Published in Acta Neuropathol on April 26, 1978
Ultrastructural studies on the neuromuscular junctions of Becker's muscular dystrophy. Acta Neuropathol (1985) 0.94
Mixed nemaline-mitochondrial "myopathy". Acta Neuropathol (1980) 0.86
Progression in nemaline myopathy. Acta Neuropathol (1989) 0.85
RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS. Neurology (1963) 2.98
Electrophysiology and electron-microscopy of rat neuromuscular junctions after nerve degeneration. Proc R Soc Lond B Biol Sci (1968) 2.90
NEMALINE MYOPATHY. A NEW CONGENITAL MYOPATHY. Brain (1963) 2.50
Adaptive transformation of rat soleus motor units during growth. J Neurol Sci (1976) 1.88
Histometric analysis of the ultrastructure of the neuromuscular junction in myasthenia gravis and in the myasthenic syndrome. Ann N Y Acad Sci (1971) 1.62
The longitudinal division of fibres in overloaded rat skeletal muscle. J Anat (1970) 1.47
A new concept of childhood nemaline myopathy. Arch Neurol (1971) 1.30
Enzyme histochemistry of skeletal muscle. J Neurol Neurosurg Psychiatry (1965) 1.29
VACUOLAR MYOPATHY: CLINICAL, HISTOCHEMICAL, AND MICROSCOPIC STUDY. Arch Neurol (1965) 1.28
Duchenne dystrophy. II. Morphometric study of motor end-plate fine structure. Brain (1974) 1.22
LIGHT AND ELECTRON MICROSCOPIC STUDIES OF "MYOGRANULES" IN A CHILD WITH HYPOTONIA AND MUSCLE WEAKNESS. Can Med Assoc J (1963) 1.22
Tenotomy. Effect on the fine structure of the soleus of the rat. Arch Neurol (1969) 1.20
THE FINE STRUCTURE OF MYO-TENDON JUNCTION IN SOME MAMMALIAN SKELETAL MUSCLES. Arch Histol Jpn (1965) 1.17
Morphology and histochemistry of the soleus muscle from normal and exercised rats. Am J Anat (1970) 1.13
Experimental core-like lesions and nemaline rods. A correlative morphological and physiological study. Arch Neurol (1972) 1.13
Longitudinal fibre splitting in muscular dystrophy: a serial cinematographic study. J Neurol Neurosurg Psychiatry (1973) 1.10
NEMALINE MYOPATHY; A SECOND CASE. Arch Neurol (1964) 1.09
Nemaline myopathy. A family study with three autopsied cases. Arch Pathol (1973) 0.98
Intra-axonal corpora amylacea in the peripheral nerve seen in a healthy woman. J Neurol Sci (1977) 0.96
Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathies. Neurology (1976) 0.93
Congenital rod disease. Further evidence of innervational abnormalities as the basis for the clinicopathologic features. J Neurol Sci (1974) 0.93
Changes in the Z disk of skeletal muscle induced by tenotomy. Neurology (1968) 0.92
Extrajunctional acetylcholine receptors. Alterations in human and experimental neuromuscular diseases. Arch Neurol (1976) 0.91
The ultrastructure of the adult and developing human myotendinous junction. Acta Neuropathol (1972) 0.90
Abnormal intrafusal muscle fibres in myotonic dystrophy: a study using serial sections. J Neurol Neurosurg Psychiatry (1975) 0.89
Ultrastructural studies on the growth of filaments and sarcomeres in mechanically overloaded human hearts. Virchows Arch B Cell Pathol (1976) 0.88
Nemaline myopathy. A histopathologic and histochemical study. Am J Clin Pathol (1967) 0.87
Nemaline myopathy. A histological and ultrastructural study of skeletal muscle from a case presenting with infantile hypotonia. Neurology (1969) 0.87
Nemaline myopathy. I. Histochemical study. Acta Neuropathol (1968) 0.86
Nemaline structures in polymyositis. A nonspecific pathological reaction of skeletal muscles. Neurology (1970) 0.86
Fine structural studies in myasthenia gravis. II. Lesions of the neuromuscular junction. Eur Neurol (1973) 0.84
Eaton-Lambert syndrome. Ultrastructural study of the motor end-plates. Arch Neurol (1972) 0.84
Nemaline (neuro) myopathy. Rod-like bodies and type I fibre atrophy in a case of congenital hypotonia with denervation. J Neurol Sci (1972) 0.82
The spectrum of rod myopathies. Arch Neurol (1968) 0.81
Fission yeast condensin complex: essential roles of non-SMC subunits for condensation and Cdc2 phosphorylation of Cut3/SMC4. Genes Dev (1999) 3.37
Characterization of fission yeast cohesin: essential anaphase proteolysis of Rad21 phosphorylated in the S phase. Genes Dev (2000) 2.94
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
Various abiotic stresses rapidly activate Arabidopsis MAP kinases ATMPK4 and ATMPK6. Plant J (2000) 2.48
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
Identification of regions on the hemagglutinin-neuraminidase protein of human parainfluenza virus type 2 important for promoting cell fusion. Virology (1995) 2.14
Hepatic dysfunction in Creutzfeldt-Jakob disease. Neurology (1992) 2.01
Case-control studies of motor neuron disease: association with mechanical injuries. Arch Neurol (1981) 1.89
Construction of nondefective adenovirus type 5 bearing a 2.8-kilobase hepatitis B virus DNA near the right end of its genome. J Virol (1985) 1.88
Estrogen inhibits bone resorption by directly inducing apoptosis of the bone-resorbing osteoclasts. J Exp Med (1997) 1.68
Neurological syndrome associated with clioquinol. Lancet (1971) 1.59
Modulation of immunoglobulin (Ig)E-mediated systemic anaphylaxis by low-affinity Fc receptors for IgG. J Exp Med (1999) 1.56
Autoantibodies against the amino terminal of alpha-enolase are a useful diagnostic marker of Hashimoto's encephalopathy. J Neuroimmunol (2005) 1.50
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
Chronic inflammatory demyelinating polyneuropathy in a patient with hyperIgEaemia. J Neurol Sci (2005) 1.42
Fcgamma receptor IIB-deficient mice develop Goodpasture's syndrome upon immunization with type IV collagen: a novel murine model for autoimmune glomerular basement membrane disease. J Exp Med (2000) 1.39
Identification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy. Am J Hum Genet (1991) 1.35
Nationwide survey of multiple sclerosis in Japan. Clinical analysis of 1,084 cases. Neurology (1975) 1.35
CD26-mediated signaling for T cell activation occurs in lipid rafts through its association with CD45RO. Proc Natl Acad Sci U S A (2001) 1.23
VP4 protein of porcine rotavirus strain OSU expressed by a baculovirus recombinant induces neutralizing antibodies. Virology (1989) 1.20
Surgical removal of submacular hemorrhage using tissue plasminogen activator and perfluorocarbon liquid. Am J Ophthalmol (1996) 1.19
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
Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism. Ann Neurol (2000) 1.13
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
Potential role of cbfa1, an essential transcriptional factor for osteoblast differentiation, in osteoclastogenesis: regulation of mRNA expression of osteoclast differentiation factor (ODF). Biochem Biophys Res Commun (1998) 1.10
Hardening and termination of long-duration γ rays detected prior to lightning. Phys Rev Lett (2013) 1.08
A eukaryotic-type protein kinase, SpkA, is required for normal motility of the unicellular Cyanobacterium synechocystis sp. strain PCC 6803. J Bacteriol (2001) 1.08
Hedgehog proteins stimulate chondrogenic cell differentiation and cartilage formation. J Bone Miner Res (2000) 1.08
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
Four-digit allele genotyping of the HLA-A and HLA-B genes in Japanese patients with Behcet's disease by a PCR-SSOP-Luminex method. Tissue Antigens (2006) 1.03
Outcomes of patients with metastatic renal cell carcinoma that do not meet eligibility criteria for clinical trials. Ann Oncol (2014) 1.03
Exophthalmos in autoimmune thyroid disease. J Clin Endocrinol Metab (1980) 1.03
AMP-Activated protein kinase is activated by the stimulations of G(q)-coupled receptors. Biochem Biophys Res Commun (2000) 1.02
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
Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease. Ann Neurol (1998) 1.02
White matter alteration in idiopathic normal pressure hydrocephalus: tract-based spatial statistics study. AJNR Am J Neuroradiol (2011) 1.02
Diagnosis of Toxoplasma meningoencephalitis in a non-AIDS patient using PCR. J Infect (2001) 1.01
Histological and compositional evaluations of three types of calcium phosphate cements when implanted in subcutaneous tissue immediately after mixing. J Biomed Mater Res (1999) 1.01
Changing mortality patterns of motor neuron disease in Japan. J Neurol Sci (1977) 0.99
Effects of capsaicin-containing yellow curry sauce on sympathetic nervous system activity and diet-induced thermogenesis in lean and obese young women. J Nutr Sci Vitaminol (Tokyo) (2000) 0.99
X-ray microbeams: Tumor therapy and central nervous system research. Nucl Instrum Methods Phys Res A (2005) 0.98
"Tail sign" associated with microembolic signals. Stroke (1999) 0.98
Observation of an energetic radiation burst from mountain-top thunderclouds. Phys Rev Lett (2009) 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
Intra-axonal corpora amylacea in the peripheral nerve seen in a healthy woman. J Neurol Sci (1977) 0.96
Distal myopathy: histochemical and ultrastructural studies. Arch Neurol (1982) 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
Basic properties of calcium phosphate cement containing atelocollagen in its liquid or powder phases. Biomaterials (1998) 0.96
Vitamin K2 inhibits osteoclastic bone resorption by inducing osteoclast apoptosis. Biochem Biophys Res Commun (1996) 0.95
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
An electrophysiological study of the locus of the interference effect in a stimulus-response compatibility paradigm. Psychophysiology (2000) 0.95
Physical performance tests after stroke: reliability and validity. Am J Phys Med Rehabil (2000) 0.94
Stimulatory function of paired immunoglobulin-like receptor-A in mast cell line by associating with subunits common to Fc receptors. J Biol Chem (1999) 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
Detection of high-energy gamma rays from winter thunderclouds. Phys Rev Lett (2007) 0.94
HLA and Japanese MS. Tissue Antigens (1978) 0.94
Joseph's disease: clinical and pathological studies in a Japanese family. Ann Neurol (1986) 0.94
Clinical significance of anomalous pancreaticobiliary union. Gastrointest Endosc (1983) 0.93
[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
Osteoclasts are present in gp130-deficient mice. Endocrinology (1997) 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
[Statistics on eye injuries]. Nihon Ganka Kiyo (1967) 0.91
Genetics of congenital nemaline myopathy. Muscle Nerve (1980) 0.91
A third-generation bisphosphonate, minodronic acid (YM529), successfully prevented the growth of bladder cancer in vitro and in vivo. Br J Cancer (2006) 0.91
Structural polypeptides of the murine coronavirus DVIM. Arch Virol (1986) 0.90
Altered microstructure in corticospinal tract in idiopathic normal pressure hydrocephalus: comparison with Alzheimer disease and Parkinson disease with dementia. AJNR Am J Neuroradiol (2011) 0.89
Preliminary experiment of fluorescent X-ray computed tomography to detect dual agents for biological study. J Synchrotron Radiat (2001) 0.89
Error-related brain potentials elicited by vocal errors. Neuroreport (2001) 0.89
Induction of OX40, a receptor of gp34, on T cells by trans-acting transcriptional activator, Tax, of human T-cell leukemia virus type I. Jpn J Cancer Res (1996) 0.88
Fabry's disease on the mechanism of the peripheral nerve involvement. Acta Neuropathol (1975) 0.88
Germinoma causing wallerian degeneration. Case report and review of the literature. J Neurosurg (1998) 0.88
Decreased expression of transcription factor GATA-2 in haematopoietic stem cells in patients with aplastic anaemia. Br J Haematol (2001) 0.87
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
Mammalian mature osteoclasts as estrogen target cells. Biochem Biophys Res Commun (1996) 0.86
Initial histological evaluation of anti-washout type fast-setting calcium phosphate cement following subcutaneous implantation. Biomaterials (1998) 0.86
Mitochondrial encephalomyopathy: elevated visual cortex lactate unresponsive to photic stimulation--a localized 1H-MRS study. Neurology (1994) 0.85