Kasapkara CS - Search Results

1

The First Case of 4H Syndrome with Type 1 Diabetes Mellitus.

Buyukyilmaz G, Erozan Cavdarlı B, Toksoy Adiguzel K, Adiguzel M, Kasapkara CS, Gurbuz F, Boyraz M, Gurkas E. Buyukyilmaz G, et al. Among authors: kasapkara cs. J Clin Res Pediatr Endocrinol. 2023 Mar 28. doi: 10.4274/jcrpe.galenos.2023.2023-1-15. Online ahead of print. J Clin Res Pediatr Endocrinol. 2023. PMID: 36974356 Free article.

2

A case with rare type of congenital disorder of glycosylation: PGM1-CDG.

Küçükçongar A, Tümer L, Ezgü FS, Kasapkara ÇS, Jaeken J, Matthijs G, Rymen D, Dalgiç B, Bıdecı A, Hasanoğlu A. Küçükçongar A, et al. Among authors: kasapkara cs. Genet Couns. 2015;26(1):87-90. Genet Couns. 2015. PMID: 26043514 No abstract available.

3

Mutational analysis of the galactose-1-phosphate uridyltransferase (GALT) gene in southeast part of Turkey: a regional report.

Akar M, Celik M, Kasapkara CS, Ozbek MN, Aldudak B, Tuzun H. Akar M, et al. Among authors: kasapkara cs. Genet Couns. 2015;26(1):91-4. Genet Couns. 2015. PMID: 26043515 No abstract available.

4

Could GSD type I expand the spectrum of disorders with elevated plasma chitotriosidase activity?

Tümer L, Kasapkara ÇS, Biberoğlu G, Ezgü F, Hasanoğlu A. Tümer L, et al. Among authors: kasapkara cs. J Pediatr Endocrinol Metab. 2013;26(11-12):1149-52. doi: 10.1515/jpem-2013-0066. J Pediatr Endocrinol Metab. 2013. PMID: 23813353

5

Variety of referral centers and diagnoses of congenital heart diseases that required intervention followed-up in neonatal intensive care unit: regional report.

Akar M, Aldudak B, Kasapkara CS, Tüzün H, Hanedan Onan S, Kanar B, Uzel VH. Akar M, et al. Among authors: kasapkara cs. Anadolu Kardiyol Derg. 2014 Feb;14(1):101-2. doi: 10.5152/akd.2013.5170. Epub 2013 Dec 18. Anadolu Kardiyol Derg. 2014. PMID: 24382504 No abstract available.

6

Transient nephrogenic diabetes insipidus caused by fetal exposure to haloperidol.

Akar M, Kasapkara ÇS, Özbek MN, Tüzün H, Aldudak B, Kanar B. Akar M, et al. Among authors: kasapkara cs. Ren Fail. 2014 Jul;36(6):951-2. doi: 10.3109/0886022X.2014.900403. Epub 2014 Mar 27. Ren Fail. 2014. PMID: 24673433

7

Hypercalcemia in glycogen storage disease type I patients of Turkish origin.

Kasapkara CS, Tümer L, Okur I, Eminoğlu T, Ezgü FS, Hasanoğlu A. Kasapkara CS, et al. Turk J Pediatr. 2012 Jan-Feb;54(1):35-7. Turk J Pediatr. 2012. PMID: 22397040

8

Hyaline fibromatosis syndrome resulting from a new homozygous missense mutation, p.Gly116Val, in ANTXR2.

Tümer L, Kasapkara C, Fong K, Serdaroğlu A, McGrath JA. Tümer L, et al. J Dermatol. 2013 Aug;40(8):677-8. doi: 10.1111/1346-8138.12182. Epub 2013 Jun 5. J Dermatol. 2013. PMID: 23734713 No abstract available.

9

Apheresis-inducible cytokine pattern change in children with homozygous familial hypercholesterolemia.

Küçükçongar A, Yenicesu I, Tümer L, Kasapkara CS, Ezgü FS, Paşaoğlu O, Demirtaş C, Celik B, Dilsiz G, Hasanoğlu A. Küçükçongar A, et al. Among authors: kasapkara cs. Transfus Apher Sci. 2013 Jun;48(3):391-6. doi: 10.1016/j.transci.2013.04.024. Epub 2013 May 4. Transfus Apher Sci. 2013. PMID: 23651865

10

Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation.

Yücel H, Genç Sel Ç, Kasapkara ÇS, Karacan Küçükali G, Savas Erdeve S, Öztoprak Ü, Ceylaner S, Şenel S, Akçaboy M. Yücel H, et al. Among authors: kasapkara cs. J Clin Res Pediatr Endocrinol. 2021 Feb 26;13(1):114-118. doi: 10.4274/jcrpe.galenos.2020.2020.0004. Epub 2020 Apr 17. J Clin Res Pediatr Endocrinol. 2021. PMID: 32302086 Free PMC article.

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