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Pervin Dinçer
Pervin Dinçer
Tıp Fakültesi Profesörü, Hacettepe Üniversitesi
Verified email at hacettepe.edu.tr
Title
Cited by
Cited by
Year
A dystroglycan mutation associated with limb-girdle muscular dystrophy
Y Hara, B Balci-Hayta, T Yoshida-Moriguchi, M Kanagawa, ...
New England Journal of Medicine 364 (10), 939-946, 2011
2792011
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
B Balci, G Uyanik, P Dincer, C Gross, T Willer, B Talim, G Haliloglu, ...
Neuromuscular Disorders 15 (4), 271-275, 2005
1952005
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.
I Richard, L Brenguier, P Dincer, C Roudaut, B Bady, JM Burgunder, ...
American journal of human genetics 60 (5), 1128, 1997
1411997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey
P Dincer, F Leturcq, I Richard, F Piccolo, D Yalnizoàlu, C De Toma, ...
Annals of Neurology: Official Journal of the American Neurological …, 1997
1341997
Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy
H Gundesli, B Talim, P Korkusuz, B Balci-Hayta, S Cirak, NA Akarsu, ...
The American Journal of Human Genetics 87 (6), 834-841, 2010
1292010
Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: a novel gene related to nuclear envelopathies
G Kayman-Kurekci, B Talim, P Korkusuz, N Sayar, T Sarioglu, I Oncel, ...
Neuromuscular Disorders 24 (7), 624-633, 2014
822014
A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies
N Cetin, B Balci-Hayta, H Gundesli, P Korkusuz, N Purali, B Talim, E Tan, ...
Journal of medical genetics 50 (7), 437-443, 2013
772013
A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan
P Dinçer, B Balcı, Y Yuva, B Talim, M Brockington, D Dinçel, S Torelli, ...
Neuromuscular Disorders 13 (10), 771-778, 2003
612003
Calpain-3 mutations in Turkey
B Balci, S Aurino, G Haliloglu, B Talim, S Erdem, Z Akcören, E Tan, ...
European journal of pediatrics 165, 293-298, 2006
562006
Calpain-3 deficiency causes a mild muscular dystrophy in childhood
H Topaloǧlu, P Dincer, I Richard, Z Akçören, D Alehan, Ş Özme, ...
Neuropediatrics 28 (04), 212-216, 1997
541997
A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families
P Dinçer, Z Akçören, E Demir, I Richard, Ö Sancak, G Kale, S Özme, ...
Journal of medical genetics 37 (5), 361-367, 2000
432000
A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F
P Dincer, CG Bönnemann, ÖE Aker, Z Akçören, V Nigro, LM Kunkel, ...
Neuromuscular Disorders 10 (4-5), 247-250, 2000
282000
Efficient transfection of mouse‐derived C2C12 myoblasts using a matrigel basement membrane matrix
B Balcı, P Dinçer
Biotechnology Journal: Healthcare Nutrition Technology 4 (7), 1042-1045, 2009
232009
Tedavi yaklaşımlarında yeni bir dönem: Kodlamayan RNA’lar ve hastalıklar
Z AKKAYA, P DİnÇer
Marmara Medical Journal 26 (1), 5-10, 2013
192013
Eosinophilic myositis in calpainopathy: Could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease?
PS Oflazer, H Gundesli, S Zorludemir, T Sabuncu, P Dincer
Neuromuscular Disorders 19 (4), 261-263, 2009
192009
Identification of muscle-specific calpain and β-sarcoglycan genes in progressive autosomal recessive muscular dystrophies
JS Beckmann, I Richard, O Broux, F Fougerousse, V Allamand, ...
Neuromuscular Disorders 6 (6), 455-462, 1996
181996
Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients
P Dinçer, H Topalogˇlu, Ş Ayter, M Özgüç, HA Tas, Y Renda
Brain and Development 18 (2), 91-94, 1996
181996
Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux
G Kayman Kürekçi, E Kural Mangit, C Koyunlar, S Unsal, B Saglam, ...
Scientific reports 11 (1), 7505, 2021
172021
Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6
FY Tuncay, GK Kurekci, SG Ergun, OT Pasaoglu, RF Akata, PR Dincer
Molecular Vision 22, 1267, 2016
172016
Higher angiotensin II type 1 receptor levels and activity in the postmortem brains of older persons with Alzheimer’s dementia
C Cosarderelioglu, LS Nidadavolu, CJ George, R Marx-Rattner, L Powell, ...
The Journals of Gerontology: Series A 77 (4), 664-672, 2022
152022
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