Vural M - Search Results

1

Correction: Clinical indicators that influence a clinician's decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia.

Yilmaz A, Ozer Y, Kaya N, Cakir AD, Culpan HC, Perk Y, Vural M, Evliyaoglu O. Yilmaz A, et al. Among authors: vural m. Ital J Pediatr. 2023 Sep 29;49(1):130. doi: 10.1186/s13052-023-01539-z. Ital J Pediatr. 2023. PMID: 37775837 Free PMC article. No abstract available.

2

Clinical indicators that influence a clinician's decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia.

Yilmaz A, Ozer Y, Kaya N, Cakir AD, Culpan HC, Perk Y, Vural M, Evliyaoglu O. Yilmaz A, et al. Among authors: vural m. Ital J Pediatr. 2023 Aug 29;49(1):105. doi: 10.1186/s13052-023-01516-6. Ital J Pediatr. 2023. PMID: 37644575 Free PMC article.

3

Evaluating of neonatal early onset sepsis through lactate and base excess monitoring.

Yilmaz A, Kaya N, Gonen I, Uygur A, Perk Y, Vural M. Yilmaz A, et al. Among authors: vural m. Sci Rep. 2023 Sep 8;13(1):14837. doi: 10.1038/s41598-023-41776-0. Sci Rep. 2023. PMID: 37684308 Free PMC article.

4

Long-term neurodevelopmental effects of exclusively high cord lactate levels in term newborn.

Yilmaz A, Cebi MN, Yilmaz G, Karacaoglu G, Aydin SN, Perk Y, Vural M. Yilmaz A, et al. Among authors: vural m. J Matern Fetal Neonatal Med. 2023 Dec;36(2):2284115. doi: 10.1080/14767058.2023.2284115. Epub 2023 Nov 21. J Matern Fetal Neonatal Med. 2023. PMID: 37989542 Free article.

5

Periviable Birth: Between Ethical and Legal Frameworks.

Koc E, Unal S, Vural M. Koc E, et al. Among authors: vural m. J Pediatr. 2024 Sep;272:114143. doi: 10.1016/j.jpeds.2024.114143. Epub 2024 Jun 12. J Pediatr. 2024. PMID: 38876154 No abstract available.

6

An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant.

Yüksel Ülker A, Uludağ Alkaya D, Çağlayan AO, Usluer E, Aykut A, Aslanger A, Vural M, Tüysüz B. Yüksel Ülker A, et al. Among authors: vural m. Am J Med Genet A. 2023 Jun;191(6):1530-1545. doi: 10.1002/ajmg.a.63180. Epub 2023 Mar 15. Am J Med Genet A. 2023. PMID: 36919607

7

Natural history and genetic spectrum of the Turkish metaphyseal dysplasia cohort, including rare types caused by biallelic COL10A1, COL2A1, and LBR variants.

Tüysüz B, Kasap B, Sarıtaş M, Alkaya DU, Bozlak S, Kıykım A, Durmaz A, Yıldırım T, Akpınar E, Apak H, Vural M. Tüysüz B, et al. Among authors: vural m. Bone. 2023 Feb;167:116614. doi: 10.1016/j.bone.2022.116614. Epub 2022 Nov 15. Bone. 2023. PMID: 36400164

8

Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes.

Tuysuz B, Uludag Alkaya D, Geyik F, Alaylıoğlu M, Kasap B, Kurugoğlu S, Akman YE, Vural M, Bilguvar K. Tuysuz B, et al. Among authors: vural m. J Med Genet. 2023 Aug;60(8):819-826. doi: 10.1136/jmg-2022-108763. Epub 2022 Dec 21. J Med Genet. 2023. PMID: 36543534

9

Biocomposites of 2D layered materials.

Vural M, Demirel MC. Vural M, et al. Nanoscale Horiz. 2025 Jan 16. doi: 10.1039/d4nh00530a. Online ahead of print. Nanoscale Horiz. 2025. PMID: 39815818 Review.

10

Navigating Resistance and Adaptation in Health Care: How Pediatricians Can Balance Transformation and Children's Needs.

Pettoello-Mantovani M, Bali D, Giardino I, Vural M, Indrio F, Buonocore G, Pastore M. Pettoello-Mantovani M, et al. Among authors: vural m. J Pediatr. 2024 Dec 24:114446. doi: 10.1016/j.jpeds.2024.114446. Online ahead of print. J Pediatr. 2024. PMID: 39725310 No abstract available.

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