Published in J Neuropathol Exp Neurol on January 01, 1972
An experimental mouse testicular teratoma as a model for neuroepithelial neoplasia and differentiation. II. Electron microscopy. Am J Pathol (1975) 1.03
The fine structure of a myxopapillary ependymoma of the filum terminale. Acta Neuropathol (1973) 0.97
In vitro characteristics of a myxopapillary ependymoma of the filum terminale maintained in tissue and organ culture systems. Light and electron microscopic observations. Acta Neuropathol (1974) 0.97
Oligodendroglioma-like cells (clear cells) in ependymoma. Acta Neuropathol (1983) 0.96
Morphologic observations of brain tumors in PD4 hamsters induced by four strains of avian sarcoma virus. Acta Neuropathol (1973) 0.92
Choroid plexus papilloma: light and electron microscopic study of three cases. Acta Neuropathol (1978) 0.88
Virus-like particles in brain tumours induced by N-ethyl-N-nitrosourea in rats. Acta Neuropathol (1974) 0.87
Ultrastructural findings in so-called ependymal rat tumors induced by transplacental administration of ethylnitrosourea (ENU). Acta Neuropathol (1982) 0.86
A novel intradural extramedullary spinal cord tumor in young dogs. Acta Neuropathol (1988) 0.84
Abnormal cilia in a fourth ventricular ependymoma. Acta Neuropathol (1986) 0.81
Synaptophysin expression in "ependymal tumors" induced by ethyl-nitrosourea in rats. Am J Pathol (1992) 0.80
Intercellular septate-like junction of neoplastic cells in myxopapillary ependymoma of the filum terminale. Acta Neuropathol (1990) 0.77
Human nervous system tumors. Observations by high voltages electron microscopy. Acta Neuropathol (1975) 0.77
Fine structure of intercellular junctions and blood vessels in medulloblastomas. Acta Neuropathol (1975) 0.77
Methylcholanthrene induced murine primitive neuroectodermal tumor: ultrastructure and nuclear RNA polymerase activity. Acta Neuropathol (1978) 0.75
The role of Schwann cells in the development of human peripheral nerves. An electron microscopic study. J Ultrastruct Res (1965) 2.18
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy. Nat Genet (1999) 2.04
A study of rod-like structures (Hirano bodies) in 240 normal and pathological brains. Acta Neuropathol (1972) 1.95
Desmin myopathy. Brain (2004) 1.79
Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy. Proc Natl Acad Sci U S A (1996) 1.44
The perineurium as a diffusion barrier. Ultrastructural correlates. Bull Los Angeles Neurol Soc (1966) 1.43
Cytokine expression profile in idiopathic inflammatory myopathies. J Neuropathol Exp Neurol (1996) 1.34
Hearing loss in facioscapulohumeral dystrophy. Eur J Pediatr (1986) 1.28
Neuromyopathy and vitamin E deficiency in man. Neuropediatrics (1981) 1.26
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies). Neuromuscul Disord (2000) 1.22
Consequences of mutations within the C terminus of the FHL1 gene. Neurology (2009) 1.18
Early lesion of Pelizaeus-Merzbacher disease: electron microscopic and biochemical study. J Neuropathol Exp Neurol (1973) 1.13
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder. Acta Neuropathol (1987) 1.13
Myopathy associated with Marfan's syndrome. Fine structural and histochemical observations. Neurology (1973) 1.12
Tumor-like amyloid formation (amyloidoma) in the brain. J Neurol (1981) 1.10
Eccrine sweat glands are not innervated in hereditary sensory neuropathy type IV. An electron-microscopic study. Acta Neuropathol (1981) 1.10
The behavior of acoustic neuroma in tissue culture. Acta Neuropathol (1969) 1.10
Inclusion body myositis presenting with isolated erector spinae paresis. Neurology (1995) 1.10
Alcohol-related acute axonal polyneuropathy: a differential diagnosis of Guillain-Barré syndrome. Arch Neurol (1998) 1.10
Mucolipidosis IV: novel mutation and diverse ultrastructural spectrum in the skin. Neuropediatrics (2002) 1.09
A mutation in myotilin causes spheroid body myopathy. Neurology (2005) 1.07
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy. Neurology (2003) 1.07
Significance of muscle biopsies in neuronal ceroid-lipofuscinoses. J Neurol Neurosurg Psychiatry (1975) 1.07
The bahavior of normal peripheral nerve in tissue culture. Z Zellforsch Mikrosk Anat (1968) 1.06
Lesions of the pontine tegmentum and conjugate gaze paralysis. Arch Neurol (1971) 1.06
Light and electron microscopic studies of experimental hydrocephalus. Ependymal and subependymal areas. Acta Neuropathol (1972) 1.05
Mallory body-like inclusions in a hereditary congenital neuromuscular disease. Muscle Nerve (1983) 1.04
The cytoplasmic bodies in a congenital myopathy can be stained with antibodies to desmin, the muscle-specific intermediate filament protein. Acta Neuropathol (1983) 1.03
Confirmation of virtual unmyelinated fiber absence in hereditary sensory neuropathy type IV. J Neuropathol Exp Neurol (1980) 1.03
On the ultrastructural diversity and essence of residual bodies in neuronal ceroid-lipofuscinosis. Mech Ageing Dev (1979) 1.02
Long-spacing fibrous collagen in human acoustic nerve tumors. In vvo and in vitro observations. J Ultrastruct Res (1968) 1.00
An ultrastructural study of the retina in the Jansky-Bielschowsky type of neuronal ceroid-lipofuscinosis. Am J Ophthalmol (1977) 0.99
Desmin splice variants causing cardiac and skeletal myopathy. J Med Genet (2000) 0.99
The ultrastructure of acoustic nerve tumors. Acta Neuropathol (1969) 0.99
Human ontogenesis. 3. Cell death in fetal muscle. Acta Neuropathol (1991) 0.99
Rigid spine syndrome in a girl. J Neurol (1982) 0.99
Congenital myopathies--a comprehensive update of recent advancements. Acta Neurol Scand (2009) 0.98
Studies on GM1-gangliosidosis, type II. Acta Neuropathol (1974) 0.98
A case of lipogranulomatosis Farber: some clinical and ultrastructural aspects. Eur J Pediatr (1985) 0.97
Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscle. J Neurol Sci (2003) 0.97
Human forms of neuronal ceroid-lipofuscinosis (Batten disease): consensus on diagnostic criteria, Hamburg 1992. J Inherit Metab Dis (1993) 0.96
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosis. Neuropediatrics (1988) 0.96
Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot. Neuropediatrics (1991) 0.96
Incidence of neuronal ceroid-lipofuscinoses in West Germany: variation of a method for studying autosomal recessive disorders. Am J Med Genet (1992) 0.96
Increased ammonia production during forearm ischemic work test in McArdle's disease. Klin Wochenschr (1981) 0.96
Wallerian degeneration: ultrastructural and histochemical studies. Bull Los Angeles Neurol Soc (1969) 0.96
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndrome. Am J Med Genet (1998) 0.95
Fibre type disproportion in the rigid spine syndrome. Neuropadiatrie (1977) 0.95
Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism. Brain (1990) 0.95
CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCL. Neurology (2010) 0.95
Experimental neurinoma in tissue culture. Acta Neuropathol (1972) 0.95
Peripheral motor and sensory neuropathy of early childhood, simulating Werdnig-Hoffmann disease. Neuropadiatrie (1976) 0.95
Diagnostic immunohistochemistry in neuromuscular disorders. Histopathology (2005) 0.94
A study of aryl sulfatase and acid phosphatase in the developing nervous system of the rat. J Histochem Cytochem (1968) 0.94
DNA-fragmentation and expression of apoptosis-related proteins in muscular dystrophies. Neuropathol Appl Neurobiol (1997) 0.93
Juvenile Huntington chorea: clinical, ultrastructural, and biochemical studies. Neurology (1978) 0.93
Morphologic studies on adult neuronal-ceroid lipofuscinosis (NCL). Clin Neuropathol (1982) 0.93
Macrophages in multiple sclerosis. Immunobiology (1996) 0.92
Retinal ultrastructure of neuronal ceroid-lipofuscinosis in the dalmatian dog. Acta Neuropathol (1985) 0.92
Pigmentoarchitectonic pathology of the isocortex in juvenile neuronal ceroid-lipofuscinosis: axonal enlargements in layer IIIab and cell loss in layer V. Acta Neuropathol (1979) 0.92
Apoptosis-related proteins in skeletal muscle fibers of spinal muscular atrophy. J Neuropathol Exp Neurol (1997) 0.92
DNA-fragmentation and expression of apoptosis-related proteins in experimentally denervated and reinnervated rat facial muscle. Neuropathol Appl Neurobiol (1997) 0.92
Congenital myopathy with cytoplasmic bodies. Neuropediatrics (1981) 0.92
The ultrastructural variability of non-specific lipopigments. Acta Neuropathol (1979) 0.92
Clinical and ultrastructural study of painful neuroma. Neurosurgery (1981) 0.91
X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene. Ann N Y Acad Sci (1995) 0.91
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient. Acta Neuropathol (1997) 0.91
Autosomal dominant "spheroid body myopathy". Muscle Nerve (1979) 0.91
Cell death and oxidative damage in inflammatory myopathies. Clin Immunol Immunopathol (1998) 0.91
A mild juvenile variant of type IV glycogenosis. Brain Dev (1992) 0.90
The fine structure of the retina in neuronal ceroid-lipofuscinosis. Am J Ophthalmol (1974) 0.90
Dense core vesicles in the desmoplastic variant of cerebral neuroblastoma. Acta Neuropathol (1980) 0.90
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation. Neurology (2001) 0.90
Inflammatory myopathies. Curr Opin Neurol (1996) 0.90
Ultrastructural pathology in emetine-induced myopathy. Acta Neuropathol (1988) 0.90
Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases. Neurology (2005) 0.89
Spinal cord infarction secondary to occlusion of the anterior spinal artery. Arch Neurol (1973) 0.89
Mitochondrial myopathy--a result of clofibrate/etofibrate treatment? Case report. Acta Neuropathol (1985) 0.88
Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1. Neuropediatrics (2010) 0.88
Rectal biopsy findings in infantile neuroaxonal dystrophy. Neuropediatrics (1980) 0.88
Ultrastructural pathology of skin biopsy and fibroblast enzyme studies in a case of GM2-gangliosidosis with deficient hexosaminidase A and thermolabile hexosaminidase B. Neuropadiatrie (1980) 0.88
Central pontine myelinolysis. A clinical and pathological study of 10 cases. Brain (1972) 0.88
Adult metachromatic leukodystrophy. III. Clinical course, final stages and first biochemical results. Eur Neurol (1980) 0.88
Late-onset metachromatic leukodystrophy: diagnostic problems elucidated by a case report. J Neurol (1981) 0.88
Amyloidoma of the gasserian ganglion as a cause of symptomatic neuralgia of the trigeminal nerve: report of three cases. J Neurol (1993) 0.87
Expression of cell adhesion molecules in inflammatory myopathies. J Neuroimmunol (1995) 0.87
Schwannoma of the sellar region. Acta Neurochir (Wien) (1979) 0.87
Dense core mitochondria in peripheral ganglia of man. Acta Neuropathol (1976) 0.87
Adult metachromatic leukodystrophy. I. Clinical manifestation in a female aged 44 years, previously diagnosed in the preclinical state. Eur Neurol (1977) 0.87
Ependymoma: internal correlations among pathological signs: the anaplastic variant. Neurosurgery (1991) 0.86
The forearm ischaemic work test--hazardous to McArdle patients? J Neurol Neurosurg Psychiatry (1982) 0.86
DNA-fragmentation and apoptosis-related proteins of muscle cells in motor neuron disorders. Acta Neurol Scand (1997) 0.86
Aberrant arrested in maturation neuromuscular junctions in centronuclear myopathy. J Neurol Sci (1994) 0.86
Immunogold EM reveals a close association of plectin and the desmin cytoskeleton in human skeletal muscle. Eur J Cell Biol (1999) 0.86
Biological characteristics of peripheral nerve tumors induced with ethylnitrosourea. Acta Neuropathol (1973) 0.86
Metachromatic leukodystrophy (sulfatide lipidoses) cultured in vitro. Science (1967) 0.85
[Acute renal failure in alcoholic myopathy (author's transl)]. Dtsch Med Wochenschr (1979) 0.85
A morphological study of non-Japanese congenital muscular dystrophy associated with cerebral lesions. Brain Dev (1983) 0.85
Nitrosourea-induced brain tumors: an in vivo and in vitro tumor model system. J Natl Cancer Inst (1978) 0.85