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MEHVEŞ PODA
MEHVEŞ PODA
Verified email at istanbul.edu.tr
Title
Cited by
Cited by
Year
Natural history of SMA IIIb: muscle strength decreases in a predictable sequence and magnitude
F Deymeer, P Serdaroglu, Y Parman, M Poda
Neurology 71 (9), 644-649, 2008
742008
Mapping of the second Friedreich's ataxia (FRDAff2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity
K Christodoulou, F Deymeer, P Serdaroğlu, C Özdemir, M Poda, ...
Neurogenetics 3, 127-132, 2001
512001
Gender-modulated impact of apolipoprotein A5 gene (APOA5) −1131T>C and c.56C>G polymorphisms on lipids, dyslipidemia and metabolic syndrome in Turkish …
E Komurcu-Bayrak, A Onat, M Poda, SE Humphries, J Palmen, F Guclu, ...
Clinical chemistry and laboratory medicine 46 (6), 778-784, 2008
462008
The S447X variant of lipoprotein lipase gene is associated with metabolic syndrome and lipid levels among Turks
E Komurcu-Bayrak, A Onat, M Poda, SE Humphries, J Acharya, ...
Clinica chimica acta 383 (1-2), 110-115, 2007
392007
Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey
H Durmuş-Tekçe, Z Matur, MM Atmaca, M Poda, A Çakar, ÜH Ulaş, ...
Neuromuscular Disorders 26 (7), 441-446, 2016
352016
Segmental distribution of muscle weakness in SMA III: implications for deterioration in muscle strength with time
F Deymeer, P Serdaroğlu, M Poda, Y Gülşen-Parman, T Özçelık, ...
Neuromuscular Disorders 7 (8), 521-528, 1997
301997
CETP TaqIB polymorphism in Turkish adults: association with dyslipidemia and metabolic syndrome.
B Özsait, E Kömürcü-Bayrak, M Poda, G Can, G Hergenç, A Onat, ...
Anatolian Journal of Cardiology/Anadolu Kardiyoloji Dergisi 8 (5), 2008
222008
Pretreatment with octreotide modulates iNOS gene expression, mimics surgical delay, and improves flap survival
A Gözü, M Poda, EI Taskin, H Turgut, N Erginel-Ünaltuna, H Dogruman, ...
Annals of plastic surgery 65 (2), 245-249, 2010
212010
A novel protein involved in heart development in Ambystoma mexicanum is localized in endoplasmic reticulum
P Jia, C Zhang, XP Huang, M Poda, F Akbas, SL Lemanski, ...
Journal of biomedical science 15, 789-799, 2008
42008
Comparison of S gene mutations in patients with occult and chronic hepatitis B virus infection
B Cakal, B Cavus, A Atasoy, D Altunok, M Poda, M Bulakci, M Gulluoglu, ...
Virus research 318, 198855, 2022
32022
The effects of IL28B rs12979860 and rs8099917 polymorphism on hepatitis B infection
B Cakal, B Cavus, A Atasoy, D Altunok, M Poda, M Bulakci, M Gulluoglu, ...
Northern Clinics of Istanbul 9 (5), 439, 2022
32022
What is the clinical impact of occult HBV infections and anti‐HBc positivity in patients with chronic hepatitis C?
B Cakal, B Cavus, A Atasoy, M Poda, M Bulakci, M Gulluoglu, M Demirci, ...
Microbiology and immunology 66 (8), 386-393, 2022
22022
OKÜLT HEPATİT B VİRÜSÜNÜN GENOTİP, SUBGENOTİP VE SUBTİP ANALİZİ
B Çakal, A Atasoy, B Çavuş, A Örmeci, M Poda, M Bulakçı, M Güllüoğlu, ...
Journal of Istanbul Faculty of Medicine 84 (3), 402-410, 2021
22021
Case report of fatal Mycobacterium tilburgii infection
T Akpinar, OK Bakkaloglu, B Ince, F Tufan, M Kose, M Poda, D Tascioglu, ...
Journal of Infection and Chemotherapy 21 (7), 538-540, 2015
22015
Kalıtsal Dislipdemi Fenotipleri ve Genetik ilişkiler Üzerine Derleme
M Poda
Deneysel Tıp Araştırma Enstitüsü Dergisi 1 (2), 14-19, 2011
22011
ANALYSIS OF GENOTYPE, SUBGENOTYPE AND SEROTYPE OF OCCULT HEPATITIS B VIRUS/OKULT HEPATIT B VIRUSUNUN GENOTIP, SUBGENOTIP VE SUBTIP ANALIZI.
B Cakal, A Atasoy, B Cavus, A Ormeci, M Poda, M Bulakci, M Gulluoglu, ...
Journal of Istanbul Faculty of Medicine 84 (3), 402-411, 2021
12021
Evaluation of dystrophin gene deletion patterns in a large Duchenne/Becker muscular dystrophy patient sample; 17 years experience from one Turkish Diagnostic Center
M Poda, FG Geyik, N Çoban, B Tüysüz, G Güven, EK Bayrak, ...
Deneysel Tıp Araştırma Enstitüsü Dergisi 7 (14), 50-61, 2017
12017
Adacık Benzeri Hücre Kümeleşmesinde Gen Anlatım Değişimleri
M Poda, BG Hasanoğulları, FY Ekici, FN Tuncer
Deneysel Tıp Araştırma Enstitüsü Dergisi 7 (13), 87-92, 2017
12017
Genotypic and phenotypic presentation of Glu89Gln mutation in Turkey
H Durmus, Z Matur, MM Atmaca, M Poda, A Cakar, P Serdaroglu-Oflazer, ...
Orphanet Journal of Rare Diseases 10, 1-1, 2015
12015
Genotypic and Phenotypic Presentation of TTR-FAP in Turkey (P2. 034)
H Durmus, Z Matur, M Poda, MM Atmaca, P Serdaroglu, F Deymeer, ...
Neurology 84 (14_supplement), P2. 034, 2015
12015
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