P. Ribaï

发表

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

P. Bauer, P. Ribai, M. Pandolfo, 2006, Neurogenetics.

Observing Huntington’s Disease: the European Huntington’s Disease Network’s REGISTRY

Alexander Münchau, Caroline Hallam, Andrea Ciarmiello, 2011, PLoS currents.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patients.

M. Vidailhet, A. Dürr, A. Brice, 2007, Archives of neurology.

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

R. Kiss, C. Decaestecker, I. Salmon, 1999, The Journal of rheumatology.

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

R. Kiss, C. Decaestecker, I. Salmon, 1999, Clinical and experimental rheumatology.

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

M. Ruberg, A. Durr, S. Forlani, 2006, Journal of Medical Genetics.

Mental deficiency in three families with SPG4 spastic paraplegia

A. Durr, C. Depienne, A. Brice, 2008, European Journal of Human Genetics.

A clinical scoring system for congenital contractural arachnodactyly

A. Green, Alison M. Male, F. McKenzie, 2019, Genetics in Medicine.

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

B. Legros, P. Tugendhaft, P. Ribaï, 2006, Journal of Neurology.

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

S. Rivaud-Pechoux, M. Koenig, A. Dürr, 2007, Archives of neurology.

NMDA receptor gene variations as modifiers in Huntington disease: a replication study

J. Schiefer, R. Barker, R. Reilmann, 2011, PLoS currents.

Hereditary Spastic Paraplegia Exon Deletions of SPG 4 are a Frequent Cause of

M. Ruberg, S. Forlani, C. Depienne, 2006 .

Brachial plexus neuritis: is prognosis worse in children?

P. van Bogaert, D. Verheulpen, P. Ribaï, 2004, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.