Publications by authors named "Fatima Rouan"

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Plectin deficient epidermolysis bullosa simplex with 27-year-history of muscular dystrophy.
Yoshie Takahashi, Fatima Rouan, Jouni Uitto, Akemi Ishida-Yamamoto, Hajime Iizuka

J Dermatol Sci· February 2005

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Severe mucous membrane involvement in epidermolysis bullosa simplex with muscular dystrophy due to a novel plectin gene mutation.
Ulrike Schara, Jens Tücke, Wilhelm Mortier, Thomas Nüsslein, Fatima Rouan

Eur J Pediatr· April 2004

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Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations.
Gabriele Richard, Nkecha Brown, Fatima Rouan, Jan-Gerrit Van der Schroeff, Emilia Bijlsma

J Invest Dermatol· April 2003

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Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy.
Rolf Schröder, Wolfram S Kunz, Fatima Rouan, Ellen Pfendner, Karen Tolksdorf

J Neuropathol Exp Neurol· June 2002

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Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.
Gabriele Richard, Fatima Rouan, Colin E Willoughby, Nkecha Brown, Pil Chung

Am J Hum Genet· May 2002

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