Published in J Neurol on December 01, 2001
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Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies. Neurology (2003) 1.46
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168th ENMC International Workshop: outcome measures and clinical trials in Charcot-Marie-Tooth disease (CMT). Neuromuscul Disord (2010) 1.23
A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS-ES Task Force. Eur J Neurol (2006) 1.22
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Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families. Neuromuscul Disord (2000) 1.09
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136th ENMC International Workshop: Charcot-Marie-Tooth disease type 1A (CMT1A)8-10 April 2005, Naarden, The Netherlands. Neuromuscul Disord (2006) 1.05
Four novel cases of periaxin-related neuropathy and review of the literature. Neurology (2010) 1.04
Diffusion tensor imaging shows different topographic involvement of the thalamus in progressive supranuclear palsy and corticobasal degeneration. AJNR Am J Neuroradiol (2009) 1.02
A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies. Am J Hum Genet (1995) 1.01
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Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies. Ann Neurol (2000) 0.96
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Activation of the contact system in cerebrospinal fluid of patients with Alzheimer disease. Alzheimer Dis Assoc Disord (1998) 0.95
17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1. Eur Neurol (1994) 0.94
Iatrogenic intraspinal epidermoid tumor: myelo-CT and MRI diagnosis. Neuroradiology (1989) 0.93
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease. Clin Genet (2007) 0.92
L-2-Hydroxyglutaric aciduria: MRI in seven cases. Neuroradiology (1998) 0.92
Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II. Neurology (2006) 0.92
Imaging degeneration of the substantia nigra in Parkinson disease with inversion-recovery MR imaging. AJNR Am J Neuroradiol (2007) 0.92
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations. Neurology (2011) 0.92
Epileptic phenotypes associated with mitochondrial disorders. Neurology (2001) 0.92
Symmetric lesions of the subthalamic nuclei in mitochondrial encephalopathies: an almost distinctive Mark of Leigh disease with COX deficiency. AJNR Am J Neuroradiol (1995) 0.91
Gait pattern classification in children with Charcot-Marie-Tooth disease type 1A. Gait Posture (2011) 0.91
Hypodense area within a meningioma: metastasis from breast cancer. Neuroradiology (1980) 0.90
Multiple system atrophy. Clinical and MR observations on 42 cases. Ital J Neurol Sci (1993) 0.90
The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegeneration. Neuropediatrics (2011) 0.90
Hemophagocytic lymphohistiocytosis with neurological presentation: MRI findings and a nearly miss diagnosis. Neurol Sci (2011) 0.90
Spinal radiological findings in nine patients with spontaneous intracranial hypotension. Neuroradiology (2002) 0.90
Basal forebrain involvement in low-functioning autistic children: a voxel-based morphometry study. AJNR Am J Neuroradiol (2011) 0.89
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Clinical features and outcomes in spontaneous intracranial hypotension: a survey of 90 consecutive patients. Neurol Sci (2009) 0.88
Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series. Eur J Neurol (2012) 0.87
A novel phenotype of sporadic Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry (2007) 0.87
Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life. J Neurol (1992) 0.87
Imaging and outcome in severe complications of lumbar epidural anaesthesia: report of 16 cases. Neuroradiology (2000) 0.85
The vascular territories in the cerebellum and brainstem: CT and MR study. AJNR Am J Neuroradiol (1987) 0.85
Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease. J Neurol (2000) 0.85
Parenchymatous neurosyphilis. Neurol Sci (2001) 0.85
Angiography and computerized tomography in the diagnosis of aneurysmal bone cyst of the skull: case report. J Neurosurg (1980) 0.84
The effects of wallerian degeneration of the optic radiations demonstrated by MRI. Neuroradiology (1992) 0.84
Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation. Gut (2004) 0.84
Subarachnoid haemorrhage and meningiomas. Report of two cases. Acta Neurochir (Wien) (1983) 0.84
Pathogenic effect of an intermediate-size SCA-6 allele (CAG)(19) in a homozygous patient. Neurology (2001) 0.84
POEMS syndrome: relapse after successful autologous peripheral blood stem cell transplantation. Neuromuscul Disord (2007) 0.84
Metastases of carcinoma to intracranial meningioma: report of two cases and review of the literature. Cancer (1981) 0.84
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. Neurol Sci (2008) 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
MR imaging and proton MR spectroscopy in adult Krabbe disease. AJNR Am J Neuroradiol (2000) 0.84
Late presentation of leucoencephalopathy with calcifications and cysts: report of two cases. J Neurol Neurosurg Psychiatry (2008) 0.84
Chronic inflammatory demyelinating polyradiculoneuropathy: long-term course and treatment of 60 patients. Neurol Sci (2000) 0.84
F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II. J Neurol Neurosurg Psychiatry (1992) 0.83
Subacute cervical myelopathy in a child with cerebral palsy. Secondary to torsion dystonia? Childs Brain (1982) 0.83
CT and MRI in maple syrup urine disease. Neurology (1988) 0.82
Dendritic cells pulsed with glioma lysates induce immunity against syngeneic intracranial gliomas and increase survival of tumor-bearing mice. Neurol Res (2006) 0.82
Acquired hemidystonia in childhood: a clinical and neuroradiological study of thirteen patients. Pediatr Neurol (1996) 0.82
Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients. Neuroradiology (1998) 0.82
Reliability of instrumented movement analysis as outcome measure in Charcot-Marie-Tooth disease: results from a multitask locomotor protocol. Gait Posture (2011) 0.82
Decreased diffusivity in the caudate nucleus of presymptomatic huntington disease gene carriers: which explanation? AJNR Am J Neuroradiol (2009) 0.81