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

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

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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Localization of laminin α2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

Acta neuropathologica, 1997-12, Vol.94 (6), p.567-571

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.1200-1203

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

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

1994

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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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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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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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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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Axonal motor and sensory neuropathy in myotonic dystrophy

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

1993

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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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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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An unusual type of primary cerebral hemihypotrophy with signs of dysfunctional neuronal migration

Acta neuropathologica, 1996-12, Vol.92 (6), p.631-634

1996

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Serum anti-brain endothelium antibodies and cognitive assessment in patients with Binswanger's encephalopathy

Journal of the neurological sciences, 1995, Vol.128 (1), p.96-102

1995

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

European neurology, 1991, Vol.31 (1), p.50-56

1991

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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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Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy

Journal of neurology, 1995-08, Vol.242 (8), p.490-496

1995

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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

Localization of laminin α2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

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

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

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

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

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

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

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

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

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

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

Axonal motor and sensory neuropathy in myotonic dystrophy

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

Neuronal intranuclear inclusion disease: neuropathologic study of a case

An unusual type of primary cerebral hemihypotrophy with signs of dysfunctional neuronal migration

Serum anti-brain endothelium antibodies and cognitive assessment in patients with Binswanger's encephalopathy

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

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

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

Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy

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