Berberoğlu M - Search Results

1

Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.

Özsu E, Çetinkaya S, Bolu S, Hatipoğlu N, Savaş Erdeve Ş, Evliyaoğlu O, Baş F, Çayır A, Dündar İ, Akbaş ED, Uçaktürk SA, Berberoğlu M, Şıklar Z, Özalkak Ş, Muratoğlu Şahin N, Keskin M, Şiraz ÜG, Turan H, Öztürk AP, Mengen E, Sağsak E, Dursun F, Akyürek N, Odabaşı Güneş S, Aycan Z. Özsu E, et al. Among authors: berberoglu m. J Clin Res Pediatr Endocrinol. 2024 Sep 5;16(3):297-305. doi: 10.4274/jcrpe.galenos.2024.2023-10-16. Epub 2024 Apr 26. J Clin Res Pediatr Endocrinol. 2024. PMID: 38665000 Free PMC article.

2

Severe hypercalcemia of an infant due to vitamin D toxicity associated with hypercholesterolemia.

Evliyaoğlu O, Berberoğlu M, Ocal G, Adiyaman P, Aycan Z. Evliyaoğlu O, et al. Among authors: berberoglu m. J Pediatr Endocrinol Metab. 2001 Jul-Aug;14(7):915-9. doi: 10.1515/jpem.2001.14.7.915. J Pediatr Endocrinol Metab. 2001. PMID: 11515734

3

Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patients.

Berberoğlu M, Aycan Z, Ocal G, Begeot M, Naville D, Akar N, Adiyaman P, Evliyaoglu O, Penhoat A. Berberoğlu M, et al. J Pediatr Endocrinol Metab. 2001 Sep-Oct;14(8):1113-8. doi: 10.1515/jpem-2001-0807. J Pediatr Endocrinol Metab. 2001. PMID: 11592568

4

Osteopetrosis, renal tubular acidosis without urinary concentration abnormality, cerebral calcification and severe mental retardation in three Turkish brothers.

Ocal G, Berberoğlu M, Adiyaman P, Cetinkaya E, Ekim M, Aycan Z, Evliyaoğlu O. Ocal G, et al. Among authors: berberoglu m. J Pediatr Endocrinol Metab. 2001 Nov-Dec;14(9):1671-7. J Pediatr Endocrinol Metab. 2001. PMID: 11795660 Review.

5

Mutations of the 5alpha-steroid reductase type 2 gene in six Turkish patients from unrelated families and a large pedigree of an isolated Turkish village.

Ocal G, Adiyaman P, Berberoğlu M, Cetinkaya E, Akar N, Uysal A, Duman T, Evliyaoğlu O, Aycan Z, Lumbroso S, Sultan C. Ocal G, et al. Among authors: berberoglu m. J Pediatr Endocrinol Metab. 2002 Apr;15(4):411-21. doi: 10.1515/jpem.2002.15.4.411. J Pediatr Endocrinol Metab. 2002. PMID: 12008688

6

No seasonality of birth in children with type 1 diabetes mellitus in Ankara, Turkey.

Evliyaoğlu O, Ocal G, Cetinkaya E, Berberoğlu M, Aycan Z, Adiyaman P, Vidinlisan S. Evliyaoğlu O, et al. Among authors: berberoglu m. J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):1033-4. doi: 10.1515/jpem.2002.15.7.1033. J Pediatr Endocrinol Metab. 2002. PMID: 12199331 No abstract available.

7

Neonatal diabetes with hyperchylomicronemia.

Aycan Z, Berberoğlu M, Ocal G, Altundas N, Adiyaman P, Evliyaoğlu O. Aycan Z, et al. Among authors: berberoglu m. Indian J Pediatr. 2002 Dec;69(12):1087-9. doi: 10.1007/BF02724395. Indian J Pediatr. 2002. PMID: 12557965

8

Effects on bone mineral density of gonadotropin releasing hormone analogs used in the treatment of central precocious puberty.

Unal O, Berberoğlu M, Evliyaoğlu O, Adiyaman P, Aycan Z, Ocal G. Unal O, et al. Among authors: berberoglu m. J Pediatr Endocrinol Metab. 2003 Mar;16(3):407-11. doi: 10.1515/jpem.2003.16.3.407. J Pediatr Endocrinol Metab. 2003. PMID: 12705366 Clinical Trial.

9

Seckel-like syndrome: a patient with precocious puberty associated with nonclassical congenital adrenal hyperplasia.

Adiyaman P, Berberoğlu M, Aycan Z, Evliyaoğlu O, Ocal G. Adiyaman P, et al. Among authors: berberoglu m. J Pediatr Endocrinol Metab. 2004 Jan;17(1):105-10. doi: 10.1515/jpem.2004.17.1.105. J Pediatr Endocrinol Metab. 2004. PMID: 14960029

10

Management of central diabetes insipidus with oral desmopressin in a premature neonate.

Atasay B, Berberoğlu M, Günlemez A, Evliyaoğlu O, Adiyaman P, Unal S, Arsan S, Ocal G. Atasay B, et al. Among authors: berberoglu m. J Pediatr Endocrinol Metab. 2004 Feb;17(2):227-30. doi: 10.1515/jpem.2004.17.2.227. J Pediatr Endocrinol Metab. 2004. PMID: 15055359

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