| 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 | 61 | 2008 |
| 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 | 51 | 2001 |
| 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 | 45 | 2008 |
| 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 | 39 | 2007 |
| 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 | 33 | 2016 |
| 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 | 29 | 1997 |
| 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 | 22 | 2008 |
| 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 | 21 | 2010 |
| Natural history of SMA IIIB F Deymeer, P Serdaroglu, Y Parman, M Poda Neurology 71, 664-649, 2008 | 11 | 2008 |
| 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 | 4 | 2008 |
| 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, ... North Clin Istanb 9, 439-44, 2022 | 3 | 2022 |
| 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 | 2 | 2022 |
| 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 | 2 | 2015 |
| Kalıtsal Dislipdemi Fenotipleri ve Genetik ilişkiler Üzerine Derleme P Mehveş Deneysel Tıp Araştırma Enstitüsü Dergisi 1 (2), 14-19, 2011 | 2 | 2011 |
| 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 | 1 | 2022 |
| Analysis of genotype, subgenotype and serotype of occult hepatitis B virus. B Çakal, A Atasoy, B Çavuş, AÇ Örmeci, M Poda, M Bulakçı, M Güllüoğlu, ... | 1 | 2021 |
| 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 | 1 | 2021 |
| 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 | 1 | 2017 |
| Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey H Durmus, A Cakar, E Sahin, Z Matur, M Poda, U Altunoglu, Y Parman WILEY, 2017 | 1 | 2017 |
| 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 | 1 | 2015 |
Nihan Erginel-UnaltunaIstanbul UniversityVerified email at istanbul.edu.tr
