La kératodermie palmo-plantaire type Méléda: à propos de dix-neuf cas = Palmoplantar transgrediens Keratodermia (Meleda). A report of nineteen casesZAHAF, A; CHARFI, C; BAKLOUTI, A et al.La Semaine des hôpitaux de Paris. 1987, Vol 63, Num 14, pp 1043-1046, issn 0037-1777Article

Kératodermie palmoplantaire aquagénique idiopathique = Idiopathic aquagenic wrinkling of the palmsTROTOT, C; STUDER, M; WATON, J et al.Annales de dermatologie et de vénéréologie. 2012, Vol 139, Num 5, pp 412-413, issn 0151-9638, 2 p.Article

Nonmutilating palmoplantar and periorificial kertoderma: a variant of Olmsted syndrome or a distinct entity?NOFAL, Ahmad; ASSAF, Magda; NASSAR, Amani et al.International journal of dermatology. 2010, Vol 49, Num 6, pp 658-665, issn 0011-9059, 8 p.Article

Peut-on traiter chirurgicalement le Mal de Meleda (kératodermie palmoplantaire diffuse de Siemens) ? = Surgical treatment of keratosis palmaris in Mal de MeledaMARCHAC, A; BLANCHET-BARDON, C; REVOL, M et al.Annales de chirurgie plastique et esthétique. 2009, Vol 54, Num 2, pp 152-155, issn 0294-1260, 4 p.Article

Papillon-Lefèvre syndromeNGUYEN, T. Q; GREER, K. E; FISHER, G. B. JR et al.Journal of the American Academy of Dermatology. 1986, Vol 15, Num 1, pp 46-49, issn 0190-9622Article

A case of Olmsted syndromeVOSYNIOTI, Vasiliki; KOSMADAKI, Maria; TAGKA, Anna et al.EJD. European journal of dermatology. 2010, Vol 20, Num 6, pp 837-838, issn 1167-1122, 2 p.Article

Haim Munk syndrome and Papillon Lefevre syndrome ― allelic mutations in cathepsin C with variation in phenotypeRAI, Reena; THIAGARAJAN, S; MOHANDAS, Soumya et al.International journal of dermatology. 2010, Vol 49, Num 5, pp 541-543, issn 0011-9059, 3 p.Article

Mutations de la kératine k6c dans les kératodermies palmoplantaires focales = Keratin k6c mutations in focal palmoplantar keratodermaDEREURE, O.Annales de dermatologie et de vénéréologie. 2010, Vol 137, Num 5, pp 423-424, issn 0151-9638, 2 p.Article

Lichen nitidus palmoplantaire Une cause rare de kératodermie palmoplantaire = Palmoplantar lichen nitidus: a rare cause of palmoplantar hyperkeratosisTHIBAUDEAU, A; MAILLARD, H; CROUE, A et al.Annales de dermatologie et de vénéréologie. 2004, Vol 131, Num 8-9, pp 822-824, issn 0151-9638, 3 p.Article

Scléroatrophie d'Huriez = Huriez syndromeBESSIS, D.Images en dermatologie. 2010, Vol 3, Num 4, pp 120-121, issn 1964-4167, 2 p.Article

Palmoplantar Keratoderma and Skin Grafting : Postsurgical Long-term Follow-up of Two Cases with Olmsted SyndromeBEDARD, Marie-Sophie; POWELL, Julie; LABERGE, Louise et al.Pediatric dermatology. 2008, Vol 25, Num 2, pp 223-229, issn 0736-8046, 7 p.Article

Le syndrome de Richner-Hanhart: à propos d'un cas familial = The Richner-Hanhart syndrome: a familial caseCHACHIA, N; KHAYRALLAH, M; HAMMAMI, M et al.Ophtalmologie (Paris). 1993, Vol 7, Num 4, pp 322-324, issn 0989-3105Article

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratodermaPOHLER, Elizabeth; MAMAI, Ons; GOH, Christabelle S. M et al.Nature genetics. 2012, Vol 44, Num 11, pp 1272-1276, issn 1061-4036, 5 p.Article

Mutilating keratodermaSCHAMROTH, J. M.International journal of dermatology. 1986, Vol 25, Num 4, pp 249-251, issn 0011-9059Article

Exome Sequencing Reveals Mutations in TRPV3 as a Cause of Olmsted SyndromeZHIMIAO LIN; QUAN CHEN; PENG ZHANG et al.American journal of human genetics. 2012, Vol 90, Num 3, pp 558-564, issn 0002-9297, 7 p.Article

Enfermedad de Thost-Unna. Consideraciones con motivo de una observación familiar = Thost-Una diseaseMIRANDA ROMERO, A; SANCHEZ-JACOB, I; DEL POZO HERNANDEZ, L. J et al.Actas dermo-sifiliográficas (Ed. impresa). 1989, Vol 80, Num 8, pp 599-603, issn 0001-7310, 5 p.Article

An Unusual Case of Palmoplantar KeratodermaGULDBAKKE, Kjetil K. S; NULDT-NYSTROM, Theis; MJONES, Patricia et al.Archives of dermatology (1960). 2010, Vol 146, Num 12, issn 0003-987X, 1419-1420, 1422-1423 [4 p.]Article

Olmsted syndrome : a case report and review of literatureJUAN TAO; HUANG, Chang-Zheng; ZHOU, You-Wen et al.International journal of dermatology. 2008, Vol 47, Num 5, pp 432-437, issn 0011-9059, 6 p.Article

Evidence for a Founder Mutation in the Cathepsin C Gene in Three Families with Papillon-Lefèvre SyndromeKURBAN, Mazen; WAJID, Muhammad; SHIMOMURA, Yutaka et al.Dermatology (Basel). 2009, Vol 219, Num 4, pp 289-294, issn 1018-8665, 6 p.Article

Aquadynie, prurit, urticaire et kératodermie palmo-plantaire aquagéniques : PEAU, MER ET SOLEIL = Aquadynia, aquagenic pruritus, aquagenic urticaria and aquagenic palmoplantar keratodermaMISERY, Laurent.Les Nouvelles dermatologiques. 2011, Vol 30, Num JUN, pp 328-330, issn 0752-5370, 3 p., CAH1Article

New Evidence for the Correlation of the p.G130V Mutation in the GJB2 Gene and Syndromic Hearing Loss With Palmoplantar KeratodermaIOSSA, Sandra; CHINETTI, Viviana; FRANZE, Annamaria et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 4, pp 685-688, issn 1552-4825, 4 p.Article

Papillon-Lefevre Syndrome and Malignant Melanoma : A High Incidence of Melanoma Development in Japanese Palmoplantar Keratoderma PatientsNAKAJIMA, Koji; NAKANO, Hajime; TAKIYOSHI, Noriko et al.Dermatology (Basel). 2008, Vol 217, Num 1, pp 58-62, issn 1018-8665, 5 p.Article

L'excès est pernicieux en tout genreBODEMER, C.Les Nouvelles dermatologiques. 2008, Vol 27, Num 2, pp 10-13, issn 0752-5370, 4 p., NSConference Paper

Richner hanhart syndromeJANAKIRAMAN, Lalitha; SATHIYASEKARAN, Malathi; DEENADAYALAN, Munirathiram et al.Indian journal of pediatrics. 2006, Vol 73, Num 2, pp 161-162, issn 0019-5456, 2 p.Article

Les kératodermies palmo-plantaires héréditaires = Hereditary palmoplantar keratodermaMOKNI, M; TRIKI, S; GUEDAMSI, S et al.Médecine et chirurgie du pied. 2005, Vol 21, Num 1, pp 14-30, issn 0759-2280, 17 p.Article