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1دورية أكاديمية
المؤلفون: Kyana Jafarabady, Arman Shafiee, Razman Arabzadeh Bahri, Ida Mohammadi, Mohammad javad Amini, Shahryar Rajai, Diba Akbarzadeh, Faeze Soltani Abhari, Emad Movahed, Soraya Parvari, Mahmood Bakhtiyari
المصدر: BMC Women's Health, Vol 24, Iss 1, Pp 1-9 (2024)
مصطلحات موضوعية: Endometriosis, Brain-derived neurotrophic factor, BDNF, Gynecology and obstetrics, RG1-991, Public aspects of medicine, RA1-1270
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1472-6874Test
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2دورية أكاديمية
المؤلفون: Rezvan Abtahi, Parvaneh Karimzadeh, Omid Aryani, Diba Akbarzadeh, Shadab Salehpour, Alireza Rezayi, Seyed Hassan Tonekaboni, Reza Zolfaghari Emameh, Massoud Houshmand
المصدر: Hereditas, Vol 159, Iss 1, Pp 1-11 (2022)
مصطلحات موضوعية: Niemann-Pick C, Molecular Study, New Mutation, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1601-5223Test
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3دورية أكاديمية
المؤلفون: Sarina Entezari, Seyedeh Mona Haghi, Narges Norouzkhani, Barsa Sahebnazar, Fatemeh Vosoughian, Diba Akbarzadeh, Muhammad Islampanah, Navid Naghsh, Mohammad Abbasalizadeh, Niloofar Deravi
المصدر: Journal of Toxicology, Vol 2022 (2022)
مصطلحات موضوعية: Toxicology. Poisons, RA1190-1270
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1687-8205Test
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4دورية أكاديمية
المؤلفون: Kyana Jafarabady, Arman Shafiee, Razman Arabzadeh Bahri, Ida Mohammadi, Mohammad javad Amini, Shahryar Rajai, Diba Akbarzadeh, Faeze Soltani Abhari, Emad Movahed, Soraya Parvari, Mahmood Bakhtiyari
مصطلحات موضوعية: Medicine, Genetics, Science Policy, Mental Health, Biological Sciences not elsewhere classified, Endometriosis, Brain-derived neurotrophic factor, BDNF
الإتاحة: https://doi.org/10.6084/m9.figshare.24995480.v1Test
https://figshare.com/articles/journal_contribution/Additional_file_1_of_Brain-derived_neurotrophic_factor_BDNF_as_a_potential_marker_of_endometriosis_a_systematic_review_and_meta-analysis/24995480Test -
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المؤلفون: Melika Mokhtari, Fatemeh Qolipour, Amir Hossein Yousefi, Dorsa Alijanzadeh, Qumars Kasnavi, Tina Sadeghi, Diba Akbarzadeh, Mohammad Sadegh Fallahi, Niloofar Deravi
المصدر: Neurology Asia. 27:535-558
مصطلحات موضوعية: Neurology, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::fca11c512fb26f60024a680e8a1ce032Test
https://doi.org/10.54029/2022psyTest -
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المؤلفون: Ali Ahmadi, Mahdyieh Naziri, Fatemeh Fallahpour, Kosar Gholami, Javad Arabpour, Fateme Pazeshgare, Diba Akbarzadeh, Arina Ansari, Hamoun Sabri, Niloofar Deravi
المصدر: Neurology Asia. 27:1-17
مصطلحات موضوعية: Neurology, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b49f19fe9708a4d2b7750ec47868bcaeTest
https://doi.org/10.54029/2022uxkTest -
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المؤلفون: Shirin Yaghoobpoor, Mobina Fathi, Kimia Vakili, Fatemeh Sayehmiri, Ramtin Hajibeygi, Hossein Hasooni, Mahsa Heidari-Foroozan, Diba Akbarzadeh, Vijay Sawlani, Mehran Anjomrooz, Arian Tavasol, Mohammadreza Hajiesmaeili
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::8923da802fc705e116d6385b39cf01afTest
https://doi.org/10.22541/au.167303809.92917586/v1Test -
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المؤلفون: Rezvan Abtahi, Parvaneh Karimzadeh, Omid Aryani, Diba Akbarzadeh, Shadab Salehpour, Alireza Rezayi, Seyed Hassan Tonekaboni, Reza Zolfaghari Emameh, Massoud Houshmand
المصدر: Hereditas
Hereditas, Vol 159, Iss 1, Pp 1-11 (2022)مصطلحات موضوعية: Molecular Study, New Mutation, Research, Computational Biology, Niemann-Pick Disease, Type C, General Medicine, Exons, QH426-470, Iran, Niemann-Pick C1 Protein, Niemann-Pick C, Mutation, Genetics, Humans
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac315a745c484672117b387471950710Test
https://pubmed.ncbi.nlm.nih.gov/35086560Test -
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المؤلفون: Diba Akbarzadeh, Seyed Hassan Tonekaboni, Rezvan Abtahi, Reza Zolfaghari Emameh, Parvaneh Karimzadeh, Shadab Salehpour, Massoud Houshmand, Alireza Rezayi
المصدر: Journal of molecular neuroscience : MN. 72(3)
مصطلحات موضوعية: Genetics, Heterozygote, Tay-Sachs Disease, beta-Hexosaminidase alpha Chain, Genotype, beta-Hexosaminidase beta Chain, General Medicine, Disease, Exons, Gene mutation, Sandhoff disease, Biology, Iran, medicine.disease, HEXB, Cellular and Molecular Neuroscience, Sphingomyelin Phosphodiesterase, Sphingolipidoses, Mutation, medicine, Humans, Sphingolipidosis, Gene
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61e9b1ec2f684fe31204771326b326ceTest
https://pubmed.ncbi.nlm.nih.gov/34554397Test