These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
160 related items for PubMed ID: 23856930
21. Atypical Phacomatosis Pigmentokeratotica as the Expression of a Mosaic RASopathy With the BRAF-Glu586Lys Mutation. Ayala D, Ramón MD, Martín JM, Jordá E. Actas Dermosifiliogr; 2016 May; 107(4):344-6. PubMed ID: 26703821 [No Abstract] [Full Text] [Related]
22. Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia. Lim YH, Ovejero D, Sugarman JS, Deklotz CM, Maruri A, Eichenfield LF, Kelley PK, Jüppner H, Gottschalk M, Tifft CJ, Gafni RI, Boyce AM, Cowen EW, Bhattacharyya N, Guthrie LC, Gahl WA, Golas G, Loring EC, Overton JD, Mane SM, Lifton RP, Levy ML, Collins MT, Choate KA. Hum Mol Genet; 2014 Jan 15; 23(2):397-407. PubMed ID: 24006476 [Abstract] [Full Text] [Related]
23. Two distinct types of speckled lentiginous nevi characterized by macular versus papular speckles. Vidaurri-de la Cruz H, Happle R. Dermatology; 2006 Jan 15; 212(1):53-8. PubMed ID: 16319475 [Abstract] [Full Text] [Related]
24. Phacomatosis pigmentokeratotica: a patient with the rare melanocytic-epidermal twin nevus syndrome. Hermes B, Cremer B, Happle R, Henz BM. Dermatology; 1997 Jan 15; 194(1):77-9. PubMed ID: 9031800 [Abstract] [Full Text] [Related]
25. Genetic and phenotypic diversities of nevus spilus phenotypes: Case series and a proposed diagnostic algorithm. Zhang J, Xu Q, Deng D. Clin Genet; 2023 Nov 15; 104(5):593-597. PubMed ID: 37501405 [Abstract] [Full Text] [Related]
26. Phacomatosis pigmentokeratotica: A very rare twin spotting phenomenon. Karia DR, Solanki AN, Jagati AG, Shah BJ. Indian J Dermatol Venereol Leprol; 2018 Nov 15; 84(1):120. PubMed ID: 28799528 [No Abstract] [Full Text] [Related]
27. Phacomatosis pigmentokeratotica: report of new cases and further delineation of the syndrome. Tadini G, Restano L, Gonzáles-Pérez R, Gonzáles-Enseñat A, Vincente-Villa MA, Cambiaghi S, Marchettini P, Mastrangelo M, Happle R. Arch Dermatol; 1998 Mar 15; 134(3):333-7. PubMed ID: 9580120 [Abstract] [Full Text] [Related]
28. Mosaic RASopathies concept: different skin lesions, same systemic manifestations? Morren MA, Fodstad H, Brems H, Bedoni N, Guenova E, Jacot-Guillarmod M, Busiah K, Giuliano F, Gilliet M, Atallah I. J Med Genet; 2024 Apr 19; 61(5):411-419. PubMed ID: 38290824 [Abstract] [Full Text] [Related]
29. Postzygotic HRAS mutation causing both keratinocytic epidermal nevus and thymoma and associated with bone dysplasia and hypophosphatemia due to elevated FGF23. Avitan-Hersh E, Tatur S, Indelman M, Gepstein V, Shreter R, Hershkovitz D, Brick R, Bergman R, Tiosano D. J Clin Endocrinol Metab; 2014 Jan 19; 99(1):E132-6. PubMed ID: 24243633 [Abstract] [Full Text] [Related]
30. Widespread nevus spilus associated with torsion dystonia: a case report. Martí N, Jordá E, Martínez E, Gámez L, Ramón MD. Pediatr Dermatol; 2010 Jan 19; 27(6):654-6. PubMed ID: 21510006 [Abstract] [Full Text] [Related]
31. Phacomatosis pigmentokeratotica: Exploring extracutaneous comorbidities and topical therapy. Camiña-Conforto G, Ivars M, Sarquella-Brugada G, Valera-Dávila C, Salvador H, Rovira C, Baselga E. Pediatr Dermatol; 2024 Jan 19; 41(5):904-907. PubMed ID: 38621679 [Abstract] [Full Text] [Related]
32. Verrucous epidermal naevus and naevus spilus associated with lower limb asymmetry and right bundle-branch block: a case of phacomatosis pigmentokeratotica? Baroni A, Staibano S, Russo T, Piccolo V, Satriano RA, Vozza A, Vozza G. Clin Exp Dermatol; 2012 Jan 19; 37(1):74-5. PubMed ID: 21790731 [No Abstract] [Full Text] [Related]
33. Optical coherence tomography confirms non-malignant pigmented lesions in phacomatosis pigmentokeratotica using a support vector machine learning algorithm. Lee J, Beirami MJ, Ebrahimpour R, Puyana C, Tsoukas M, Avanaki K. Skin Res Technol; 2023 Jun 19; 29(6):e13377. PubMed ID: 37357662 [Abstract] [Full Text] [Related]
34. Phacomatosis pigmentokeratotica: a further case without extracutaneous anomalies and review of the condition. Chantorn R, Shwayder T. Pediatr Dermatol; 2011 Jun 19; 28(6):715-719. PubMed ID: 22082467 [Abstract] [Full Text] [Related]
35. Novel postzygotic KRAS mutation in a Japanese case of epidermal nevus syndrome presenting with two distinct clinical features, keratinocytic epidermal nevi and sebaceous nevi. Igawa S, Honma M, Minami-Hori M, Tsuchida E, Iizuka H, Ishida-Yamamoto A. J Dermatol; 2016 Jan 19; 43(1):103-4. PubMed ID: 26498739 [No Abstract] [Full Text] [Related]
36. Phacomatosis pigmentokeratotica without extracutaneous abnormalities: a case study involving a preterm baby. Oh GN, Kim JY, Choi JE, Ahn HH, Kye YC, Seo SH. J Korean Med Sci; 2012 Nov 19; 27(11):1444-6. PubMed ID: 23166433 [Abstract] [Full Text] [Related]
37. Gene Mutation Mapping in a Fatal Case of Phacomatosis Pigmentokeratotica Happle. Hayani K, Giehl K, Kumbrink J, Fischer J, Schlaak M, French LE, Wollenberg A. Acta Derm Venereol; 2020 Aug 18; 100(15):adv00241. PubMed ID: 32725253 [Abstract] [Full Text] [Related]
38. Phacomatosis pigmentokeratotica associated with hemihypertrophy and a rhabdomyosarcoma of the abdominal wall. Gruson LM, Orlow SJ, Schaffer JV. J Am Acad Dermatol; 2006 Aug 18; 55(2 Suppl):S16-20. PubMed ID: 16843117 [Abstract] [Full Text] [Related]
39. Agminated Spitz nevus arising in normal skin with redundant HRAS mutation. Pontoizeau J, Stefan A, Comoz F, Houlier A, Haddad V, Pissaloux D, de la Fouchardiere A. Eur J Dermatol; 2017 Feb 01; 27(1):73-74. PubMed ID: 27694096 [No Abstract] [Full Text] [Related]
40. Familial papular epidermal nevus with "skyline" basal cell layer. Brena M, Besagni F, Boneschi V, Tadini G. Pediatr Dermatol; 2014 Feb 01; 31(1):e33-5. PubMed ID: 24274825 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]