Biberoglu G[au] - Search Results

Year	Number of Results
1995	1
1996	2
1998	3
1999	3
2002	1
2003	1
2004	2
2005	2
2006	1
2007	4
2008	5
2009	2
2010	1
2011	4
2012	1
2013	5
2014	3
2018	1
2019	4
2020	2
2021	8
2022	2
2023	1
2024	2

1

Two patients from Turkey with a novel variant in the GM2A gene and review of the literature.

İnci A, Cengiz Ergin FB, Biberoğlu G, Okur İ, Ezgü FS, Tümer L. İnci A, et al. Among authors: biberoglu g. J Pediatr Endocrinol Metab. 2021 Apr 6;34(6):805-812. doi: 10.1515/jpem-2020-0655. Print 2021 Jun 25. J Pediatr Endocrinol Metab. 2021. PMID: 33819415 Review.

2

Ultra-Rare Disorder in a Young Girl with Lipodystrophy: Analbuminemia.

İnci A, Arslan B, Okur İ, Biberoğlu G, Şanlı ME, Aktaşoğlu E, Kılıç A, Tümer L, Ezgü FS. İnci A, et al. Among authors: biberoglu g. Indian J Pediatr. 2021 Jul;88(7):723. doi: 10.1007/s12098-021-03729-1. Epub 2021 Apr 27. Indian J Pediatr. 2021. PMID: 33905091 No abstract available.

3

Hypophosphatasia: is it an underdiagnosed disease even by expert physicians?

İnci A, Ergin FBC, Yüce BT, Çiftçi B, Demir E, Buyan N, Okur İ, Biberoğlu G, Öktem RM, Tümer L, Ezgü FS. İnci A, et al. Among authors: biberoglu g. J Bone Miner Metab. 2021 Jul;39(4):598-605. doi: 10.1007/s00774-020-01193-z. Epub 2021 Jan 6. J Bone Miner Metab. 2021. PMID: 33404770

4

A possible biomarker of neurocytolysis in infantile gangliosidoses: aspartate transaminase.

Kılıç M, Kasapkara ÇS, Kılavuz S, Mungan NÖ, Biberoğlu G. Kılıç M, et al. Among authors: biberoglu g. Metab Brain Dis. 2019 Apr;34(2):495-503. doi: 10.1007/s11011-019-0391-y. Epub 2019 Feb 2. Metab Brain Dis. 2019. PMID: 30712135

5

A Case of Glycogen Storage Disease Type 1a Mimicking Familial Chylomicronemia Syndrome.

Olgac A, Okur I, Biberoğlu G, Ezgü FS, Tümer L. Olgac A, et al. Among authors: biberoglu g. Balkan J Med Genet. 2021 Jul 27;24(1):103-106. doi: 10.2478/bjmg-2021-0013. eCollection 2021 Jun. Balkan J Med Genet. 2021. PMID: 34447667 Free PMC article.

6

Neonatal multiple sulfatase deficiency with a novel mutation and review of the literature.

Nur BG, Mıhçı E, Pepe S, Biberoğlu G, Ezgü FS, Ballabio A, Öztekin O, Dursun O. Nur BG, et al. Among authors: biberoglu g. Turk J Pediatr. 2014 Jul-Aug;56(4):418-22. Turk J Pediatr. 2014. PMID: 25818962 Review.

7

Autism: Screening of inborn errors of metabolism and unexpected results.

İnci A, Özaslan A, Okur İ, Biberoğlu G, Güney E, Ezgü FS, Tümer L, İşeri E. İnci A, et al. Among authors: biberoglu g. Autism Res. 2021 May;14(5):887-896. doi: 10.1002/aur.2486. Epub 2021 Feb 19. Autism Res. 2021. PMID: 33605552

8

Beneficial Effects of Modified Atkins Diet in Glycogen Storage Disease Type IIIa.

Olgac A, İnci A, Okur İ, Biberoğlu G, Oğuz D, Ezgü FS, Kasapkara ÇS, Aktaş E, Tümer L. Olgac A, et al. Among authors: biberoglu g. Ann Nutr Metab. 2020;76(4):233-241. doi: 10.1159/000509335. Epub 2020 Jul 24. Ann Nutr Metab. 2020. PMID: 32712609

9

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: biberoglu g. 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

10

A 7-year-old Boy with Hand Tremors and a Novel Mutation for L-2-hydroxyglutaric Aciduria.

Olgac A, Tekin OL, Ezgü FS, Biberoǧlu G, Tümer L. Olgac A, et al. Among authors: biberoglu g. Balkan J Med Genet. 2019 Dec 21;22(2):93-96. doi: 10.2478/bjmg-2019-0015. eCollection 2019 Dec. Balkan J Med Genet. 2019. PMID: 31942424 Free PMC article.

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