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Scale for the assessment and rating of ataxia: development of a new clinical scale

Neurology, 2006-06, Vol.66 (11), p.1717-1720

2006

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Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms

Neurology, 2008-09, Vol.71 (13), p.982-989

2008

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Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

Journal of medical genetics, 2007-04, Vol.44 (4), p.281-284

2007

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

Neurology, 2006-01, Vol.66 (1), p.112-114

2006

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Chorea associated with anti-phospholipid antibodies: case report

Acta clinica belgica (English ed. Online), 2010-09, Vol.65 (5), p.350-353

2010

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A new phenotype linked to SPG27 and refinement of the critical region on chromosome

Journal of neurology, 2006-06, Vol.253 (6), p.714-719

2006

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Acute Balint's syndrome is not always caused by a stroke

European journal of neurology, 2006-03, Vol.13 (3), p.310-312

2006

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Usefulness of prolonged video-EEG monitoring and provocative procedure with saline injection for the diagnosis of non epileptic seizures of psychogenic origin

Journal of neurology, 2006-03, Vol.253 (3), p.328-332

2006

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A novel locus for autosomal dominant uncomplicated hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3

Human genetics, 2007-11, Vol.122 (3-4), p.261-273

2007

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Second polar body inclusion results in diploid/triploid mixoploidy

Genetic counseling, 2003, Vol.14 (4), p.425

2003

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A new phenotype linked to SPG27 and refinement of the critical region on chromosome 10

Journal of neurology, 2006-06, Vol.253 (6), p.714-719

2006

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Congenital stationary night blindness: Report of an autosomal recessive family and linkage analysis

American journal of medical genetics, 2005-01, Vol.132A (1), p.76-79

2005

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Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up

Archives of neurology (Chicago), 2007-04, Vol.64 (4), p.558

2007

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A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene

Neurogenetics, 2006-05, Vol.7 (2), p.131-132

2006

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Transient cerebral arteriopathy in infancy associated with enteroviral infection

European journal of paediatric neurology, 2003-01, Vol.7 (2), p.73-75

2003

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D-mannose and N-acetylglucosamine moieties and their respective binding sites in salivary glands of Sjögren's syndrome

Journal of rheumatology, 1999-04, Vol.26 (4), p.833

1999

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Sialic acid residues in the labial salivary glands from Sjögren's syndrome patients

Clinical and experimental rheumatology, 1999-11, Vol.17 (6), p.713

1999

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Brachial plexus neuritis: is prognosis worse in children?

European journal of paediatric neurology, 2004-01, Vol.8 (3), p.165-165

2004

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Genetic analysis of candidate genes modifying the age-at-onset in Huntington's Disease: results of a large European association study

Aktuelle Neurologie, 2005, Vol.32 (S 4)

2005

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CHOREA ASSOCIATED WITH ANTI-PHOSPHOLIPID ANTIBODIES: CASE REPORT

Acta Clinica Belgica, 2010, Vol.65 (5), p.350-353

2010

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Acute Balint's syndrome is not always caused by a stroke

European journal of neurology, 2006, Vol.13 (3), p.310-312

2006

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Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6

Movement disorders, 2008-11, Vol.23 (15), p.2232-2238

2008

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Scale for the assessment and rating of ataxia: development of a new clinical scale

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms

Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

Chorea associated with anti-phospholipid antibodies: case report

A new phenotype linked to SPG27 and refinement of the critical region on chromosome

Acute Balint's syndrome is not always caused by a stroke

Usefulness of prolonged video-EEG monitoring and provocative procedure with saline injection for the diagnosis of non epileptic seizures of psychogenic origin

A novel locus for autosomal dominant uncomplicated hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3

Second polar body inclusion results in diploid/triploid mixoploidy

A new phenotype linked to SPG27 and refinement of the critical region on chromosome 10

Congenital stationary night blindness: Report of an autosomal recessive family and linkage analysis

Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up

A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene

The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease

Transient cerebral arteriopathy in infancy associated with enteroviral infection

D-mannose and N-acetylglucosamine moieties and their respective binding sites in salivary glands of Sjögren's syndrome

Sialic acid residues in the labial salivary glands from Sjögren's syndrome patients

Brachial plexus neuritis: is prognosis worse in children?

Genetic analysis of candidate genes modifying the age-at-onset in Huntington's Disease: results of a large European association study

CHOREA ASSOCIATED WITH ANTI-PHOSPHOLIPID ANTIBODIES: CASE REPORT

Acute Balint's syndrome is not always caused by a stroke

Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6

Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings

Self-rated health status in spinocerebellar ataxia-Results from a European multicenter study

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