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Evidence-based recommendations for the diagnosis and treatment of pediatric acne.
Eichenfield LF, Krakowski AC, Piggott C, Del Rosso J, Baldwin H, Friedlander SF, Levy M, Lucky A, Mancini AJ, Orlow SJ, Yan AC, Vaux KK, Webster G, Zaenglein AL, Thiboutot DM; American Acne and Rosacea Society. Eichenfield LF, et al. Among authors: levy m. Pediatrics. 2013 May;131 Suppl 3:S163-86. doi: 10.1542/peds.2013-0490B. Pediatrics. 2013. PMID: 23637225
Incontinentia pigmenti in male patients.
Pacheco TR, Levy M, Collyer JC, de Parra NP, Parra CA, Garay M, Aprea G, Moreno S, Mancini AJ, Paller AS. Pacheco TR, et al. Among authors: levy m. J Am Acad Dermatol. 2006 Aug;55(2):251-5. doi: 10.1016/j.jaad.2005.12.015. Epub 2006 May 15. J Am Acad Dermatol. 2006. PMID: 16844507
Inpatient management of epidermolysis bullosa: Consensus-based hands-on instructions for neonates and postneonates.
Abreu Molnar B, Levin L, Yun D, Morel K, Wiss K, Wieser J, Ward C, Trice H, Garcia-Romero MT, Stephenson A, Provost A, Price HN, Perman MJ, Moxon M, Moeves B, McCuaig CC, McCarthy C, Lucky AW, Levy ML, Lee M, Lara-Corrales I, Henner N, Halliburton N, Griffith E, Gorell E, Glick S, Eichenfield L, Collins C, Bruckner AL, Boulrice B, Bayliss S, Badger K, Paller AS. Abreu Molnar B, et al. Among authors: levy ml. J Am Acad Dermatol. 2024 Apr 9:S0190-9622(24)00583-8. doi: 10.1016/j.jaad.2024.04.014. Online ahead of print. J Am Acad Dermatol. 2024. PMID: 38604489
Pediatric Intensive Care Unit follow-up: thinking before acting.
Mortamet G, Birsan S, Zini J, Morin L, Kolev K, Pelluau S, Pouletty M, Thiberghien D, Beldjilali S, Brissaud O, Milési C, Brotelande C, Dupont A, Giraud M, Hassid SA, Tsapis M, Essid A, Villemain C, De Sampaio S, Troff S, Micaelli D, Levy M. Mortamet G, et al. Among authors: levy m. Anaesth Crit Care Pain Med. 2024 May 30:101401. doi: 10.1016/j.accpm.2024.101401. Online ahead of print. Anaesth Crit Care Pain Med. 2024. PMID: 38823635 Free article.
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature.
Karayol R, Borroto MC, Haghshenas S, Namasivayam A, Reilly J, Levy MA, Relator R, Kerkhof J, McConkey H, Shvedunova M, Petersen AK, Magnussen K, Zweier C, Vasileiou G, Reis A, Savatt JM, Mulligan MR, Bicknell LS, Poke G, Abu-El-Haija A, Duis J, Hannig V, Srivastava S, Barkoudah E, Hauser NS, van den Born M, Hamiel U, Henig N, Baris Feldman H, McKee S, Krapels IPC, Lei Y, Todorova A, Yordanova R, Atemin S, Rogac M, McConnell V, Chassevent A, Barañano KW, Shashi V, Sullivan JA, Peron A, Iascone M, Canevini MP, Friedman J, Reyes IA, Kierstein J, Shen JJ, Ahmed FN, Mao X, Almoguera B, Blanco-Kelly F, Platzer K, Treu AB, Quilichini J, Bourgois A, Chatron N, Januel L, Rougeot C, Carere DA, Monaghan KG, Rousseau J, Myers KA, Sadikovic B, Akhtar A, Campeau PM. Karayol R, et al. Among authors: levy ma. Am J Hum Genet. 2024 May 28:S0002-9297(24)00164-2. doi: 10.1016/j.ajhg.2024.05.001. Online ahead of print. Am J Hum Genet. 2024. PMID: 38815585
5,891 results