Kılıç M - Search Results

1

First manifestation of citrullinemia type I as Sandifer syndrome.

Kılıç M, Altınel-Açoğlu E, Zorlu P, Yüksel D, Bülbül S, Haeberle J. Kılıç M, et al. Turk J Pediatr. 2017;59(6):696-698. doi: 10.24953/turkjped.2017.06.013. Turk J Pediatr. 2017. PMID: 30035404 Free article.

Kilic M, Altinel-Acoglu E, Zorlu P, Yuksel D, Bulbul S, Haeberle J. First manifestation of citrullinemia type I as Sandifer syndrome. ...

Kilic M, Altinel-Acoglu E, Zorlu P, Yuksel D, Bulbul S, Haeberle J. First manifestation of citrullinemia type I as Sandifer sy …

2

3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures.

Coşkun T, Aydin HI, Kiliç M, Dursun A, Haliloğlu G, Topaloğlu H, Karli-Oğuz K, de Koning TJ. Coşkun T, et al. Among authors: kilic m. Turk J Pediatr. 2009 Nov-Dec;51(6):587-92. Turk J Pediatr. 2009. PMID: 20196394

3

A novel mutation in the DGUOK gene in a Turkish newborn with mitochondrial depletion syndrome.

Kiliç M, Sivri HS, Dursun A, Tokatli A, De Meirleir L, Seneca S, Akçören Z, Yiğit S, Topaloğlu H, Coşkun T. Kiliç M, et al. Turk J Pediatr. 2011 Jan-Feb;53(1):79-82. Turk J Pediatr. 2011. PMID: 21534344

4

Conventional and advanced MR imaging in infantile Refsum disease.

Kılıç M, Karlı-Oğuz K, Haliloğlu G, Topçu M, Wanders RJ, Coşkun T. Kılıç M, et al. Turk J Pediatr. 2015 May-Jun;57(3):294-9. Turk J Pediatr. 2015. PMID: 26701952

5

Hypoalbuminemia and Malnutrition Associated With Cow's Milk Allergy: A Case Report.

Altinel Acoglu E, Akcaboy M, Melek Oguz M, Kilic M, Zorlu P, Senel S. Altinel Acoglu E, et al. Among authors: kilic m. Iran Red Crescent Med J. 2016 May 17;18(6):e34810. doi: 10.5812/ircmj.34810. eCollection 2016 Jun. Iran Red Crescent Med J. 2016. PMID: 27621935 Free PMC article.

6

Successful treatment of a patient with ethylmalonic encephalopathy by intravenous N-acetylcysteine.

Kılıç M, Dedeoğlu Ö, Göçmen R, Kesici S, Yüksel D. Kılıç M, et al. Metab Brain Dis. 2017 Apr;32(2):293-296. doi: 10.1007/s11011-016-9928-5. Epub 2016 Nov 9. Metab Brain Dis. 2017. PMID: 27830356

7

A patient with mitochondrial disorder due to a novel mutation in MRPS22.

Kılıç M, Oğuz KK, Kılıç E, Yüksel D, Demirci H, Sağıroğlu MŞ, Yücel-Yılmaz D, Özgül RK. Kılıç M, et al. Among authors: kilic e. Metab Brain Dis. 2017 Oct;32(5):1389-1393. doi: 10.1007/s11011-017-0074-5. Epub 2017 Jul 27. Metab Brain Dis. 2017. PMID: 28752220

8

PMM2-CDG and sensorineural hearing loss.

Kasapkara ÇS, Barış Z, Kılıç M, Yüksel D, Keldermans L, Matthijs G, Jaeken J. Kasapkara ÇS, et al. Among authors: kilic m. J Inherit Metab Dis. 2017 Sep;40(5):629-630. doi: 10.1007/s10545-017-0073-z. Epub 2017 Jul 31. J Inherit Metab Dis. 2017. PMID: 28762107 No abstract available.

9

Primary trimethylaminuria (fish odor syndrome) and hypothyroidism in an adolescent.

Kılıç M. Kılıç M. Turk J Pediatr. 2017;59(5):614-616. doi: 10.24953/turkjped.2017.05.020. Turk J Pediatr. 2017. PMID: 29745129 Free article.

10

Nonketotic hyperglycinemia: Clinical range and outcome of a rare neurometabolic disease in a single-center.

Genç Sel Ç, Kılıç M, Yüksel D, Aksoy A, Kasapkara ÇS, Ceylaner S, Oğuz KK. Genç Sel Ç, et al. Among authors: kilic m. Brain Dev. 2018 Nov;40(10):865-875. doi: 10.1016/j.braindev.2018.06.007. Epub 2018 Jun 19. Brain Dev. 2018. PMID: 29929752

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