Sagi L - Search Results

1

Glucagon-like peptide-1 analog therapy in rare genetic diseases: monogenic obesity, monogenic diabetes, and spinal muscular atrophy.

Zaitoon H, Lubetzky R, Amir AZ, Moran-Lev H, Sagi L, Yacobi-Bach M, Borger O, Chorna E, Lebenthal Y, Brener A. Zaitoon H, et al. Among authors: sagi l. Acta Diabetol. 2023 Aug;60(8):1099-1108. doi: 10.1007/s00592-023-02109-9. Epub 2023 May 9. Acta Diabetol. 2023. PMID: 37160786 Review.

2

Clinical significance of the parental origin of the X chromosome in turner syndrome.

Sagi L, Zuckerman-Levin N, Gawlik A, Ghizzoni L, Buyukgebiz A, Rakover Y, Bistritzer T, Admoni O, Vottero A, Baruch O, Fares F, Malecka-Tendera E, Hochberg Z. Sagi L, et al. J Clin Endocrinol Metab. 2007 Mar;92(3):846-52. doi: 10.1210/jc.2006-0158. Epub 2006 Dec 27. J Clin Endocrinol Metab. 2007. PMID: 17192299

3

Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3.

Sellick GS, Longman C, Brockington M, Mahjneh I, Sagi L, Bushby K, Topaloğlu H, Muntoni F, Houlston RS. Sellick GS, et al. Among authors: sagi l. Hum Genet. 2005 Jul;117(2-3):207-12. doi: 10.1007/s00439-005-1301-4. Epub 2005 May 11. Hum Genet. 2005. PMID: 15886997

4

The endocrine manifestations of spinal muscular atrophy, a real-life observational study.

Brener A, Lebenthal Y, Shtamler A, Levy S, Stein R, Fattal-Valevski A, Sagi L. Brener A, et al. Among authors: sagi l. Neuromuscul Disord. 2020 Apr;30(4):270-276. doi: 10.1016/j.nmd.2020.02.011. Epub 2020 Feb 24. Neuromuscul Disord. 2020. PMID: 32273202

5

Insulin-like growth factor-1 status is associated with insulin resistance in young patients with spinal muscular atrophy.

Brener A, Sagi L, Shtamler A, Levy S, Fattal-Valevski A, Lebenthal Y. Brener A, et al. Among authors: sagi l. Neuromuscul Disord. 2020 Nov;30(11):888-896. doi: 10.1016/j.nmd.2020.09.025. Epub 2020 Sep 20. Neuromuscul Disord. 2020. PMID: 33071067

6

Nutritional Therapy in Children With Spinal Muscular Atrophy in the Era of Nusinersen.

Yerushalmy-Feler A, Levy D, Sagi L, Fattal-Valevski A, Shiff YE, Brener A, Cohen S. Yerushalmy-Feler A, et al. Among authors: sagi l. J Pediatr Gastroenterol Nutr. 2021 Jun 1;72(6):e154-e160. doi: 10.1097/MPG.0000000000003055. J Pediatr Gastroenterol Nutr. 2021. PMID: 33492038

7

Choosing Life with Spinal Muscular Atrophy Type 1.

Lavie M, Nisnkorn H, Sagi L, Amirav I. Lavie M, et al. Among authors: sagi l. Adv Ther. 2020 May;37(5):1708-1713. doi: 10.1007/s12325-020-01340-y. Epub 2020 Apr 18. Adv Ther. 2020. PMID: 32306245 Free PMC article.

8

Nusinersen for spinal muscular atrophy type 1: Real-world respiratory experience.

Lavie M, Diamant N, Cahal M, Sadot E, Be'er M, Fattal-Valevski A, Sagi L, Domany KA, Amirav I. Lavie M, et al. Among authors: sagi l. Pediatr Pulmonol. 2021 Jan;56(1):291-298. doi: 10.1002/ppul.25140. Epub 2020 Nov 5. Pediatr Pulmonol. 2021. PMID: 33111497

9

Nonrespiratory complications of nusinersen-treated spinal muscular atrophy type 1 patients.

Lavie M, Rochman M, Sagi L, Yerushalmy Feler A, Ovadia D, Cahal M, Be'er M, Sadot E, Fattal-Valevski A, Amirav I. Lavie M, et al. Among authors: sagi l. Pediatr Pulmonol. 2022 Mar;57(3):686-694. doi: 10.1002/ppul.25795. Epub 2022 Jan 3. Pediatr Pulmonol. 2022. PMID: 34921596

10

Muscle microRNAs in the cerebrospinal fluid predict clinical response to nusinersen therapy in type II and type III spinal muscular atrophy patients.

Magen I, Aharoni S, Yacovzada NS, Tokatly Latzer I, Alves CRR, Sagi L, Fattal-Valevski A, Swoboda KJ, Katz J, Bruckheimer E, Nevo Y, Hornstein E. Magen I, et al. Among authors: sagi l. Eur J Neurol. 2022 Aug;29(8):2420-2430. doi: 10.1111/ene.15382. Epub 2022 Jun 7. Eur J Neurol. 2022. PMID: 35510740 Free PMC article.

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