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Autosomal dominant lamellar ichthyosis due to a missense mutation in the gene NKPD1.
Komlosi K, Glocker C, Hsu-Rehder HH, Alter S, Kopp J, Hotz A, Zimmer AD, Hausser-Siller I, Sandhoff R, Oji V, Fischer J. Komlosi K, et al. Among authors: hotz a. J Invest Dermatol. 2024 Apr 18:S0022-202X(24)00303-8. doi: 10.1016/j.jid.2024.03.041. Online ahead of print. J Invest Dermatol. 2024. PMID: 38642798 Free article.
Categorization of a Universal Coding System to Distinguish Use of Durable Medical Equipment and Supplies in Pediatric Patients.
Hotz A, Sprecher E, Bastianelli L, Rodean J, Stringfellow I, Barkoudah E, Cohen LE, Estrada C, Graham R, Greenwood J, Kyle J, Mann N, Pinkham M, Solari T, Rosen R, Saleeb S, Shah AS, Watters K, Wells S, Berry JG. Hotz A, et al. JAMA Netw Open. 2023 Oct 2;6(10):e2339449. doi: 10.1001/jamanetworkopen.2023.39449. JAMA Netw Open. 2023. PMID: 37874565 Free PMC article.
Reduced Postdischarge Incidents After Implementation of a Hospital-to-Home Transition Intervention for Children With Medical Complexity.
Huth K, Hotz A, Emara N, Robertson B, Leaversuch M, Mercer AN, Khan A, Campos ML, Liss I, Hahn PD, Graham DA, Rossi L, Thomas MV, Elias N, Morris M, Glader L, Pinkham A, Bardsley KM, Wells S, Rogers J, Berry JG, Mauskar S, Starmer AJ. Huth K, et al. Among authors: hotz a. J Patient Saf. 2023 Oct 1;19(7):493-500. doi: 10.1097/PTS.0000000000001155. Epub 2023 Sep 5. J Patient Saf. 2023. PMID: 37729645
Reflective multi-immersion microscope objectives inspired by the Schmidt telescope.
Voigt FF, Reuss AM, Naert T, Hildebrand S, Schaettin M, Hotz AL, Whitehead L, Bahl A, Neuhauss SCF, Roebroeck A, Stoeckli ET, Lienkamp SS, Aguzzi A, Helmchen F. Voigt FF, et al. Among authors: hotz al. Nat Biotechnol. 2024 Jan;42(1):65-71. doi: 10.1038/s41587-023-01717-8. Epub 2023 Mar 30. Nat Biotechnol. 2024. PMID: 36997681 Free PMC article.
Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis.
Hotz A, Kopp J, Bourrat E, Oji V, Süßmuth K, Komlosi K, Bouadjar B, Tantcheva-Poór I, Hellström Pigg M, Betz RC, Giehl K, Schedel F, Weibel L, Schulz S, Stölzl DV, Tadini G, Demiral E, Berggard K, Zimmer AD, Alter S, Fischer J. Hotz A, et al. Genes (Basel). 2023 Mar 15;14(3):717. doi: 10.3390/genes14030717. Genes (Basel). 2023. PMID: 36980989 Free PMC article.
67 results