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American Journal of Medical Genetics. Part A|February 12, 2026
Insights Into Poikiloderma With Neutropenia: Genotypic and Phenotypic Analysis of 90 Cases With a New Case ReportMareike Becker, Lisa M Koehler, Peter H Hoeger
Frontiers in Pediatrics|March 20, 2018
Update on Genetic Conditions Affecting the Skin and the KidneysAntonia Reimer, Yinghong He, Cristina Has
Lancet (London, England)|January 17, 2017
Infantile haemangiomaChristine Léauté-Labrèze, John I Harper, Peter H Hoeger
Orphanet Journal of Rare Diseases|November 10, 2018
Mapping health care of rare diseases: the example of epidermolysis bullosa in GermanyAntonia Reimer, Leena Bruckner-Tuderman, Hagen Ott
Pediatric Dermatology|May 1, 2021
Multicentric dermatofibrosarcoma protuberans in a child with severe combined immunodeficiency due to adenosine deaminase deficiencyTatjana D Wahjudi, Heinz Kutzner, Matthias Bleeke, et al.
Pediatric Dermatology|September 14, 2022
Hereditary fibrosing poikiloderma (POIKTMP syndrome) report of a new mutation and review of the literaturePeter H Hoeger, Lisa M Koehler, Maria Reipschlaeger, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|February 17, 2025
Fulminant parvovirus B19 myocarditis in infants -report of three post-pandemic casesTatjana Wahjudi, Alex Nitsch, Jan-Peter Sperhake, et al.
European Journal of Pediatrics|September 9, 2006
Zinc-deficiency dermatitis in breast-fed infantsAntonia Kienast, Bernhard Roth, Christiane Bossier, et al.
JAAD Case Reports|July 10, 2018
Combined neodymium-doped yttrium aluminum garnet laser and sclerotherapy in Gorham-Stout syndromeMaria Reipschläger, Uwe Huebner, Joerg Seemann, et al.
Pediatric Dermatology|March 23, 2023
A call for implementing augmented intelligence in pediatric dermatologyChristopher J Issa, Antonia Reimer-Taschenbrecker, Amy S Paller
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