Published in J Neurol Sci on April 01, 1977
Generalized giant axonal neuropathy: a filament-forming disease of neuronal, endothelial, glial, and schwann cells in a patient without kinky hair. Acta Neuropathol (1977) 1.16
N-hexane neuropathy in offset printers. J Neurol Neurosurg Psychiatry (1993) 0.88
Animal models of peripheral neuropathy due to environmental toxicants. ILAR J (2014) 0.83
Giant axonal neuropathy (GAN): an immunohistochemical and ultrastructural study report of a Latin American case. Acta Neuropathol (1990) 0.78
Recovery from 2,5-hexanediol intoxication of the retinotectal tract of the rat. An ultrastructural study. Acta Neuropathol (1982) 0.75
n-Hexane intoxication in a Chinese medicine pharmaceutical plant: a case report. J Med Case Rep (2017) 0.75
Paired helical filaments from Alzheimer disease patients contain cytoskeletal components. Proc Natl Acad Sci U S A (1985) 2.86
Critical illness myopathy and neuropathy. Lancet (1996) 2.71
Multiple sclerosis associated with duplicated CMT1A: a report of two cases. J Neurol Neurosurg Psychiatry (1997) 1.67
The role of muscle biopsy in investigating isolated muscle pain. Neurology (2007) 1.54
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study. Neurol Sci (2006) 1.48
Inhibition of lymphocytic neuropathy target esterase predicts the development of organophosphate-induced delayed polyneuropathy. Arch Toxicol (1986) 1.34
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. Neurology (2007) 1.16
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy. J Neurol Neurosurg Psychiatry (1978) 1.16
Neuroaxonal dystrophy with dystonia and pallidal involvement. Neuropediatrics (1999) 1.16
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study. Neurology (2006) 1.15
Hereditary neuropathy with liability to pressure palsies: electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation. Neurol Sci (2003) 1.13
Eclamptic encephalopathy: imaging and pathogenetic considerations. Acta Neurol Scand (1997) 1.11
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease. J Biol Chem (2001) 1.10
Activation of NF-kappaB and c-jun transcription factors in multiple sclerosis lesions. Implications for oligodendrocyte pathology. Am J Pathol (1999) 1.10
Locked-in syndrome in multiple sclerosis with sparing of the ventral portion of the pons. Ann Neurol (1982) 1.09
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia. Neuromuscul Disord (2001) 1.09
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E. Neurology (2004) 1.08
Human peripheral nerve macrophages in normal and pathological conditions. J Neurol Sci (1993) 1.02
Glial cell and macrophage reactions in rat spinal ganglion after peripheral nerve lesions: an immunocytochemical and morphometric study. Arch Ital Biol (2001) 0.99
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. Hum Genet (1995) 0.99
Natural history of CMT1A including QoL: a 2-year prospective study. Neuromuscul Disord (2008) 0.99
Hepatitis C virus infection of peripheral nerves in type II cryoglobulinaemia. Virchows Arch (1999) 0.97
Clinical features of Kleine-Levin syndrome with localized encephalitis. Neuropediatrics (1993) 0.94
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. Ital J Neurol Sci (1988) 0.93
An unusual case of meningeal gliomatosis. Acta Neuropathol Suppl (1981) 0.93
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. Neurology (2010) 0.91
Charcot-Marie-Tooth disease: study of a large kinship with an intermediate form. J Neurol (1985) 0.91
Neuropathy in Tangier disease: A clinicopathologic study and a review of the literature. Acta Neurol Scand (1985) 0.91
Decerebrate rigidity in acute head injury. J Neurosurg (1977) 0.90
Bovine spongiform encephalopathy and Creutzfeldt-Jakob disease: facts and uncertainties underlying the causal link between animal and human diseases. Neurol Sci (2004) 0.90
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathy. J Neuroimmunol (1997) 0.90
[The anatomo-clinical association of hypertrophic neuritis and multiple sclerosis]. Acta Neurol (Napoli) (1969) 0.90
Ultrastructural study of effect of methionine sulfoximine on developing and adult rat cerebral cortex. J Neuropathol Exp Neurol (1974) 0.89
Lumbar epidural Ewing sarcoma. Light and electron microscopic investigation. J Neurol (1981) 0.89
Charcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entity. Neurology (2003) 0.88
Prosopagnosia. Report of four cases. Eur Neurol (1982) 0.88
A distinctive cutaneous malignant neoplasm expressing the Langerhans cell phenotype. Synchronous occurrence with B-chronic lymphocytic leukemia. Cancer (1985) 0.88
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy. Brain Pathol (2001) 0.88
Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families. Hum Mutat (2001) 0.88
Amyotrophy in Shy-Drager syndrome. Acta Neurol Belg (1983) 0.87
Simultaneous occurrence of spongiform encephalopathy in a man and his cat in Italy. Lancet (1998) 0.87
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero. Acta Neuropathol (2000) 0.87
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. Neurology (2009) 0.87
Charcot-Marie-Tooth disease: an intermediate form. Neuromuscul Disord (1998) 0.86
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve function. J Bone Joint Surg Br (1997) 0.85
MELAS: clinical phenotype and morphological brain abnormalities. Acta Neuropathol (2003) 0.85
Opsoclonus and palatal myoclonus during prolonged post-traumatic coma. A clinico-pathologic study. Eur Neurol (1977) 0.85
Methyl bromide induced neuropathy: a clinical, neurophysiological, and morphological study. J Neurol Neurosurg Psychiatry (1995) 0.84
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. Neurol Sci (2009) 0.84
Brain metastases from post-radiation malignant peripheral nerve sheath tumour. Ital J Neurol Sci (1995) 0.84
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. Neurol Sci (2008) 0.84
Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy. Neuropediatrics (2000) 0.83
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat. Acta Neuropathol (1983) 0.83
Phosphorylated 14-3-3zeta protein in the CSF of neuroleptic-treated patients. Neurology (2005) 0.82
Prevalence of dementia and apolipoprotein e genotype distribution in the elderly of buttapietra, verona province, Italy. Neuroepidemiology (2002) 0.82
Peripheral neuropathy associated with immunoglobulin disorders an immunological and ultrastructural study. Acta Neuropathol Suppl (1981) 0.82
Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype. Ital J Neurol Sci (1989) 0.82
DNA fragmentation in normal development of the human central nervous system: a morphological study during corticogenesis. Neuropathol Appl Neurobiol (1997) 0.82
A somatic and germline mosaic mutation in MPZ/P(0) mimics recessive inheritance of CMT1B. Neurology (2001) 0.82
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathy. Neurology (2004) 0.82
Hepatitis C virus infection and myositis: a virus localization study. Neuromuscul Disord (2003) 0.81
Friedreich's ataxia. A light- and electron microscopic study of peripheral nerve biopsies. Acta Neuropathol Suppl (1981) 0.81
[On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation]. Acta Neuropathol (1967) 0.81
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations. Hum Mutat (2000) 0.81
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy. Acta Neuropathol (1995) 0.81
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseases. Neuropathol Appl Neurobiol (2003) 0.81
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases. Neuropediatrics (1988) 0.81
Expression and regulation of glial-cell-line-derived neurotrophic factor (GDNF) mRNA in human astrocytes in vitro. Cell Tissue Res (1996) 0.81
Nerve conduction changes during lower limb lengthening. Somatosensory evoked potentials (SEPs) and F-wave results. Electromyogr Clin Neurophysiol (1999) 0.81
Peripheral nerve vasculitis: a clinico-pathological study. Clin Neuropathol (1995) 0.81
BAEP and autopsy findings in Wallenberg syndrome. Ital J Neurol Sci (1982) 0.80
Diffuse Rosenthal fiber formation in adults. A case report. Acta Neuropathol (1980) 0.80
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases. Muscle Nerve (1998) 0.80
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain. Microsc Res Tech (1999) 0.80
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22. Neuromuscul Disord (1999) 0.80
Ponto-cerebellar hypoplasia with dystonia: clinico-pathological findings in a sporadic case. Childs Nerv Syst (1998) 0.80
Experimental induction of myelin changes by anti-MAG antibodies and terminal complement complex. J Neuropathol Exp Neurol (1995) 0.80
Microgyria associated with Sturge-Weber angiomatosis. Childs Nerv Syst (1994) 0.79
Cytoskeletal changes and ubiquitin expression in dystrophic axons of Seitelberger's disease. Clin Neuropathol (1993) 0.79
Status spongiosus of rat central nervous system induced by actinomycin D. Acta Neuropathol (1976) 0.79
[Seitelberger's infantile neuroaxonal dystrophy: anatomoclinical study of a sibling group]. Acta Neurol Psychiatr Belg (1969) 0.79
Motor neuron disease with pyramidal tract dysfunction involves the cortical generators of the early somatosensory evoked potential to tibial nerve stimulation. Neurology (1996) 0.79
Atypical phenotype of Refsum's disease: clinical, biochemical, neurophysiological and pathological study. Eur Neurol (1985) 0.79
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. J Neuroimmunol (2002) 0.79
Genetic and molecular features of Su(P), a gene that interacts with ref(2)P in male fertility of Drosophila melanogaster. Mol Genet Genomics (2001) 0.79
PMP22 related congenital hypomyelination neuropathy. J Neurol Neurosurg Psychiatry (2001) 0.78
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL. Neuropediatrics (2000) 0.78
Spinal somatosensory evoked potentials in patients with tethered cord syndrome. Can J Neurol Sci (1994) 0.78
Chronic inflammatory demyelinating polyneuropathy. Int J Tissue React (1985) 0.78
Expression and distribution of GAP-43 in human astrocytes in culture. Neuropathol Appl Neurobiol (1995) 0.78
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin. Acta Neuropathol (1998) 0.78
Sensory and motor peripheral neuropathy in olivopontocerebellar atrophy. Acta Neurol Scand (1986) 0.78
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy. Neuropathol Appl Neurobiol (2005) 0.78
n-hexane polyneuropathy. An occupational disease of shoemakers. Eur Neurol (1980) 0.78
Coeliac disease associated with peripheral neuropathy in a child: a case report. Neuropediatrics (1998) 0.78
Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsies. Eur J Neurol (2007) 0.77