Mungan NÖ - Search Results

1

Erratum to `Recommendations on phenylketonuria in Turkey` [Turk J Pediatr 2022; 64: 413-434].

Coşkun T, Çoker M, Mungan NÖ, Özel HG, Sivri HS. Coşkun T, et al. Among authors: mungan no. Turk J Pediatr. 2022;64(6):1175. Turk J Pediatr. 2022. PMID: 36583907 No abstract available.

2

Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders.

Yılmaz BŞ, Ceylaner S, Mungan NÖ. Yılmaz BŞ, et al. Among authors: mungan no. Turk J Pediatr. 2021;63(2):314-318. doi: 10.24953/turkjped.2021.02.016. Turk J Pediatr. 2021. PMID: 33929122 Free article.

3

Recommendations on phenylketonuria in Turkey.

Coşkun T, Çoker M, Mungan NÖ, Özel HG, Sivri HS. Coşkun T, et al. Among authors: mungan no. Turk J Pediatr. 2022;64(3):413-434. doi: 10.24953/turkjped.2021.4098. Turk J Pediatr. 2022. PMID: 35899555 Free article.

4

Expert-opinion-based guidance for the care of children with lysosomal storage diseases during the COVID-19 pandemic: An experience-based Turkey perspective.

Akgun A, Gokcay G, Mungan NO, Sivri HS, Tezer H, Zeybek CA, Ezgu F. Akgun A, et al. Among authors: mungan no. Front Public Health. 2023 Jan 30;11:1092895. doi: 10.3389/fpubh.2023.1092895. eCollection 2023. Front Public Health. 2023. PMID: 36794069 Free PMC article. Review.

5

Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin.

Horoz OO, Mungan NO, Yildizdas D, Hergüner Ö, Ceylaner S, Kör D, Waterham H, Coskun T. Horoz OO, et al. Among authors: mungan no. J Pediatr Endocrinol Metab. 2016 Feb;29(2):227-31. doi: 10.1515/jpem-2015-0198. J Pediatr Endocrinol Metab. 2016. PMID: 26444347

6

Combination of two different homozygote mutations in Pompe disease.

Arslan A, Poyrazoğlu HG, Kiraz A, Özcan A, Işık H, Ergul AB, Mungan NÖ, Streubel B, Ceylaner S, Altuner Torun Y. Arslan A, et al. Among authors: mungan no. Pediatr Int. 2016 Mar;58(3):241-243. doi: 10.1111/ped.12873. Pediatr Int. 2016. PMID: 26946079

7

Urinary N-acetyl-beta-D-glucosaminidase activity in type I diabetes mellitus.

Mungan N, Yuksel B, Bakman M, Topaloglu AK, Ozer G. Mungan N, et al. Indian Pediatr. 2003 May;40(5):410-4. Indian Pediatr. 2003. PMID: 12768043 Free article.

8

Chromium levels in healthy and newly diagnosed type 1 diabetic children.

Karagun BS, Temiz F, Ozer G, Yuksel B, Topaloglu AK, Mungan NO, Mazman M, Karagun GM. Karagun BS, et al. Among authors: mungan no. Pediatr Int. 2012 Dec;54(6):780-5. doi: 10.1111/j.1442-200X.2012.03696.x. Epub 2012 Oct 9. Pediatr Int. 2012. PMID: 22783884

9

Glycogen storage disease type XII; an ultra rare cause of hemolytic anemia and rhabdomyolysis: one new case report.

Kara E, Kor D, Bulut FD, Hergüner Ö, Ceylaner S, Köşeci B, Burgaç E, Mungan NÖ. Kara E, et al. Among authors: mungan no. J Pediatr Endocrinol Metab. 2021 Jun 28;34(10):1335-1339. doi: 10.1515/jpem-2021-0258. Print 2021 Oct 26. J Pediatr Endocrinol Metab. 2021. PMID: 34171939

10

Diagnostic value of plasma lysosphingolipids levels in a Niemann-Pick disease type C patient with transient neonatal cholestasis.

Bulut FD, Bozbulut NE, Özalp Ö, Dalgiç B, Mungan NÖ, Koç Uçar H, Biberoğlu G. Bulut FD, et al. Among authors: mungan no. J Pediatr Endocrinol Metab. 2022 Feb 2;35(5):681-685. doi: 10.1515/jpem-2021-0580. Print 2022 May 25. J Pediatr Endocrinol Metab. 2022. PMID: 35107903

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