Published in J Neurol Sci on November 01, 1987
An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A. Korean J Pediatr (2010) 0.91
A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G). J Korean Med Sci (2005) 0.84
Lysosomal glycogen storage disease with normal acid maltase. Neurology (1981) 2.13
Intermolecular interactions in two (ferrocenylmethyl)benzimidazoles incorporating the 4-MeOC6H4 and 3,4-(MeO)2C6H3 groups: analysis of MeO-C-C distortions from ideal 120 degrees geometry. Acta Crystallogr C (2001) 1.90
Early features of zidovudine-associated myopathy: histopathological findings and clinical correlations. Acta Neuropathol (1995) 1.26
Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA. Neurology (1992) 1.10
Inclusion body myositis. A corticosteroid-resistant idiopathic inflammatory myopathy. Arch Neurol (1982) 1.03
Phosphodiesters in muscular dystrophies. Ann N Y Acad Sci (1979) 1.01
Somatosensory evoked potentials for the prognosis of coma in humans. Exp Neurol (1978) 0.88
Hydrocephalus as a cause of dementia: evaluation by computerised tomography and intracranial pressure monitoring. J Neurol Neurosurg Psychiatry (1977) 0.87
Cell adhesion and neurite extension in response to two proteolytic fragments of laminin. J Neurosci Res (1989) 0.87
Clenbuterol reduces degeneration of exercised or aged dystrophic (mdx) muscle. Muscle Nerve (2000) 0.84
Characterization of the enzymatic defect in late-onset muscle phosphofructokinase deficiency. New subtype of glycogen storage disease type VII. J Clin Invest (1987) 0.82
Nonprogressive congenital neuromuscular disease with uniform type 1 fiber. Arch Neurol (1983) 0.82
Treatment of aneurysmal hemiplegia with dopamine and mannitol. J Neurosurg (1978) 0.82
Adult-onset nemaline rods in a patient treated for suspected dermatomyositis. Study with two-dimensional electrophoresis. Arch Neurol (1981) 0.82
Inclusion body myositis associated with systemic sarcoidosis. Can J Neurol Sci (1986) 0.80
Effect of sodium nitroprusside on cerebral blood flow in conscious human beings. Surg Neurol (1977) 0.80
Juvenile-onset acid maltase deficiency with unusual familial features. Neurology (1986) 0.80
The expression of myosin light chains and tropomyosin in human muscle biopsies with histochemical type 1 and type 2 fiber deficiency. Muscle Nerve (1990) 0.79
Fatal infantile glycogen storage disease: deficiency of phosphofructokinase and phosphorylase b kinase. Neurology (1981) 0.79
Management of 136 consecutive supratentorial berry aneurysms. J Neurosurg (1978) 0.79
Tubular aggregates: their association with myalgia. J Neurol Neurosurg Psychiatry (1985) 0.78
Nemaline rod myopathy and Charcot-Marie-Tooth disease. Report of a case in a 10-year-old girl. Arch Neurol (1980) 0.78
Erythrocytes in muscular dystrophy. Investigation with 31P nuclear magnetic resonance spectroscopy. Arch Neurol (1981) 0.77
Use of fructose-2,6-diphosphate to assay for phosphofructokinase activity in human muscle. Clin Biochem (1996) 0.77
Heterogeneity of human skeletal muscle tropomyosin. Ann Neurol (1985) 0.76
Inclusion body myositis with cricopharyngeus muscle involvement and severe dysphagia. Muscle Nerve (1992) 0.75
Human muscle proteins: analysis by two-dimensional electrophoresis. Neurology (1983) 0.75
Muscle glycogen of steroid myopathy patients. J Neurol Sci (1996) 0.75
Treatment of grade III and IV astrocytomas with BCNU alone and in combination with VM-26 following surgery and radiation therapy. Cancer Treat Rep (1980) 0.75
Lysophospholipase activity in rabbit skeletal muscle. Life Sci (1982) 0.75
Lysophosphatidylcholine-induced lysis of erythrocytes in Duchenne and myotonic dystrophies and in Huntington's disease. J Neurol Sci (1982) 0.75
Peripheral polyneuropathy associated with primary malignant lymphoma of the brain. Arch Neurol (1978) 0.75
Description and uses of intracranial pressure monitoring. Heart Lung (1976) 0.75
Intracranial pressure gradients in a patient with a thalamic tumor. Surg Neurol (1976) 0.75
The significance of pulmonary changes associated with cerebral perfusion with hypoxic blood in monkeys. Surgery (1977) 0.75
Intracranial compliance interpretation and clinical application. J Neurosurg Nurs (1977) 0.75
Fast to slow change of myosin in nemaline rod myopathy. Neurology (1983) 0.75
Heterotopic neogenesis of skeletal muscle induced in the adult rat diaphragmatic peritoneum: ultrastructural and transplantation studies. Histol Histopathol (1999) 0.75
Clonal evolution and tumor progression in 2 human colorectal adenoma-derived cell-lines invitro - the involvement of chromosome-1 abnormalities. Int J Oncol (1992) 0.75
Erythrocyte membrane lysophospholipase activity in muscular dystrophy. J Neurol Sci (1983) 0.75
Maintaining sexuality after spinal cord injury. Nursing (1975) 0.75
Muscle protein analysis. II. Two-dimensional electrophoresis of normal and diseased human skeletal muscle. Clin Chem (1980) 0.75
Hereditary sensory neuropathy: biopsy study of an autosomal dominant variety. Neurology (1985) 0.75
Erythrocyte metabolism in muscular dystrophy. Arch Neurol (1978) 0.75
Acute quadriplegic myopathy with thick filament loss spares moving muscles: an autopsy study. Acta Myol (2006) 0.75