Zobrazeno 1 - 10
of 68
pro vyhledávání: '"I, Moraillon"'
Autor:
Michel Rybojad, M.D. Vignon-Pennamen, V. Baudoin, S. Cambiaghi, I. Moraillon, Patrice Morel, C. Loirat
Publikováno v:
British Journal of Dermatology. 135:124-127
Omenn's reticulosis is an inherited severe combined immunodeficiency characterized by neonatal exfoliative erythroderma. A newborn baby who had minimal change nephrotic syndrome and Omenn's reticulosis is reported. Abnormalities in lymphocyte functio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::374955e00bb592e2f82dc19e92b20ccb
https://doi.org/10.1111/j.1365-2133.1996.tb03623.x
https://doi.org/10.1111/j.1365-2133.1996.tb03623.x
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 142:S542
Introduction La maladie de Meleda (MM) est une keratodermie palmo-plantaire (KPP) genetique rare, decrite initialement sur l’ile croate de Meleda, en rapport avec des mutations du gene SLURP-1 . Cette KPP autosomique recessive, diffuse, transgredie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::382a2a23cefcd7114bbd5a38e9b1a278
https://doi.org/10.1016/j.annder.2015.10.254
https://doi.org/10.1016/j.annder.2015.10.254
Autor:
M.D. Vignon-Pennamen, Patrice Morel, Michel Rybojad, S. Cambiaghi, I. Moraillon, C. Blanchet-Bardon
Publikováno v:
British Journal of Dermatology. 135:340-342
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75566caa4421b6f55dfa69d12700a70c
https://doi.org/10.1111/j.1365-2133.1996.tb01189.x
https://doi.org/10.1111/j.1365-2133.1996.tb01189.x
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 139:B173-B174
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7e35e36ff5464d4f7dadb2691ad7d8b
https://doi.org/10.1016/j.annder.2012.10.276
https://doi.org/10.1016/j.annder.2012.10.276
Publikováno v:
Annales de dermatologie et de venereologie. 129(2)
Polyarteritis nodosa is a necrotizing vasculitis of small and medium-size arteries. The cutaneous form of polyarteritis nodosa follows a chronic course, characterized by recurrent episodes limited to skin, muscles and joints. This entity differs from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f9782d30972f139a538e36f27091850
https://pubmed.ncbi.nlm.nih.gov/11937959
https://pubmed.ncbi.nlm.nih.gov/11937959
Autor:
F. Guibal, Matthieu Resche-Rigon, M Baccard, I Moraillon, C. Juillard, Florence Cordoliani, D. Lehucher-Ceyrac, A.-M. Heudes, Martine Bagot, F. Ramel
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 141:S249
Introduction Le risque de depression induit par l’isotretinoine est sujet a controverse. Nous rapportons les resultats de la premiere etude prospective controlee en pratique de ville utilisant le score Adolescent Depression Rating Scale (ADRS) chez
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba75a529b44402d01d6bab4ad981efd
https://doi.org/10.1016/j.annder.2014.09.066
https://doi.org/10.1016/j.annder.2014.09.066
Publikováno v:
Annales de dermatologie et de venereologie. 126(4)
Congenital cutis laxa is an exceptional condition. No large scale series has been reported in the French literature. We report 5 cases observed between 1993 and 1997.Five children with a morphotype compatible with congenital generalized cutis laxa we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1aaee85a429f3ba2038a91befb0fc07
https://pubmed.ncbi.nlm.nih.gov/10421933
https://pubmed.ncbi.nlm.nih.gov/10421933
Publikováno v:
Annales de dermatologie et de venereologie. 126(1)
We report a case of a large blue mongolian spot which led to early diagnosis of Hurler's syndrome. This association is uncommon and should be recognized by dermatologists for early diagnosis and management.A male infant from Guinea, born to first-cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccd6e191f6f587aca40ff01b9b0bb8fd
https://pubmed.ncbi.nlm.nih.gov/10095889
https://pubmed.ncbi.nlm.nih.gov/10095889
Autor:
M, Rybojad, G, Ducloy, J L, Reymond, I, Moraillon, B, Flageul, M D, Vignon-Pennamen, P, Morel, E, Bourrat
Publikováno v:
Annales de dermatologie et de venereologie. 126(1)
Excepting the endemic foliaceus form, childhood pemphigus is uncommon. We report two cases of pemphigus foliaceus in children with typical clinical manifestations.Case n(o) 1. A 5-year-old girl was seen for a vesiculobullous crusted dermatosis involv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e29d0af8954c4e6dc61d6249866d3a6b
https://pubmed.ncbi.nlm.nih.gov/10095891
https://pubmed.ncbi.nlm.nih.gov/10095891
Publikováno v:
Annales de dermatologie et de venereologie. 125(12)
Giant axonal neuropathy is an autosomal recessive condition characterized by progressive degeneration of the central and peripheral nervous system. Sensoromotor neuropathy develops around 3 years of age. Children have particular faces with curly hair
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::173431c5c1d80c49a9a2caf931f8c3fd
https://pubmed.ncbi.nlm.nih.gov/9922862
https://pubmed.ncbi.nlm.nih.gov/9922862