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Page 1
Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency.
Parvaneh N, Teimourian S, Jacomelli G, Badalzadeh M, Bertelli M, Zakharova E, Tabatabaei P, Parvaneh L, Pourakbari B, Yeganeh M, Tamizifar B, Mamishi S, Micheli V. Parvaneh N, et al. Among authors: badalzadeh m. Clin Biochem. 2008 Mar;41(4-5):350-2. doi: 10.1016/j.clinbiochem.2007.11.007. Epub 2007 Nov 21. Clin Biochem. 2008. PMID: 18067860 No abstract available.
Molecular diagnosis of X-linked chronic granulomatous disease in Iran.
Teimourian S, Rezvani Z, Badalzadeh M, Kannengiesser C, Mansouri D, Movahedi M, Zomorodian E, Parvaneh N, Mamishi S, Pourpak Z, Moin M. Teimourian S, et al. Among authors: badalzadeh m. Int J Hematol. 2008 May;87(4):398-404. doi: 10.1007/s12185-008-0060-0. Int J Hematol. 2008. PMID: 18322777
Inheritance pattern and clinical aspects of 93 Iranian patients with chronic granulomatous disease.
Fattahi F, Badalzadeh M, Sedighipour L, Movahedi M, Fazlollahi MR, Mansouri SD, Khotaei GT, Bemanian MH, Behmanesh F, Hamidieh AA, Bazargan N, Mamishi S, Zandieh F, Chavoshzadeh Z, Mohammadzadeh I, Mahdaviani SA, Tabatabaei SA, Kalantari N, Tajik S, Maddah M, Pourpak Z, Moin M. Fattahi F, et al. Among authors: badalzadeh m. J Clin Immunol. 2011 Oct;31(5):792-801. doi: 10.1007/s10875-011-9567-x. Epub 2011 Jul 26. J Clin Immunol. 2011. PMID: 21789723
Genetic and molecular findings of 38 Iranian patients with chronic granulomatous disease caused by p47-phox defect.
Tajik S, Badalzadeh M, Fazlollahi MR, Houshmand M, Bazargan N, Movahedi M, Mahlouji Rad M, Mahdaviani SA, Mamishi S, Khotaei GT, Mansouri D, Zandieh F, Pourpak Z. Tajik S, et al. Among authors: badalzadeh m. Scand J Immunol. 2019 Jul;90(1):e12767. doi: 10.1111/sji.12767. Epub 2019 Apr 25. Scand J Immunol. 2019. PMID: 30963593 Free article.
Lupus Erythematosus and Chronic Granulomatous Disease: Report of Four Iranian Patients with AR-CGD and One XL-CGD.
Maddah M, Fazlollahi MR, Shiari R, Shahram F, Mamishi S, Babaie D, Monajemzadeh M, Sotudeh S, Hamidieh AA, Badalzadeh M, Tajik S, Sedighipour L, Pourpak Z. Maddah M, et al. Among authors: badalzadeh m. Iran J Allergy Asthma Immunol. 2019 Aug 17;18(4):452-458. doi: 10.18502/ijaai.v18i4.1426. Iran J Allergy Asthma Immunol. 2019. PMID: 31522454 Free article.
Investigation of ITGB2 gene in 12 new cases of leukocyte adhesion deficiency-type I revealed four novel mutations from Iran.
Taghizade Mortezaee F, Esmaeli B, Badalzadeh M, Ghadami M, Fazlollahi MR, Alizade Z, Hamidieh AA, Chavoshzadeh Z, Movahedi M, Heydarzadeh M, Sadeghi Shabestari M, Tavassoli M, Nabavi M, Nasiri Kalmarzi R, Pourpak Z. Taghizade Mortezaee F, et al. Among authors: badalzadeh m. Arch Iran Med. 2015 Nov;18(11):760-4. Arch Iran Med. 2015. PMID: 26497373
A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran.
Tajik S, Badalzadeh M, Fazlollahi MR, Houshmand M, Zandieh F, Khandan S, Pourpak Z. Tajik S, et al. Among authors: badalzadeh m. Iran J Allergy Asthma Immunol. 2016 Oct;15(5):426-429. Iran J Allergy Asthma Immunol. 2016. PMID: 27917630 Free article.
Clinical, Laboratory, and Molecular Findings for 63 Patients With Severe Combined Immunodeficiency: A Decade´s Experience.
Fazlollahi MR, Pourpak Z, Hamidieh AA, Movahedi M, Houshmand M, Badalzadeh M, Nourizadeh M, Mahloujirad M, Arshi S, Nabavi M, Gharagozlou M, Khayatzadeh A, Dabbaghzade A, Atarod L, Zandieh F, Sadeghi Shabestary M, Mesdaghi M, Mohammadzadeh I, Mahdaviani SA, Eslamian MH, Pesaran F, Bahraminia E, Abolnezhadian F, Arij Z, Moin M. Fazlollahi MR, et al. Among authors: badalzadeh m. J Investig Allergol Clin Immunol. 2017;27(5):299-304. doi: 10.18176/jiaci.0147. Epub 2017 Mar 7. J Investig Allergol Clin Immunol. 2017. PMID: 28266921 Free article.
25 results