Hamid M - Search Results

1

Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family.

Akbari MT, Hamid M, Izadyar M. Akbari MT, et al. Among authors: hamid m. Ann Hematol. 2011 Mar;90(3):349-51. doi: 10.1007/s00277-010-1003-4. Epub 2010 Jun 3. Ann Hematol. 2011. PMID: 20521148 Free article. No abstract available.

2

The Cretan type of nondeletional hereditary persistence of fetal hemoglobin in an Iranian family.

Hamid M, Mahjoubi F, Akbari MT, Zeinali S, Karimipoor M. Hamid M, et al. Ann Hematol. 2009 Dec;88(12):1267-8. doi: 10.1007/s00277-009-0756-0. Epub 2009 May 26. Ann Hematol. 2009. PMID: 19468729 No abstract available.

3

A 13-bp deletion in the 3' untranslated region of the β-globin gene causes β-thalassemia major in compound heterozygosity with IVSII-1 mutation.

Hamid M, Akbari MT. Hamid M, et al. Med Princ Pract. 2011;20(5):488-90. doi: 10.1159/000328425. Epub 2011 Jul 11. Med Princ Pract. 2011. PMID: 21757944 Free article.

4

Identification of α-globin chain variants: a report from Iran.

Akbari MT, Hamid M. Akbari MT, et al. Among authors: hamid m. Arch Iran Med. 2012 Sep;15(9):564-7. Arch Iran Med. 2012. PMID: 22924376

5

Molecular analysis of gamma-globin promoters, HS-111 and 3'HS1, in beta-thalassemia intermedia patients associated with high levels of Hb F.

Hamid M, Mahjoubi F, Akbari MT, Arab A, Zeinali S, Karimipoor M. Hamid M, et al. Hemoglobin. 2009;33(6):428-38. doi: 10.3109/03630260903336479. Hemoglobin. 2009. PMID: 19958188

6

Clinical features, DYT1 mutation screening and genotype-phenotype correlation in patients with dystonia from Iran.

Akbari MT, Zand Z, Shahidi GA, Hamid M. Akbari MT, et al. Among authors: hamid m. Med Princ Pract. 2012;21(5):462-6. doi: 10.1159/000336783. Epub 2012 Apr 6. Med Princ Pract. 2012. PMID: 22487959 Free article.

7

A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients.

Hamid M, Karimipoor M, Chaleshtori MH, Akbari MT. Hamid M, et al. J Genet. 2009 Dec;88(3):359-62. doi: 10.1007/s12041-009-0054-6. J Genet. 2009. PMID: 20086306 No abstract available.

8

Determination of exon 7 SMN1 deletion in Iranian patients and heterozygous carriers by quantitative real-time PCR.

Akbari MT, Noruzinia M, Mozdarani H, Hamid M. Akbari MT, et al. Among authors: hamid m. J Genet. 2011 Apr;90(1):133-6. doi: 10.1007/s12041-011-0038-1. J Genet. 2011. PMID: 21677399 Free article. No abstract available.

9

The Frequency of DYT1 (GAG Deletion) Mutation in Primary Dystonia Patients from Iran.

Hamid M, Akbari MT, Shahidi GA, Zand Z. Hamid M, et al. Cell J. 2011 Spring;13(1):55-8. Epub 2011 Apr 21. Cell J. 2011. PMID: 23671828 Free PMC article.

10

Transient expression assay of Agamma-588 (A/G) mutations in the K562 cell line.

Hamid M, Mahjoubi F, Akbari MT, Khanahmad H, Jamshidi F, Zeinali S, Karimipoor M. Hamid M, et al. Iran Biomed J. 2011;15(1-2):15-21. Iran Biomed J. 2011. PMID: 21725495 Free PMC article.

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