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A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

Neurology, 1999-07, Vol.53 (1), p.38

1999

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IL-6 detection in multiple sclerosis brain

Journal of the neurological sciences, 1997-02, Vol.146 (1), p.59-65

1997

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Early synthesis and correlation of serum anti-thyroid antibodies with clinical parameters in multiple sclerosis

Journal of the neurological sciences, 1999-09, Vol.168 (1), p.32-36

1999

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Interleukin-6 levels in the cerebrospinal fluid and serum of patients with Guillain-Barré syndrome and chronic inflammatory demyelinating polyradiculoneuropathy

Journal of neuroimmunology, 1993-08, Vol.47 (1), p.55-61

1993

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The potential role of hepatitis C virus in the pathogenesis of the neurological syndrome in chronic hepatitis C

Gut, 1997-09, Vol.41 (3), p.411-412

1997

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Detection of Borrelia burgdorferi DNA and complement membrane attack complex deposits in the sural nerve of a patient with chronic polyneuropathy and tertiary lyme disease

Muscle & nerve, 1997-08, Vol.20 (8), p.969-975

1997

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Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy

Neurology, 1997-05, Vol.48 (5), p.1200

1997

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Involvement of peripheral sensory fibers in amyotrophic lateral sclerosis : electrophysiological study of 64 cases

Muscle & nerve, 1993-02, Vol.16 (2), p.166-172

1993

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Three-dimensional analysis of pulmonary nodules by MSCT with Advanced Lung Analysis (ALA1) software

Radiologia medica, 2006-04, Vol.111 (3), p.343-354

2006

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Cerebrotendinous xanthomatosis (van Bogaert-Scherer-Epstein disease): CT and MR findings

American journal of neuroradiology : AJNR, 1994-10, Vol.15 (9), p.1721-1726

1994

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Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities

Journal of the neurological sciences, 1996-09, Vol.140 (1), p.129-131

1996

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Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy

Virchows Archiv : an international journal of pathology, 1995-12, Vol.427 (4), p.415-421

1995

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Association of polyclonal anti-GM1 IgM and anti-neurofilament antibodies with CSF oligoclonal bands in a young with amyotrophic lateral sclerosis

Acta neurologica Scandinavica, 1995-11, Vol.92 (5), p.387-393

1995

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Hypoplasia of the corpus callosum in Niemann-Pick type C disease

Neuroradiology, 1994, Vol.36 (1), p.20-22

1994

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Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy

Acta neuropathologica, 1996-08, Vol.92 (2), p.115-122

1996

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Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)

Acta neuropathologica, 1999-07, Vol.98 (1), p.78-84

1999

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High levels of cerebrospinal fluid IgM binding to myelin basic protein are associated with early benign course in multiple sclerosis

Journal of neuroimmunology, 1997-07, Vol.77 (1), p.128-133

1997

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Neuronal intranuclear inclusion disease: neuropathologic study of a case

Brain & development (Tokyo. 1979), 1998-08, Vol.20 (5), p.290-294

1998

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Cloning and sequence analysis of the human liver rhodanese: Comparison with the bovine and chicken enzymes

Biochemical and biophysical research communications, 1991-10, Vol.180 (2), p.887-893

1991

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Neuronal intranuclear inclusion disease : polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case

Acta neuropathologica, 1996-02, Vol.91 (2), p.215-218

1996

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Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report

Journal of the neurological sciences, 1998-03, Vol.155 (2), p.218-221

1998

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Axonal motor and sensory neuropathy in myotonic dystrophy

Acta neurologica Scandinavica, 1993-08, Vol.88 (2), p.141-148

1993

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ATAXIA‐TELANGIECTASIA: SOMATOSENSORY,‘BRAINSTEM AUDITORY. AND MOTOR EVOKED POTENTIALS IN SIX PATIENTS

Developmental medicine and child neurology, 1996-01, Vol.38 (1), p.65-73

1996

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Giant axonal neuropathy in 2 siblings: a generalized disorder of intermediate filaments

European neurology, 1991, Vol.31 (1), p.50

1991

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Autosomal recessive paraparesis with amyotrophy of hands and feet and white matter lesions

Acta neurologica Scandinavica, 1996-07, Vol.94 (1), p.60-62

1996

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A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

IL-6 detection in multiple sclerosis brain

Early synthesis and correlation of serum anti-thyroid antibodies with clinical parameters in multiple sclerosis

Interleukin-6 levels in the cerebrospinal fluid and serum of patients with Guillain-Barré syndrome and chronic inflammatory demyelinating polyradiculoneuropathy

The potential role of hepatitis C virus in the pathogenesis of the neurological syndrome in chronic hepatitis C

Detection of Borrelia burgdorferi DNA and complement membrane attack complex deposits in the sural nerve of a patient with chronic polyneuropathy and tertiary lyme disease

Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy

Involvement of peripheral sensory fibers in amyotrophic lateral sclerosis : electrophysiological study of 64 cases

Three-dimensional analysis of pulmonary nodules by MSCT with Advanced Lung Analysis (ALA1) software

Cerebrotendinous xanthomatosis (van Bogaert-Scherer-Epstein disease): CT and MR findings

Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities

Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy

Association of polyclonal anti-GM1 IgM and anti-neurofilament antibodies with CSF oligoclonal bands in a young with amyotrophic lateral sclerosis

Hypoplasia of the corpus callosum in Niemann-Pick type C disease

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy

Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)

High levels of cerebrospinal fluid IgM binding to myelin basic protein are associated with early benign course in multiple sclerosis

Neuronal intranuclear inclusion disease: neuropathologic study of a case

Cloning and sequence analysis of the human liver rhodanese: Comparison with the bovine and chicken enzymes

Neuronal intranuclear inclusion disease : polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case

Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report

Axonal motor and sensory neuropathy in myotonic dystrophy

ATAXIA‐TELANGIECTASIA: SOMATOSENSORY,‘BRAINSTEM AUDITORY. AND MOTOR EVOKED POTENTIALS IN SIX PATIENTS

Giant axonal neuropathy in 2 siblings: a generalized disorder of intermediate filaments

Autosomal recessive paraparesis with amyotrophy of hands and feet and white matter lesions

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