Juhani Rapola
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Biology
Juhani Rapola's Degrees
- PhD Molecular Biology University of Helsinki
- Masters Biochemistry University of Helsinki
- Bachelors Biochemistry University of Helsinki
Why Is Juhani Rapola Influential?
(Suggest an Edit or Addition)Juhani Rapola'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
- Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis (1995) (698)
- Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients. (2000) (265)
- Infantile Type of So‐called Neuronal Ceroid‐lipofuscinosis (1973) (234)
- Muscle-eye-brain disease (MEB) (1989) (224)
- Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies. (1973) (220)
- Microscopic hematuria in school children: epidemiology and clinicopathologic evaluation. (1979) (197)
- Long-term outcome of primary nephrotic syndrome. (1982) (184)
- Neuronal ceroid-lipofuscinoses in childhood. (1993) (167)
- Supplementary creatine as a treatment for gyrate atrophy of the choroid and retina. (1981) (167)
- Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology (1998) (161)
- Henoch-Schönlein nephritis: long-term prognosis of unselected patients. (1981) (152)
- "Salla disease": a new lysosomal storage disorder. (1979) (134)
- Cellular expression of xanthine oxidoreductase protein in normal human tissues. (1999) (131)
- A variant of Jansky-Bielschowsky disease. (1982) (122)
- Isolated proteinuria: analysis of a school-age population. (1982) (122)
- Immunohistochemical Spectrum of Rhabdomyosarcoma and Rhabdomyosarcoma‐like Tumors: Expression of Cytokeratin and the 68‐kD Neurofilament Protein (1989) (121)
- Osteitis caused by bacille Calmette-Guérin vaccination: a retrospective analysis of 222 cases. (1995) (120)
- Gyrate atrophy of the choroid and retina. A five-year follow-up of creatine supplementation. (1985) (115)
- The spectrum of Jansky-Bielschowsky disease. (1991) (100)
- Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria (1998) (100)
- Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology. (1998) (99)
- Causes of stillbirth: a clinicopathological study of 243 patients (1983) (99)
- Apoptotic Cell Death in the Normal and Cryptorchid Human Testis: The Effect of Human Chorionic Gonadotropin on Testicular Cell Survival (1996) (96)
- Mice with Ppt1 Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons (2005) (96)
- Correlation between the Clinical Symptoms and the Proportion of Mitochondrial DNA Carrying the 8993 Point Mutation in the NARP Syndrome (1995) (92)
- CONGENITAL NEPHROTIC SYNDROME: PRENATAL DIAGNOSIS AND GENETIC COUNSELLING BY ESTIMATION OF AMNIOTIC-FLUID AND MATERNAL SERUM ALPHA-FETOPROTEIN (1976) (91)
- Histopathological changes in rats and pigs fed rapeseed oil (1960) (89)
- MATERNAL ALPHA-FETOPROTEIN AND FETAL EXOMPHALOS (1976) (88)
- A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging. (2004) (84)
- Infantile type of so-called neuronal ceroid-lipofuscinosis (1973) (82)
- Chronic osteomyelitislike disease with negative bacterial cultures. (1988) (81)
- C-reactive protein compared with white blood cell count and erythrocyte sedimentation rate in the diagnosis of acute appendicitis in children. (1986) (77)
- Familial congenital diaphragmatic defects: aspects of etiology, prenatal diagnosis, and treatment. (1984) (77)
- Gyrate atrophy of the choroid and retina with hyperornithinemia (1979) (74)
- Kidneys with heavy proteinuria show fibrosis, inflammation, and oxidative stress, but no tubular phenotypic change. (2005) (73)
- Gene deletions in X-linked muscular dystrophy. (1989) (72)
- Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations (2002) (71)
- Infantile type of so-called neuronal ceroid-lipofuscinosis. (1974) (70)
- Pathology of congenital nemaline myopathy A follow-up study (1988) (69)
- Lysinuric protein intolerance: a two-year trial of dietary supplementation therapy with citrulline and lysine. (1980) (66)
- Congenital muscular dystrophy: a clinico-pathological and follow-up study of 15 patients. (1975) (66)
- Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-coa dehydrogenase deficiency with the G1528C mutation (1996) (65)
- Congenital nephrotic syndrome. (1973) (65)
- Renal pathology in congenital nephrotic syndrome of Finnish type: a quantitative light microscopic study on 50 patients. (1980) (64)
- Hematopoietic stem cell transplantation in infantile neuronal ceroid lipofuscinosis (2001) (61)
- Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy (1995) (60)
- Frequent Myocardial Lesions in Shwachman's Syndrome (1984) (59)
- RESPONSE OF THE JEJUNAL MUCOSA TO COW'S MILK IN THE MALABSORPTION SYNDROME WITH COW'S MILK INTOLERANCE A Light‐ and Electron‐Microscopic Study (1973) (58)
- Mulibrey Heart Disease: Clinical Manifestations, Long-Term Course, and Results of Pericardiectomy in a Series of 49 Patients Born Before 1985 (2003) (56)
- Salla disease (1983) (55)
- Bronchial epithelial inflammation in children with chronic cough after early lower respiratory tract illness. (1990) (54)
- Intraneural muscular hamartoma: report of two cases in small children. (1972) (51)
- Suction biopsy of rectal mucosa in the diagnosis of infantile and juvenile types of neuronal ceroid lipofuscinoses. (1984) (51)
- High‐frequency ultrasonography of skeletal muscle in children with neuromuscular disease. (1988) (51)
- SCLERODERMA-LIKE GRAFT-VERSUS-HOST DISEASE AS LATE CONSEQUENCE OF BONE-MARROW GRAFTING (1977) (50)
- Familial third and fourth pharyngeal pouch syndrome with truncus arteriosus: DiGeorge syndrome. (1981) (50)
- Characterization of high endothelial-like properties of peritubular capillary endothelium during acute renal allograft rejection. (1990) (50)
- Antioxidant treatment in Spielmeyer‐Sjögren's disease (1985) (47)
- Letter: Maternal alpha-fetoprotein and fetal exomphalos. (1976) (46)
- Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1). (2006) (46)
- Antenatal screening for congenital nephrosis in Finland by maternal serum α‐fetoprotein (1983) (45)
- RENAL INVOLVEMENT IN SCHÖNLEIN‐HENOCH PURPURA (1974) (45)
- Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villi (1990) (45)
- Prenatal diagnosis of Batten's disease (1996) (43)
- Prenatal diagnosis of congenital nephrosis in 23 high-risk families. (1978) (43)
- Cytoplasmic inclusions in the vermiform appendix and skeletal muscle in two types of so-called neuronal ceroid-lipofuscinosis. (1973) (42)
- ASSOCIATION OF POSTMEDICATION HYPOCORTISOLISM WITH EARLY FIRST RELAPSE OF IDIOPATHIC NEPHROTIC SYNDROME (1977) (42)
- Cyclophosphamide and the pubertal testis. (1973) (41)
- Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA) (1994) (41)
- Embryonic Enzyme Patterns: Characterization of the Single Lactate Dehydrogenase Isozyme in Preimplanted Mouse Ova (1967) (39)
- Renal pathology of fetuses with congenital nephrotic syndrome of the Finnish type. A qualitative and quantitative light microscopic study. (1981) (39)
- Visceral anomalies in the Meckel syndrome. (1985) (39)
- Extracardiac malformations associated with congenital heart disease. (1978) (38)
- Renal cysts in pediatric autopsy material. (1983) (38)
- Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II). (1975) (37)
- Polycystic disease of the kidney. Evaluation and classification based on nephron segment and cell-type specific markers. (1990) (37)
- THE ADRENAL CORTEX AND METAMORPHOSIS OF XENOPUS LAEVIS DAUDIN. (1963) (36)
- Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients. (1998) (35)
- Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation. (1997) (35)
- Genetics of congenital nemaline myopathy: a study of 10 families. (1990) (34)
- Pathology of fetal congenital nephrosis: immunohistochemical and ultrastructural studies. (1984) (34)
- Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy (1992) (34)
- Hepatotoxicity in patients with juvenile idiopathic arthritis receiving longterm methotrexate therapy. (2002) (34)
- Fetal gonadal histology in XXXXY, XYY and XXX syndromes (1980) (33)
- Congenital and infantile nephrotic syndromes. (1989) (33)
- Bone-marrow transplantation in aspartylglucosaminuria (1997) (33)
- Extracellular matrix and epithelial differentiation of Wilms' tumor. (1985) (33)
- Morphology of the placenta in fetal I‐cell disease (1977) (33)
- Treatment with human chorionic gonadotrophin for cryptorchidism: clinical and histological effects. (1996) (32)
- Early prenatal detection of diastrophic dysplasia (1983) (32)
- Post-transplantation nephrosis in congenital nephrotic syndrome of the Finnish type (1993) (32)
- The rectourogenital connection in anorectal malformations is an ectopic anal canal. (1990) (31)
- The cardiopathy of mulibrey nanism, a new inherited syndrome. (1974) (31)
- Demonstration of laminin, a basement membrane glycoprotein, in routinely processed formalin-fixed human tissues (2004) (31)
- Salla disease variants. Sialoylaciduric encephalopathy with increased sialidase activity in two non-Finnish children. (1986) (30)
- Cell kinetics in the jejunal crypt epithelium in malabsorption syndrome with cow's milk protein intolerance and in coeliac disease of childhood. (1980) (30)
- Reversible mitochondrial myopathy with cytochrome c oxidase deficiency. (1992) (29)
- X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28. (1990) (29)
- Prenatal diagnosis of the Meckel syndrome. (1977) (29)
- Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation. (1997) (29)
- Disturbed calcium and phosphate homeostasis during treatment with ACTH of infantile spasms. (1986) (28)
- Neuronal intestinal dysplasia. (1989) (28)
- DNA‐based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1) (1991) (27)
- NEMALINE MYOPATHY: Report of Four 1Cases and Review of the Literature (1972) (27)
- Lysosomal storage diseases in adults. (1994) (26)
- Observations on the metabolism of adrenal and gonadal steroids in Xenopus laevis and Bufo bufo. (1962) (25)
- Glomerular basement membrane antigens in congenital and acquired nephrotic syndrome in childhood. (1976) (25)
- Nonspecific diskitis in children. A nonmicrobial disease? (1993) (25)
- IMMUNOFLUORESCENT AND MORPHOLOGICAL STUDIES IN CONGENITAL NEPHROTIC SYNDROME1 (1971) (25)
- The thickness of the glomerular basement membrane in congenital nephrotic syndrome of the Finnish type. (1983) (25)
- Pathology of lethal fetal growth retardation syndrome with aminoaciduria, iron overload, and lactic acidosis (GRACILE). (2002) (25)
- Use of nonviral promoters in adenovirus‐mediated gene therapy: reduction of lysosomal storage in the aspartylglucosaminuria mouse (2006) (24)
- Neonatal benign sacrococcygeal teratoma may recur in adulthood and give rise to malignancy (1993) (24)
- CAUSES OF NEONATAL DEATHS IN A PEDIATRIC HOSPITAL NEONATAL UNIT (1983) (23)
- Prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCLFinnish; CLN5) (1999) (23)
- FIBROMUSCULAR DYSPLASIA IN A CHILD: A GENERALIZED ARTERIAL DISEASE (1980) (22)
- CLUSTER OF SEVERE AMNIOTIC ADHESION MALFORMATIONS IN FINLAND (1980) (22)
- Synaptophysin--an immuno-histochemical marker for childhood neuroblastoma. (2009) (22)
- Diagnosis of fatal infantile defects of the mitochondrial respiratory chain: age dependence and postmortem analysis of enzyme activities (1995) (21)
- Capillary circulation and morphology in Duchenne muscular dystrophy. (1979) (20)
- Changes in lactate dehydrogenase and esterase-specific activities, isozymic patterns, and cellular distribution during the growth cycle of PK cells in vitro. (1970) (20)
- Duchenne‐like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritance (1985) (20)
- Production of basement membrane laminin and type IV collagen by tumors of striated muscle: an immunohistochemical study of rhabdomyosarcomas of different histologic types and a benign vaginal rhabdomyoma. (1986) (20)
- Nephronophthisis in Finland: epidemiology and comparison of genetically classified subgroups (1999) (20)
- Lymphotic inclusions in I-cell disease. (1974) (19)
- Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorder. (1984) (19)
- Scanning electron microscopic study of normal human glomerulogenesis and of fetal glomeruli in congenital nephrotic syndrome of the Finnish type. (1981) (19)
- Antenatal screening for congenital nephrosis in Finland by maternal serum alpha-fetoprotein. (1983) (18)
- Renal pathology of fetal congenital nephrosis. (1981) (18)
- The glycosaminoglycan content of renal basement membranes in the congenital nephrotic syndrome of the Finnish type (2004) (18)
- Bone marrow transplantation in aspartylglucosaminuria--histopathological and MRI study. (1999) (17)
- Prenatal diagnosis and fetal pathology of aspartylglucosaminuria. (1984) (17)
- Non‐Hodgkin's lymphomas in childhood a clinicopathologic and epidemiologic study in finland (1987) (17)
- Atypical juvenile neuronal ceroid liposfuscinosis with granular osmiophilic deposit-like inclusions in the autonomic nerve cells of the gut wall (1998) (17)
- Palcental pathology and prenatal diagnosis of infantile type of neuronal ceroid‐lipofuscinosis (1988) (16)
- Polycystic kidney disease (1988) (15)
- CLN5 – Finnish variant late infantile NCL (1999) (15)
- Accumulation of laminin and type IV collagen in the kidney in congenital nephrosis. (1985) (15)
- Correction of peripheral lysosomal accumulation in mice with aspartylglucosaminuria by bone marrow transplantation. (1999) (14)
- Chronic arthritis in patients with aspartylglucosaminuria. (1998) (14)
- Congenital nephrotic syndrome (1987) (14)
- Chronic rejection of rat renal allograft. III. Ultrastructure of vascular and glomerular changes. (1992) (13)
- Pathology of renal arteries of dyslipidemic children with congenital nephrosis (1994) (12)
- Muscle membrane–skeleton protein changes and histopathological characterization of muscle-eye-brain disease (2000) (12)
- Nonspecific diskitis in children : a nonmicrobial disease ? : Advances in Finland (1993) (11)
- Amniotic fluid pregnancy‐specific β1‐glycoprotein (SP1) in Meckel's syndrome: A new test for prenatal diagnosis? (1982) (11)
- Bone marrow transplantation in young aspartylglucosaminuria mice: improved clearance of lysosomal storage in brain by using wild type as compared to heterozygote donors (2004) (11)
- Early juvenile neuronal ceroid-lipofuscinosis or variant Jansky-Bielschowsky disease: Diagnostic criteria and nomenclature (1993) (10)
- Cell differentiation in sacrococcygeal teratomas. An immunohistochemical and follow-up study. (1990) (9)
- Clinical quiz (1991) (9)
- Kidney biopsy findings in cyclosporine-treated patients with insulin-dependent diabetes mellitus (1991) (8)
- Fibrosarcoma in a girl with celiac disease and IgA deficiency. (1985) (8)
- Polycystic kidney disease. Morphological diagnosis of recessive and dominant polycystic kidney disease in infancy and childhood. (1988) (8)
- Four patients with a new lysosomal storage disorder (Salla disease). (1978) (8)
- Morphological Diagnostic and Pathological Considerations (2011) (7)
- PATHOLOGY OF LETHAL FETAL GROWTH RETARDATION SYNDROME WITH AMINOACIDURIA, IRON OVERLOAD, AND LACTIC ACIDOSIS (GRACILE) (2002) (7)
- The neuronal ceroid lipofuscinoses: unfolding the genetic defect. (1991) (6)
- Characterization of neoplastic and reactive cells in T‐cell lymphomas with cytogenetic, surface marker, and DNA methods (1989) (6)
- Selectivity of proteinuria in congenital nephrotic syndrome of the Finnish type. (1975) (6)
- Kidneys in Meckel's syndrome as a model of abnormal renal differentiation. (1989) (6)
- Particulate fraction in amniotic fluid at second trimester. (1985) (5)
- Why is congenital nephrotic syndrome associated with a rise in the concentration of alpha-fetoprotein in the amniotic fluid? (1990) (5)
- DIAGNOSIS OF HIRSCHSPRUNG'S DISEASE (1979) (5)
- Glomerular anionic charge in congenital nephrotic syndrome of the Finnish type (2004) (5)
- Glomerular anionic charge in congenital nephrotic syndrome of the Finnish type (1995) (5)
- PRENATAL SCREENING FOR CONGENITAL NEPHROSIS (1978) (5)
- Inevitable and Avoidable Deaths in Childhood ALL (1986) (5)
- Congenital nephrotic syndrome: prenatal diagnosis and genetic counselling by estimation of aminotic-fluid and maternal serum alpha-fetoprotein. (1976) (5)
- Polycystic kidney disease in children: differential diagnosis between the dominantly and recessively inherited forms. (1989) (5)
- Clinical quiz. Congenital nephrotic syndrome, microcephaly, brain malformations and diaphragmatic abnormality associated with histological features of diffuse mesangial sclerosis. (1991) (5)
- Lymphocyte inclusions in Finnish-variant late infantile neuronal ceroid lipofuscinosis (CLN5). (2000) (5)
- Studies in kidney tubulogenesis (1965) (4)
- Placental pathology and prenatal diagnosis of infantile type of neuronal ceroid-lipofuscinosis. (1988) (4)
- Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis, INCL: Morphological aspects (1993) (4)
- METAMORPHOSIS AND NEUROSECRETION OF XENOPUS LAEVIS. (1965) (4)
- Causes of death in transposition of the great arteris. A clinical and autopsy study of 140 cases. (1975) (4)
- Further studies on chronic osteitis in infancy caused by BCG-vaccination in newborns. (1976) (4)
- Nonendemic Burkitt's lymphoma with jaw involvement: case report. (1987) (4)
- Infantile SPASMS as presenting symptom of mitochondrial DNA 8993 T → G point mutation (1994) (3)
- [Gene localization will explain the basic causes of neuronal ceroid lipofuscinoses]. (1991) (2)
- ANTENATAL DIAGNOSIS OF CONGENITAL NEPHROSIS (1975) (2)
- Presence of apocrine epithelial antigen (AEA) in type II pneumocytes and in hyaline membranes of neonatal RDS (1986) (2)
- Renal involvement in Schölein-Henoch purpura. (1974) (2)
- Should we prescribe antioxidants to patients with coronary heart disease? (1998) (2)
- Adrenocortical function during anuran metamorphosis. (1962) (2)
- Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and liver of aspartylglucosaminuria (AGU) mouse (1998) (2)
- CAUSES OF DEATH IN TRANSPOSITION OF THE GREAT ARTERIES (1975) (1)
- Muscle-Eye-Brain (MEB) Disease: A New Form of Congenital Muscular Dystrophy with Ophthalmic and Cerebral Manifestations (1987) (1)
- Prenatal diagnosis of congenital nephrosis. (1985) (1)
- Treatment of patients with gyrate atrophy of the choroid and retina with hyperornithinemia (GA) with creatine, a clinical trial (1980) (1)
- Improved technique for the expression of fragile-X in cultured amniotic fluid cells (2004) (1)
- Genetics ofcongenital nemaline myopathy: a studyof10families (1990) (1)
- Congenital cervical cysts and fistulas. (1974) (1)
- Cyclosporin reduces renal prostanoid excretion in type 1 diabetic patients (2004) (1)
- Condyloma acuminatum giganticum: Buschke-Loewenstein tumour. (1970) (1)
- 25. CONGENITAL HEART MALFORMATIONS IN AN AUTOPSY MATERIAL (1970) (1)
- Studies on the elevated amniotic fluid SP1 in Meckel's syndrome: modified glycosylation of SP1. (1987) (1)
- Combined immunodeficiency associated with adenosine deaminase enzyme with altered kinetic properties (1979) (1)
- Renal tumours in children. (2009) (1)
- [Time is our most important capital]. (2002) (0)
- [Multiple abnormalities]. (1980) (0)
- [Congenital nephrotic syndrome - Finnish type]. (1982) (0)
- Fetal Growth Retardation, Lactacidosis, Aminoaciduria and Hemosiderosis- A New Iron Storage Disease? 82 (1996) (0)
- METAMORPHOSIS AND NEUROSECRETION OF XENOPUS LAEVIS. NEUROSECRETORY ACTIVITY OF PRAEOPTIC NUCLEI DURING AND AFTER PROLONGED THIOUREA TREATMENT. (1965) (0)
- Extracellular Matrix and Epithelial Djferentiation of Wilms' Tumor (2007) (0)
- Disturbed calcium andphosphate homeostasis during treatment withACTH ofinfantile spasms (1986) (0)
- [The improving diagnostics in Hirschsprung's disease]. (1979) (0)
- Subject Index, Vol. 16, 1976 (1976) (0)
- Osteitis as a complication of neonatal BCG vaccination (1994) (0)
- 869 FIVE YEAR FOLLOW-UP OF CREATINE SUPPLEMENTATION IN GYRATE ATROPHY OF THE CHOROID AND RETINA (GA) (1985) (0)
- [Clinico-pathological conference XLIII. Abdominal tumor, sudden coma and hypertension in a child]. (1977) (0)
- [Cystic diseases of the kidney]. (1983) (0)
- A.F.P. AND CONGENITAL NEPHROSIS FINNISH TYPE (1979) (0)
- Succinic dehydrogenase activity in male accessory sex organs of intact, testosterone-treated and castrated rat; a histochemical study. (1956) (0)
- Light and electron micropscopical changes in congenital nephrotic syndrome (1973) (0)
- Expectations, objectives and use of digital marketing in Finnish ice hockey sponsorship - Case Liiga Oy (2019) (0)
- Ask the expert (2004) (0)
- SCLERODERMA LIKE GRAFT VERSUS HOST DISEASE (GVHD): A LATE CONSEQUENCE OF BONE HARROW GRAFTING (1978) (0)
- [Detection of diastrophic dysplasia in early pregnancy]. (1983) (0)
- Muscle pathology in hyperornithinemia with gyrate atrophy of the choroid and retina (HOGA) (1979) (0)
- Contents, Vol. 16, 1976 (2004) (0)
- GDNF AND p 75 NEUROTROPHIN RECEPTOR IN DEVELOPMENT AND DISEASE (1999) (0)
- An infant with X-linked myotubular myopathy. (1993) (0)
- [Salla disease - a new inherited Finnish disease]. (1981) (0)
- [Immunologic deficiency in a child and generalized BCG infection]. (1982) (0)
- Antioxidants and ischaemic heart disease (Letter) (1997) (0)
- Letter: Antenatal diagnosis of congenital nephrosis. (1975) (0)
- Toxoplasmosis as a cause of foetal death. (1971) (0)
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What Schools Are Affiliated With Juhani Rapola?
Juhani Rapola is affiliated with the following schools:
