Mihci E - Search Results

1

[Influence of percutaneous coronary intervention in non ST-elevation acute coronary syndromes on prescription of secondary prevention medications. Data from the S-Témoin Registry].

Danchin N, Thébaut JF, Diévart F, Grenier O, Mihci E, Herrmann MA, Ferrières J. Danchin N, et al. Among authors: mihci e. Ann Cardiol Angeiol (Paris). 2007 Jan;56(1):30-5. doi: 10.1016/j.ancard.2006.10.002. Ann Cardiol Angeiol (Paris). 2007. PMID: 17343036 French.

2

Predictors of long-term use of evidence-based therapies after non-ST-segment elevation acute coronary syndrome. The S-Témoin survey.

Danchin N, Diévart F, Thébaut JF, Grenier O, Mihci E, Herrmann MA, Ferrières J. Danchin N, et al. Among authors: mihci e. Int J Cardiol. 2009 Mar 20;133(1):32-40. doi: 10.1016/j.ijcard.2007.11.060. Epub 2008 Mar 28. Int J Cardiol. 2009. PMID: 18375000

3

Prevalence of peripheral arterial disease in high-risk patients using ankle-brachial index in general practice: a cross-sectional study.

Cacoub P, Cambou JP, Kownator S, Belliard JP, Beregi JP, Branchereau A, Carpentier P, Léger P, Luizy F, Maïza D, Mihci E, Herrmann MA, Priollet P. Cacoub P, et al. Among authors: mihci e. Int J Clin Pract. 2009 Jan;63(1):63-70. doi: 10.1111/j.1742-1241.2008.01953.x. Int J Clin Pract. 2009. PMID: 19125994 Free PMC article.

4

A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism Due to a Novel Homozygous Variant in the SCNN1B Gene.

Singin B, Donbaloğlu Z, Barsal Çetiner E, Çetin K, Özkan Zarif N, Çelik K, Mıhçı E, Altıok Clark Ö, Tuhan H, Parlak M. Singin B, et al. Among authors: mihci e. J Clin Res Pediatr Endocrinol. 2024 Dec 26. doi: 10.4274/jcrpe.galenos.2024.2024-10-5. Online ahead of print. J Clin Res Pediatr Endocrinol. 2024. PMID: 39723761 Free article.

5

Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas.

Güneş N, Uludağ Alkaya D, Toylu A, Özüdoğru P, Çifçi Sunamak E, Şeker A, Demir B, Kuruğoğlu S, Mıhçı E, Tüysüz B. Güneş N, et al. Among authors: mihci e. Turk Arch Pediatr. 2023 Jul;58(4):376-381. doi: 10.5152/TurkArchPediatr.2023.23011. Turk Arch Pediatr. 2023. PMID: 37317574 Free PMC article.

6

The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review.

Karamik G, Tuysuz B, Isik E, Yilmaz A, Alanay Y, Sunamak EC, Durmusalioglu EA, Ozkinay F, Cetin GO, Ozturk N, Mihci E, Nur B. Karamik G, et al. Among authors: mihci e. Am J Med Genet A. 2023 Jul;191(7):1814-1825. doi: 10.1002/ajmg.a.63207. Epub 2023 Apr 13. Am J Med Genet A. 2023. PMID: 37053206 Review.

7

Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variant.

Öztürk N, Karamık G, Mutlu H, Bayer ÖY, Mıhçı E, Çetin GO, Nur B. Öztürk N, et al. Among authors: mihci e. Turk J Pediatr. 2023;65(1):81-95. doi: 10.24953/turkjped.2022.793. Turk J Pediatr. 2023. PMID: 36866988 Free article.

8

Novel Gene Variants Associated with Primary Ciliary Dyskinesia.

Demir Eksi D, Yilmaz E, Basaran AE, Erduran G, Nur B, Mihci E, Karadag B, Bingol A, Alper OM. Demir Eksi D, et al. Among authors: mihci e. Indian J Pediatr. 2022 Jul;89(7):682-691. doi: 10.1007/s12098-022-04098-z. Epub 2022 Mar 3. Indian J Pediatr. 2022. PMID: 35239159

9

Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMA.

Arikan Y, Berker Karauzum S, Uysal H, Mihci E, Nur B, Duman O, Haspolat S, Altiok Clark O, Toylu A. Arikan Y, et al. Among authors: mihci e. Gene. 2022 May 20;823:146322. doi: 10.1016/j.gene.2022.146322. Epub 2022 Feb 25. Gene. 2022. PMID: 35219815

10

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.

Dundar M, Fahrioglu U, Yildiz SH, Bakir-Gungor B, Temel SG, Akin H, Artan S, Cora T, Sahin FI, Dursun A, Sezer O, Gurkan H, Erdogan M, Gunduz CNS, Bisgin A, Ozdemir O, Ulgenalp A, Percin EF, Yildirim ME, Tekes S, Bagis H, Yuce H, Duman N, Bozkurt G, Yararbas K, Yildirim MS, Arman A, Mihci E, Eraslan S, Altintas ZM, Aymelek HS, Ruhi HI, Tatar A, Ergoren MC, Cetin GO, Altunoglu U, Caglayan AO, Yuksel B, Ozkul Y, Saatci C, Kenanoglu S, Karasu N, Dundar B, Ozcelik F, Demir M, Siniksaran BS, Kulak H, Kiranatlioglu K, Baysal K, Kazimli U, Akalin H, Dundar A, Boz M, Bayram A, Subasioglu A, Colak FK, Karaduman N, Gunes MC, Kandemir N, Aynekin B, Emekli R, Sahin IO, Ozdemir SY, Onal MG, Senel AS, Poyrazoglu MH, Kisaarslan ANP, Gursoy S, Baskol M, Calis M, Demir H, Zararsiz GE, Erdogan MO, Elmas M, Solak M, Ulu MS, Thahir A, Aydin Z, Atasever U, Sag SO, Aliyeva L, Alemdar A, Dogan B, Erguzeloglu CO, Kaya N, Ozkinay F, Cogulu O, Durmaz A, Onay H, Karaca E, Durmaz B, Aykut A, Cilingir O, Aras BD, Gokalp EE, Arslan S, Temena A, Haziyeva K, Kocagil S, Bas H, Susam E, Keklikci AR, Sarac E, Kocak N, Nergiz S, Terzi YK, Dincer SA, Baskin ES, Genc GC, Bahadir O, Sanri A, Yigit S, Tozkir H, Y… See abstract for full author list ➔ Dundar M, et al. Among authors: mihci e. Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31. Funct Integr Genomics. 2022. PMID: 35098403

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

97 results

Search Page

Filters