Cansever MS - Search Results

1

Altered immune response in organic acidemia.

Altun I, Kiykim A, Zubarioglu T, Burtecene N, Hopurcuoglu D, Topcu B, Cansever MS, Kiykim E, Cokugras HC, Aktuglu Zeybek AC. Altun I, et al. Among authors: cansever ms. Pediatr Int. 2022 Jan;64(1):e15082. doi: 10.1111/ped.15082. Pediatr Int. 2022. PMID: 34861062

2

Determination of NTBC in serum samples from patients with hereditary tyrosinemia type I by capillary electrophoresis.

Cansever MS, Aktuğlu-Zeybek AC, Erim FB. Cansever MS, et al. Talanta. 2010 Mar 15;80(5):1846-8. doi: 10.1016/j.talanta.2009.10.032. Epub 2009 Oct 24. Talanta. 2010. PMID: 20152421

3

Biotinidase deficiency mimicking primary immune deficiencies.

Kiykim E, Kiykim A, Cansever MS, Zeybek CA. Kiykim E, et al. Among authors: cansever ms. BMJ Case Rep. 2015 May 8;2015:bcr2014209275. doi: 10.1136/bcr-2014-209275. BMJ Case Rep. 2015. PMID: 25956498 Free PMC article.

4

Screening Mucopolysaccharidosis Type IX in Patients with Juvenile Idiopathic Arthritis.

Kiykim E, Barut K, Cansever MS, Zeybek CA, Zubarioglu T, Aydin A, Kasapcopur O. Kiykim E, et al. Among authors: cansever ms. JIMD Rep. 2016;25:21-24. doi: 10.1007/8904_2015_467. Epub 2015 Jun 30. JIMD Rep. 2016. PMID: 26122630 Free PMC article.

5

Neonatal nonketotic hyperglycinemia: diffusion-weighted magnetic resonance imaging and diagnostic clues.

Zubarioglu T, Kiykim E, Cansever MS, Aktuglu Zeybek C, Yalcinkaya C. Zubarioglu T, et al. Among authors: cansever ms. Acta Neurol Belg. 2016 Dec;116(4):671-673. doi: 10.1007/s13760-015-0583-0. Epub 2015 Dec 24. Acta Neurol Belg. 2016. PMID: 26702626 No abstract available.

6

Clinical and neuroradiological approach to fucosidosis in a child with atypical presentation.

Zubarioglu T, Kiykim E, Zeybek CA, Cansever MS, Benbir G, Aydin A, Yalcinkaya C. Zubarioglu T, et al. Among authors: cansever ms. Ann Indian Acad Neurol. 2015 Oct-Dec;18(4):471-4. doi: 10.4103/0972-2327.160090. Ann Indian Acad Neurol. 2015. PMID: 26713028 Free PMC article.

7

Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation.

Zubarioglu T, Kiykim E, Cansever MS, Aktuglu Zeybek C. Zubarioglu T, et al. Among authors: cansever ms. Indian J Pediatr. 2016 Jul;83(7):754-5. doi: 10.1007/s12098-016-2077-3. Epub 2016 Apr 1. Indian J Pediatr. 2016. PMID: 27037922 No abstract available.

8

Evaluation of dynamic thiol/disulphide homeostasis as a novel indicator of oxidative stress in maple syrup urine disease patients under treatment.

Zubarioglu T, Kiykim E, Cansever MS, Neselioglu S, Aktuglu-Zeybek C, Erel O. Zubarioglu T, et al. Among authors: cansever ms. Metab Brain Dis. 2017 Feb;32(1):179-184. doi: 10.1007/s11011-016-9898-7. Epub 2016 Aug 18. Metab Brain Dis. 2017. PMID: 27535382

9

Hereditary Tyrosinemia Type 1 in Turkey.

Aktuglu-Zeybek AC, Kiykim E, Cansever MS. Aktuglu-Zeybek AC, et al. Among authors: cansever ms. Adv Exp Med Biol. 2017;959:157-172. doi: 10.1007/978-3-319-55780-9_15. Adv Exp Med Biol. 2017. PMID: 28755194 Review.

10

Early diagnosed cerebrotendinous xanthomatosis patients: clinical, neuroradiological characteristics and therapy results of a single center from Turkey.

Zubarioglu T, Kiykim E, Yesil G, Demircioglu D, Cansever MS, Yalcinkaya C, Aktuglu-Zeybek C. Zubarioglu T, et al. Among authors: cansever ms. Acta Neurol Belg. 2019 Sep;119(3):343-350. doi: 10.1007/s13760-017-0851-2. Epub 2017 Oct 22. Acta Neurol Belg. 2019. PMID: 29058268

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