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Top papers

Rank Title Journal Year PubWeight™‹?›
1 Paired helical filaments from Alzheimer disease patients contain cytoskeletal components. Proc Natl Acad Sci U S A 1985 2.86
2 Critical illness myopathy and neuropathy. Lancet 1996 2.71
3 Multiple sclerosis associated with duplicated CMT1A: a report of two cases. J Neurol Neurosurg Psychiatry 1997 1.67
4 The role of muscle biopsy in investigating isolated muscle pain. Neurology 2007 1.54
5 Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study. Neurol Sci 2006 1.48
6 Inhibition of lymphocytic neuropathy target esterase predicts the development of organophosphate-induced delayed polyneuropathy. Arch Toxicol 1986 1.34
7 Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. Neurology 2007 1.16
8 Stiff-man syndrome associated with nocturnal myoclonus and epilepsy. J Neurol Neurosurg Psychiatry 1978 1.16
9 Neuroaxonal dystrophy with dystonia and pallidal involvement. Neuropediatrics 1999 1.16
10 Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study. Neurology 2006 1.15
11 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
12 Eclamptic encephalopathy: imaging and pathogenetic considerations. Acta Neurol Scand 1997 1.11
13 pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease. J Biol Chem 2001 1.10
14 Activation of NF-kappaB and c-jun transcription factors in multiple sclerosis lesions. Implications for oligodendrocyte pathology. Am J Pathol 1999 1.10
15 Locked-in syndrome in multiple sclerosis with sparing of the ventral portion of the pons. Ann Neurol 1982 1.09
16 A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia. Neuromuscul Disord 2001 1.09
17 Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E. Neurology 2004 1.08
18 Human peripheral nerve macrophages in normal and pathological conditions. J Neurol Sci 1993 1.02
19 A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. Hum Genet 1995 0.99
20 Glial cell and macrophage reactions in rat spinal ganglion after peripheral nerve lesions: an immunocytochemical and morphometric study. Arch Ital Biol 2001 0.99
21 Natural history of CMT1A including QoL: a 2-year prospective study. Neuromuscul Disord 2008 0.99
22 Hepatitis C virus infection of peripheral nerves in type II cryoglobulinaemia. Virchows Arch 1999 0.97
23 Clinical features of Kleine-Levin syndrome with localized encephalitis. Neuropediatrics 1993 0.94
24 Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. Ital J Neurol Sci 1988 0.93
25 Toxic polyneuropathies in Italy due to leather cement poisoning in shoe industries. A light- and electron-microscopic study. J Neurol Sci 1977 0.93
26 An unusual case of meningeal gliomatosis. Acta Neuropathol Suppl 1981 0.93
27 Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. Neurology 2010 0.91
28 Charcot-Marie-Tooth disease: study of a large kinship with an intermediate form. J Neurol 1985 0.91
29 Neuropathy in Tangier disease: A clinicopathologic study and a review of the literature. Acta Neurol Scand 1985 0.91
30 Bovine spongiform encephalopathy and Creutzfeldt-Jakob disease: facts and uncertainties underlying the causal link between animal and human diseases. Neurol Sci 2004 0.90
31 Decerebrate rigidity in acute head injury. J Neurosurg 1977 0.90
32 T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathy. J Neuroimmunol 1997 0.90
33 [The anatomo-clinical association of hypertrophic neuritis and multiple sclerosis]. Acta Neurol (Napoli) 1969 0.90
34 Lumbar epidural Ewing sarcoma. Light and electron microscopic investigation. J Neurol 1981 0.89
35 Ultrastructural study of effect of methionine sulfoximine on developing and adult rat cerebral cortex. J Neuropathol Exp Neurol 1974 0.89
36 Charcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entity. Neurology 2003 0.88
37 Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy. Brain Pathol 2001 0.88
38 Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families. Hum Mutat 2001 0.88
39 A distinctive cutaneous malignant neoplasm expressing the Langerhans cell phenotype. Synchronous occurrence with B-chronic lymphocytic leukemia. Cancer 1985 0.88
40 Prosopagnosia. Report of four cases. Eur Neurol 1982 0.88
41 Simultaneous occurrence of spongiform encephalopathy in a man and his cat in Italy. Lancet 1998 0.87
42 Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero. Acta Neuropathol 2000 0.87
43 Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. Neurology 2009 0.87
44 Amyotrophy in Shy-Drager syndrome. Acta Neurol Belg 1983 0.87
45 Charcot-Marie-Tooth disease: an intermediate form. Neuromuscul Disord 1998 0.86
46 Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve function. J Bone Joint Surg Br 1997 0.85
47 MELAS: clinical phenotype and morphological brain abnormalities. Acta Neuropathol 2003 0.85
48 Opsoclonus and palatal myoclonus during prolonged post-traumatic coma. A clinico-pathologic study. Eur Neurol 1977 0.85
49 Methyl bromide induced neuropathy: a clinical, neurophysiological, and morphological study. J Neurol Neurosurg Psychiatry 1995 0.84
50 Brain metastases from post-radiation malignant peripheral nerve sheath tumour. Ital J Neurol Sci 1995 0.84
51 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
52 Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. Neurol Sci 2008 0.84
53 Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy. Neuropediatrics 2000 0.83
54 The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat. Acta Neuropathol 1983 0.83
55 Phosphorylated 14-3-3zeta protein in the CSF of neuroleptic-treated patients. Neurology 2005 0.82
56 Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathy. Neurology 2004 0.82
57 DNA fragmentation in normal development of the human central nervous system: a morphological study during corticogenesis. Neuropathol Appl Neurobiol 1997 0.82
58 Prevalence of dementia and apolipoprotein e genotype distribution in the elderly of buttapietra, verona province, Italy. Neuroepidemiology 2002 0.82
59 Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype. Ital J Neurol Sci 1989 0.82
60 A somatic and germline mosaic mutation in MPZ/P(0) mimics recessive inheritance of CMT1B. Neurology 2001 0.82
61 Peripheral neuropathy associated with immunoglobulin disorders an immunological and ultrastructural study. Acta Neuropathol Suppl 1981 0.82
62 Hepatitis C virus infection and myositis: a virus localization study. Neuromuscul Disord 2003 0.81
63 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
64 Nerve conduction changes during lower limb lengthening. Somatosensory evoked potentials (SEPs) and F-wave results. Electromyogr Clin Neurophysiol 1999 0.81
65 Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations. Hum Mutat 2000 0.81
66 Expression and regulation of glial-cell-line-derived neurotrophic factor (GDNF) mRNA in human astrocytes in vitro. Cell Tissue Res 1996 0.81
67 [On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation]. Acta Neuropathol 1967 0.81
68 Cerebro-ocular dysplasia and muscular dystrophy: report of two cases. Neuropediatrics 1988 0.81
69 Peripheral nerve vasculitis: a clinico-pathological study. Clin Neuropathol 1995 0.81
70 Friedreich's ataxia. A light- and electron microscopic study of peripheral nerve biopsies. Acta Neuropathol Suppl 1981 0.81
71 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
72 Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain. Microsc Res Tech 1999 0.80
73 Ponto-cerebellar hypoplasia with dystonia: clinico-pathological findings in a sporadic case. Childs Nerv Syst 1998 0.80
74 Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22. Neuromuscul Disord 1999 0.80
75 Diffuse Rosenthal fiber formation in adults. A case report. Acta Neuropathol 1980 0.80
76 BAEP and autopsy findings in Wallenberg syndrome. Ital J Neurol Sci 1982 0.80
77 Experimental induction of myelin changes by anti-MAG antibodies and terminal complement complex. J Neuropathol Exp Neurol 1995 0.80
78 Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. J Neuroimmunol 2002 0.79
79 [Seitelberger's infantile neuroaxonal dystrophy: anatomoclinical study of a sibling group]. Acta Neurol Psychiatr Belg 1969 0.79
80 Atypical phenotype of Refsum's disease: clinical, biochemical, neurophysiological and pathological study. Eur Neurol 1985 0.79
81 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
82 Status spongiosus of rat central nervous system induced by actinomycin D. Acta Neuropathol 1976 0.79
83 Cytoskeletal changes and ubiquitin expression in dystrophic axons of Seitelberger's disease. Clin Neuropathol 1993 0.79
84 Microgyria associated with Sturge-Weber angiomatosis. Childs Nerv Syst 1994 0.79
85 Coeliac disease associated with peripheral neuropathy in a child: a case report. Neuropediatrics 1998 0.78
86 n-hexane polyneuropathy. An occupational disease of shoemakers. Eur Neurol 1980 0.78
87 Chronic inflammatory demyelinating polyneuropathy. Int J Tissue React 1985 0.78
88 PMP22 related congenital hypomyelination neuropathy. J Neurol Neurosurg Psychiatry 2001 0.78
89 Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy. Neuropathol Appl Neurobiol 2005 0.78
90 Expression and distribution of GAP-43 in human astrocytes in culture. Neuropathol Appl Neurobiol 1995 0.78
91 Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin. Acta Neuropathol 1998 0.78
92 Spinal somatosensory evoked potentials in patients with tethered cord syndrome. Can J Neurol Sci 1994 0.78
93 A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL. Neuropediatrics 2000 0.78
94 Sensory and motor peripheral neuropathy in olivopontocerebellar atrophy. Acta Neurol Scand 1986 0.78
95 Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsies. Eur J Neurol 2007 0.77
96 Sensory involvement in X-linked spino-bulbar muscular atrophy (Kennedy's syndrome): an electrophysiological study. J Neurol 1996 0.77
97 Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study. Ann Neurol 1997 0.77
98 Striato-nigral degeneration. Report of a case with an unusually short course and multiple system degenerations. J Neurol Sci 1975 0.77
99 Novel mutation of the P0 extracellular domain causes a Déjérine-Sottas syndrome. J Neurol Neurosurg Psychiatry 1999 0.77
100 Synapses and malnutrition: quantitative ultrastructural study of rat cerebral cortex. Exp Neurol 1974 0.77
101 T-cell anti-apoptotic mechanisms in inflammatory myopathies. J Neuroimmunol 2000 0.77
102 Demyelinating polyradiculoneuritis following Coxiella burnetti infection (Q fever). Ital J Neurol Sci 1991 0.77
103 Tau protein immunolocalization in fetal and adult human spinal cord. Neurosci Res 1995 0.77
104 An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2. Toxicol Appl Pharmacol 1978 0.77
105 Paired transcranial magnetic stimulation for the early diagnosis of corticobasal degeneration. Clin Neurophysiol 2003 0.77
106 Familial spastic paraplegia with peroneal amyotrophy. A family with hypersensitivity to pyrexia. Ital J Neurol Sci 1990 0.77
107 Polyneuropathy in hypereosinophilic syndrome. Neurology 1988 0.77
108 Choroid plexus papilloma of the cerebello-pontine angle. Neurochirurgia (Stuttg) 1983 0.76
109 Stereotactic brain biopsy in human immunodeficiency virus-infected patients. Arch Intern Med 1996 0.76
110 Cytoskeletal pathology in ataxia-telangiectasia. Clin Neuropathol 1988 0.76
111 Complement neoantigen and vitronectin are components of plaques in amyloid AL neuropathy. Ital J Neurol Sci 1992 0.76
112 Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene. Neurology 2004 0.76
113 Neuronal ceroid lipofuscinoses: pathological features of bioptic specimens from 28 patients. Neurol Sci 2000 0.76
114 Neuropsychological and neuroimaging correlates in corticobasal degeneration. Ital J Neurol Sci 1998 0.76
115 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study. Eur Neurol 2008 0.76
116 Two novel missense mutations causing adrenoleukodystrophy in Italian patients. Mol Cell Probes 1999 0.76
117 Myelin oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy. J Neuroimmunol 2000 0.76
118 Human neoplastic Schwann cells: changes in the expression of neurotrophins and their low-affinity receptor p75. Neuropathol Appl Neurobiol 1997 0.76
119 [Flaccid paralysis of the foot in rolandic parasagittal tumors]. G Psichiatr Neuropatol 1965 0.76
120 Splicing mutation causes infantile Sandhoff disease. Am J Med Genet 1998 0.75
121 Möbius-like syndrome due to multiple cerebral abnormalities including hypoplasia of the descending tracts. A case report. J Neurol 1982 0.75
122 Gliomatosis cerebri diffusa. A case report. Acta Neuropathol 1981 0.75
123 Binding of monoclonal anti-myelin-associated glycoprotein antibodies to human foetal peripheral neurons in culture. Acta Neuropathol 1987 0.75
124 Peripheral and segmental spinal abnormalities of median and ulnar somatosensory evoked potentials in Hirayama's disease. J Neurol Neurosurg Psychiatry 2003 0.75
125 Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation and show different phenotypes; description of a novel null-type mutation. Hum Genet 1998 0.75
126 Changes in systemic arterial pressure during sleep in Shy-Drager syndrome. Sleep 1981 0.75
127 Sudanophilic leucodystrophy: report of a case with tigroid demyelination of the centrum ovale. Acta Neuropathol 1976 0.75
128 Neurotoxic effects of 2,5-hexanedione in rats: early morphological and functional changes in nerve fibres and neuromuscular junctions. Neurotoxicology 1981 0.75
129 [Histopathologic and ultrastructural study of various amputation neuromas]. Riv Patol Nerv Ment 1983 0.75
130 Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients. J Neurol Sci 1999 0.75
131 Seitelberger's infantile neuroaxonal dystrophy. A case report. Eur Neurol 1973 0.75
132 [Myoclonic form of Hallervorden-Spatz disease. Clinical aspect simulating a subacute spongiform encephalitis]. Rev Neurol (Paris) 1967 0.75
133 [Juvenile thrombosis of the basilar artery]. Sist Nerv 1970 0.75
134 [Acute traumatic pontine syndromes. Clinical, electroencephalographic, and neuropathological study]. Riv Neurol 1979 0.75
135 [Electromyographic study of 2 cases of nystagmus-myoclonus of the velum palatinum]. Riv Neurol 1970 0.75
136 Familiar microcephaly with bilateral heterotopias of gray matter in the centrum ovale. Acta Neurol (Napoli) 1980 0.75
137 [Myoclonic cerebellar dyssnergia]. Riv Neurobiol 1980 0.75
138 [Rapid evolution of presenile dementia in a case of Hallervorden-Spatz disease]. Acta Neurol (Napoli) 1969 0.75
139 Blood lymphocytes in neuronal ceroid lipofuscinosis. Ital J Neurol Sci 1988 0.75
140 Familial infantile myoclonic epilepsy in a family suffering from tuberous sclerosis. Epilepsia 1968 0.75
141 Autoimmune paraneoplastic cerebellar degeneration: immunohistological localization of antibody-binding sites. Clin Neurol Neurosurg 1995 0.75
142 Dermatomyositis and retroperitoneal germ cell cancer. Eur Neurol 2001 0.75
143 [Hypertrophic neuropathies beginning in infancy: a study of 3 cases (author's transl)]. Riv Patol Nerv Ment 1982 0.75
144 Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report. Neurol Sci 2001 0.75
145 Histopathological and ultrastructural study of a case of infantile metachromatic leukodystrophy. Ital J Neurol Sci 1983 0.75
146 [The problem of fetal cystic encephalopathy occurring in the second third of pregnancy]. Biol Neonat 1967 0.75
147 A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease. Mol Cell Probes 2001 0.75
148 Involvement of the central nervous system in non-Hodgkin's lymphoma. Tumori 1981 0.75
149 [Spino-olivo-cerebello-nigral degeneration. Study of a case begining in infancy]. Acta Neurol (Napoli) 1977 0.75
150 [Some encephalopathies and neuropathies caused by toxic agents]. Pathologica 1977 0.75
151 [Recurrent chronic polyneuritis. Neuropathologic models]. Riv Neurobiol 1985 0.75
152 Arteriovenous aneurysm of the vein of Galen. A clinical, angiographic CT scan and neuropathological study. J Neurol Sci 1979 0.75
153 [Oculo-facio-cervical dystonia syndrome revealed by plurisystematized degeneration of the central nervous system with pallidoreticular pigmentary condition]. Acta Neurol Psychiatr Belg 1969 0.75
154 Cytoskeletal changes induced by 2,5-hexanedione on developing human neurons in vitro. Arch Toxicol 1991 0.75
155 Pattern of nervous tissue immunostaining by human anti-glycolipid antibodies. J Neurol Sci 1994 0.75
156 Immunohistochemical demonstration of spinal ventral horn cells involvement in a case of "myoclonus epilepsy with ragged red fibers" (MERRF). Clin Neuropathol 2000 0.75
157 Polyglucosan body myopathy: a new case. Neuromuscul Disord 1992 0.75
158 [Diffuse sclerosis. Anatomo-clinical study of a subacute case with a striated demyelination]. Acta Neurol (Napoli) 1976 0.75
159 [Thrombosis of the extracranial carotid caused by traumatic lesions of the soft palate in childhood]. Sist Nerv 1970 0.75
160 Progressive peroneal muscular atrophy (Charcot-Marie-Tooth disease) associated with beta-thalassemia trait and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. A clinical and nerve biopsy case. Ital J Neurol Sci 1981 0.75
161 [Alzheimer's disease. Histopathological and ultrastructural study of 6 cases (author's transl)]. Riv Patol Nerv Ment 1978 0.75
162 [Experimental neuropathy due to acrilamide. Histological and ultrastructural studies (author's transl)]. Riv Patol Nerv Ment 1978 0.75
163 Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion. Brain Res 1982 0.75
164 Cytoskeletal changes in cultured human fibroblasts following exposure to 2,5-hexanedione. Neuropathol Appl Neurobiol 1996 0.75
165 Inherited neuroaxonal dystrophy in C6 deficient rabbits. J Neuropathol Exp Neurol 1992 0.75
166 Remitting infratentorial leukoencephalopathy in a patient with HIV infection. AIDS 1998 0.75
167 Systemic passive transfer studies using IgM monoclonal antibodies to sulfatide. J Neuroimmunol 1995 0.75
168 Evaluating endothelial function of the common carotid artery: an in vivo human model. Nutr Metab Cardiovasc Dis 2008 0.75
169 HIV-associated PML presenting as epilepsia partialis continua. J Neurol Sci 1998 0.75
170 [Progressive myoclonic epilepsy: anatomo - clinical study of a sporadic case with a marked cerebellar symptomatology (author's transl)]. Riv Patol Nerv Ment 1976 0.75
171 Neuromuscular complications of kidney diseases. Nephrol Dial Transplant 1998 0.75
172 Reversible upper limb muscle weakness with selective loss of thick filaments. Neurology 2003 0.75
173 A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene. Mol Cell Probes 1997 0.75
174 A novel missense mutation in the L1CAM gene in a boy with L1 disease. Neurol Sci 2006 0.75
175 Nuroaxonal degeneration induced by sodium diethyldithiocarbamate in cultures of central nervous tissue. J Neuropathol Exp Neurol 1975 0.75
176 [Infantile neuro-axonal dystrophy: anatomo clinical study of one case (author's transl)]. Riv Patol Nerv Ment 1977 0.75
177 IDPN impairs post-traumatic regeneration of rat sciatic nerve. Neuropathol Appl Neurobiol 1993 0.75
178 Recurrent familial brachial plexus palsies as the only clinical expression of 'tomaculous' neuropathy. Eur Neurol 1989 0.75
179 A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease. Hum Mutat 1995 0.75
180 [Polyneuropathies due to adhesives. Histopathological and ultrastructural studies]. Acta Neurol (Napoli) 1976 0.75
181 Bilateral infarction of pyramidal tracts (a case report). Acta Neurol (Napoli) 1978 0.75
182 Mutations associated with very late-onset metachromatic leukodystrophy. Clin Genet 1999 0.75
183 [Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations]. Riv Neurobiol 1983 0.75
184 The epidemiology of inflammatory polyradiculoneuropathy. A critical review of the distribution, characteristics and outcome of the disease. Plasmapheresis Study Group. Ital J Neurol Sci 1991 0.75
185 [Four cases of Creutzfeldt-Jakob's disease (author's transl)]. Riv Patol Nerv Ment 1980 0.75
186 Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report. Clin Neuropathol 1986 0.75
187 [Atonic diplegia caused by antipoliomyelitic oral vaccination. Anatomo-clinical study]. Acta Neurol (Napoli) 1970 0.75
188 [4 cases of Jakob-Creutzfeldt's disease]. Acta Neurol (Napoli) 1976 0.75
189 Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22. Neurology 1999 0.75
190 [Clinical and biopsy study of 4 cases of chronic recurrent polyradiculoneuritis]. Riv Neurobiol 1985 0.75
191 Peripheral neuropathy associated with allergic granulomatous angiitis (Churg-Strauss syndrome): clinical features and histological findings. Ital J Neurol Sci 1988 0.75
192 Hyperpyrexia-triggered relapses in an unusual case of ataxic chronic inflammatory demyelinating polyradiculoneuropathy. Neurol Sci 2006 0.75
193 Chronic relapsing polyneuritis. A light- and electron-microscopic study. Acta Neuropathol 1982 0.75
194 Congenital toxoplasmosis: histological and ultrastructural study. Ital J Neurol Sci 1982 0.75
195 [Myopathy with lipid accumulation and type-II glutaric aciduria]. Minerva Pediatr 1991 0.75
196 [Cerebral calcinosis in postoperative hypoparathyroidism. Presentation of an anatomo-clinical case]. Acta Neurol (Napoli) 1970 0.75
197 Axillary injection of botulinum A toxin in a patient with muscle cramps associated with severe axillary hyperhidrosis. Acta Neurol Belg 2001 0.75
198 Neurotoxicity of idiopathic hypereosinophilia on a case with simultaneous CNS and PNS involvement. Ital J Neurol Sci 1993 0.75