Publications by authors named "A Dusser"

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Movement disorders in patients with alternating hemiplegia: "Soft" and "stiff" at the same time.
Eleni Panagiotakaki, Diane Doummar, Erika Nogue, Nicolas Nagot, Gaetan Lesca, Anne Dusser

Neurology· March 2020

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Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiency.
Frédérique Sabourdy, Lionel Mourey, Emmanuelle Le Trionnaire, Nathalie Bednarek, Catherine Caillaud, Anne Dusser

Orphanet J Rare Dis· March 2015

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Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures.
Gaelle Thierry, Claire Bénéteau, Olivier Pichon, Elisabeth Flori, Bertrand Isidor, Anne Dusser

Am J Med Genet A· July 2012

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Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females.
Christel Depienne, Oriane Trouillard, Delphine Bouteiller, Isabelle Gourfinkel-An, Karine Poirier, Anne Dusser

Hum Mutat· January 2011

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[Diagnostic trap and difficulties of genetic counseling in a family with neuromuscular disease carriers].
G Lesca, E Ollagnon-Roman, J Lachanat, A Dusser, P Edery

Arch Pediatr· September 2001

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