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1دورية أكاديمية
المؤلفون: Sepehr Javadikooshesh, Hooshang Zaimkohan, Parisa Pourghorban, Fatemeh Bahramim, Nader Ebadi
المصدر: Iranian Journal of Medical Sciences, Vol 46, Iss 6, Pp 493-497 (2021)
مصطلحات موضوعية: leukodystrophy, hypomyelinating, 2, mutation, whole exome sequencing, central nervous system diseases, Medicine (General), R5-920
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Mirsajjad MOUSAVI-ASL GERMEH CHESHMEH, Ali NAJIZADEH, Saied HOSSEINI-ASL, Hooshang ZAIMKOHAN, Roshanak JAZAYERI
المصدر: Iranian Journal of Public Health, Vol 48, Iss 7 (2019)
مصطلحات موضوعية: Nail dysplasia, FZD6 gene, Autosomal recessive, Iran, Public aspects of medicine, RA1-1270
وصف الملف: electronic resource
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3
المؤلفون: Ali Najizadeh, Mirsajjad Mousavi-Asl Germeh Cheshmeh, Saied Hosseini-Asl, Roshanak Jazayeri, Hooshang Zaimkohan
المصدر: Iranian Journal of Public Health
Iranian Journal of Public Health, Vol 48, Iss 7 (2019)مصطلحات موضوعية: medicine.medical_specialty, Nail dysplasia, integumentary system, business.industry, lcsh:Public aspects of medicine, Autosomal recessive, Public Health, Environmental and Occupational Health, Abnormal Nails, lcsh:RA1-1270, Case Report, Iran, medicine.disease, Dermatology, medicine.anatomical_structure, FZD6 gene, Dysplasia, Nail (anatomy), Medicine, business, skin and connective tissue diseases, Gene, NAIL DYSTROPHY
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4
المؤلفون: Nami Mohammadian Khonsari, Shahab Noorian, Farzaneh Rohani, Sharham Savad, Kourosh Kabir, Benyamin Hakak-Zargar, Nima Ghanipour, Mehri Gholami, Hooshang Zaimkohan
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::38795a19cc2fae2c539c792e02df302f
https://doi.org/10.21203/rs.2.22066/v1 -
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المؤلفون: Shahab Noorian, Farzaneh Rohani, Shahram Savad, Kourosh Kabir, Nami Mohammadian Khonsari, Nima Ghanipour, Mehri Gholami, Hooshang Zaimkohan
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2d8c6a1c97567c9c416a6baa3bb1acab
https://doi.org/10.21203/rs.2.16842/v1 -
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المؤلفون: Maryam Pirhoushiaran, Mohsen Moohebati, Hamideh Ghazizadeh, Alireza Pasdar, Mahdi Nohtani, Hooshang Zaimkohan, Khadijeh Jamialahmadi, Amir Avan, Gordon A. Ferns, Majid Ghayour-Mobarhan, Marzieh Ghalandari, Maryam Mardan Nik, Hassan Rooki, Seyed Reza Mirhafez
المصدر: Cytokine. 139
مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Genotype, Immunology, Coronary Artery Disease, Iran, Biochemistry, Polymorphism, Single Nucleotide, Coronary artery disease, 03 medical and health sciences, 0302 clinical medicine, Polymorphism (computer science), Internal medicine, Genetic model, Immunology and Allergy, Medicine, Humans, Genetic Predisposition to Disease, Allele, Molecular Biology, Alleles, Cause of death, business.industry, Case-control study, Hematology, Middle Aged, medicine.disease, Atherosclerosis, Interleukin-10, 030104 developmental biology, Cross-Sectional Studies, 030220 oncology & carcinogenesis, Meta-analysis, Case-Control Studies, Female, business, Polymorphism, Restriction Fragment Length
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7
المؤلفون: Mohammad Piryaei, Hooshang Zaimkohan, Javad Tavakkoly-Bazzaz, Majid Ghayour-Mobarhan, Azadeh Tahooni, Mohammad Keramatipour, Seyed Reza Mirhafez, Seyed Mohammad Hossein Ghaderian
المصدر: Iranian Red Crescent Medical Journal
مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Population, Coronary Artery Disease, Proprotein Convertase Subtilisin/Kexin Type 9, Coronary artery disease, 03 medical and health sciences, PCSK9 Gene, Internal medicine, Medicine, cardiovascular diseases, Polymorphism, education, Genotyping, education.field_of_study, business.industry, PCSK9, Melanoma inhibitory activity, General Medicine, medicine.disease, 3. Good health, Kowsar, 030104 developmental biology, Endocrinology, Kexin, business, Research Article