Kucukcongar A - Search Results

1

Desensitisation of the youngest patient with Pompe disease in response to alglucosidase alfa.

Karagol IH, Bakirtas A, Yilmaz O, Topal E, Kucukcongar A, Ezgu FS, Demirsoy MS, Turktas I. Karagol IH, et al. Among authors: kucukcongar a. Allergol Immunopathol (Madr). 2014 Jul-Aug;42(4):372-5. doi: 10.1016/j.aller.2013.02.012. Epub 2013 Jun 14. Allergol Immunopathol (Madr). 2014. PMID: 23769736 No abstract available.

2

BCS1L gene mutation causing GRACILE syndrome: case report.

Kasapkara ÇS, Tümer L, Ezgü FS, Küçükçongar A, Hasanoğlu A. Kasapkara ÇS, et al. Among authors: kucukcongar a. Ren Fail. 2014 Jul;36(6):953-4. doi: 10.3109/0886022X.2014.900422. Epub 2014 Mar 24. Ren Fail. 2014. PMID: 24655110 Free article.

3

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. 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

4

Home sleep study characteristics in patients with mucopolysaccharidosis.

Kasapkara ÇS, Tümer L, Aslan AT, Hasanoğlu A, Ezgü FS, Küçükçongar A, Tunca Z, Köktürk O. Kasapkara ÇS, et al. Among authors: kucukcongar a. Sleep Breath. 2014 Mar;18(1):143-9. doi: 10.1007/s11325-013-0862-z. Epub 2013 May 22. Sleep Breath. 2014. PMID: 23690022

5

Diagnosis of glycine encephalopathy in a pediatric patient by detection of a GLDC mutation during initial next generation DNA sequencing.

Ezgu F, Çiftci B, Topçu B, Adıyaman G, Gökmenoğlu H, Küçükçongar A, Kasapkara Ç, Biberoğlu G, Tümer L, Hasanoğlu A. Ezgu F, et al. Among authors: kucukcongar a. Metab Brain Dis. 2014 Mar;29(1):211-3. doi: 10.1007/s11011-014-9482-y. Epub 2014 Jan 11. Metab Brain Dis. 2014. PMID: 24407464

6

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. Genet Couns. 2015;26(1):87-90. Genet Couns. 2015. PMID: 26043514 No abstract available.

7

High incidence of co-existing factors significantly modifying the phenotype in patients with Fabry disease.

Koca S, Tümer L, Okur İ, Erten Y, Bakkaloğlu S, Biberoğlu G, Kasapkara Ç, Küçükçongar A, Dalgıç B, Oktar SÖ, Öner Y, Atalay T, Cemri M, Çiftçi B, Topçu B, Hasanoğlu A, Ezgü F. Koca S, et al. Among authors: kucukcongar a. Gene. 2019 Mar 1;687:280-288. doi: 10.1016/j.gene.2018.11.054. Epub 2018 Nov 20. Gene. 2019. PMID: 30468909

8

Congenital defects of glycosylation: Novel presentations with mainly neurological involvement and variable dysmorphic features.

İnci A, Cengiz B, Biberoğlu G, Okur İ, Arhan E, Öner AY, Kasapkara ÇS, Küçükçongar A, Tümer L, Ezgu F. İnci A, et al. Among authors: kucukcongar a. Am J Med Genet A. 2021 Sep;185(9):2739-2747. doi: 10.1002/ajmg.a.62247. Epub 2021 May 7. Am J Med Genet A. 2021. PMID: 33960646

9

Breastfeeding and Childhood Cancer: Is Breastfeeding Preventative to Childhood Cancer?

Küçükçongar A, Oğuz A, Pınarlı FG, Karadeniz C, Okur A, Kaya Z, Çelik B. Küçükçongar A, et al. Pediatr Hematol Oncol. 2015;32(6):374-81. Epub 2015 Aug 13. Pediatr Hematol Oncol. 2015. PMID: 26269940

10

Kasapkara CS, Tümer L, Küçükçongar A, Hasanoğlu A, Seneca S, De Meirleir L. Kasapkara CS, et al. Among authors: kucukcongar a. J Pediatr Gastroenterol Nutr. 2013 Nov;57(5):e28-9. doi: 10.1097/MPG.0b013e31826bd4ed. J Pediatr Gastroenterol Nutr. 2013. PMID: 22868686 No abstract available.

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