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Turner syndrome phenotype with 47,XXX karyotype: further investigation warranted?
Wallerstein R, Musen E, McCarrier J, Aisenberg J, Chartoff A, Hutcheon RG, Tepperberg J, Pappenhausen P, Griffin S. Wallerstein R, et al. Among authors: aisenberg j. Am J Med Genet A. 2004 Feb 15;125A(1):106-7. doi: 10.1002/ajmg.a.20362. Am J Med Genet A. 2004. PMID: 14755478 No abstract available.
Atypical GH insensitivity syndrome and severe insulin-like growth factor-I deficiency resulting from compound heterozygous mutations of the GH receptor, including a novel frameshift mutation affecting the intracellular domain.
Aisenberg J, Auyeung V, Pedro HF, Sugalski R, Chartoff A, Rothenberg R, Derr MA, Hwa V, Rosenfeld RG. Aisenberg J, et al. Horm Res Paediatr. 2010;74(6):406-11. doi: 10.1159/000314968. Epub 2010 Jul 7. Horm Res Paediatr. 2010. PMID: 20606392
Management of pediatric patients with type 1 diabetes.
Ghanny S, Aisenberg J. Ghanny S, et al. Among authors: aisenberg j. Pediatr Ann. 2014 Mar;43(3):115-20. doi: 10.3928/00904481-20140221-11. Pediatr Ann. 2014. PMID: 24605859 Review. No abstract available.
Longitudinal Changes in Continuous Glucose Monitoring Use Among Individuals With Type 1 Diabetes: International Comparison in the German and Austrian DPV and U.S. T1D Exchange Registries.
Miller KM, Hermann J, Foster N, Hofer SE, Rickels MR, Danne T, Clements MA, Lilienthal E, Maahs DM, Holl RW; T1D Exchange and DPV Registries. Miller KM, et al. Diabetes Care. 2020 Jan;43(1):e1-e2. doi: 10.2337/dc19-1214. Epub 2019 Oct 31. Diabetes Care. 2020. PMID: 31672703 Free PMC article. No abstract available.
88 results