Published in Rinsho Shinkeigaku on July 01, 1974
Fabry's disease on the mechanism of the peripheral nerve involvement. Acta Neuropathol (1975) 0.88
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene. Nat Genet (2001) 2.79
The Crow-Fukase syndrome: a study of 102 cases in Japan. Neurology (1984) 2.65
Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature. J Neurol Sci (1980) 2.34
Case-control studies of motor neuron disease: association with mechanical injuries. Arch Neurol (1981) 1.89
Neurological syndrome associated with clioquinol. Lancet (1971) 1.59
TAL1 and LIM-only proteins synergistically induce retinaldehyde dehydrogenase 2 expression in T-cell acute lymphoblastic leukemia by acting as cofactors for GATA3. Mol Cell Biol (1998) 1.49
Nationwide survey of multiple sclerosis in Japan. Clinical analysis of 1,084 cases. Neurology (1975) 1.35
Identification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy. Am J Hum Genet (1991) 1.35
VP4 protein of porcine rotavirus strain OSU expressed by a baculovirus recombinant induces neutralizing antibodies. Virology (1989) 1.20
Rimmed vacuoles. Acta Neuropathol (1980) 1.16
Involvement of the zinc-binding capacity of Sendai virus V protein in viral pathogenesis. J Virol (2000) 1.15
Identification of temperature-sensitive dnaD mutants of Staphylococcus aureus that are defective in chromosomal DNA replication. Mol Genet Genomics (2004) 1.13
TS-071 is a novel, potent and selective renal sodium-glucose cotransporter 2 (SGLT2) inhibitor with anti-hyperglycaemic activity. Br J Pharmacol (2011) 1.11
Characterization of monoclonal antibodies against human rotavirus hemagglutinin. J Med Virol (1986) 1.08
Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9. Ann Neurol (1997) 1.07
Hereditary lipo-muscular atrophy with joint contracture, skin eruptions and hyper-gamma-globulinemia: a new syndrome. Intern Med (1993) 1.07
Kugelberg-welander syndrome with dominant inheritance. Arch Neurol (1966) 1.04
Transcriptional activity of TAL1 in T cell acute lymphoblastic leukemia (T-ALL) requires RBTN1 or -2 and induces TALLA1, a highly specific tumor marker of T-ALL. J Biol Chem (1997) 1.02
Changing mortality patterns of motor neuron disease in Japan. J Neurol Sci (1977) 0.99
"Tail sign" associated with microembolic signals. Stroke (1999) 0.98
Controlled trial of thyrotropin releasing hormone tartrate in ataxia of spinocerebellar degenerations. J Neurol Sci (1983) 0.97
Slow cord dorsum potentials elicited by descending volleys in man. J Neurol Neurosurg Psychiatry (1979) 0.97
Evidence of duplication and deletion in super short segment 11 of rabbit rotavirus Alabama strain. Virology (1989) 0.97
Adrenoleukodystrophy: a clinical variant presenting as olivopontocerebellar atrophy. J Neurol (1984) 0.96
Identification of a highly specific surface marker of T-cell acute lymphoblastic leukemia and neuroblastoma as a new member of the transmembrane 4 superfamily. Int J Cancer (1995) 0.96
Distal myopathy: histochemical and ultrastructural studies. Arch Neurol (1982) 0.96
Intra-axonal corpora amylacea in the peripheral nerve seen in a healthy woman. J Neurol Sci (1977) 0.96
Hexasulfonated calix[6]arene derivatives: a new class of catalysts, surfactants, and host molecules. J Am Chem Soc (1986) 0.95
Serologic characteristics of a human rotavirus isolate, AU-1, which has a "long" RNA pattern and subgroup I specificity. J Med Virol (1987) 0.95
Ultrastructural studies on the neuromuscular junctions of Becker's muscular dystrophy. Acta Neuropathol (1985) 0.94
HLA and Japanese MS. Tissue Antigens (1978) 0.94
A fulminant case of Guillain-Barré syndrome: topographic and fibre size related analysis of demyelinating changes. J Neurol Neurosurg Psychiatry (1989) 0.94
[Sibling cases with lipodystrophic skin change, muscular atrophy, recurrent skin eruptions, and deformities and contractures of the joints. A possible new clinical entity]. Rinsho Shinkeigaku (1984) 0.93
Mitochondrial encephalomyopathy: fluctuating symptoms and CT. Neurology (1984) 0.92
Strong induction of ICAM-1 in human T cells transformed by human T-cell-leukemia virus type 1 and depression of ICAM-1 or LFA-1 in adult T-cell-leukemia-derived cell lines. Int J Cancer (1992) 0.92
Structural polypeptides of the murine coronavirus DVIM. Arch Virol (1986) 0.90
Fabry's disease on the mechanism of the peripheral nerve involvement. Acta Neuropathol (1975) 0.88
The Ryukyuan muscular atrophy. An obscure heritable neuromuscular disease found in the islands of southern Japan. J Neurol Sci (1970) 0.87
Amyotrophic lateral sclerosis: oculomotor function in patients in respirators. Neurology (1987) 0.86
Nemaline myopathy: histological, histochemical and ultrastructural studies. Acta Neuropathol (1978) 0.86
Blood--nerve barrier: effect of ligation of the peripheral nerve. Exp Neurol (1979) 0.85
Eaton-Lambert syndrome. Ultrastructural study of the motor end-plates. Arch Neurol (1972) 0.84
Oculopharyngeal muscular dystrophy and distal myopathy. Intrafamilial difference in the onset and distribution of muscular involvement. Acta Neurol Scand (1982) 0.84
An improved synthesis of taurine- and glycine-conjugated bile acids. Lipids (1997) 0.84
An autopsy case of mitochondrial encephalomyopathy: biochemical and electron microscopic studies of the brain. J Neurol Sci (1988) 0.84
Creatine kinase (CK)-linked IgA in Isaacs' syndrome. An immune complex disease? J Neurol Sci (1985) 0.84
[A family of spino-cerebellar degeneration with disturbance of ocular movement, choreoathetosis, amyotrophy and dementia--a consideration in clinical features]. No To Shinkei (1988) 0.84
Strokelike episodes in MERRF. Ann Neurol (1985) 0.83
Involvement of dopamine, N-methyl-D-aspartate and sigma receptor mechanisms in methamphetamine-induced anticipatory activity rhythm in rats. J Pharmacol Exp Ther (1995) 0.83
[Adrenomyeloneuropathy associated with congenital cataract--report of a family with MRI study]. Rinsho Shinkeigaku (1988) 0.83
[Organic mercurial poisoning along the River Agano]. Naika (1968) 0.82
A new myopathy with tubulomembranous inclusions. J Neurol Sci (1981) 0.81
Scanning electron microscopic study of skeletal muscle. Normal, destrophic, and neurogenic atrophic muscle in mice and humans. Arch Neurol (1973) 0.81
[A case of spinal osteomyelitis detected by MRI]. Rinsho Shinkeigaku (1991) 0.81
Transient recurrent ventricular fibrillation due to hypopotassemia with a special note on the U wave. Jpn Heart J (1967) 0.81
Electron microscopical demonstration of nucleic acids in virus-like particles in the skeletal muscle of a traffic accident victim. Acta Neuropathol (1979) 0.80
Familial Creutzfeldt-Jakob disease in Japan. Three cases in a family with white matter involvement. J Neurol Sci (1985) 0.80
Core/targetoid fibres and multiple cytoplasmic bodies in organophosphate neuropathy. Acta Neuropathol (1977) 0.80
Reduced glycine receptor in the spinal cord in amyotrophic lateral sclerosis. Ann Neurol (1981) 0.80
Chronic recurrent demyelinating encephalomyelitis associated with hemophagocytic lymphohistiocytosis. Acta Neuropathol (1983) 0.80
Creatinine-clearance estimates for predicting gentamicin pharmacokinetic values in obese patients. Am J Hosp Pharm (1994) 0.80
[Clinical and electrophysiological studies on a case of myokymia evidence suggesting the hyperexcitability of the proximal alpha motor fibers (author's transl)]. Rinsho Shinkeigaku (1980) 0.79
Uniform tissue distribution of tRNA(Lys) mutation in mitochondrial DNA in MERRF patients. Neurology (1993) 0.79
Experimental chloroquine myopathy: morphological and biochemical studies. Eur Neurol (1989) 0.79
Immunohistochemical localization of senescence marker protein-30 (SMP30) in the submandibular gland and ultrastructural changes of the granular duct cells in SMP30 knockout mice. Histol Histopathol (2005) 0.79
Experimental neuropathy induced by methyl mercury compounds: autoradiographic study of GABA uptake by dorsal root ganglia. Eur Neurol (1986) 0.79
Binding of iodine 125 alpha-bungarotoxin to the thymus of mice. Arch Neurol (1978) 0.78
[Clinical features of organic mercury poisoning in the Agano River area]. Shinkei Kenkyu No Shimpo (1969) 0.78
Proteolytic enhancement of human rotavirus infectivity. Clin Infect Dis (1993) 0.78
Clinical and immunologic studies on multiple sclerosis. Neurology (1976) 0.78
Facio-scapulo-humeral muscular dystrophy in a patient with one paretic leg due to poliomyelitis. J Neurol Sci (1970) 0.78
[Atypical Guillain-Barré syndrome associated with ophthalmoplegia and visual impairment following herpes simplex virus type 1 infection]. Rinsho Shinkeigaku (1994) 0.77
Study of liver function in infants with atopic dermatitis using the 13C-methacetin breath test. Int Arch Allergy Immunol (1995) 0.77
Histometrical studies on the kidneys in diabetes mellitus. Tohoku J Exp Med (1968) 0.77
Quantitative study of intermediolateral column cell counts in Machado-Joseph disease. J Neurol Sci (1996) 0.77
A case of myocardial infarction, precipitated by orthostatic hypotension in the presence of essential hypertension, with the autopsy. Jpn Heart J (1967) 0.77
Analysis of sputum taken from wheezy and asthmatic infants and children, with special reference to respiratory infections. Pediatr Allergy Immunol (2001) 0.77
A patient with dementia with Lewy bodies and codon 232 mutation of PRNP. Neurology (2002) 0.76
[Case of adrenoleukodystrophy (ALD) with clinical features of olivopontocerebellar atrophy]. Rinsho Shinkeigaku (1983) 0.76
Morphological studies of peripheral nerves and skeletal muscles of an adult case with adrenoleukomyeloneuropathy. Eur Neurol (1985) 0.76
A family with adult type ceroid lipofuscinosis (Kufs' disease) and heart muscle disease: report of two autopsy cases. Intern Med (1995) 0.76
The peripheral neuropathy in De Sanctis-Cacchione syndrome. Histological, ultrastructural, and morphometric studies. Acta Neuropathol (1982) 0.76
Nocturnal decrease in vasopressin secretion into plasma in patients with multiple system atrophy. J Neurol Neurosurg Psychiatry (1999) 0.76
[A case of neurofibromatosis associated with Parkinson disease showing myokymia-like movement and hypertrophy of the lower extremities]. Rinsho Shinkeigaku (1987) 0.76
Reduced morning cortisol secretion in patients with multiple system atrophy. Clin Auton Res (2001) 0.76
Endocrinologic regulation of carbohydrate metabolism. Amyotrophic lateral sclerosis and Parkinsonism-dementia on Guam. Arch Neurol (1979) 0.75
[Distribution of C 14 -chinoform in various organs of rats]. Igaku To Seibutsugaku (1971) 0.75
[Abnormal carbohydrate metabolism in amyotrophic lateral sclerosis and parkinsonism-dementia complex on Guam (author's transl)]. Rinsho Shinkeigaku (1978) 0.75
[Successfully treated case of cryptococcal meningitis: clinical course and amphotericin B nephropathy]. Naika (1971) 0.75