Ulgenalp A - Search Results

1

MIRAGE syndrome in a 10-year-old girl with a novel Lys1024Glu missense variant in SAMD9.

Cinleti T, Gülen A, Sönmez B, Gürsoy S, Boyacioğlu ÖK, Asilsoy S, Ulgenalp A, Bozkaya ÖG, Çağlayan AO. Cinleti T, et al. Among authors: ulgenalp a. Clin Dysmorphol. 2023 Jul 1;32(3):133-138. doi: 10.1097/MCD.0000000000000460. Epub 2023 May 1. Clin Dysmorphol. 2023. PMID: 37195360 No abstract available.

2

Protracted febrile myalgia syndrome in a patient with familial Mediterranean fever homozygous for the E148Q mutation.

Soylu A, Kasap B, Türkmen M, Ulgenalp A, Uzuner N, Kavukçu S. Soylu A, et al. Among authors: ulgenalp a. Semin Arthritis Rheum. 2008 Oct;38(2):161-2. doi: 10.1016/j.semarthrit.2007.10.009. Epub 2008 Jan 14. Semin Arthritis Rheum. 2008. PMID: 18191992 No abstract available.

3

Long-standing fever and Angelman syndrome: report of two cases.

Yiş U, Giray O, Kurul SH, Bora E, Ulgenalp A, Erçal D, Dirik E. Yiş U, et al. Among authors: ulgenalp a. J Paediatr Child Health. 2008 May;44(5):308-10. doi: 10.1111/j.1440-1754.2008.01302.x. J Paediatr Child Health. 2008. PMID: 18416709

4

Myalgia as a symptom of familial Mediterranean fever in children.

Kavukçu S, Turkmen MA, Soylu A, Bayram MT, Ulgenalp A. Kavukçu S, et al. Among authors: ulgenalp a. Rheumatol Int. 2012 Nov;32(11):3705-6. doi: 10.1007/s00296-011-2167-5. Epub 2011 Oct 22. Rheumatol Int. 2012. PMID: 22020390 No abstract available.

5

Lack of association of childhood partial epilepsy with brain derived neurotrophic factor gene.

Unalp A, Bora E, Cankaya T, Giray Bozkaya O, Ercal D, Ozturk A, Ulgenalp A. Unalp A, et al. Among authors: ulgenalp a. ScientificWorldJournal. 2012;2012:414797. doi: 10.1100/2012/414797. Epub 2012 May 1. ScientificWorldJournal. 2012. PMID: 22654603 Free PMC article.

6

Prolonged unconjugated hyperbilirubinaemia associated with the haem oxygenase-1 gene promoter polymorphism.

Bozkaya OG, Kumral A, Yesilirmak DC, Ulgenalp A, Duman N, Ercal D, Ozkan H. Bozkaya OG, et al. Among authors: ulgenalp a. Acta Paediatr. 2010 May;99(5):679-683. doi: 10.1111/j.1651-2227.2009.01678.x. Epub 2010 Feb 1. Acta Paediatr. 2010. PMID: 20121710

7

Lymphoid tissue histology in a patient with ICF syndrome.

Makay B, Anal O, Köse G, Bozkaya O, Ozer E, Bora E, Ulgenalp A, Erçal D. Makay B, et al. Among authors: ulgenalp a. J Investig Allergol Clin Immunol. 2012;22(3):220-1. J Investig Allergol Clin Immunol. 2012. PMID: 22697015 Free article. No abstract available.

8

Three novel mutations of CHD7 gene in two turkish patients with charge syndrome; A double point mutation and an insertion.

Bozkaya OG, Ataman E, Randa C, Cura DO, Gürsoy S, Aksel O, Ulgenalp A. Bozkaya OG, et al. Among authors: ulgenalp a. Balkan J Med Genet. 2015 Dec 30;18(1):65-70. doi: 10.1515/bjmg-2015-0007. eCollection 2015 Jun. Balkan J Med Genet. 2015. PMID: 26929907 Free PMC article.

9

Serum motilin levels and motilin gene polymorphisms in children with functional constipation.

Ulusoy E, Arslan N, Küme T, Ülgenalp A, Çirali C, Bozkaya Ö, Ercal D. Ulusoy E, et al. Among authors: ulgenalp a. Minerva Pediatr (Torino). 2021 Oct;73(5):420-425. doi: 10.23736/S2724-5276.16.04369-X. Epub 2016 Oct 5. Minerva Pediatr (Torino). 2021. PMID: 27706119

10

Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy.

Gursoy S, Ataman E, Baysal BT, Özyılmaz B, Gençpınar P, Hız AS, Yiş U, Ünalp A, Dündar NO, Ülgenalp A, Erçal D. Gursoy S, et al. Among authors: ulgenalp a. Ann Indian Acad Neurol. 2020 Mar-Apr;23(2):206-210. doi: 10.4103/aian.AIAN_465_19. Epub 2020 Feb 25. Ann Indian Acad Neurol. 2020. PMID: 32189863 Free PMC article.

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