Gucer S - Search Results

1

A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutation.

Dursun A, Yalnizoglu D, Gerdan OF, Yucel-Yilmaz D, Sagiroglu MS, Yuksel B, Gucer S, Sivri S, Ozgul RK. Dursun A, et al. Among authors: gucer s. Clin Dysmorphol. 2017 Jan;26(1):1-12. doi: 10.1097/MCD.0000000000000149. Clin Dysmorphol. 2017. PMID: 27547915

2

Zellweger syndrome with unusual findings: non-immune hydrops fetalis, dermal erythropoiesis and hypoplastic toe nails.

Dursun A, Gucer S, Ebberink MS, Yigit S, Wanders RJ, Waterham HR. Dursun A, et al. Among authors: gucer s. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S345-8. doi: 10.1007/s10545-009-9010-0. Epub 2009 Dec 23. J Inherit Metab Dis. 2009. PMID: 20033294 Review.

3

Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation.

Eroglu FK, Ozaltin F, Gönç N, Nalçacıoğlu H, Özçakar ZB, Yalnızoğlu D, Güçer Ş, Orhan D, Eminoğlu FT, Göçmen R, Alikaşifoğlu A, Topaloğlu R, Düzova A. Eroglu FK, et al. Among authors: gucer s. Pediatr Neurol. 2018 Nov;88:71-74. doi: 10.1016/j.pediatrneurol.2018.07.008. Epub 2018 Jul 27. Pediatr Neurol. 2018. PMID: 30337132

4

Erratum to 'Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation' [Pediatric Neurology 88 (2018) 71-74].

Eroglu FK, Ozaltin F, Gönç N, Nalçacıoğlu H, Özçakar ZB, Yalnızoğlu D, Güçer Ş, Orhan D, Eminoğlu FT, Göçmen R, Alikaşifoğlu A, Topaloğlu R, Düzova A. Eroglu FK, et al. Among authors: gucer s. Pediatr Neurol. 2019 May;94:84. doi: 10.1016/j.pediatrneurol.2018.12.017. Epub 2019 Feb 15. Pediatr Neurol. 2019. PMID: 30777605 No abstract available.

5

Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing.

Guleray N, Kosukcu C, Taskiran ZE, Simsek Kiper PO, Utine GE, Gucer S, Tokatli A, Boduroglu K, Alikasifoglu M. Guleray N, et al. Among authors: gucer s. Fetal Pediatr Pathol. 2020 Apr;39(2):163-171. doi: 10.1080/15513815.2019.1639089. Epub 2019 Jul 15. Fetal Pediatr Pathol. 2020. PMID: 31303091

6

Association of prothrombin gene mutation with sepsis in a preterm with multiple intracardiac thrombi.

Cinar A, Dilber E, Karagoz T, Bahadir N, Gucer S, Tekinalp G, Gurgey A. Cinar A, et al. Among authors: gucer s. Echocardiography. 2005 Apr;22(4):340-4. doi: 10.1111/j.1540-8175.2005.03107.x. Echocardiography. 2005. PMID: 15839991

7

A suprarenal mass in a child.

Gucer S, Caliskan U, Ucar C, Koksal Y, Dilsiz A, Kale G. Gucer S, et al. Eur J Pediatr. 2006 Oct;165(10):736-8. doi: 10.1007/s00431-006-0149-5. Epub 2006 Aug 16. Eur J Pediatr. 2006. PMID: 16912900 No abstract available.

8

Giant lymphadenopathy infiltrated by gaucher cells mimicking lymphoma.

Yağci B, Salor O, Yalçin B, Gürakan F, Güçer S, Büyükpamukçu M. Yağci B, et al. Among authors: gucer s. Pediatr Blood Cancer. 2009 Jul;52(7):870-1. doi: 10.1002/pbc.21948. Pediatr Blood Cancer. 2009. PMID: 19213078

9

A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome.

Balci S, Güçer S, Orhan D, Karagöz T. Balci S, et al. Among authors: gucer s. Turk J Pediatr. 2008 Nov-Dec;50(6):595-9. Turk J Pediatr. 2008. PMID: 19227428

10

Different features of lung involvement in Niemann-Pick disease and Gaucher disease.

Gülhan B, Ozçelik U, Gürakan F, Güçer S, Orhan D, Cinel G, Yalçin E, Ersöz DD, Kiper N, Yüce A, Kale G. Gülhan B, et al. Among authors: gucer s. Respir Med. 2012 Sep;106(9):1278-85. doi: 10.1016/j.rmed.2012.06.014. Epub 2012 Jul 10. Respir Med. 2012. PMID: 22784405 Free article.

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