Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Masoumeh Falah"'
Publikováno v:
Journal of Research & Health, Vol 13, Iss 6, Pp 427-436 (2023)
Background: Difficulty regulating emotion has been identified as a trans-diagnostic factor common to various psychiatric diagnoses and behavior problems. This study aims to implement emotion regulation training techniques on adolescents with a disrup
Externí odkaz:
https://doaj.org/article/20b46c61bfac41cba94e66373078d32f
Autor:
Ahmad Daneshi, Masoud Garshasbi, Mohammad Farhadi, Khalil Ghasemi Falavarjani, Mohammad Vafaee-Shahi, Navid Almadani, MohammadSina Zabihi, Mohammad Amin Ghalavand, Masoumeh Falah
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-22 (2023)
Abstract Background Mutations in ABHD12 (OMIM: 613,599) are associated with polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract (PHARC) syndrome (OMIM: 612674), which is a rare autosomal recessive neurodegenerative disease. PHARC
Externí odkaz:
https://doaj.org/article/3d3039bb6e094fa08737ec43ea18b442
Autor:
Mohammad Amin Ghalavand, Alimohamad Asghari, Mohammad Farhadi, Farzad Taghizadeh-Hesary, Masoud Garshasbi, Masoumeh Falah
Publikováno v:
Cancer Cell International, Vol 23, Iss 1, Pp 1-27 (2023)
Abstract Neurofibromatosis type 2 (NF2) is a genetic condition marked by the development of multiple benign tumors in the nervous system. The most common tumors associated with NF2 are bilateral vestibular schwannoma, meningioma, and ependymoma. The
Externí odkaz:
https://doaj.org/article/4f8195ce18a6490e80e5475a4770417e
Autor:
Sima Rayat, Nasim Ramezanidoraki, Nima Kazemi, Mohammad H. Modarressi, Masoumeh Falah, Safoura Zardadi, Saeid Morovvati
Publikováno v:
BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Coronary artery disease (CAD) is the most common heart disease. Several studies have shown association between some polymorphism in different genes with CAD. Finding this association can be used in order to early diagnosis and pre
Externí odkaz:
https://doaj.org/article/3aa47ba280404fde85368c446927b64f
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-10 (2022)
Abstract Background Transmembrane inner ear (TMIE) protein is an essential component of the mechanotransduction complex. In collaboration with other components, TMIE aids the maintenance and function of the sensory hair cells. Autosomal recessive dea
Externí odkaz:
https://doaj.org/article/e92d8271d23e48c3aef2735fd677ac22
Publikováno v:
پژوهش در دین و سلامت, Vol 6, Iss 4, Pp 88-100 (2020)
سابقه و هدف: بي‌توجهي به جنبه‌هاي اجتماعي سلامت سالمندان در عصر ارتباطات و جهاني‌سازي، موجب افزایش آسيب‌پذیري این قشر از افراد جامعه د
Externí odkaz:
https://doaj.org/article/c9c4d5cf048f400a812c3c3c801a4ccc
Publikováno v:
Journal of Research & Health; Nov/Dec2023, Vol. 13 Issue 6, p427-435, 9p
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 34, Iss 382, Pp 526-535 (2016)
کاهش شنوایی حسی- عصبی پیش‌رونده در طی افزایش سن، پیرگوشی نامیده می‌شود. پیرگوشی، یکی از شایع‌ترین بیماری‌های مزمن کهن‌سالی است. این بی
Externí odkaz:
https://doaj.org/article/a92a815fbf6f46b7bbe7eee9a36b651c
Publikováno v:
Journal of Cellular and Molecular Medicine
Different cellular mechanisms contribute to the hearing sense, so it is obvious that any disruption in such processes leads to hearing impairment that greatly influences the global economy and quality of life of the patients and their relatives. In t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d71d9b6e7a693c1f0f16a6d1faa93c3
https://doi.org/10.1111/jcmm.16610
https://doi.org/10.1111/jcmm.16610
Autor:
Masoumeh Falah Nodehi
Publikováno v:
Journal of Occupational Health and Epidemiology. 9:61-67
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8f09e6b0833e7781282f86e8544ec5b
https://doi.org/10.29252/johe.9.1.61
https://doi.org/10.29252/johe.9.1.61