fire (1995) (160)
Amplitude fluctuations of dual-component EPSCs in hippocampal pyramidal cells: implications for long-term potentiation. (1994) (149)
Kainate receptor-dependent axonal depolarization and action potential initiation in interneurons (2001) (142)
Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures (2015) (142)
Hippocampal synapses: do they talk to their neighbours? (1999) (137)
Synaptically released glutamate reduces gamma-aminobutyric acid (GABA)ergic inhibition in the hippocampus via kainate receptors. (1999) (128)
Differential triggering of spontaneous glutamate release by P/Q-, N-, and R-type Ca2+ channels (2013) (127)
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis (2009) (125)
Chemical–genetic attenuation of focal neocortical seizures (2014) (124)
Progressive Motor Neuron Pathology and the Role of Astrocytes in a Human Stem Cell Model of VCP-Related ALS (2017) (124)
Genetics of epilepsy (2002) (120)
Outwardly Rectifying Tonically Active GABAA Receptors in Pyramidal Cells Modulate Neuronal Offset, Not Gain (2009) (119)
The clinical and genetic heterogeneity of paroxysmal dyskinesias (2015) (114)
Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions. (2007) (112)
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders (2019) (111)
Presynaptic GABAA receptors enhance transmission and LTP induction at hippocampal mossy fiber synapses (2010) (108)
PRRT2 gene mutations (2012) (106)
Neurological channelopathies: new insights into disease mechanisms and ion channel function (2010) (101)
Clinical relevance of serum antibodies to extracellular N-methyl-d-aspartate receptor epitopes (2014) (98)
dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice. (2020) (98)
Interneuron networks in the hippocampus (2011) (97)
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia. (2005) (95)
Spillover and synaptic cross talk mediated by glutamate and GABA in the mammalian brain. (2000) (95)
Oscillatory dynamics in the hippocampus support dentate gyrus–CA3 coupling (2012) (94)
Role of Ionotropic Glutamate Receptors in Long-Term Potentiation in Rat Hippocampal CA1 Oriens-Lacunosum Moleculare Interneurons (2009) (94)
Endogenous zinc inhibits GABA(A) receptors in a hippocampal pathway. (2004) (93)
Nanoscale-Targeted Patch-Clamp Recordings of Functional Presynaptic Ion Channels (2013) (90)
The role of mammalian ionotropic receptors in synaptic plasticity: LTP, LTD and epilepsy (2000) (87)
Nerve excitability studies characterize Kv1.1 fast potassium channel dysfunction in patients with episodic ataxia type 1. (2010) (87)
Genetic neurological channelopathies: molecular genetics and clinical phenotypes (2015) (85)
Anti-N-methyl-D-aspartate receptor antibodies: A potentially treatable cause of encephalitis in the intensive care unit (2010) (83)
Target-Cell Specificity of Kainate Autoreceptor and Ca2+-Store-Dependent Short-Term Plasticity at Hippocampal Mossy Fiber Synapses (2008) (82)
Knockout of NMDA-receptors from parvalbumin interneurons sensitizes to schizophrenia-related deficits induced by MK-801 (2016) (82)
GABA and GABAA receptors at hippocampal mossy fibre synapses (2003) (81)
Neurological disorders caused by inherited ion-channel mutations (2002) (79)
Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy (2010) (78)
LTP and LTD in cortical GABAergic interneurons: Emerging rules and roles (2011) (78)
Episodic ataxia type 1: A neuronal potassium channelopathy (2007) (78)
Efficient “Communication through Coherence” Requires Oscillations Structured to Minimize Interference between Signals (2012) (74)
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment (2019) (73)
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment (2019) (73)
Variable K+ channel subunit dysfunction in inherited mutations of KCNA1 (2002) (73)
Autoimmune synaptopathies (2016) (71)
Cholinergic Axons Modulate GABAergic Signaling among Hippocampal Interneurons via Postsynaptic α7 Nicotinic Receptors (2007) (71)
Electric Fields Due to Synaptic Currents Sharpen Excitatory Transmission (2008) (70)
Independent Regulation of Basal Neurotransmitter Release Efficacy by Variable Ca2+ Influx and Bouton Size at Small Central Synapses (2012) (69)
Outcome of ventilatory support for acute respiratory failure in motor neurone disease (2002) (68)
Cortical inhibition, pH and cell excitability in epilepsy: what are optimal targets for antiepileptic interventions? (2013) (67)
Gene therapy in epilepsy—is it time for clinical trials? (2014) (67)
Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants (2018) (66)
Spike-Timing Dependent Plasticity in Inhibitory Circuits (2010) (64)
Analog Modulation of Mossy Fiber Transmission Is Uncoupled from Changes in Presynaptic Ca2+ (2008) (64)
NMDA receptor‐dependent long‐term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca2+/calmodulin‐dependent kinases (2007) (64)
Andersen–Tawil syndrome (2005) (63)
KCC2 overexpression prevents the paradoxical seizure-promoting action of somatic inhibition (2018) (63)
CA1 Oriens-Lacunosum Moleculare Interneurons Role of Ionotropic Glutamate Receptors in Long-Term Potentiation in Rat Hippocampal (2015) (63)
Endogenous Neurotrophin-3 Regulates Short-Term Plasticity at Lateral Perforant Path–Granule Cell Synapses (1998) (63)
Plasticity of GABAB Receptor-Mediated Heterosynaptic Interactions at Mossy Fibers After Status Epilepticus (2003) (60)
GABAergic Interneurons in Seizures: Investigating Causality With Optogenetics (2018) (59)
Ih-mediated depolarization enhances the temporal precision of neuronal integration (2011) (58)
Myasthenia and related disorders of the neuromuscular junction (2010) (57)
Epileptogenesis is associated with enhanced glutamatergic transmission in the perforant path. (2006) (57)
Focal cortical seizures start as standing waves and propagate respecting homotopic connectivity (2017) (56)
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study (2018) (56)
Clinical, pathological and functional characterization of riboflavin-responsive neuropathy (2017) (55)
Epilepsy Gene Therapy Using an Engineered Potassium Channel (2019) (55)
Action potential broadening in a presynaptic channelopathy (2016) (53)
Roles of distinct glutamate receptors in induction of anti‐Hebbian long‐term potentiation (2008) (52)
In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsy (2018) (52)
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing (2009) (51)
Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A (2005) (51)
Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4‐1.1/Kvβ1.1 and Kv1.4‐1.1/Kvβ1.2 (2006) (50)
Group I mGluR Agonist-Evoked Long-Term Potentiation in Hippocampal Oriens Interneurons (2011) (49)
Applications of the expectation-maximization algorithm to quantal analysis of postsynaptic potentials (1989) (49)
Thymectomy: role in the treatment of myasthenia gravis (2013) (48)
Release of Neurotransmitters (2004) (46)
Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1 (2013) (45)
Clinical neurophysiology of the episodic ataxias: Insights into ion channel dysfunction in vivo (2009) (44)
Creutzfeldt-Jakob disease presenting as complex partial status epilepticus: a report of two cases (1999) (44)
Optogenetic and chemogenetic therapies for epilepsy (2020) (43)
Quantal variability of excitatory transmission in the hippocampus: implications for the opening probability of fast glutamate-gated channels (1993) (43)
Biochemical autoregulatory gene therapy for focal epilepsy (2018) (42)
Glutamatergic Modulation of GABAergic Signaling Among Hippocampal Interneurons: Novel Mechanisms Regulating Hippocampal Excitability (2002) (42)
Silent synapses: what are they telling us about long-term potentiation? (2003) (42)
NMDA receptor-dependent function and plasticity in inhibitory circuits (2013) (42)
Episodic ataxia type 1 mutations differentially affect neuronal excitability and transmitter release (2009) (39)
Optogenetic approaches to treat epilepsy (2016) (38)
Hippocampal–prefrontal coherence mediates working memory and selective attention at distinct frequency bands and provides a causal link between schizophrenia and its risk gene GRIA1 (2019) (37)
Admission to neurological intensive care: who, when, and why? (2003) (37)
Alternative Splicing Modulates Inactivation of Type 1 Voltage-gated Sodium Channels by Toggling an Amino Acid in the First S3-S4 Linker* (2011) (36)
Neurological channelopathies. (2010) (36)
Heterogeneity and specificity of presynaptic Ca2+ current modulation by mGluRs at individual hippocampal synapses. (2004) (36)
Glycine receptor autoantibodies disrupt inhibitory neurotransmission (2019) (36)
Do Mossy Fibers Release GABA? (2002) (35)
Short- and long-term depression at glutamatergic synapses on hippocampal interneurons by group I mGluR activation (2011) (35)
Non-genomic effects of sex hormones on CLC-1 may contribute to gender differences in myotonia congenita (2008) (34)
Olanzapine: A potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogenetics (2019) (33)
Functional Characterization of a Novel Mutation in KCNA1 in Episodic Ataxia Type 1 Associated with Epilepsy (1999) (33)
Dendritic NMDA receptors in parvalbumin neurons enable strong and stable neuronal assemblies (2018) (32)
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination (2019) (32)
Tonic GABAA Receptor-Mediated Signaling in Epilepsy (2012) (32)
Plasticity of GABA(B) receptor-mediated heterosynaptic interactions at mossy fibers after status epilepticus. (2003) (30)
Functional characterization of compound heterozygosity for GlyRα1 mutations in the startle disease hyperekplexia (2002) (29)
Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2 (2008) (29)
Designer receptor technology for the treatment of epilepsy (2019) (29)
Relative picrotoxin insensitivity distinguishes ionotropic GABA receptor-mediated IPSCs in hippocampal interneurons (2002) (29)
Febrile convulsions: a 'benign' condition? (1999) (28)
Long-term potentiation in hippocampal oriens interneurons: postsynaptic induction, presynaptic expression and evaluation of candidate retrograde factors (2014) (27)
Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity (2017) (26)
Pathogenic potential of antibodies to the GABAB receptor (2017) (26)
What's wrong with the amygdala in temporal lobe epilepsy? (2011) (25)
Imaging pathological activities of human brain tissue in organotypic culture (2018) (24)
Personalized translational epilepsy research — Novel approaches and future perspectives Part I: Clinical and network analysis approaches (2017) (24)
Optogenetic induction of the schizophrenia-related endophenotype of ventral hippocampal hyperactivity causes rodent correlates of positive and cognitive symptoms (2018) (23)
Induction of Anti-Hebbian LTP in CA1 Stratum Oriens Interneurons: Interactions between Group I Metabotropic Glutamate Receptors and M1 Muscarinic Receptors (2015) (23)
Ionotropic receptors at hippocampal mossy fibers: roles in axonal excitability, synaptic transmission, and plasticity (2013) (23)
The Inherited Episodic Ataxias: How Well Do We Understand the Disease Mechanisms? (2001) (23)
The Mother of All Battles 20 years on: is LTP expressed pre‐ or postsynaptically? (2012) (22)
Novel therapies for epilepsy in the pipeline (2019) (22)
Kv1.1 channelopathy abolishes presynaptic spike width modulation by subthreshold somatic depolarization (2017) (22)
Open letter to prime minister David Cameron and health secretary Andrew Lansley (2010) (22)
Can N-Methyl-D-Aspartate Receptor Hypofunction in Schizophrenia Be Localized to an Individual Cell Type? (2019) (22)
Comment on "Role of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity" (2004) (21)
A tortuous and viscous route to understanding diffusion in the brain (1998) (20)
Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders (1998) (20)
Synapsin- and Actin-Dependent Frequency Enhancement in Mouse Hippocampal Mossy Fiber Synapses (2008) (20)
Myasthenia gravis (2012) (20)
Learning to live with Dale’s principle: ANNs with separate excitatory and inhibitory units (2020) (19)
Quantal analysis using maximum entropy noise deconvolution (1992) (18)
Dysfunction of the CaV2.1 calcium channel in cerebellar ataxias (2010) (18)
Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities (2018) (18)
T‐type calcium channels contribute to NMDA receptor independent synaptic plasticity in hippocampal regular‐spiking oriens‐alveus interneurons (2017) (17)
In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission. (2012) (17)
Slow channel congenital myasthenic syndrome responsive to a combination of fluoxetine and salbutamol (2013) (17)
Spider toxin inhibits gating pore currents underlying periodic paralysis (2018) (16)
Personalized translational epilepsy research — Novel approaches and future perspectives Part II: Experimental and translational approaches (2017) (16)
Myasthenia gravis and neuromyelitis opica: A causal link. (2013) (16)
Gene therapy in status epilepticus (2013) (15)
Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene (2015) (15)
Analogue closed-loop optogenetic modulation of hippocampal pyramidal cells dissociates gamma frequency and amplitude (2018) (15)
CD8+ encephalitis: a severe but treatable HIV-related acute encephalopathy (2016) (14)
Another migraine gene (2005) (14)
Excitatory synapses: Neither too loud nor too quiet (1999) (13)
Lambert-Eaton syndrome IgG inhibits transmitter release via P/Q Ca2+ channels (2015) (13)
Presynaptic fluctuations and release-independent depression (2006) (12)
De novo KCNA2 mutations cause hereditary spastic paraplegia (2017) (12)
Semiology, clustering, periodicity and natural history of seizures in an experimental occipital cortical epilepsy model (2018) (12)
Late recurrent thymoma in myasthenia gravis: a case series (2012) (11)
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation (2019) (11)
Changes in the severity and subtype of Guillain-Barré syndrome admitted to a specialist Neuromedical ICU over a 25 year period (2017) (11)
A PATIENT WITH EPISODIC ATAXIA AND PARAMYOTONIA CONGENITA DUE TO MUTATIONS IN KCNA1 AND SCN4A (2009) (10)
In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2 (2016) (10)
Central nervous system histoplasmosis in an immunocompetent patient (2010) (10)
Neurological manifestation of vitamin B12 deficiency. (2010) (10)
Nicotinic receptor activation induces NMDA receptor independent long‐term potentiation of glutamatergic signalling in hippocampal oriens interneurons (2020) (9)
The Enlightened Brain: Novel Imaging Methods Focus on Epileptic Networks at Multiple Scales (2018) (9)
Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins (2011) (9)
A 'sustain pedal' in the hippocampus? (2010) (8)
On-demand cell-autonomous gene therapy for brain circuit disorders (2022) (8)
Activity Clamp Provides Insights into Paradoxical Effects of the Anti-Seizure Drug Carbamazepine (2017) (8)
GABAA receptor mutations in epilepsy (Commentary on Lachance‐Touchette et al.) (2011) (7)
Interneurons go plastic (2011) (6)
CHAPTER 8 – Release of Neurotransmitters (2004) (6)
Just a graze? Cephalic tetanus presenting as a stroke mimic (2013) (6)
Impaired Pre‐Motor Circuit Activity and Movement in a Drosophila Model of KCNMA1‐Linked Dyskinesia (2021) (6)
Evaluating first seizures in adults in primary care. (2011) (5)
Synaptically released glutamate reduces g-aminobutyric acid (GABA)ergic inhibition in the hippocampus via kainate receptors (disinhibitionyguinea pigs) (1999) (5)
Catastrophic primary antiphospholipid syndrome presenting as status epilepticus (2005) (5)
GABA(A) receptor mutations in epilepsy (2011) (5)
Bortezomib for anti-NMDAR encephalitis following daclizumab treatment in a patient with multiple sclerosis (2021) (4)
Gene-Environment Interaction in a Conditional NMDAR-Knockout Model of Schizophrenia (2019) (4)
Benign neonatal convulsions and spontaneous network activity in the developing brain: is there a link? (2008) (4)
Cortical seizure propagation respects functional connectivity underlying sensory processing (2016) (4)
Clinical, pathological and functional characterization of riboﬂavin-responsive neuropathy (2017) (4)
Chapter 15 – Release of Neurotransmitters (2014) (4)
Brain. Editorial. (2014) (3)
How much inhibition in an epileptiform burst? (2010) (3)
Interneurons Expressing either Parvalbumin or CB1 Cannabinoid Receptor Cell Type-Specific Long-Term Plasticity at Glutamatergic Synapses onto Hippocampal (2010) (3)
Cell-Free Expression of Sodium Channel Domains for Pharmacology Studies. Noncanonical Spider Toxin Binding Site in the Second Voltage-Sensing Domain of Human Nav1.4 Channel (2019) (3)
Silent synapse (2011) (3)
Editorial. (2020) (3)
Long‐term potentiation in neurogliaform interneurons modulates excitation–inhibition balance in the temporoammonic pathway (2022) (3)
Tonic GABAA receptor–mediated signaling (2010) (3)
Disorders of Consciousness, Intensive Care Neurology and Sleep (2009) (3)
Lentiviral expression of GAD67 and CCK promoter‐driven opsins to target interneurons in vitro and in vivo (2016) (2)
Editorial. (2020) (2)
Glutamate and GABA spillover onto ionotropic and metabotropic receptors (2003) (2)
Computational Sophistication at a Single GABAergic Connection (2009) (2)
Extracellular glutamate and GABA transients at the transition from interictal spiking to seizures (2020) (2)
ION CHANNELS | Channelopathies in Epilepsy (2009) (2)
Sodium channel mutations and epilepsy: Association and causation (2010) (2)
Alternative splicing tunes sodium channels to support channel- and neuron-specific effects (2020) (2)
A retrospective cohort study of super-refractory status epilepticus in a tertiary neuro-ICU setting (2021) (2)
Translating genetic and functional data into clinical practice: a series of 223 families with myotonia (2021) (2)
Rhombencephalitis and Myeloradiculitis Caused by a European Subtype of Tick-Borne Encephalitis Virus (2019) (2)
CRISPRa-mediated Kcna1 upregulation decreases neuronal excitability and suppresses seizures in a rodent model of temporal lobe epilepsy (2018) (2)
Olanzapine: a full and potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogenetics (2018) (2)
Long-term synaptic plasticity in hippocampal neurogliaform interneurons (2019) (2)
Hypokalemic periodic paralysis: an omega pore mutation affects inactivation (2015) (2)
History central to diagnosing myasthenia gravis. (2010) (2)
Sodium channelopathy of peripheral nerve: tightening the genotype-phenotype relationship. (2009) (2)
Developmental instability of CA1 pyramidal cells in Dravet Syndrome (2022) (2)
Presynaptic GABAA receptors enhance glutamatergic transmission and facilitate LTP induction at hippocampal mossy fibre synapses (2010) (1)
GABA(B) receptor-mediated heterosynaptic depression at the mossy fibre-CA3 synapse is absent after status epilepticus (2001) (1)
Functional analysis of compound heterozygosity in hyperekplexia mutations of the human glycine receptor alpha 1 subunit. (2000) (1)
170 Diaphragmatic weakness following thymectomy: due to myasthenia gravis or phrenic nerve injury? (2012) (1)
Vasculitis of the central and peripheral nervous system mimicking brain death (2012) (1)
061 Management of NMDA-receptor encephalitis on the neurological ICU (2019) (1)
Mapping out hippocampal inhibition (2012) (1)
CHANGING FORMS OF GUILLAIN-BARRé SYNDROME IN NEURO-ICU (2014) (1)
Epilepsy gene therapy using non-integrating lentiviral delivery of an engineered potassium channel gene (2018) (1)
Volume-transmitted GABA waves pace epileptiform rhythms in the hippocampal network (2021) (1)
CHAPTER 10:Optogenetic and Chemogenetic Tools for Drug Discovery in Schizophrenia (2015) (1)
OPTOGENETIC INHIBITION OF EPILEPTIC ACTIVITY (2011) (1)
LAMBERT EATON MYASTHENIC SYNDROME ANTIBODIES DECREASE SYNAPTIC VESICLE EXOCYTOSIS IN NEURONAL CULTURES (2013) (1)
Density functional and spectroscopic studies of nitrogen inversion in substituted dizocilpines (2009) (1)
Inherited Channelopathies of the CNS. Lessons for Clinical Neurology (2005) (1)
Epilepsy Optogenetic and Potassium Channel Gene Therapy in a Rodent Model of (2012) (1)
Editorial. (2020) (1)
Febrile convulsions: a 'benign' condition? A new rodent model of hyperthermia-induced seizures (page 888) raises questions about the role of GABAergic inhibition in epilepsy. (1999) (1)
Semiology, clustering, periodicity and natural history of seizures in an experimental visual cortical epilepsy model (2018) (1)
LENTIVIRAL-MEDIATED OVEREXPRESSION OF THE POTASSIUM CHANNEL KV1.1 AS A TREATMENT FOR FOCAL NEOCORTICAL EPILEPSY (2011) (1)
171 Myasthenic crisis in the intensive care unit: a 10-year review (2012) (1)
A novel voltage-sensing mutation in Kv1.1 is associated with episodic ataxia type 1 (2007) (0)
P31 Synaptic mechanisms in P/Q deficient neuromuscular junctions (2011) (0)
De novo KCNA6 variants with attenuated KV 1.6 channel deactivation in patients with epilepsy (2022) (0)
Letters to EditorReply (2000) (0)
Optogenetic Treatment Approaches for Focal Neocortical Epilepsy (2012) (0)
Biomedicine is plagued by failure of replication. (2015) (0)
N-methyl-D-aspartate limbic encephalitis: Diagnosis should respect well-recognized criteria. Author's reply (2010) (0)
Brain. Editorial. (2016) (0)
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders (2019) (0)
Brain. Editorial. (2015) (0)
Glutamatergic Transmission in the Perforant Path Epileptogenesis Is Associated With Enhanced (2015) (0)
A clinical, genetic and electrophysiological study of a new UK episodic ataxia type 1 pedigree (2007) (0)
Rat Dentate Gyrus Mediated Facilitation of High-Frequency Input in the - Kindling Induces Transient NMDA Receptor (2015) (0)
Catastrophic antiphospholipid syndrome: A very unusual presentation with status epilepticus (2004) (0)
Unusual use-dependent plasticity of GABAergic synaptic signals related to the hippocampal mossy fibre system (2000) (0)
Editorial. (2020) (0)
Modulation of action potential-dependent Ca 2+ transients in hippocampal mossy fibres by granule cell membrane potential and ionotropic receptors (2003) (0)
JUST A GRAZE? (2013) (0)
Contents page + Editorial Board (2004) (0)
PAW31 Clinical and genetic spectrum of the episodic ataxias: the UK perspective (2010) (0)
Tonic GABA(A) receptor mediated currents modulate cortical excitability (2003) (0)
Difficulty breathing and moving (2016) (0)
PONM08 Late recurrent thymoma: a case series (2010) (0)
Epilepsy genetics. (2003) (0)
Editorial. (2020) (0)
KCC2 overexpression prevents the paradoxical seizure-promoting action of somatic inhibition (2019) (0)
Brain. Editorial. (2015) (0)
Focal cortical seizures start as standing waves and propagate respecting homotopic connectivity (2017) (0)
114 Neuro-critical care: a 4-year experience (2022) (0)
Clinical and Genetic Heterogeneity of Paroxysmal Dyskinesias (S30.008) (2016) (0)
Premature termination in the CACNA1A gene observed in episodic ataxia type 2 (EA2) results in a loss of alpha1A calcium channel function (2000) (0)
A genetically encoded fluorescent sensor for in vivo imaging of GABA (2019) (0)
PN03 Mitochondrial dysfunction in a treatable childhood neuronopathy (2017) (0)
P48 Late recurrent thymoma: a case series (2010) (0)
Tornado-FLIM acquisition for monitoring single-synapse presynaptic calcium dynamics in a mouse model of a migraine (2019) (0)
Two novel mutations in the CACNA1A gene leading to identical functional consequences but with different phenotypic expression. (2002) (0)
Mitochondrial impairment and rescue in riboflavin responsive neuropathy (2017) (0)
Gene therapy in experimental focal neocortical epilepsy (2013) (0)
P47 Thymectomy – role in the management of myasthenia gravis (2010) (0)
Editorial. (2020) (0)
From Reticulospinal Axons in Lamprey Calcium Channels Involved in Synaptic Transmission (2015) (0)
Brain editorial. (2014) (0)
Functional analysis of interactions between wild-type and mutant subunits of hKv1.1 in episodic ataxia type 1 (2000) (0)
Brain. Editorial. (2016) (0)
Brain. Editorial. (2014) (0)
Episodic ataxia type 1 in identical twins: genotype-phenotype correlation (2008) (0)
N-methyl-d-aspartate limbic encephalitis: Diagnosis should respect well-recognized criteria (2010) (0)
Neuronal computation in the mammalian spinal cord (1989) (0)
Advances in Synaptic Plasticity edited by M. Baudry, J.L. Davis and R.F. Thompson (2000) (0)
Non-functional alpha(1A) calcium channel in episodic ataxia type 2 (2000) (0)
Brain. Editorial. (2016) (0)
A clinical, genetic and electrophysiological study of a new UK episodic ataxia type 1 (EA1) pedigree (2007) (0)
PO190 Anti-musk positive myasthenia gravis at a tertiary centre (2017) (0)
Editorial. (2020) (0)
Brain. Editorial. (2014) (0)
Manole et al., KCNA2 in hereditary spastic paraplegia De-novo KCNA2 mutations cause hereditary spastic paraplegia Running head: KCNA2 in hereditary spastic paraplegia (2017) (0)
042 Familial generalized myokymia: A new potassium channelopathy (1999) (0)
Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants (2018) (0)
OutwardlyRectifyingTonicallyActiveGABA A Receptorsin PyramidalCellsModulateNeuronalOffset,NotGain (2009) (0)
Voltage-gated ion channels: molecular biology and role of mutations in epilepsy (2008) (0)
GABAergic synapses between hippocampal interneurons detect extracellular glutamate: A possible mechanism for interneuron disinhibition (2000) (0)
Functional characterisation of mutant Kv1.1 subunits from two families with episodic ataxia type 1 (2000) (0)
172 An unusual case of congenital myasthenic syndrome: the mechanism for treatment response (2012) (0)
NEUROLOGIC CATASTROPHES IN THE EMERGENCY DEPARTMENT. (2000) (0)
PO221 Pathological mechanisms of glycine receptor antibodies (2017) (0)
Anti-seizure Gene Therapy for Focal Cortical Dysplasia (2023) (0)
One Quantum Is One Vesicle (2003) (0)
Brain. Editorial. (2014) (0)
Brain. Editorial. (2014) (0)
Neural Responses in the Inferotemporal Cortex of Macaque Monkeys State-Dependent Effects of Stimulus Presentation Duration on the Temporal Dynamics of (2010) (0)
STATUS EPILEPTICUS IN THE INTENSIVE CARE UNIT: FREQUENCY, MANAGEMENT AND IMPACT ON OUTCOME (2011) (0)
PO007 Neuro-critical care: an 11-year experience (2017) (0)
[Prevention of functional disturbances after operative treatment of habitual shoulder dislocation]. (1966) (0)
Do extracellular Ca2+ signals carry information through neural tissue? Reply (2000) (0)
Brain. Editorial. (2014) (0)
The excitatory neurotransmitter glutamate tunes its interaction with AMPA receptors via a novel mechanism during synaptic activation (2008) (0)
Biochemical autoregulatory gene therapy for focal epilepsy (2018) (0)
C 72 Hebbian LTP in inhibitory hippocampal interneurons of α CaMKII-T 286 A mutant mice (2006) (0)
Nerve Excitability Measurements Can Distingush Genetic Channelopathies in the Episodic Ataxias (2009) (0)
Both evoked and spontaneous NMDA receptor responses are tuned by the ion passage through NMDA channels during synaptic activation (2008) (0)
CRISPRa-mediated overexpression of the voltage-gated channels Kv1.1 and Nav1.1 as a new therapeutic strategy to restore excitation/inhibition balance in epileptic neuronal circuits (2016) (0)
Allosteric Metabotropic Glutamate Receptor 7 Antagonists In Vitro Pharmacological Characterization of Novel Isoxazolopyridone Derivatives as (2010) (0)
Pathological mechanisms in patients with antibodies to glycine receptors (2014) (0)
by Toggling an Amino Acid in the First S3-S4 Linker Alternative Splicing Modulates Inactivation of Type 1 Voltage-gated Sodium Channels (2015) (0)
SYNAPTIC, EXTRASYNAPTIC AND NONSYNAPTIC ION CHANNELS IN EPILEPSY (2009) (0)
N-methyl-D-aspartate receptor antibody-mediated encephalitis. (2012) (0)
Mechanisms of Neurological Disease (2016) (0)
Preserve Your Health, Not Your Vegetables (2017) (0)
Brain. Editorial. (2014) (0)
D.P.2.12 Episodic ataxia type 1 in identical twins (2008) (0)
Episodic ataxia type 1 in twins: Genotype-phenotype correlation (2008) (0)
Editorial. (2020) (0)
Brain. Editorial. (2014) (0)
The role of the brain P/Q-type calcium channel in human epilepsy (2006) (0)
Brain editorial. (2014) (0)
(2017). Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity. Cell 97-109. (2017) (0)
PATHOLOGICAL MECHANISMS OF GLYCINE RECEPTOR ANTIBODIES (2014) (0)
Figure 3, Tonic GABAA receptor-mediated currents in interneurons of the hippocampus are relatively larger and more sensitive to low ambient GABA concentrations than are currents in pyramidal cells (2012) (0)
P32 Myasthenic crisis in the intensive care unit – a ten year review (2011) (0)
The Functional Effect of R1648H, a Sodium Channel Mutation that Causes Generalized Epilepsy with Febrile Seizures Plus in Splice Variants of SCN1A (2010) (0)
GABAA Receptors at Hippocampal Mossy Fibers processing (2003) (0)
PO006 Encephalitis on the neuro-icu: changing patterns (2017) (0)
New mutations in the voltage-gated calcium channel gene CACNA1A in british families with episodic ataxia type 2. (1999) (0)
Brain. Editorial. (2015) (0)
Cellular / Molecular Role of Ionotropic Glutamate Receptors in Long-Term Potentiation in Rat Hippocampal CA 1 Oriens-Lacunosum Moleculare Interneurons (2009) (0)
Variation in CACNA1A associated with episodic ataxia and epilepsy (2009) (0)
A knock-in Drosophila model supports a conserved link between potassium channelopathy and involuntary movement (2020) (0)
Figure 1, Voltage-clamp recording from a dentate gyrus granule cell in the presence of glutamate receptor blockers (2012) (0)
Episodic ataxia type 1 in identical twins (2008) (0)
Editorial. (2020) (0)
Presynaptic channelopathies causing ataxia and migraine (2015) (0)
Episodic ataxia type 2 (EA2) is associated with epilepsy (2007) (0)
Paradoxical effects of a CACNA1A mutation on neurotransmitter exocytosis in hippocampal neurons (2008) (0)
Sodium channels open in response to depolarization and then inactivate rapidly. (2015) (0)
Long-term potentiation in neurogliaform cells modulates excitation-inhibition balance in the temporoammonic pathway (2019) (0)
Modulation of axonal signalling in type 1 episodic ataxia (2016) (0)
A Lady with Head Drop (2017) (0)
Optogenetic induction of the schizophrenia-related endophenotype of ventral hippocampal hyperactivity causes rodent correlates of positive and cognitive symptoms (2018) (0)
Brain. Editorial. (2015) (0)
Figure 2, The input-output function of a pyramidal cell can be represented by the probability of neuronal firing plotted against the amplitude of the input (black curve) (2012) (0)
Statistical and Computational Methods for Quantal Analysis of Synaptic Transmission (1992) (0)
D.P.2.09 Non-genomic effects of sex hormones on ClC-1 may contribute to gender differences in myotonia congenita (2008) (0)
Editorial. (2020) (0)

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University College London

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