Hereditary Palmoplantar Keratodermas;Hereditäre Palmoplantarhyperkeratosen

JDDG - Journal of the German Society of Dermatology

Volumn 7, Issue 11, 2009, Pages 971-984

  Braun Falco, Markus ^a  

^a UNIVERSITY OF MUNICH   (Germany)

Author keywords

Cathepsins; Connexins; Cornified envelope; Cytokeratins; Desmosomes; Epidermal differentiation; Genodermatosis

Indexed keywords

CATHEPSIN; GAP JUNCTION PROTEIN; KERATIN; LORICRIN;

ACROKERATOELASTOSIS; ARTICLE; CARDIOMYOPATHY; CARVAJAL SYNDROME; CELL DIFFERENTIATION; COLLAGEN DISEASE; CONGENITAL PACHYONYCHIA; CONGENITAL SKIN DISEASE; DESMOSOME; DIAGNOSTIC PROCEDURE; DISEASE CLASSIFICATION; EPIDERMIS CELL; ERYTHROKERATODERMA FIGURATA VARIABILIS; ESOPHAGUS CARCINOMA; FOCAL PALMOPLANTAR; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GINGIVAL KERATOSIS; GREITHER DISEASE; HEARING IMPAIRMENT; HIDROTIC ECTODERMAL DYSPLASIA; HUMAN; HURIEZ SYNDROME; KERATODERMA; KERATOSIS PALMOPLANTARIS DIFFUSA; KERATOSIS PALMOPLANTARIS MUTILANS; KERATOSIS PALMOPLANTARIS PAPULOSA; KERATOSIS PALMOPLANTARIS STRIATA; KERATOSIS PALMOPLANTARIS TRANSGREDIENS ET PROGREDIENS; KLICK SYNDROME; LORICRIN KERATODERMA; NAEGELI FRANCESCHETTI JADASSOHN SYNDROME; NAXOS SYNDROME; NEOPLASM; OCULOCUTANEOUS TYROSINEMIA; OLMSTED SYNDROME; PALMOPLANTAR KERATODERMA; PAPILLON LEFEVRE SYNDROME; PATHOPHYSIOLOGY; PROTEIN DEFECT; PROTEIN FUNCTION; PROTEIN STRUCTURE; PUNCTATE PALMOPLANTAR KERATODERMA; SCHOPF SCHULZ PASSARGE SYNDROME; SKIN FRAGILITY SYNDROME; SYNDROME KID; TOOTH MALFORMATION;

DERMATOLOGIC AGENTS; HUMANS; KERATODERMA, PALMOPLANTAR; OINTMENTS; RETINOIDS;

EID: 70350490794     PISSN: 16100379     EISSN: 16100387     Source Type: Journal    
DOI: 10.1111/j.1610-0387.2009.07058.x     Document Type: Article

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