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201 results

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Page 1
Alport syndrome: Expanding diagnosis and treatment.
Huang HX, Tsai IJ, Greenbaum LA. Huang HX, et al. Among authors: greenbaum la. Pediatr Neonatol. 2024 Oct 30:S1875-9572(24)00191-8. doi: 10.1016/j.pedneo.2024.10.005. Online ahead of print. Pediatr Neonatol. 2024. PMID: 39521677 Free article.
Management of childhood onset nephrotic syndrome.
Gipson DS, Massengill SF, Yao L, Nagaraj S, Smoyer WE, Mahan JD, Wigfall D, Miles P, Powell L, Lin JJ, Trachtman H, Greenbaum LA. Gipson DS, et al. Among authors: greenbaum la. Pediatrics. 2009 Aug;124(2):747-57. doi: 10.1542/peds.2008-1559. Epub 2009 Jul 27. Pediatrics. 2009. PMID: 19651590
Atypical hemolytic uremic syndrome.
Greenbaum LA. Greenbaum LA. Adv Pediatr. 2014 Aug;61(1):335-56. doi: 10.1016/j.yapd.2014.04.001. Epub 2014 May 17. Adv Pediatr. 2014. PMID: 25037136 Review. No abstract available.
Renin Angiotensin System Blocker Fetopathy: A Midwest Pediatric Nephrology Consortium Report.
Nadeem S, Hashmat S, Defreitas MJ, Westreich KD, Shatat IF, Selewski DT, Onder AM, Chiang M, Weaver DJ Jr, Steinke J, Barcia J, Hernandez J, Hidalgo G, Ingraham SE, Abitbol CL, Pan C, Greenbaum LA. Nadeem S, et al. Among authors: greenbaum la. J Pediatr. 2015 Oct;167(4):881-5. doi: 10.1016/j.jpeds.2015.05.045. Epub 2015 Jun 27. J Pediatr. 2015. PMID: 26130112
Nephrotic Syndrome.
Wang CS, Greenbaum LA. Wang CS, et al. Among authors: greenbaum la. Pediatr Clin North Am. 2019 Feb;66(1):73-85. doi: 10.1016/j.pcl.2018.08.006. Pediatr Clin North Am. 2019. PMID: 30454752 Review.
Diagnosis, Treatment, and Outcomes in Children With Congenital Nephrogenic Diabetes Insipidus: A Pediatric Nephrology Research Consortium Study.
D'Alessandri-Silva C, Carpenter M, Ayoob R, Barcia J, Chishti A, Constantinescu A, Dell KM, Goodwin J, Hashmat S, Iragorri S, Kaspar C, Mason S, Misurac JM, Muff-Luett M, Sethna C, Shah S, Weng P, Greenbaum LA, Mahan JD. D'Alessandri-Silva C, et al. Among authors: greenbaum la. Front Pediatr. 2020 Jan 21;7:550. doi: 10.3389/fped.2019.00550. eCollection 2019. Front Pediatr. 2020. PMID: 32039113 Free PMC article.
Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations.
Cason RK, Williams A, Chryst-Stangl M, Wu G, Huggins K, Brathwaite KE, Lane BM, Greenbaum LA, D'Agati VD, Gbadegesin RA. Cason RK, et al. Among authors: greenbaum la. Front Pediatr. 2022 Jul 7;10:915174. doi: 10.3389/fped.2022.915174. eCollection 2022. Front Pediatr. 2022. PMID: 35874595 Free PMC article.
Clinical presentation and management of nephrotic syndrome in the first year of life: A report from the Pediatric Nephrology Research Consortium.
Constantinescu AR, Mattoo TK, Smoyer WE, Greenbaum LA, Niu J, Howard N, Muff-Luett M, Benoit EB, Traum A, Annaim AA, Wenderfer SE, Plautz E, Rheault MN, Myette RL, Twombley KE, Kamigaki Y, Wandique-Rapalo B, Kallash M, Vasylyeva TL. Constantinescu AR, et al. Among authors: greenbaum la. Front Pediatr. 2022 Sep 14;10:988945. doi: 10.3389/fped.2022.988945. eCollection 2022. Front Pediatr. 2022. PMID: 36210940 Free PMC article.
201 results