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Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.
J Inherit Metab Dis. 2018 Nov;41(6):1159-1167. doi: 10.1007/s10545-018-0228-6. Epub 2018 Aug 29.
J Inherit Metab Dis. 2018.
PMID: 30159852
The treatment and clinical follow-up outcome in Iranian patients with tetrahydrobiopterin deficiency.
Khani S, Barzegari M, Esmaeilizadeh Z, Farsian P, Alaei M, Salehpour S, Setoodeh A, Rohani F, Samavat A, Zekri A, Mirzazadeh R, Sadeghi S, Khatami S.
Khani S, et al. Among authors: samavat a.
J Pediatr Endocrinol Metab. 2021 Jul 2;34(9):1157-1167. doi: 10.1515/jpem-2021-0155. Print 2021 Sep 27.
J Pediatr Endocrinol Metab. 2021.
PMID: 34214291
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Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients.
Khatami S, Dehnabeh SR, Zeinali S, Thöny B, Alaei M, Salehpour S, Setoodeh A, Rohani F, Hajivalizadeh F, Samavat A.
Khatami S, et al. Among authors: samavat a.
JIMD Rep. 2017;32:7-14. doi: 10.1007/8904_2016_572. Epub 2016 Jun 1.
JIMD Rep. 2017.
PMID: 27246466
Free PMC article.
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Iranian national program for the prevention of thalassemia and prenatal diagnosis : mandatory premarital screening and legal medical abortion.
Fallah MS, Samavat A, Zeinali S.
Fallah MS, et al. Among authors: samavat a.
Prenat Diagn. 2009 Dec;29(13):1285-6. doi: 10.1002/pd.2373.
Prenat Diagn. 2009.
PMID: 19953581
No abstract available.
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Iranian national thalassaemia screening programme.
Samavat A, Modell B.
Samavat A, et al.
BMJ. 2004 Nov 13;329(7475):1134-7. doi: 10.1136/bmj.329.7475.1134.
BMJ. 2004.
PMID: 15539666
Free PMC article.
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Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort.
Yazdani R, Abolhassani H, Kiaee F, Habibi S, Azizi G, Tavakol M, Chavoshzadeh Z, Mahdaviani SA, Momen T, Gharagozlou M, Movahedi M, Hamidieh AA, Behniafard N, Nabavi M, Bemanian MH, Arshi S, Molatefi R, Sherkat R, Shirkani A, Amin R, Aleyasin S, Faridhosseini R, Jabbari-Azad F, Mohammadzadeh I, Ghaffari J, Shafiei A, Kalantari A, Mansouri M, Mesdaghi M, Babaie D, Ahanchian H, Khoshkhui M, Soheili H, Eslamian MH, Cheraghi T, Dabbaghzadeh A, Tavassoli M, Kalmarzi RN, Mortazavi SH, Kashef S, Esmaeilzadeh H, Tafaroji J, Khalili A, Zandieh F, Sadeghi-Shabestari M, Darougar S, Behmanesh F, Akbari H, Zandkarimi M, Abolnezhadian F, Fayezi A, Moghtaderi M, Ahmadiafshar A, Shakerian B, Sajedi V, Taghvaei B, Safari M, Heidarzadeh M, Ghalebaghi B, Fathi SM, Darabi B, Bazregari S, Bazargan N, Fallahpour M, Khayatzadeh A, Javahertrash N, Bashardoust B, Zamani M, Mohsenzadeh A, Ebrahimi S, Sharafian S, Vosughimotlagh A, Tafakoridelbari M, Rahim M, Ashournia P, Razaghian A, Rezaei A, Samavat A, Mamishi S, Khazaei HA, Mohammadi J, Negahdari B, Parvaneh N, Rezaei N, Lougaris V, Giliani S, Plebani A, Ochs HD, Hammarström L, Aghamohammadi A.
Yazdani R, et al. Among authors: samavat a.
J Allergy Clin Immunol Pract. 2019 Mar;7(3):864-878.e9. doi: 10.1016/j.jaip.2018.09.004. Epub 2018 Sep 19.
J Allergy Clin Immunol Pract. 2019.
PMID: 30240888
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Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity.
Asgardoon MH, Azizi G, Yazdani R, Sohani M, Pashangzadeh S, Kalantari A, Shariat M, Shafiei A, Salami F, Jamee M, Rasouli SE, Mohammadi J, Hassanpour G, Tavakol M, Chavoshzadeh Z, Mahdaviani SA, Momen T, Behniafard N, Nabavi M, Bemanian MH, Arshi S, Molatefi R, Sherkat R, Shirkani A, Alyasin S, Jabbari-Azad F, Ghaffari J, Mesdaghi M, Ahanchian H, Khoshkhui M, Eslamian MH, Cheraghi T, Dabbaghzadeh A, Nasiri Kalmarzi R, Esmaeilzadeh H, Tafaroji J, Khalili A, Sadeghi-Shabestari M, Darougar S, Moghtaderi M, Ahmadiafshar A, Shakerian B, Heidarzadeh M, Ghalebaghi B, Fathi SM, Darabi B, Fallahpour M, Mohsenzadeh A, Ebrahimi S, Sharafian S, Vosughimotlagh A, Tafakoridelbari M, Rahimi Haji-Abadi M, Ashournia P, Razaghian A, Rezaei A, Delavari S, Shirmast P, Babaha F, Samavat A, Mamishi S, Khazaei HA, Negahdari B, Rezaei N, Abolhassani H, Aghamohammadi A.
Asgardoon MH, et al. Among authors: samavat a.
Int Arch Allergy Immunol. 2020;181(9):706-714. doi: 10.1159/000508817. Epub 2020 Jul 2.
Int Arch Allergy Immunol. 2020.
PMID: 32615565
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Fourteen-year experience of prenatal diagnosis of thalassemia in Iran.
Najmabadi H, Ghamari A, Sahebjam F, Kariminejad R, Hadavi V, Khatibi T, Samavat A, Mehdipour E, Modell B, Kariminejad MH.
Najmabadi H, et al. Among authors: samavat a.
Community Genet. 2006;9(2):93-7. doi: 10.1159/000091486.
Community Genet. 2006.
PMID: 16612059
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