Ryabets-Lienhard A - Search Results

1

Obesity Management in Youth with Duchenne Muscular Dystrophy: A Review of Metformin and Alternative Pharmacotherapies.

Goldman V, Ryabets-Lienhard A, Howard L, Kohli R, Sousa E, Patel P, Marpuri I, Vidmar AP. Goldman V, et al. Among authors: ryabets lienhard a. Child Obes. 2024 Oct 11. doi: 10.1089/chi.2024.0297. Online ahead of print. Child Obes. 2024. PMID: 39392010 Review.

2

Pediatric Endocrine Society Statement on Considerations for Use of Teplizumab (Tzield™) in Clinical Practice.

Mehta S, Ryabets-Lienhard A, Patel N, Breidbart E, Libman I, Haller MJ, Simmons KM, Sims EK, DiMeglio LA, Gitelman SE, Griffin KJ, Tonyushkina KN. Mehta S, et al. Among authors: ryabets lienhard a. Horm Res Paediatr. 2024 Apr 30:1-12. doi: 10.1159/000538775. Online ahead of print. Horm Res Paediatr. 2024. PMID: 38663372 Free article.

3

Cushing Syndrome in Childhood.

Parish A, Cheung C, Ryabets-Lienhard A, Zamiara P, Kim MS. Parish A, et al. Among authors: ryabets lienhard a. Pediatr Rev. 2024 Jan 1;45(1):14-25. doi: 10.1542/pir.2022-005732. Pediatr Rev. 2024. PMID: 38161162 Review.

4

A Novel De Novo Frameshift Pathogenic Variant in the FAM111B Resulting in Progressive Osseous Heteroplasia Phenotype.

Ryabets-Lienhard A, Panjawatanan P, Vogt K, Ji J, Georgia S, Pitukcheewanont P. Ryabets-Lienhard A, et al. Calcif Tissue Int. 2023 Apr;112(4):518-523. doi: 10.1007/s00223-022-01053-0. Epub 2022 Dec 27. Calcif Tissue Int. 2023. PMID: 36575358

5

A Unique Case of Aggressive Central Giant Cell Granuloma in a 10-Year-Old Boy With 16p13.11 Microdeletion Syndrome.

Shum BJ, Kim MS, Kondra K, Hammoudeh JA, Strom C, Ryabets-Lienhard A. Shum BJ, et al. Among authors: ryabets lienhard a. J Investig Med High Impact Case Rep. 2022 Jan-Dec;10:23247096221123146. doi: 10.1177/23247096221123146. J Investig Med High Impact Case Rep. 2022. PMID: 36154495 Free PMC article.

6

Evaluating RANKL and OPG levels in patients with Duchenne muscular dystrophy.

Akhtar Ali S, Kang H, Olney R, Ramos-Platt L, Ryabets-Lienhard A, Cheung C, Georgia S, Pitukcheewanont P. Akhtar Ali S, et al. Among authors: ryabets lienhard a. Osteoporos Int. 2019 Nov;30(11):2283-2288. doi: 10.1007/s00198-019-05077-5. Epub 2019 Aug 7. Osteoporos Int. 2019. PMID: 31392399

7

Quantifying RANKL and OPG levels in healthy children: A large cross-sectional analysis.

Akhtar Ali S, Kang H, Olney R, Ramos-Platt L, Ryabets-Lienhard A, Georgia S, Pitukcheewanont P. Akhtar Ali S, et al. Among authors: ryabets lienhard a. Bone. 2019 Oct;127:215-219. doi: 10.1016/j.bone.2019.06.012. Epub 2019 Jun 15. Bone. 2019. PMID: 31212033 Free PMC article.

8

Meeting Report: 2018 Annual Meeting of the Pediatric Endocrine Society, Toronto, Canada, May 5-8, 2018, Selected Highlights.

Ryabets-Lienhard A, Akhtar S, Monzavi R, Austin J. Ryabets-Lienhard A, et al. Pediatr Endocrinol Rev. 2018 Dec;16(2):284-293. doi: 10.17458/per.vol16.2018.lama.mr.pestoronto. Pediatr Endocrinol Rev. 2018. PMID: 30556661

9

A case of severe TBCE-negative hypoparathyroidism-retardation-dysmorphism syndrome: Case report and literature review.

Ryabets-Lienhard A, Issaranggoon Na Ayuthaya S, Graham JM, Pitukcheewanont P. Ryabets-Lienhard A, et al. Am J Med Genet A. 2018 Aug;176(8):1768-1772. doi: 10.1002/ajmg.a.38851. Epub 2018 Jul 28. Am J Med Genet A. 2018. PMID: 30055029

10

The Optic Nerve Hypoplasia Spectrum: Review of the Literature and Clinical Guidelines.

Ryabets-Lienhard A, Stewart C, Borchert M, Geffner ME. Ryabets-Lienhard A, et al. Adv Pediatr. 2016 Aug;63(1):127-46. doi: 10.1016/j.yapd.2016.04.009. Adv Pediatr. 2016. PMID: 27426898 Review. No abstract available.

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