Canda E - Search Results

1

A Patient with MSUD: Acute Management with Sodium Phenylacetate/Sodium Benzoate and Sodium Phenylbutyrate.

Köse M, Canda E, Kagnici M, Uçar SK, Çoker M. Köse M, et al. Among authors: canda e. Case Rep Pediatr. 2017;2017:1045031. doi: 10.1155/2017/1045031. Epub 2017 May 15. Case Rep Pediatr. 2017. PMID: 28589054 Free PMC article.

2

Molecular analysis in X-linked adrenoleukodystrophy patients: identification of a novel mutation.

Durmaz A, Atik T, Onay H, Canda EE, Uçar SK, Bademkıran F, Coker M, Coğulu Ö, Özkınay F. Durmaz A, et al. Metab Brain Dis. 2014 Sep;29(3):809-12. doi: 10.1007/s11011-014-9552-1. Epub 2014 May 1. Metab Brain Dis. 2014. PMID: 24788897

3

One Year Experience of Pheburane(®) (Sodium Phenylbutyrate) Treatment in a Patient with Argininosuccinate Lyase Deficiency.

Uçar SK, Ozbaran B, Altinok YA, Kose M, Canda E, Kagnici M, Coker M. Uçar SK, et al. Among authors: canda e. JIMD Rep. 2015;19:31-3. doi: 10.1007/8904_2014_361. Epub 2015 Feb 10. JIMD Rep. 2015. PMID: 25665834 Free PMC article.

4

Previously Unreported Biallelic Mutation in DNAJC19: Are Sensorineural Hearing Loss and Basal Ganglia Lesions Additional Features of Dilated Cardiomyopathy and Ataxia (DCMA) Syndrome?

Ucar SK, Mayr JA, Feichtinger RG, Canda E, Çoker M, Wortmann SB. Ucar SK, et al. Among authors: canda e. JIMD Rep. 2017;35:39-45. doi: 10.1007/8904_2016_23. Epub 2016 Dec 8. JIMD Rep. 2017. PMID: 27928778 Free PMC article.

5

Patients with Gaucher type 1: Switching from imiglucerase to miglustat therapy.

Canda E, Kose M, Kagnici M, Ucar SK, Sozmen EY, Coker M. Canda E, et al. Blood Cells Mol Dis. 2018 Feb;68:180-184. doi: 10.1016/j.bcmd.2017.01.007. Epub 2017 Jan 16. Blood Cells Mol Dis. 2018. PMID: 28111116 No abstract available.

6

A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiency.

Yilmaz S, Serin M, Canda E, Eraslan C, Tekin H, Ucar SK, Gokben S, Tekgul H, Serdaroglu G. Yilmaz S, et al. Among authors: canda e. Metab Brain Dis. 2017 Jun;32(3):675-678. doi: 10.1007/s11011-017-9984-5. Epub 2017 Mar 9. Metab Brain Dis. 2017. PMID: 28281033

7

Preliminary Screening Results of Fabry Disease in Kidney Transplantation Patients: A Single-Center Study.

Yılmaz M, Uçar SK, Aşçı G, Canda E, Tan FA, Hoşcoşkun C, Çoker M, Töz H. Yılmaz M, et al. Among authors: canda e. Transplant Proc. 2017 Apr;49(3):420-424. doi: 10.1016/j.transproceed.2017.01.025. Transplant Proc. 2017. PMID: 28340804

8

[33 Questions about Triglycerides and Cardiovascular Effects: Expert Answers].

Çetinkalp Ş, Koylan N, Özer N, Onat A, Özgen AG, Koldaş ZL, Sain Güven G, Özdoğan Ö, Karşıdağ K, Yiğit Z, Kayıkçıoğlu M, Tokgözoğlu L, Can LH, Tartan Z, Kültürsay H, Karpuz B, Kırılmaz B, Ersanlı M, Ural D, Erbakan AN, Oğuz A, Kayıkçıoğlu ÖR, Temizhan A, Sansoy V, Ceyhan C, Öngen Z, Bayram F, Örem C, Sönmez A, Beyaz Ş, Ükinç K, Şarer Yürekli B, Çoker M, Canda E, Yıldırım Şimşir I. Çetinkalp Ş, et al. Among authors: canda e. Turk Kardiyol Dern Ars. 2017 Mar;45(Suppl 1):1-63. doi: 10.5543/tkda.2017.77459. Turk Kardiyol Dern Ars. 2017. PMID: 28446733 Free article. Turkish. No abstract available.

9

Single center experience of biotinidase deficiency: 259 patients and six novel mutations.

Canda E, Yazici H, Er E, Kose M, Basol G, Onay H, Ucar SK, Habif S, Ozkinay F, Coker M. Canda E, et al. J Pediatr Endocrinol Metab. 2018 Aug 28;31(8):917-926. doi: 10.1515/jpem-2018-0148. J Pediatr Endocrinol Metab. 2018. PMID: 29995633 Free article. Clinical Trial.

10

Coexistence of Gaucher Disease and severe congenital neutropenia.

Kose MD, Canda E, Kağnıcı M, Uçar SK, Onay H, Yıldırım Sozmen E, Karapınar D, Özkınay F, Çoker M. Kose MD, et al. Among authors: canda e. Blood Cells Mol Dis. 2019 May;76:1-6. doi: 10.1016/j.bcmd.2018.07.001. Epub 2018 Aug 10. Blood Cells Mol Dis. 2019. PMID: 30473482

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