Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Farzad, Ahmadabadi"'
Autor:
Mohammad Jahanpanah, Diana Mokhtari, Haleh Mokaber, Sara Arish, Farzad Ahmadabadi, Behzad Davarnia
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 4, Pp n/a-n/a (2024)
Abstract Background The ASNS (ASNS, MIM 108370) gene variations are responsible for asparagine synthetase deficiency (ASNSD, MIM 615574), a very rare autosomal recessive disease characterized by cerebral anomalies. These patients have congenital micr
Externí odkaz:
https://doaj.org/article/a14c84459ae3489ab47b8dd356746982
Autor:
Farhad Salehzadeh, Farhad Pourfarzi, Rasool Molatefi, Behzad Davarnia, Ehsan Shahbazfar, Farzad Ahmadabadi
Publikováno v:
Iranian Journal of Medical Sciences, Vol 48, Iss 1, Pp 43-48 (2023)
Background: In December 2019, an outbreak of pneumonia caused by the novel coronavirus disease 2019 (COVID-19) became a pandemic and caused a global health crisis. This study evaluates the immunogenic potential of the Mediterranean fever (MEFV) gene
Externí odkaz:
https://doaj.org/article/5a1c109d6f6849b18216ea22e7fcf728
Autor:
Yuji Nakamura, Issei S. Shimada, Reza Maroofian, Henry Houlden, Micol Falabella, Masanori Fujimoto, Emi Sato, Hiroshi Takase, Shiho Aoki, Akihiko Miyauchi, Eriko Koshimizu, Satoko Miyatake, Yuko Arioka, Mizuki Honda, Takayoshi Higashi, Fuyuki Miya, Yukimune Okubo, Isamu Ogawa, Annarita Scardamaglia, Mohammad Miryounesi, Sahar Alijanpour, Farzad Ahmadabadi, Peter Herkenrath, Hormos Salimi Dafsari, Clara Velmans, Mohammed Balwi, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Médéric Jeanne, Antoine Civit, Maha S. Zaki, Hossein Darvish, Somayeh Bakhtiari, Michael Kruer, Christopher J Carroll, Ehsan Ghayoor Karimiani, Rozhgar A Khailany, Talib Adil Abdulqadir, Mehmet Ozaslan, Peter Bauer, Giovanni Zifarelli, Tahere Seifi, Mina Zamani, Chadi Al Alam, Robert D S Pitceathly, Kazuhiro Haginoya, Tamihide Matsunaga, Hitoshi Osaka, Naomichi Matsumoto, Norio Ozaki, Yasuyuki Ohkawa, Shinya Oki, Tatsuhiko Tsunoda, Yoshitaka Taketomi, Makoto Murakami, Yoichi Kato, Shinji Saitoh
PNPLA8, one of the calcium-independent phospholipase A2 enzymes, is involved in various physiological processes through the maintenance of membrane phospholipids. However, little is known about its role in brain development. Here, we report 12 indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3166c6dd5bfac2bccc9f569d1910b079
https://doi.org/10.1101/2023.04.26.23288947
https://doi.org/10.1101/2023.04.26.23288947
Publikováno v:
Pharmaceutical Sciences, Vol 22, Iss 2, Pp 132-137 (2016)
Background: Poisoning is a major cause of morbidity and mortality in children. Medicines and household cleaning products are responsible for the majority of cases. The aim of the present study is to analyze poisoning cases presenting to Tabriz childr
Externí odkaz:
https://doaj.org/article/fffbee0e8253410489092c884f26402b
Autor:
Samareh Panjeshahi, Parvaneh Karimzadeh, Abolfazl Movafagh, Farzad Ahmadabadi, Elham Rahimian, Sahar Alijanpour, Mohammad Miryounesi
Neuronal ceroid lipofuscinoses (NCLs) are neurodegenerative lysosomal storage diseases witch considered among the most frequent cause of dementia in childhood worldwide This study aimed to identify the gene variants, molecular etiologies, and clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3496a054d9ac750d34661f9224710008
https://doi.org/10.21203/rs.3.rs-2514013/v1
https://doi.org/10.21203/rs.3.rs-2514013/v1
Autor:
Farzad Ahmadabadi, Mehrdad Mirzarahimi, Mehdi Samadzadeh, Ashkan Nikaeen, Bita Shahbazzadegan, Mahshid Hajiali
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 31, Iss 262, Pp 1910-1918 (2014)
Background: Seizure is accompany with neurons function disorder and abnormal electrical action. However, febrile convulsion seizure is usually benign and causes no important problem for patients; but all children with febrile convulsion are usually f
Externí odkaz:
https://doaj.org/article/6a0672c454934c62b47f61aef9d33959
Autor:
Maryam Motezarre, Ahad Azami, Farhad Salehzadeh, Farzad Ahmadabadi, Roghayeh Nematdoust Haghi
Publikováno v:
Open Access Rheumatology: Research and Reviews. 12:15-19
Background and aims Familial Mediterranean Fever (FMF) is a periodic auto-inflammatory disease with an autosomal recessive hereditary pattern. The aim of this study is to explain the spectrum of possible neurological manifestations and its genotype-p
Publikováno v:
Acta Medica Iranica, Vol 50, Iss 1, Pp 21-25 (2012)
Clofibrate is a glucuronosyl transferase inducer that has been proposed to increase the elimination of bilirubin in neonates with hyperbilirubinemia. This study was conducted to determine the therapeutic effect of clofibrate in term neonates with non
Externí odkaz:
https://doaj.org/article/b4a3c01973c246d1a0f85834823b6de7
Autor:
Hamid, Nemati, Farzad, Ahmadabadi, Mina, Shahisavandi, Mohsen, Farjoud Kouhanjani, Mahtab, Rostamihosseinkhani
Publikováno v:
Iranian journal of child neurology. 16(2)
Gratification disorder is a group of self-stimulatory behaviors tending to form a habit. These normal behaviors are common and have various differential diagnoses, including epilepsy. Hence, misdiagnosis may lead to performing unnecessary workups and
Autor:
Farzad, Ahmadabadi, Abdullah, Motamedi, Ghazal, Zahed, Akram, Motamedi, Farshid, Shahriari, Farhad, Pourfarzi, Narjes, Jafari, Mohammad Mehdi, Hosseini
Publikováno v:
Iranian journal of child neurology. 16(3)
Stuttering is a common problem at all ages that is required to be treated since childhood. Atomoxetine is currently used for the treatment of attention deficit hyperactivity disorder (ADHD). It can be effective for the treatment of stuttering due to