Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Spinal müsküler atrofi"'
Publikováno v:
Ebelik ve Sağlık Bilimleri Dergisi, Vol 7, Iss 3, Pp 541-547 (2024)
SMA, a genetic neuromuscular disease that affects the control of muscle movement and results in severe motor disorders, is among the rare diseases. Due to the low prevalence of rare diseases and serious problems with correct diagnosis, there may be d
Externí odkaz:
https://doaj.org/article/1953c805dd0a49f1ba11e96b3565a5f9
Autor:
KİPOĞLU, Osman, KARAKILIÇ ÖZTURHAN, Esin, COŞKUN, Orhan, ÖZTÜRK, Ayşe Pınar, PEMBEGÜL YILDIZ, Edibe, BAŞ, Firdevs, AYDINLI, Nur, ÇALIŞKAN, Mine
Publikováno v:
Volume: 85, Issue: 1 22-28
Journal of Istanbul Faculty of Medicine
Journal of Istanbul Faculty of Medicine
Objective: Spinal muscular atrophy is a lower motor neuron disease, but other parts of the body could be affected. This study compared bone mineral density with bone metabolism and physical growth rates in patients diagnosed with spinal muscular atro
Spinal müsküler atrofi hastalarının fibroblast kültürlerinde mikrotübül stabilitesinin araştırılması
Autor:
Zobaroğlu, Pelin
Spinal müsküler atrofi (SMA) motor nöron kaybı ve kas atrofisi ile karakterize olan, çoğunlukla yenidoğan ve çocukları etkileyen, otozomal resesif kalıtım gösteren nörodejeneratif bir hastalıktır. SMA 5q13.3 kromozom bölgesinde yer al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7628a79771042216ac40c4fe64b36d8f
https://acikbilim.yok.gov.tr/handle/20.500.12812/489211
https://acikbilim.yok.gov.tr/handle/20.500.12812/489211
Autor:
Yeşbek Kaymaz, Ayşe
Yeşbek Kaymaz, A. Spinal Muscular Atrophy Phenotype Variations and Insulin Like Growth Factors/Binding Proteins. Hacettepe University Institute of Health Sciences Medical Biology Programme, Doctor of Philosophy Thesis, Ankara, 2017. Spinal muscular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::42594c9b8401f43ab9a8a759fc2daa13
https://acikbilim.yok.gov.tr/handle/20.500.12812/491353
https://acikbilim.yok.gov.tr/handle/20.500.12812/491353