Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
Alef, Thomas, Torres, Serena, Hausser, Ingrid, Metze, Dieter, Türsen, Ümit, Lestringant, Gilles G., Hennies, Hans Christian
Published in Journal of investigative dermatology (01.04.2009)
Published in Journal of investigative dermatology (01.04.2009)
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Journal Article
Pathogenicity of POFUT1 in Dowling-Degos Disease: Additional Mutations and Clinical Overlap with Reticulate Acropigmentation of Kitamura
Buket Basmanav, F., Fritz, Günter, Lestringant, Gilles G., Pachat, Divya, Hoffjan, Sabine, Fischer, Johannes, Wehner, Maria, Wolf, Sabrina, Thiele, Holger, Altmüller, Janine, Pulimood, Susanne A., Rütten, Arno, Kruse, Roland, Hanneken, Sandra, Frank, Jorge, Danda, Sumita, Bygum, Anette, Betz, Regina C.
Published in Journal of investigative dermatology (01.02.2015)
Published in Journal of investigative dermatology (01.02.2015)
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Journal Article
Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates
ECKL, Katja Martina, STEVENS, Howard P, REIS, André, HENNIES, Hans Christian, LESTRINGANT, Gilles G, WESTENBERGER-TREUMANN, Margaretha, TRAUPE, Heiko, HINZ, Britta, FROSSARD, Philippe M, STADLER, Rudolf, LEIGH, Irene M, NÜRNBERG, Peter
Published in Human genetics (2003)
Published in Human genetics (2003)
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Journal Article
Junctional epidermolysis bullosa in the Middle East: Clinical and genetic studies in a series of consanguineous families
Nakano, Aoi, Lestringant, Gilles G., Paperna, Tamar, Bergman, Reuven, Gershoni, Ruth, Frossard, Philippe, Kanaan, Moien, Meneguzzi, Guerrino, Richard, Gabriele, Pfendner, Ellen, Uitto, Jouni, Pulkkinen, Leena, Sprecher, Eli
Published in Journal of the American Academy of Dermatology (01.04.2002)
Published in Journal of the American Academy of Dermatology (01.04.2002)
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Journal Article
Identification, by Homozygosity Mapping, of a Novel Locus for Autosomal Recessive Congenital Ichthyosis on Chromosome 17p, and Evidence for Further Genetic Heterogeneity
Krebsová, Alice, Küster, Wolfgang, Lestringant, Gilles G., Schulze, Bernt, Hinz, Britta, Frossard, Philippe M., Reis, André, Hennies, Hans Christian
Published in American journal of human genetics (01.07.2001)
Published in American journal of human genetics (01.07.2001)
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Journal Article
l-2-hydroxyglutaric aciduria in two siblings
Sztriha, László, Gururaj, Aithala, Vreken, Peter, Nork, Michael, Lestringant, Gilles G
Published in Pediatric neurology (01.08.2002)
Published in Pediatric neurology (01.08.2002)
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Journal Article
Human renin gene BglI dimorphism associated with hypertension in two independent populations
Frossard, Philippe M, Lestringant, Gilles G, Malloy, Mary J, Kane, John P
Published in Clinical genetics (01.12.1999)
Published in Clinical genetics (01.12.1999)
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Journal Article
Association of an Apolipoprotein B Gene Marker With Essential Hypertension
Frossard, Philippe M, Obineche, Enyioma N, Lestringant, Gilles G
Published in Hypertension (Dallas, Tex. 1979) (01.04.1999)
Published in Hypertension (Dallas, Tex. 1979) (01.04.1999)
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Journal Article
Conference Proceeding
Associations of angiotensinogen gene mutations with hypertension and myocardial infarction in a gulf population
Frossard, Philippe M, Hill, Susan H, Elshahat, Yassin I, Obineche, Eniyoma N, Bokhari, Awais M, Lestringant, Gilles G, John, Anne, Abdulle, Abdishakur M
Published in Clinical genetics (01.10.1998)
Published in Clinical genetics (01.10.1998)
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Journal Article
Allergic contact dermatitis in the United Arab Emirates
Lestringant, Gilles G., Bener, Abdulbari, Sawaya, Maha, Galadari, Ibrahim H., Frossard, Philippe M.
Published in International journal of dermatology (01.03.1999)
Published in International journal of dermatology (01.03.1999)
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Journal Article