Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Maryam Malakouti Nejad"'
Autor:
Farhang Aliakbari, Hassan Bardania, Alireza Baradaran-Rafii, Daniela Monti, Elahe Elahi, Maryam Malakouti-Nejad, Dina Morshedi
Publikováno v:
International journal of pharmaceutics. 590
Bevacizumab (Avastin®), an anti-vascular endothelial growth factor, is one of the most effective drugs widely used to inhibit ocular angiogenesis. Nanoliposomes were recruited to improve the accessibility of bevacizumab (BVZ) during treatment. To op
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb602bcaf46f503962e0cf2c32820c1a
https://pubmed.ncbi.nlm.nih.gov/32956821
https://pubmed.ncbi.nlm.nih.gov/32956821
Publikováno v:
Neurobiology of aging. 54
Various neurodegenerative disorders share some clinical features that sometimes renders differential diagnosis challenging. Genetic-based classification also has limitations as mutations in the same gene are sometimes associated with different clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12897bb3d87e85d35918474385d2de77
https://pubmed.ncbi.nlm.nih.gov/28365006
https://pubmed.ncbi.nlm.nih.gov/28365006
Autor:
Mehrdad Hashemi, Maryam Malakouti-Nejad, Jian-Bing Fan, Mohammad Rohani, Gholam Ali Shahidi, Brandy Klotzle, Seyed Mehdi Shojaee, Elahe Elahi
Publikováno v:
Neuroscience letters. 577
We present results of homozygosity mapping in two siblings affected with early onset Parkinson's disease (EOPD) and mutation screening of ATP13A2 in these and other Iranian EOPD patients. Genome-wide SNP homozygosity analysis revealed linkage to a lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::428617c27e128a4347dcb8a5bf3d7438
https://pubmed.ncbi.nlm.nih.gov/24949580
https://pubmed.ncbi.nlm.nih.gov/24949580
Autor:
Brandy Klotzle, Elham Jaberi, Masoud Houshmand, Elahe Elahi, Mohammad Rohani, Iman Safari, Maryam Malakouti Nejad, Farzad Sina, Fereshteh Chitsazian, Gholam Ali Shahidi
Publikováno v:
Journal of human genetics. 58(8)
SUCLA2 is one of several nuclear-encoded genes that can cause encephalomyopathy accompanied by mitochondrial DNA depletion. The disorder usually manifests in early childhood and leads to early death. The gene encodes one of the subunits of succinyl-C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a7a0386080bde260e9fd686edac5dd1
https://pubmed.ncbi.nlm.nih.gov/23759946
https://pubmed.ncbi.nlm.nih.gov/23759946