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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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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

1997

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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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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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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

Volltextzugriff (PDF)

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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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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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

Volltextzugriff (PDF)

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

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

1991

Volltextzugriff (PDF)

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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Choreo-acanthocytosis like phenotype without acanthocytes : clinicopathological case report : a contribution to the knowledge of the functional pathology of the caudate nucleus

Acta neuropathologica, 1993-11, Vol.86 (6), p.651-658

1993

Volltextzugriff (PDF)

A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers

Brain & development (Tokyo. 1979), 1997-04, Vol.19 (3), p.209-211

1997

Volltextzugriff (PDF)

Ultrastructural study of enteric ganglia in three patients with Rett syndrome

Brain & development (Tokyo. 1979), 1998-12, Vol.20 (8), p.586-588

1998

Volltextzugriff (PDF)

Cherry-red spot myoclonus syndrome (type I sialidosis)

Developmental neuroscience, 1991, Vol.13 (4-5), p.320

1991

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Clinicopathological study of familial late infantile Hallervorden-Spatz disease : a particular form of neuroacanthocytosis

Child's nervous system, 1996-03, Vol.12 (3), p.155-160

1996

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Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy

Brain & development (Tokyo. 1979), 1996, Vol.18 (1), p.59-63

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

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

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)

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

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

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

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

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

Choreo-acanthocytosis like phenotype without acanthocytes : clinicopathological case report : a contribution to the knowledge of the functional pathology of the caudate nucleus

A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers

Ultrastructural study of enteric ganglia in three patients with Rett syndrome

Cherry-red spot myoclonus syndrome (type I sialidosis)

Clinicopathological study of familial late infantile Hallervorden-Spatz disease : a particular form of neuroacanthocytosis

Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy

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