K. I. Suzuki
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Biology
K. I. Suzuki's Degrees
- PhD Neuroscience University of Tokyo
- Masters Biology Stanford University
- Bachelors Biochemistry University of Tokyo
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(Suggest an Edit or Addition)K. I. Suzuki'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
- TNF alpha promotes proliferation of oligodendrocyte progenitors and remyelination. (2001) (511)
- Adrenoleukodystrophy. A clinical and pathological study of 17 cases. (1975) (466)
- Microglial/macrophage accumulation during cuprizone-induced demyelination in C57BL/6 mice (1998) (350)
- Interleukin-1beta promotes repair of the CNS. (2001) (272)
- Insulin-Like Growth Factor-1 Inhibits Mature Oligodendrocyte Apoptosis during Primary Demyelination (2000) (233)
- Immunohistochemical localization of oxytocin receptors in human brain (2013) (227)
- Progressive accumulation of toxic metabolite in a genetic leukodystrophy. (1984) (218)
- Mature oligodendrocyte apoptosis precedes IGF‐1 production and oligodendrocyte progenitor accumulation and differentiation during demyelination/remyelination (2000) (211)
- Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase. (1999) (209)
- Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids. (1996) (206)
- The type II epithelial cells of the lung. II. Chemical composition and phospholipid synthesis. (1975) (175)
- Donor-derived cells in the central nervous system of twitcher mice after bone marrow transplantation. (1988) (173)
- Cerebellar degeneration in the Niemann-Pick type C mouse (2004) (172)
- Status spongiosus of CNS and hepatic changes induced by cuprizone (biscyclohexanone oxalyldihydrazone). (1969) (170)
- Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease. (1994) (167)
- Episodic demyelination and subsequent remyelination within the murine central nervous system: changes in axonal calibre (2001) (164)
- Paired helical filament tau (PHFtau) in Niemann-Pick type C disease is similar to PHFtau in Alzheimer's disease (2004) (163)
- A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorder. (1999) (155)
- Generalized CNS disease and massive GM1-ganglioside accumulation in mice defective in lysosomal acid beta-galactosidase. (1997) (152)
- Ultrastructural studies of multiple sclerosis. (1969) (146)
- Bone marrow transplantation prolongs life span and ameliorates neurologic manifestations in Sandhoff disease mice. (1998) (143)
- Sphingolipid activator protein D (sap-D) stimulates the lysosomal degradation of ceramide in vivo. (1994) (142)
- A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse. (2001) (140)
- Adult (chronic) GM2 gangliosidosis. Atypical spinocerebellar degeneration in a Jewish sibship. (1976) (133)
- Demyelination and remyelination in the rat central nervous system following ethidium bromide injection. (1979) (125)
- Mouse model for the lysosomal disorder galactosialidosis and correction of the phenotype with overexpressing erythroid precursor cells. (1995) (123)
- Structure of full-length cDNA coding for sulfatide activator, a Co-beta-glucosidase and two other homologous proteins: two alternate forms of the sulfatide activator. (1989) (116)
- An apoptotic depletion of oligodendrocytes in the twitcher, a murine model of globoid cell leukodystrophy. (1999) (107)
- Infantile Niemann-Pick disease. A chemical study with isolation and characterization of membranous cytoplasmic bodies and myelin. (1969) (106)
- Mice with type 2 and 3 Gaucher disease point mutations generated by a single insertion mutagenesis procedure. (1998) (103)
- Alleviation of neuronal ganglioside storage does not improve the clinical course of the Niemann-Pick C disease mouse. (2000) (100)
- Isolation, characterization, and expression of cDNA clones that encode rat UDP‐galactose: Ceramide galactosyltransferase (1994) (96)
- Brain ceramide hexosides in Tay-Sachs disease and generalized gangliosidosis (GM1-gangliosidosis). (1967) (96)
- CHEMICAL STUDIES ON ALZHEIMER'S DISEASE (1965) (92)
- Morphological, histochemical and biochemical studies on a case of systemic late infantile lipidosis (generalized gangliosidosis). (1968) (92)
- Variant of GM2‐gangliosidosis with hexosaminidase A having a severely changed substrate specificity. (1983) (89)
- Sphingolipid activator proteins. (1995) (87)
- Presenile dementia with "Lafora-like" intraneuronal inclusions. (1971) (87)
- Progressive myoclonus epilepsy with Lafora inclusion bodies. I. Clinical, genetic, histopathologic, and biochemical aspects. (1967) (87)
- Mouse model of GM2 activator deficiency manifests cerebellar pathology and motor impairment. (1997) (83)
- Sulfatide activator protein. Alternative splicing that generates three mRNAs and a newly found mutation responsible for a clinical disease. (1991) (82)
- Ballooned neurons in select neurodegenerative diseases contain phosphorylated neurofilament epitopes (2004) (76)
- Immunocytochemical and ultrastructural studies of lower motor neurons in amyotrophic lateral sclerosis. (1989) (76)
- Distribution and characterization of GFP(+) donor hematogenous cells in Twitcher mice after bone marrow transplantation. (2000) (71)
- Occurrence of two molecular forms of human acid sphingomyelinase. (1994) (71)
- The twitcher mouse: determination of genetic status by galactosylceramidase assays on clipped tail. (1982) (70)
- Adreno-leukodystrophy (sex-linked Schilder disease). Ultrastructural demonstration of specific cytoplasmic inclusions in the central nervous system. (1974) (70)
- GM1-gangliosidosis (genetic beta-galactosidase deficiency): identification of four mutations in different clinical phenotypes among Japanese patients. (1991) (61)
- Microtubule disarray in cortical dendrites and neurobehavioral failure. I. Golgi and electron microscopic studies. (1982) (59)
- In utero diagnosis of globoid cell leukodystrophy (Krabb's disease). (1971) (58)
- Chemokine receptors on infiltrating leucocytes in inflammatory pathologies of the central nervous system (CNS) (2003) (58)
- The twitcher mouse. A model of human globoid cell leukodystrophy (krabbe's disease). (1983) (57)
- A unique pattern of astrocytosis in the primary motor area in amyotrophic lateral sclerosis (1991) (54)
- Isolation of a cDNA encoding the human GM2 activator protein (1989) (53)
- Over-expression of a functionally active human GM2-activator protein in Escherichia coli. (1993) (52)
- Tyrosine hydroxylase-immunoreactive neurons in the mouse cerebral cortex during the postnatal period. (1990) (52)
- The twitcher mouse. Central nervous system pathology after bone marrow transplantation. (1988) (52)
- Targeted disruption of the mouse prosaposin gene affects the development of the prostate gland and other male reproductive organs. (2000) (52)
- The twitcher mouse. Central nervous system pathology after bone marrow transplantation. (1988) (52)
- Krabbe's leukocystrophy (globoid cell leukodystrophy). An ultrastructural study. (1970) (51)
- CHEMICAL STUDIES ON JAKOB‐CREUTZFELDT DISEASE (1966) (51)
- GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene abnormalities in seven patients. (1990) (50)
- Acute multiple sclerosis. Confirmation of "paramyxovirus-like" intranuclear inclusions. (1974) (50)
- Dramatic phenotypic improvement during pregnancy in a genetic leukodystrophy: estrogen appears to be a critical factor. (2001) (49)
- Early-onset, rapidly progressive familial tauopathy with R406W mutation (2002) (48)
- Ultrastructural study of experimental globoid cells. (1970) (48)
- Familial neuromyelitis optica (Devic’s syndrome) with late onset in Japan (2000) (47)
- Studies in globoid (Krabbe) leukodystrophy (GLD). V. Controlled enzymic studies in ten human cases. (1970) (46)
- Molecular cloning, chromosomal mapping, and characterization of the mouse UDP-galactose:ceramide galactosyltransferase gene. (1996) (46)
- GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene mutations in 11 patients from a defined region in Portugal. (1991) (45)
- ULTRASTRUCTURAL AND BIOCHEMICAL STUDIES OF SCHILDER'S DISEASE: I. Ultrastructure (1970) (44)
- Pathological study of mice with total deficiency of sphingolipid activator proteins (SAP knockout mice) (1998) (42)
- Immunocytochemical and ultrastructural studies of Werdnig-Hoffmann disease (1991) (42)
- The twitcher mouse: degeneration of oligodendrocytes in vitro. (1986) (42)
- Expression of the neu oncogene under the transcriptional control of the myelin basic protein gene in transgenic mice: Generation of transformed glial cells (1992) (41)
- ULTRASTRUCTURAL AND BIOCHEMICAL STUDIES OF SCHILDER'S DISEASE: II. Biochemistry (1970) (40)
- Mutations in acid beta-galactosidase cause GM1-gangliosidosis in American patients. (1993) (39)
- Paradoxical influence of acid beta-galactosidase gene dosage on phenotype of the twitcher mouse (genetic galactosylceramidase deficiency). (2000) (37)
- Extracerebral leptomeningeal astrocytoma mimicking a meningioma. (1979) (37)
- Analysis of galactosylsphingosine (psychosine) in the brain. (1984) (35)
- Effect of Steroid on Ischemic Brain Edema: Analysis of Cytotoxic and Vasogenic Edema Occurring During Ischemia and After Restoration of Blood Flow (1980) (35)
- Abnormal accumulation of galactosylceramide in the kidney of twitcher mouse. (1983) (35)
- Multiple abnormal beta-hexosaminidase alpha chain mRNAs in a compound-heterozygous Ashkenazi Jewish patient with Tay-Sachs disease. (1988) (34)
- Lipocalin‐type prostaglandin D synthase (β‐trace) is upregulated in the αB‐crystallin‐positive oligodendrocytes and astrocytes in the chronic multiple sclerosis (2006) (33)
- Cellular degeneration in developing central nervous system of rats produced by hypocholesteremic drug AY9944. (1971) (33)
- Genetic galactosylceramidase deficiency (globoid cell leukodystrophy, Krabbe disease) in different mammalian species. (1983) (33)
- Immunocytochemical and ultrastructural studies of upper motor neurons in amyotrophic lateral sclerosis (1992) (33)
- Mice deficient in all forms of lysosomal beta-hexosaminidase show mucopolysaccharidosis-like pathology. (1997) (33)
- NEURONAL DEGENERATION IN THE BRAIN OF THE BRINDLED MOUSE—A LIGHT MICROSCOPE STUDY (1979) (33)
- Biochemical and molecular aspects of late-onset GM2-gangliosidosis: B1 variant as a prototype. (1991) (31)
- Giant neuronal mitochondria in a infant with microcephaly and seizure disorder. (1969) (30)
- Fetal globoid cell leukocystrophy (Krabbe disease). Pathological and biochemical examination. (1973) (30)
- GM1-gangliosidosis (gneralized gangliosidosis). Morphology and chemical pathology. (1968) (29)
- The effect of aging on the healing of hydroxylapatite implants. (1993) (28)
- A case of juvenile lipidosis: Electron microscopic, histochemical and biochemical studies (1968) (28)
- Lipids of developing brain of twitcher mouse. An authentic murine model of human Krabbe disease. (1983) (27)
- Age-related changes in attachment and proliferation of mouse Schwann cells in vitro. (1991) (26)
- Cerebro-ocular dysplasia —Muscular dystrophy (COD-MD) syndrome (2004) (25)
- Hemophagocytic syndrome and adult Still's disease associated with meningoencephalitis and unconsciousness. (2001) (25)
- Late infantile neuronal storage disease with curvilinear bodies. (1976) (25)
- Non-specific familial presenile dementia. (1968) (25)
- Radial component of the central myelin in neurologic mutant mice. (1982) (25)
- Molecular analysis of the acid sphingomyelinase deficiency in a family with an intermediate form of Niemann-Pick disease. (1995) (24)
- Neuropathology of late onset gangliosidoses. A review. (1991) (24)
- Lack of PPCA expression only partially coincides with lysosomal storage in galactosialidosis mice: indirect evidence for spatial requirement of the catalytic rather than the protective function of PPCA. (1998) (24)
- Rapid conversion of drebrin isoforms during synapse formation in primary culture of cortical neurons. (1998) (23)
- Ultrastructural study of neurons in metachromatic leukodystrophy. (1987) (23)
- Metabolism of glycolipids: the role of glycolipid-binding proteins in the function and pathobiochemistry of lysosomes. (1992) (22)
- Alteration of cellular and acellular alveolar and bronchiolar walls produced by hypocholesteremic drug AY9944. (1972) (22)
- Animal models of lysosomal disease: An overview (1998) (22)
- Enzymic activities associated with membranous cytoplasmic bodies and isolated brain lysosomes (1971) (22)
- The Major Mutation Among Japanese Patients with Infantile Tay-Sachs Disease: A G-to-T Transversion at the Acceptor Site of Intron 5 of the β-Hexosaminidase α-Gene (1993) (21)
- Immunocytochemical and ultrastructural studies of eosinophilic granular bodies in astrocytic tumors (2004) (20)
- Degeneration of oligodendroglia in the central nervous system of rats treated with AY9944 or triparanol. (1974) (20)
- Gangliosides and disease: a review. (1984) (19)
- Metabolic studies of adrenoleukodystrophy. (1978) (18)
- Studies in Tay-Sachs disease. I. A. methods. (1963) (18)
- The blood brain barrier in human leukodystrophies and allied diseases. Ultrastructural and morphometric studies on the capillaries in brain biopsies. (1993) (18)
- Alleviation of neurologic symptoms after bone marrow transplantation in twitcher mice. (1989) (17)
- Biochemical pathogenesis of genetic leukodystrophies: comparison of metachromatic leukodystrophy and globoid cell leukodystrophy (Krabbe's disease). (1984) (16)
- A new point mutation in the beta-hexosaminidase alpha subunit gene responsible for infantile Tay-Sachs disease in a non-Jewish Caucasian patient (a Kpn mutant). (1990) (16)
- Adrenoleukodystrophy: a clinical, pathological and biochemical study. (1976) (15)
- Autosomal recessive neuromuscular disorder in a transgenic line of mice (1994) (15)
- Immunophenotype Characterization for Swine Selected Line, Which is Resistant for the Mycoplasma Pneumonia (2011) (14)
- Tay-Sachs disease: intron 7 splice junction mutation in two Portuguese patients. (1995) (14)
- Ultrastructural changes in the lung in Niemann-Pick type C mouse (2004) (14)
- Studies on the copper binding affinity of fibers in the peripheral nervous system of the quaking mouse (1978) (14)
- Effect of liposome-mediated macrophage depletion on Schwann cell proliferation during Wallerian degeneration. (2000) (14)
- Amyotrophic lateral sclerosis with diffuse neurofibrillary changes. Report of a case. (1974) (14)
- Isolation and morphologic characterization in vitro of Schwann cells of the twitcher mouse. (1990) (13)
- Are animal models useful for understanding the pathophysiology of lysosomal storage disease? (2003) (13)
- Heterotypic sprouting of serotonergic forebrain fibers in the brindled mottled mutant mouse. (1994) (12)
- Genetic analysis of myelin galactolipid function. (1999) (12)
- The twitcher mouse: An ultrastructural study on the oligodendroglia (2004) (12)
- Myelin degeneration in sciatic nerve of rats treated with hypocholesteremic drug AY9944. (1972) (12)
- Murine globoid cell leukodystrophy (the twitcher mouse). The presence of characteristic inclusions in the kidney and lymph nodes. (1983) (12)
- Sensory neuropathy with onion-bulb formation. Report of a case with onset in infancy. (1978) (12)
- Pathological study of corticospinal‐tract degeneration in Friedreich's ataxia (1992) (11)
- AN EXPERIMENTAL PROCEDURE FOR THE MEASUREMENT OF THE GANGLIOSIDE RADIOACTIVITY LABELLED IN VIVO * (1967) (11)
- Status marmoratus and Bielschowsky bodies (1982) (11)
- Molecular genetics of Tay-Sachs disease in Japan (1994) (11)
- Induced mouse models of abnormal sphingolipid metabolism. (1998) (11)
- Neuronal degeneration in the brain of the brindled mouse (1979) (10)
- Demyelinating diseases, leukodystrophies, and other myelin disorders. (2001) (9)
- Expression of the beta-hexosaminidase alpha subunit gene with the four-base insertion of infantile Jewish Tay-Sachs disease. (1991) (9)
- The major mutation among Japanese patients with infantile Tay-Sachs disease: a G-to-T transversion at the acceptor site of intron 5 of the beta-hexosaminidase alpha gene. (1993) (9)
- Murine globoid cell leukodystrophy: the twitcher mouse. An ultrastructural study of the kidney. (1984) (9)
- GM2-gangliosidosis B1 variant: a wide geographic and ethnic distribution of the specific beta-hexosaminidase alpha chain mutation originally identified in a Puerto Rican patient. (1988) (8)
- Schwann cells and peripheral nervous system myelin in the rat retina (1978) (8)
- A search for a chemical correlate of amyloid in senile plaques of Alzheimer's disease. (1964) (8)
- An ultrastructural and biochemical investigation of Lafora's disease. (1965) (7)
- Metachromatic leukodystrophy: isolation and chemical characterization of metachromatic granules. (1967) (7)
- Onion bulb formation in the initial complex of neurons in human dorsal root ganglion: their significance and alterations in amyotrophic lateral sclerosis (1991) (7)
- LACTOSYLCERAMIDASES IN CANINE GLOBOID CELL LEUKODYSTROPHY 1 (1977) (7)
- A splicing defect due to an exon-intron junctional mutation results in abnormal beta-hexosaminidase alpha chain mRNAs in Ashkenazi Jewish patients with Tay-Sachs disease. (1988) (7)
- Quantification of mRNAs encoding proteins of the glycosphingolipid catabolism in mouse models of GM2 gangliosidoses and sphingolipid activator protein precursor (prosaposin) deficiency. (2000) (7)
- RADIAL COMPONENT OF CENTRAL MYELIN IN NORMAL AND QUAKING MICE (1981) (6)
- Selective sparing of Betz cells in primary motor area in hypoxic-ischemic encephalopathy (1990) (5)
- Immunohistochemical evaluation of the marbled state in childhood hypoxic encephalopathy (1999) (5)
- Neuronal degeneration in the brain of the brindled mouse. II. Ultrastructure of neuronal inclusions in the cerebral cortex. (1979) (5)
- Glycolipid metabolism in the canine form of globoid cell leukodystrophy. (1976) (5)
- A point mutation in the coding sequence of the beta-hexosaminidase alpha gene results in defective processing of the enzyme protein in an unusual GM2-gangliosidosis variant. (1988) (5)
- The female brindled mouse as a model of Menkes' disease: the relationship of fur pattern to behavioral and neurochemical abnormalities. (1991) (4)
- Accumulation of smooth cisterns, multivesicular bodies and "zebra" bodies in neurons. A case of peculiar storage condition. (1971) (4)
- Cerebellar infarction in a young boy (1999) (4)
- DEMYELINATION AND REMYELINATION IN RAT CNS FOLLOWING ETHIDIUM BROMIDE INJECTION: 146 (1979) (4)
- Ultrastructural Methods for Neurotoxicology and Neuropathology (1995) (4)
- Spinal epidermoid cyst in the mouse (1981) (4)
- ASSOCIATION OF ACTIN WITH HIRANO BODIES IN HUMAN AND BRINDLED MOUSE CNS: 54 (1982) (4)
- Morphological characteristics of senile plaques in familial Alzheimer's disease (2004) (4)
- The specificity of beta-galactosidase in the degradation of gangliosides. (1980) (3)
- A case of adult neuronal ceroid-lipofuscinosis with the appearance of membranous cytoplasmic bodies localized in the spinal anterior horn (2004) (3)
- A new point mutation within exon 5 of beta-hexosaminidase alpha gene in a Japanese infant with Tay-Sachs disease. (1990) (3)
- 71 Murine Globoid Cell Leukodystrophy, The Twiteher: Presence of Inclusions in the Kidney and Lymphnode (1983) (3)
- Membranous cytoplasmic bodies from Tay-Sachs disease. Gm-1-gangliosidosis (generalized gangliosidosis). (1968) (3)
- A case of late infantile systemic lipidosis. (1967) (2)
- Pexid-induced rat retinal pathology (1979) (2)
- Megalencephaly, hydrocephalus and cortical dysplasia in severe dwarfism mimicking leprechaunism (1998) (2)
- Expression of immune-related molecules in a murine genetic demyelinating disease. (1995) (2)
- Presence of β-hexosaminidase. A α-chain mRNA in two different variants of GM2-gangliosidosis (1988) (2)
- Demonstration of non-infections hemagglutinating particles of rabies virus and isolation of the hemagglutinin by disruption of the virion with Nonidet P-40 (2005) (2)
- Genetic leukodystrophies. (1976) (1)
- Nitric oxide exacerbates the course of pathology in a mouse model of demyelinating disesase (1998) (1)
- Trilobate placenta and an abnormal fetal heart rate pattern. (1973) (1)
- BALLOONED NEURONS IN NEUROLOGICAL DISEASE CONTAIN PHOSPHORYLATED NEUROFILAMENTS(NF) (1986) (1)
- PROLIFERATIVE RESPONSES OF TWITCHER SCHWANN CELLS IN VITRO FOLLOWING ADMINISTRATION OF GROWTH FACTORS: 175 (1995) (1)
- Recognition and delineation of beta-hexosaminidase alpha-chain variants: a historical and personal perspective. (2001) (1)
- [Galactosylceramide synthase (CGT) knockout mouse]. (1998) (1)
- PURIFICATION AND SPECIFICITY OF HATCHING ENZYME OF THE SEA URCHIN HEMICENTROTUS PULCHERRIMUS : Developmental Biology (1990) (1)
- AN IMMUN0HISTOCHEMICAL STUDY ON MURINE GLOBOID CELL LEUKODYSTROPHY, THE TWITCHER (1985) (1)
- Cerebellar changes of the female mice heterozygous for brindled gene (2004) (1)
- Characteristic inclusions in the kidney of canine globoid cell leukodystrophy (2004) (1)
- UNUSUAL PATTERNS OF MYELINATION IN THE PERIPHERAL NERVES OF QUAKING MICE: 46 (1976) (1)
- Microglial r macrophage accumulation during cuprizone-induced demyelination in C57BL r 6 mice (1998) (0)
- IMMUNOCYTOCHEMICAL EXPRESSIONS OF TYROSINE HYDROXYLASE IN THE BRINDLED MOUSE: 222 (1989) (0)
- MOLECULAR GENETICS OF INHERITED NEUROLOGICAL DISORDERS (1996) (0)
- Cryptococcal meningoencephalitis and the other opportunistic infections in a patient with AIDS : in association with interesting lesioned distribution, and fiber gliosis (1995) (0)
- THE TWITCHER MOUSE: SCHWANN CELLS IN PRIMARY CULTURE (1989) (0)
- UNUSUAL ULTRASTRUCTURAL FEATURES OF OLIGODENDROCYTES IN A CASE OF LEUKODYSTROPHY.: 82 (1987) (0)
- Fundamental investigation on wave making interactions around multi-hull vessel (2004) (0)
- The function of MHC class II molecules on microglia during demyelination (1998) (0)
- 22 APPARENT DIFFERENCE IN THE RESPONSE OF QUAKING AND CONTROL MICE TO TET (1981) (0)
- Quaking mouse: Vacuolar degeneration of spinal roots (2004) (0)
- [2 cases of emphysematous pyelonephritis demonstrated by computed tomography]. (1983) (0)
- Giant mitochondria and abnormal "lipid" in a microcephalic infant. (1968) (0)
- NATURAL HISTORY OF YOUNG-ADULT AMYOTROPHIC LATERAL SCLEROSIS (2009) (0)
- Detection of Mouse MGL1/CD301a by a Specific Monoclonal Antibody (2008) (0)
- 105 PREVENTION OF NEURONAL DEGENERATION IN THE BRAIN OF BRINDLED MOUSE BY COPPER SUPPLEMENTATION (1981) (0)
- Oligodendrocytes with aberrant cytoplasmic processes in a human white matter disorder. (1988) (0)
- 104 Abnormal Arborization of Purkinje Cell in the Brindled Mouse (1984) (0)
- 126 CHRONOLOGICAL STUDY OF OLIGODENDROGLIAL ALTERATIONS AND MYELINATION IN QUAKING MOUSE (1980) (0)
- Developmentally regulated expression of a novel GCK family kinase, MINK, in postnatal mouse cerebellum (2000) (0)
- Two novel (1334delC and 1363G to A, G455R) mutations in exon 12 of the beta-hexosaminidase alpha-chain gene in two Portuguese patients. (1997) (0)
- Glycosphingolipid beta-galactosidases. 3. Canine form of globoid cell leukodystrophy; comparison with the human disease. (1974) (0)
- [Genetic deficiencies of beta-N-acetylhexosaminidase A and B: Tay-Sachs and Sandhoff diseases (GM2-gangliosidosis)]. (1988) (0)
- Scientific meeting of the Netherlands Society of Child Neurology held in Heeze, 7th of April 1989 Bone marrow transplantation in the treatment of lysosomal enzyme deficiencies with neurological involvement (1989) (0)
- Ultrastructural study of experimental globoid cells. (1970) (0)
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