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GENODERMATOSIS EN COCARDA DE DEGOS = GENODERMATOSE EN COCARDE DE DEGOSENRIQUE LUINI R; ALTOPIEDI A; JOSE MANGANO O et al.1973; ARCH. ARGENT. DERMATOL.; ARGENT.; DA. 1973; VOL. 23; NO 4; PP. 46-48Article

Photosensibilité: quand évoquer une génodermatose ?LORETTE, Gérard.Les Nouvelles dermatologiques. 2012, Vol 31, Num SEP, pp 24-27, issn 0752-5370, 4 p., CAH2Article

Genodermatoses with profound malignant potentialTOKAR, I. P; FRASER, M. C; BALE, S. J et al.Seminars in oncology nursing. 1992, Vol 8, Num 4, pp 272-280, issn 0749-2081Article

Erythrokeratodermia anularis migrans : eine neue Genodermatose ?VAKILZADEH, F; ROSE, I.Hautarzt. 1991, Vol 42, Num 10, pp 634-637, issn 0017-8470Article

ERYTHROKERATODERMIE VARIABLE. GENODERMATOSE EN COCARDE. ETUDE ULTRASTRUCTURALE. EFFET FAVORABLE DE L'ETRETINATEREYMOND JL; BEANI JC; STOEBNER P et al.1982; ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE; ISSN 0151-9638; FRA; DA. 1982; VOL. 109; NO 9; PP. 805-806; BIBL. 3 REF.Article

Genodermatoses in paediatric age groupKUMAR, S; SHARMA, R. C.Indian Journal of Dermatology Venereology and Leprology. 1996, Vol 62, Num 4, pp 235-236, issn 0378-6323Article

Rothmund-Thomson syndrome in fraternal twins. Case reportsTONG, M.Pediatric dermatology. 1995, Vol 12, Num 2, pp 134-137, issn 0736-8046Article

Maladie de Dowling-Degos : amélioration sous acitrétine = Dowling Degos disease: a case report improving on acitretinDINET, Y; DELESCLUSE, J.Les Nouvelles dermatologiques. 1990, Vol 9, Num 7, pp 556-557, issn 0752-5370, 2 p.Article

Trichoépithéliomes multiples familiaux: nouvelle mutation du gène CYLD = Multiple familial trichoepithelioma: A new CYLD gene mutationDUPARC, A; LASEK-DURIEZ, A; WIART, T et al.Annales de dermatologie et de vénéréologie. 2013, Vol 140, Num 4, pp 274-277, issn 0151-9638, 4 p.Article

Retikuläre pigmentdermatose der beugen. M. Dowling-Degos vom intertriginösen Typ in Assoziation mit Acne inversa = Reticulated pigmented anomaly of the flexures. M. Dowling-Degos disease in association with acne inversaKLEEMAN, D; TRÜEB, R. M; SCHMID-GRENDELMEIER, P et al.Hautarzt. 2001, Vol 52, Num 7, pp 642-645, issn 0017-8470Article

Muir-Torr syndrome in patients with hematologic malignanciesCOHEN, P. R.American journal of hematology. 1992, Vol 40, Num 1, pp 64-65, issn 0361-8609Article

Diagnosis in dysmorphology: clues from the skinSMITHSON, S. F; WINTER, R. M.British journal of dermatology (1951). 2004, Vol 151, Num 5, pp 953-960, issn 0007-0963, 8 p.Article

Maladies dermatologiques chroniques: le défi des parents soignants ? = Chronic skin diseases: The challenge for the caring parents?DUFRESNE, Hélène; HADJ-RABIA, Smail; BODEMER, Christine et al.Medecine palliative. 2010, Vol 9, Num 1, pp 10-12, issn 1636-6522, 3 p.Conference Paper

Progress in heritable skin diseases: Molecular bases and clinical implicationsPULKKINEN, Leena; RINGPFEIL, Franziska; UITTO, Jouni et al.Journal of the American Academy of Dermatology. 2002, Vol 47, Num 1, pp 91-104, issn 0190-9622Article

Les troubles mentaux de la maladie de Darier. Discussion = Mental disorders of Darier's illness. DiscussionBOUR, F; KOSADINOS, E; HACHE, E et al.Annales médico-psychologiques. 2006, Vol 164, Num 8, pp 696-701, issn 0003-4487, 6 p.Conference Paper

Epidermolysis bullosa with congenital pyloric atresia: Novel mutations in the β4 integrin gene (ITGB4) and genotype/phenotype correlationsNAKANO, Aoi; PULKKINEN, Leena; MURRELL, Dedee et al.Pediatric research. 2001, Vol 49, Num 5, pp 618-626, issn 0031-3998Article

Tricho-épithéliomes multiples et dystrophie unguéale congénitale chez deux frères = Trichoepithelioma multiplex and dystrophia unguis congenita in two brothersYEDOMON, H. G; DO ANGO-PADONOU, F; BOURLOND, A et al.Annales de dermatologie et de vénéréologie. 1991, Vol 118, Num 2, pp 119-120, issn 0151-9638, 2 p.Article

X-Linked Ichthyosis along with Recessive Dystrophic Epidermolysis Bullosa in the Same PatientHERNANDEZ-MARTIN, A; CUADRADO-CORRALES, N; CIRIA-ABAD, S et al.Dermatology (Basel). 2010, Vol 221, Num 2, pp 113-116, issn 1018-8665, 4 p.Article

Recherche de gènes responsables de génodermatoses : Exemple de la kératodermie naso-plantaire chez le dogue de bordeaux = Identification of genes involved in genodermatoses : Example of naso-plantar keratodermia in the french breed dogue de bordeauxANDRE, Catherine; GUAGUERE, Eric; THOMAS, Anne et al.Bulletin de l'Académie vétérinaire de France. 2007, Vol 160, Num 3, pp 245-250, issn 0001-4192, 6 p.Article

Progress towards genetic and pharmacological therapies for keratin genodermatoses: current perspective and future promiseCHRISTOPHER CHAMCHEU, Jean; WOOD, Gary S; SIDDIQUI, Imtiaz A et al.Experimental dermatology. 2012, Vol 21, Num 7, pp 481-489, issn 0906-6705, 9 p.Article

Klinik und Ätiologie der Ichthyosen: Grundlage der neuen Nomenklatur und Klassifikation = Clinical presentation and etiology of ichthyoses · Overview of the new nomenclature and classificationOJI, V.Der Hautarzt. 2010, Vol 61, Num 10, pp 891-902, issn 0017-8470, 12 p.Article

Kindler-Syndrom Eine neue bullöse Dermatose : Bullöse Dermatosen = Kindler syndrome. A new bullous dermatosis : Bullous dermatosesHAS, C.Der Hautarzt. 2009, Vol 60, Num 8, pp 622-626, issn 0017-8470, 5 p.Article

An unusual Ala12Thr polymorphism in the 1A α-helical segment of the companion layer-specific keratin K6hf: Evidence for a risk factor in the etiology of the common hair disorder pseudofolliculitis barbaeWINTER, Hermelita; SCHISSEL, Daniel; WILDE, Joseph et al.Journal of investigative dermatology. 2004, Vol 122, Num 3, pp 652-657, issn 0022-202X, 6 p.Article

Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasiaHARRISON, Shannon; SINCLAIR, Rodney.Australasian journal of dermatology. 2004, Vol 45, Num 2, pp 103-105, issn 0004-8380, 3 p.Article

Incontinentia Pigmenti ou syndrome de Bloch-Sulzberçer : A propos d'un cas = Incontinentia pitmenti or bloch-sulzberter syndrome : Case reportCHHOUL, Hakima; EL HASSAN, Aziz Moulay; AMEZIANE, Rachida et al.RFOP Revue francophone d'odontologie pédiatrique. 2006, Vol 1, Num 3, pp 164-168, issn 1954-5010, 5 p.Article

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