Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mohammad Kahani"'
Autor:
Seyyed Mohammad Kahani, Ali Rabbizadeh Saray, Mir Salar Kahaei, Ali Dehghani, Pouria Mohammadi, Masoud Garshasbi
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-14 (2024)
Abstract Background Hermansky-Pudlak Syndrome (HPS), a rare autosomal recessive disorder, is characterized by oculocutaneous albinism, bleeding diathesis, and sometimes severe lung problems and inflammatory bowel disease. Symptoms include skin and ha
Externí odkaz:
https://doaj.org/article/41e03dc6fff14af98a32c56322293656
Autor:
Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-18 (2023)
Abstract Background Phospholipase-associated neurodegeneration (PLAN) caused by mutations in the PLA2G6 gene is a rare neurodegenerative disorder that presents with four sub-groups. Infantile neuroaxonal dystrophy (INAD) and PLA2G6-related dystonia-p
Externí odkaz:
https://doaj.org/article/33b08d5b1a9846ac9b6a4cfa26acdbbd
Autor:
Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani, Afshin Bahramy, Seyed Mohammad Salar Zaheryani, Javad Behroozi, Seyyed Mohammad Kahani, Pouria Mohammadi, Masoud Garshasbi
Publikováno v:
Clinical Case Reports, Vol 11, Iss 10, Pp n/a-n/a (2023)
Key Clinical Message Congenital myasthenic syndromes‐5 (CMS5) is a rare autosomal recessive heterogeneous disorder, caused by pathogenic variants in the COLQ that lead to skeletal muscle weakness and abnormal fatigability. The onset is usually from
Externí odkaz:
https://doaj.org/article/df4b91691d194b778f63d76417dd44d8
Autor:
Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/1a7e2a9cd0cb490ba3fb6216410a703b
Autor:
Ali Reza Tavasoli, Ali Zare Dehnavi, Maryam Bemanalizadeh, Mohammad Kahani, Mohammad Rohani, Mehran Beriraghi Toosi, Mahmoud Reza Ashrafi, Morteza Heidari, Man Amanat, Sareh Hosseinpour
Publikováno v:
Sunday, April 23.
Autor:
Ali, Dehghani, Elham, Zokaei, Seyyed Mohammad, Kahani, Elaheh, Alavinejad, Mohammad, Dehghani, Gholam Hossein, Meftahi, Mohammad Reza, Afarinesh
Publikováno v:
Asian Journal of Psychiatry. 72:103097
Due to its high prevalence and fatality, the current Severe Acute Respiratory Syndrome-coronavirus-2 (SARS-CoV-2) virus, which first emerged in China in 2019, quickly spread around the world and immediately became a serious global health concern. Alt