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Pediatric Dermatology|October 28, 2008
A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome?Tamara Lazic, Kimberly A Horii, Gabriele Richard, et al.Pediatric Dermatology|October 28, 2008
Microphthalmia with linear skin defects: a case report and reviewVishakha M Sharma, Arlene M Ruiz de Luzuriaga, Darrel Waggoner, et al.Pediatric Dermatology|March 1, 1991
Childhood scleromyositis: an overlap syndrome associated with PM-Scl antibodyM Błaszczyk, S Jabłońska, W Szymańska-Jagiełło, et al.Pediatric Dermatology|September 30, 2005
Progressive hemifacial atrophy with linear sclerodermaEmine Dervis, Emel DervisPediatric Dermatology|September 30, 2005
Ecthyma gangrenosum-like lesions in a healthy child after infection treated with antibioticsTomoaki Ishikawa, Yoshihiko Sakurai, Maki Tanaka, et al.Pediatric Dermatology|September 30, 2005
Successful treatment of refractory childhood pemphgus vulgaris with anti-CD20 monoclonal antibody (rituximab)Heidi H Kong, Neil S Prose, Russell E Ware, et al.Pediatric Dermatology|May 29, 2004
Dermatitis artefacta in pediatric patients: experience at the national institute of pediatricsMarimar Saez-de-Ocariz, Luz Orozco-Covarrubias, Ignacio Mora-Magaña, et al.Pediatric Dermatology|May 29, 2004
Three children with CD30 cutaneous anaplastic large cell lymphomas bearing the t(2;5)(p23;q35) translocationMolly Hinshaw, Andrea B Trowers, Eric Kodish, et al.Pediatric Dermatology|May 29, 2004
Dermatologic signs of biotin deficiency leading to the diagnosis of multiple carboxylase deficiencyKatia Seymons, Anja De Moor, Hendrik De Raeve, et al.Pediatric Dermatology|May 29, 2004
An unusual case of factitious onychodystrophyJack L Lesher, Christopher M Peterson, Joshua E LanePageof 624