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Ashraf Samavat

Showing results (1-10 of 9) with videos related to

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BMJ (Clinical Research Ed.)|November 13, 2004
Iranian national thalassaemia screening programmeAshraf Samavat, Bernadette Modell
Prenatal Diagnosis|December 3, 2009
Iranian national program for the prevention of thalassemia and prenatal diagnosis : mandatory premarital screening and legal medical abortionMohammad-Sadegh Fallah, Ashraf Samavat, Sirous Zeinali
Medical Journal of the Islamic Republic of Iran|March 24, 2022
Effectiveness of the Preventive Intervention of Chromosomal Disorders of Iran's Community Genetics Program: Application of Bayesian NetworkSeyyedeh Sara Azimi, Sama Ashraf Samavat, Vahid Rezaei Tabar, et al.
JIMD Reports|June 2, 2016
Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian PatientsShohreh Khatami, Soghra Rouhi Dehnabeh, Sirous Zeinali, et al.
Community Genetics|April 14, 2006
Fourteen-year experience of prenatal diagnosis of thalassemia in IranHossein Najmabadi, Alireza Ghamari, Farhad Sahebjam, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 2, 2021
The treatment and clinical follow-up outcome in Iranian patients with tetrahydrobiopterin deficiencySoghra Khani, Mina Barzegari, Zahra Esmaeilizadeh, et al.
Journal of Inherited Metabolic Disease|August 31, 2018
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous populationTina Shirzadeh, Amir Hossein Saeidian, Hamideh Bagherian, et al.
International Archives of Allergy and Immunology|July 3, 2020
Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and AutoimmunityMohammad Hossein Asgardoon, Gholamreza Azizi, Reza Yazdani, et al.
The Journal of Allergy and Clinical Immunology. in Practice|September 22, 2018
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency CohortReza Yazdani, Hassan Abolhassani, Fatemeh Kiaee, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
BMJ (Clinical Research Ed.)|November 13, 2004
Iranian national thalassaemia screening programmeAshraf Samavat, Bernadette Modell
Prenatal Diagnosis|December 3, 2009
Iranian national program for the prevention of thalassemia and prenatal diagnosis : mandatory premarital screening and legal medical abortionMohammad-Sadegh Fallah, Ashraf Samavat, Sirous Zeinali
Medical Journal of the Islamic Republic of Iran|March 24, 2022
Effectiveness of the Preventive Intervention of Chromosomal Disorders of Iran's Community Genetics Program: Application of Bayesian NetworkSeyyedeh Sara Azimi, Sama Ashraf Samavat, Vahid Rezaei Tabar, et al.
JIMD Reports|June 2, 2016
Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian PatientsShohreh Khatami, Soghra Rouhi Dehnabeh, Sirous Zeinali, et al.
Community Genetics|April 14, 2006
Fourteen-year experience of prenatal diagnosis of thalassemia in IranHossein Najmabadi, Alireza Ghamari, Farhad Sahebjam, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 2, 2021
The treatment and clinical follow-up outcome in Iranian patients with tetrahydrobiopterin deficiencySoghra Khani, Mina Barzegari, Zahra Esmaeilizadeh, et al.
Journal of Inherited Metabolic Disease|August 31, 2018
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous populationTina Shirzadeh, Amir Hossein Saeidian, Hamideh Bagherian, et al.
International Archives of Allergy and Immunology|July 3, 2020
Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and AutoimmunityMohammad Hossein Asgardoon, Gholamreza Azizi, Reza Yazdani, et al.
The Journal of Allergy and Clinical Immunology. in Practice|September 22, 2018
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency CohortReza Yazdani, Hassan Abolhassani, Fatemeh Kiaee, et al.
Pageof 1