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Pediatric Dermatology|December 21, 2000
Coexistence of disseminated superficial porokeratosis in childhood with congenital linear porokeratosisD H Suh, H S Lee, S D Kim, et al.Pediatric Dermatology|December 16, 2022
Cutaneous lesions and mitochondrial hearing loss: A case reportEster Moreno-Artero, Teresa Imizcoz, Carlos Prieto, et al.Pediatric Dermatology|January 2, 2023
Cutaneous presentation of bullous multisystem inflammatory syndrome in a child: A diagnosis not to "MIS-C"Nadia S El-Hamdi, Nicole N Dacy, Shannon C Brown, et al.Pediatric Dermatology|January 4, 2023
Annular erythema of infancy: A rare and challenging diagnosisSophia Ly, Mavinder Guram, Nicholas Zoumberos, et al.Pediatric Dermatology|November 21, 2022
Enterokinase deficiency with novel TMPRSS15 gene mutation masquerading as acrodermatitis enteropathicaYusha Chen, Zhongtao Li, Chuangwen Liu, et al.Pediatric Dermatology|March 1, 1994
Infantile systemic hyalinosis in a black infantE E Sahn, C F Salinas, M A Sens, et al.Pediatric Dermatology|September 1, 1995
Unilateral Beau's lines in childhood reflex sympathetic dystrophyE A O'Toole, S Gormally, B Drumm, et al.Pediatric Dermatology|September 1, 1995
Congenital apocrine hamartoma: an unusual clinical variant of organoid nevus with apocrine differentiationJ J Herrmann, L R EramoPageof 629