Karatas E - Search Results

1

Brain malformation, neurodevelopmental disorder and epilepsy in a case of two rare genetic diseases: overlapping phenotype.

Karatas E, Gulec A, Korkmaz M, Karaman ZF, Kiraz A, Per H, Dundar M. Karatas E, et al. Neurogenetics. 2024 Dec 26;26(1):16. doi: 10.1007/s10048-024-00795-3. Neurogenetics. 2024. PMID: 39724270

2

A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort.

Şahin İO, Karataş E, Demir M, Tan B, Per H, Özkul Y, Dündar M. Şahin İO, et al. Among authors: karatas e. Turk J Med Sci. 2023 Dec 18;54(1):86-98. doi: 10.55730/1300-0144.5769. eCollection 2024. Turk J Med Sci. 2023. PMID: 38812636 Free PMC article.

3

Corrigendum to "A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort": [Turkish Journal of Medical Sciences 54 (1) 2024 86-98].

Şahin İO, Karataş E, Demir M, Tan B, Per H, Özkul Y, Dündar M. Şahin İO, et al. Among authors: karatas e. Turk J Med Sci. 2024 Sep 30;54(4):880. doi: 10.55730/1300-0144.5861. eCollection 2024. Turk J Med Sci. 2024. PMID: 39351509 Free PMC article.

4

A Case of Short Stature Caused by a Mutation in the ACAN Gene.

Karatas E, Demir M, Ozcelik F, Kara L, Akyurek E, Berber U, Hatipoglu N, Ozkul Y, Dundar M. Karatas E, et al. Mol Syndromol. 2023 Apr;14(2):123-128. doi: 10.1159/000526166. Epub 2022 Oct 21. Mol Syndromol. 2023. PMID: 37064332 Free PMC article.

5

Myasthenia gravis with acute respiratory failure in the emergency department.

Kozak HH, Uca AU, Teke T, Altas M, Karatas E. Kozak HH, et al. Among authors: karatas e. Turk J Emerg Med. 2016 May 8;16(2):80-82. doi: 10.1016/j.tjem.2015.03.002. eCollection 2016 Jun. Turk J Emerg Med. 2016. PMID: 27896329 Free PMC article.

6

Communication dynamics and media interactions of young adults who have attempted suicide: a qualitative thematic analysis.

Arık E, İnce M, Koçak MC, Bilişli Y, Karataş EO, Akgün H, Aşlakçı F. Arık E, et al. Among authors: karatas eo. Front Psychol. 2024 Nov 1;15:1460348. doi: 10.3389/fpsyg.2024.1460348. eCollection 2024. Front Psychol. 2024. PMID: 39554706 Free PMC article.

7

Outcomes of pregnancies diagnosed with absent or abnormal fetal gallbladder in a tertiary center.

Karataş E, Tanaçan A, Özkavak OO, Şerbetçi H, Haksever M, Atalay A, Kara Ö, Şahin D. Karataş E, et al. Int J Gynaecol Obstet. 2024 Oct 18. doi: 10.1002/ijgo.15949. Online ahead of print. Int J Gynaecol Obstet. 2024. PMID: 39422567

8

Association between Behçet's disease and apical periodontitis: A cross-sectional study.

Sümbüllü M, Kul A, Karataş E, Memiş M. Sümbüllü M, et al. Among authors: karatas e. Dent Med Probl. 2024 Sep-Oct;61(5):679-685. doi: 10.17219/dmp/163127. Dent Med Probl. 2024. PMID: 39364625 Free article.

9

Congenital hereditary endothelial dystrophy with progressive sensorineural deafness: a case report of Harboyan syndrome.

Karataş E, Utine CA. Karataş E, et al. Arq Bras Oftalmol. 2024 Sep 23;88(2):e20230078. doi: 10.5935/0004-2749.2023-0078. eCollection 2024. Arq Bras Oftalmol. 2024. PMID: 39319907 Free article.

10

Foveal Hypoplasia in Presumed Xeroderma Pigmentosum: A Case Report.

Karatas E, Utine CA, Lebe B, Kaya M. Karatas E, et al. Beyoglu Eye J. 2024 Sep 1;9(3):172-177. doi: 10.14744/bej.2024.58224. eCollection 2024. Beyoglu Eye J. 2024. PMID: 39239625 Free PMC article.

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