Dalgiç B - Search Results

1

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

2

An infantile case of Zellweger syndrome presented with Kabuki-like phenotype.

Ezgu F, Eminoglu T, Okur I, Gunduz M, Tumer L, Hasanoglu A, Dalgic B. Ezgu F, et al. Among authors: dalgic b. Genet Couns. 2011;22(2):217-20. Genet Couns. 2011. PMID: 21848015

3

Multisystem involvement in a patient due to accumulation of amylopectin-like material with diminished branching enzyme activity.

Eminoglu TF, Tumer L, Okur I, Olgunturk R, Hasanoglu A, Gonul II, Dalgic B. Eminoglu TF, et al. Among authors: dalgic b. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S255-9. doi: 10.1007/s10545-008-0819-8. Epub 2008 Apr 4. J Inherit Metab Dis. 2008. PMID: 18392749

4

Cholesteryl ester storage disease in a young child presenting as isolated hepatomegaly treated with simvastatin.

Dalgiç B, Sari S, Gündüz M, Ezgü F, Tümer L, Hasanoğlu A, Akyol G. Dalgiç B, et al. Turk J Pediatr. 2006 Apr-Jun;48(2):148-51. Turk J Pediatr. 2006. PMID: 16848116

5

Expected or unexpected clinical findings in liver glycogen storage disease type IX: distinct clinical and molecular variability.

İnci A, Kılıç Yıldırım G, Cengiz Ergin FB, Sarı S, Eğritaş Gürkan Ö, Okur İ, Biberoğlu G, Bükülmez A, Ezgü FS, Dalgıç B, Tümer L. İnci A, et al. Among authors: dalgic b. J Pediatr Endocrinol Metab. 2022 Jan 17;35(4):451-462. doi: 10.1515/jpem-2021-0278. Print 2022 Apr 26. J Pediatr Endocrinol Metab. 2022. PMID: 35038814

6

The co-existence of Fabry and celiac diseases: a case report.

Tümer L, Ezgü FS, Hasanoğlu A, Dalgiç B, Bakkaloğlu SA, Memiş L, Dursun A. Tümer L, et al. Among authors: dalgic b. Pediatr Nephrol. 2004 Jun;19(6):679-81. doi: 10.1007/s00467-004-1462-8. Epub 2004 Apr 15. Pediatr Nephrol. 2004. PMID: 15085421

7

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): case report with a new mutation.

Bariş Z, Eminoğlu T, Dalgiç B, Tümer L, Hasanoğlu A. Bariş Z, et al. Among authors: dalgic b. Eur J Pediatr. 2010 Nov;169(11):1375-8. doi: 10.1007/s00431-010-1237-0. Epub 2010 Jun 29. Eur J Pediatr. 2010. PMID: 20585803

8

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: dalgic b. Gene. 2019 Mar 1;687:280-288. doi: 10.1016/j.gene.2018.11.054. Epub 2018 Nov 20. Gene. 2019. PMID: 30468909

9

Cirrhosis in an infant heterozygous for classical citrullinaemia.

Ezgü FS, Tümer L, Dalgiç B, Hasanoĝlu A, Kobayashi K, Saheki T. Ezgü FS, et al. Among authors: dalgic b. Acta Paediatr. 2005 Dec;94(12):1849-51. doi: 10.1111/j.1651-2227.2005.tb01868.x. Acta Paediatr. 2005. PMID: 16421053

10

Relation between ghrelin level and treatment response in functional constipation.

Gürkan OE, Dalgıç B, Bideci A. Gürkan OE, et al. Among authors: dalgic b. Turk J Gastroenterol. 2013;24(6):515-20. Turk J Gastroenterol. 2013. PMID: 24623291 Free article.

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