Balci B - Search Results

1

Balci B, Aurino S, Haliloglu G, Talim B, Erdem S, Akcören Z, Tan E, Caglar M, Richard I, Nigro V, Topaloglu H, Dincer P. Balci B, et al. Eur J Pediatr. 2006 May;165(5):293-8. doi: 10.1007/s00431-005-0046-3. Epub 2006 Jan 13. Eur J Pediatr. 2006. PMID: 16411092

2

Beta-sarcoglycan gene mutations in Turkey.

Balci B, Wilichowski E, Haliloğlu G, Talim B, Aurino S, Kremer E, Ebinger F, Senbil N, Anlar B, Kale G, Nigro V, Topaloğlu H, Bonnemann C, Dinçer P. Balci B, et al. Acta Myol. 2004 Dec;23(3):154-8. Acta Myol. 2004. PMID: 15938573

3

A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan.

Dinçer P, Balci B, Yuva Y, Talim B, Brockington M, Dinçel D, Torelli S, Brown S, Kale G, Haliloglu G, Gerçeker FO, Atalay RC, Yakicier C, Longman C, Muntoni F, Topaloglu H. Dinçer P, et al. Among authors: balci b. Neuromuscul Disord. 2003 Dec;13(10):771-8. doi: 10.1016/s0960-8966(03)00161-5. Neuromuscul Disord. 2003. PMID: 14678799

4

An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene.

Balci B, Uyanik G, Dincer P, Gross C, Willer T, Talim B, Haliloglu G, Kale G, Hehr U, Winkler J, Topaloğlu H. Balci B, et al. Neuromuscul Disord. 2005 Apr;15(4):271-5. doi: 10.1016/j.nmd.2005.01.013. Neuromuscul Disord. 2005. PMID: 15792865

5

Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from the Eastern Black Sea Region in Turkey.

Balci B, Gerçeker FO, Aksoy S, Sennaroğlu G, Kalay E, Sennaroğlu L, Dinçer P. Balci B, et al. Turk J Pediatr. 2005 Jul-Sep;47(3):213-21. Turk J Pediatr. 2005. PMID: 16250304

6

Prenatal diagnosis of muscle-eye-brain disease.

Balci B, Morris-Rosendahl DJ, Celebi A, Talim B, Topaloglu H, Dinçer P. Balci B, et al. Prenat Diagn. 2007 Jan;27(1):51-4. doi: 10.1002/pd.1622. Prenat Diagn. 2007. PMID: 17154333

7

Efficient transfection of mouse-derived C2C12 myoblasts using a matrigel basement membrane matrix.

Balci B, Dinçer P. Balci B, et al. Biotechnol J. 2009 Jul;4(7):1042-5. doi: 10.1002/biot.200800269. Biotechnol J. 2009. PMID: 19360711

8

Short-term outcomes of pregnant women with convalescent COVID-19 and factors associated with false-negative polymerase chain reaction test: A prospective cohort study.

Sahin O, Yildirmak T, Karacalar S, Aydın E, Ciftci MA, Bagci H, Yildirim S, Emeklioglu C, Balci BG, Genc S, Cingillioglu B, Mihmanli V, Khalil A, Kalafat E. Sahin O, et al. Among authors: balci bg. Int J Clin Pract. 2021 Nov;75(11):e14670. doi: 10.1111/ijcp.14670. Epub 2021 Aug 26. Int J Clin Pract. 2021. PMID: 34342119 Free PMC article.

9

Accelerometer-measured physical activity patterns in daily life and their association with factors of sedentary behavior in people with epilepsy.

Aktar B, Balci B, Eraslan Boz H, Ferik Ozalan S, Oztura I, Baklan B. Aktar B, et al. Among authors: balci b. Epilepsy Behav. 2024 Dec 11;163:110198. doi: 10.1016/j.yebeh.2024.110198. Online ahead of print. Epilepsy Behav. 2024. PMID: 39667124

10

Nationwide prospective audit for the evaluation of appendicitis risk prediction models in adults: right iliac fossa treatment (RIFT)-Turkey.

Yalcinkaya A, Yalcinkaya A, Balci B, Keskin C, Erkan I, Yildiz A, Kamer E, Leventoglu S; RIFT TURKEY Study Collaboration. Yalcinkaya A, et al. Among authors: balci b. BJS Open. 2024 Sep 3;8(5):zrae120. doi: 10.1093/bjsopen/zrae120. BJS Open. 2024. PMID: 39383358 Free PMC article.

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