Published in Acta Neuropathol on January 01, 1980
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12. Am J Hum Genet (1997) 1.17
Inflammatory and non-inflammatory inclusion body myositis. Characterization of the mononuclear cells and expression of the immunoreactive class I major histocompatibility complex product. Acta Neuropathol (1990) 0.94
Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1. Am J Hum Genet (1999) 0.90
Inclusion body myositis: an underdiagnosed condition? Ann Rheum Dis (1993) 0.88
Abnormal increases of lysosomal cysteinine proteinases in rimmed vacuoles in the skeletal muscle. Am J Pathol (1986) 0.87
Progression in nemaline myopathy. Acta Neuropathol (1989) 0.85
Intranuclear and cytoplasmic filamentous inclusions in distal myopathy (Welander). Acta Neuropathol (1991) 0.83
Intranuclear inclusions in muscle, nervous tissue, and adrenal gland. Acta Neuropathol (1984) 0.81
Tubulomembranous and fingerprint-like inclusions in biopsied muscle of distal myopathy with rimmed vacuoles. Acta Neuropathol (1984) 0.78
Myopathy with mitochondrial abnormalities and rimmed vacuoles. Acta Neuropathol (1986) 0.77
Muscle fiber degradation in distal myopathy with rimmed vacuoles. Acta Neuropathol (1994) 0.75
Molecular markers for granulovacuolar degeneration are present in rimmed vacuoles. PLoS One (2013) 0.75
Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathy. Neurology (1978) 1.65
The histographic analysis of human muscle biopsies with regard to fiber types. 2. Diseases of the upper and lower motor neuron. Neurology (1969) 1.64
Hereditary muscular atrophy with ataxia, retinitis pigmentosa, and diabetes mellitus. A clinical report of a family. Neurology (1968) 1.49
Tubular aggregates in type II muscle fibers: ultrastructural and histochemical correlation. J Ultrastruct Res (1970) 1.42
Inclusion body myositis. Lab Invest (1971) 1.39
Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations. Mayo Clin Proc (1968) 1.33
Experimental chloroquine myopathy. J Neuropathol Exp Neurol (1970) 1.30
Distal myopathy: electron microscopic and histochemical studies. Neurology (1977) 1.17
Familial hypokalemic periodic paralysis with permanent myopathy. A clinical and ultrastructural study. J Neuropathol Exp Neurol (1967) 1.07
Sporadic distal myopathy with early adult onset. Ann Neurol (1979) 1.05
The fine structure of spheromembranous degeneration of skeletal muscle induced by vincristine. J Neuropathol Exp Neurol (1967) 0.92
The effect of vincristine on skeletal muscle in the rat. A correlative histochemical, ultrastructural and chemical study. J Neuropathol Exp Neurol (1972) 0.89
Ultrastructure of dystrophic skeletal muscle. Isr J Med Sci (1977) 0.84
Mass occurrence of multilamellar bodies in myopathy. Virchows Arch B Cell Pathol (1976) 0.83
Inflammatory myopathy in oculopharyngeal dystrophy. Muscle Nerve (1980) 0.83
[A case report of oculo-pharyngo-distal type myopathy, with vacuolar degeneration and myelin figure in muscle fibers (author's transl)]. Rinsho Shinkeigaku (1979) 0.81
Identification of a novel, dendritic cell-associated molecule, dectin-1, by subtractive cDNA cloning. J Biol Chem (2000) 2.83
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
Distinct mechanisms of neonatal tolerance induced by dendritic cells and thymic B cells. J Exp Med (1991) 1.82
Increased production of cysteinyl leukotrienes and prostaglandin D2 during human anaphylaxis. Clin Exp Allergy (2009) 1.71
Sarcoidosis presenting as bilateral hydronephrosis. Intern Med (1996) 1.63
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
Elevated expression of interleukin-18 in the granulomatous lesions of muscular sarcoidosis. Clin Immunol (2001) 1.44
Results of a total aortic arch replacement for an acute aortic arch dissection. J Thorac Cardiovasc Surg (2000) 1.41
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
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
Motor neuron disease in the Kii peninsula, Japan. Proc Aust Assoc Neurol (1968) 1.04
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
Slow cord dorsum potentials elicited by descending volleys in man. J Neurol Neurosurg Psychiatry (1979) 0.97
Controlled trial of thyrotropin releasing hormone tartrate in ataxia of spinocerebellar degenerations. J Neurol Sci (1983) 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
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
Ultrastructural studies on the neuromuscular junctions of Becker's muscular dystrophy. Acta Neuropathol (1985) 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
Interleukin-2 receptor levels indicating relapse in multiple sclerosis. Lancet (1989) 0.93
Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Ann Neurol (1994) 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
Ontogeny of thymic B cells in normal mice. Cell Immunol (1991) 0.91
Neurologic features of chronic Minamata disease (organic mercury poisoning) certified at autopsy. Intern Med (1995) 0.91
[A case of adult-onset tethered cord syndrome accompanied with slowly progressive muscular atrophy in the lower limbs]. Rinsho Shinkeigaku (1991) 0.91
Characterization of a mitochondrial matrix protease catalyzing the processing of adrenodoxin precursor. J Biochem (1986) 0.91
Structural polypeptides of the murine coronavirus DVIM. Arch Virol (1986) 0.90
Clinical manifestations associated with human herpesvirus 7 infection. Arch Dis Child (1995) 0.90
Immunosuppressive properties of CD95L-transduced "killer" hybrids created by fusing donor- and recipient-derived dendritic cells. Blood (2001) 0.89
A statistical evaluation on the age and sex distribution of basal serum gastrin and gastric acid secretion in subjects with or without peptic ulcer disease. Hiroshima J Med Sci (1984) 0.89
Interleukin-4-producing cells in idiopathic pulmonary fibrosis: an immunohistochemical study. Respirology (1999) 0.89
R1 resection for aggressive or advanced colorectal liver metastases is justified in combination with effective prehepatectomy chemotherapy. Eur J Surg Oncol (2011) 0.89
Expression of three calpain isoform genes in human skeletal muscles. J Neurol Sci (1998) 0.88
A new dysferlin gene mutation in two Japanese families with limb-girdle muscular dystrophy 2B and Miyoshi myopathy. Neuromuscul Disord (2001) 0.88
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
Isolated third nerve palsy due to sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis (1997) 0.87
Effects of coronary artery bypass grafting using internal mammary arteries for diabetic patients. J Am Coll Cardiol (1999) 0.86
Protective effect of thiopental against cerebral ischemia during circulatory arrest. Thorac Cardiovasc Surg (1999) 0.86
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
A pivotal role of Rho GTPase in the regulation of morphology and function of dendritic cells. J Immunol (2001) 0.86
Blood--nerve barrier: effect of ligation of the peripheral nerve. Exp Neurol (1979) 0.85
Oculopharyngeal muscular dystrophy and distal myopathy. Intrafamilial difference in the onset and distribution of muscular involvement. Acta Neurol Scand (1982) 0.84
HTLV-1 associated myelopathy in an HTLV-1 and HBV double carrier family: report of a case and the mode of vertical transmission of both viruses. J Gastroenterol Hepatol (1991) 0.84
An improved synthesis of taurine- and glycine-conjugated bile acids. Lipids (1997) 0.84
The reconstitution of CD45RBhiCD4+ naive T cells is inversely correlated with donor age in murine allogeneic haematopoietic stem cell transplantation. Br J Haematol (2000) 0.84
Eaton-Lambert syndrome. Ultrastructural study of the motor end-plates. Arch Neurol (1972) 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
[Adrenomyeloneuropathy associated with congenital cataract--report of a family with MRI study]. Rinsho Shinkeigaku (1988) 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
Elevated concentrations of CCR7 ligands in patients with eosinophilic pneumonia. Allergy (2013) 0.83
Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation. J Neurol Sci (1996) 0.83
Human muscle protein degradation in vitro by eosinophil cationic protein (ECP). Muscle Nerve (2001) 0.83
Two cytotoxic pathways of natural killer cells in human cord blood: implications in cord blood transplantation. Br J Haematol (1997) 0.82
Structural requirement for recognition of the precursor proteins by the mitochondrial processing peptidase. J Biol Chem (1994) 0.82
[An adult with type III glycogenosis with lobulated fibers]. Rinsho Shinkeigaku (1986) 0.82
[Organic mercurial poisoning along the River Agano]. Naika (1968) 0.82
Stroke after coronary artery bypass grafting in patients with cerebrovascular disease. Ann Thorac Surg (2000) 0.81
Scanning electron microscopic study of skeletal muscle. Normal, destrophic, and neurogenic atrophic muscle in mice and humans. Arch Neurol (1973) 0.81
Transient recurrent ventricular fibrillation due to hypopotassemia with a special note on the U wave. Jpn Heart J (1967) 0.81
Aortic arch repair using hypothermic circulatory arrest technique associated with pharmacological brain protection. Eur J Cardiothorac Surg (2000) 0.81
[A case of neuro-Behçet's disease presenting with chorea]. Rinsho Shinkeigaku (2001) 0.81
A new myopathy with tubulomembranous inclusions. J Neurol Sci (1981) 0.81
[A case of spinal osteomyelitis detected by MRI]. Rinsho Shinkeigaku (1991) 0.81