Galehdari H - Search Results

1

Whole-exome sequencing deciphers the genetic profile of visual impairments in patients from Southwest Iran.

Zamani M, Sedighzadeh S, Seifi T, Negahdari S, Zeighami J, Sedaghat A, Shariati G, Galehdari H. Zamani M, et al. Among authors: galehdari h. Mol Genet Genomics. 2022 Sep;297(5):1289-1300. doi: 10.1007/s00438-022-01917-y. Epub 2022 Jun 26. Mol Genet Genomics. 2022. PMID: 35754085

2

Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],a new hemoglobin variant of the α2-globin gene.

Hamid M, Shariati G, Saberi A, Galehdari H, Kaikhaei B, Mohammadi-Anaei M. Hamid M, et al. Among authors: galehdari h. Hemoglobin. 2013;37(5):477-80. doi: 10.3109/03630269.2013.792095. Epub 2013 May 15. Hemoglobin. 2013. PMID: 23672273

3

Identification of IVS-I (-1) (G > C) or Hb Monroe as a report on the beta-globin gene with a beta-thalassemia minor phenotype in south of Iran.

Hamid M, Shariati G, Saberi A, Kaikhaei B, Galehdari H, Mohammadi-Anaei M. Hamid M, et al. Among authors: galehdari h. Arch Iran Med. 2013 Sep;16(9):563-4. Arch Iran Med. 2013. PMID: 23981164

4

Exon sequencing of PKD1 gene in an Iranian patient with autosomal-dominant polycystic kidney disease.

Hafizi A, Khatami SR, Galehdari H, Shariati G, Saberi AH, Hamid M. Hafizi A, et al. Among authors: galehdari h. Iran Biomed J. 2014 Jul;18(3):143-50. doi: 10.6091/ibj.1317.2014. Iran Biomed J. 2014. PMID: 24842140 Free PMC article.

5

A novel alpha-thalassemia nonsense mutation in HBA2: C.382 A > T globin gene.

Hamid M, Bokharaei Merci H, Galehdari H, Saberi AH, Kaikhaei B, Mohammadi-Anaei M, Ahmadzadeh A, Shariati G. Hamid M, et al. Among authors: galehdari h. Arch Iran Med. 2014 Jul;17(7):475-6. Arch Iran Med. 2014. PMID: 24979558

6

Wolf-Hirschhorn syndrome: a case with normal karyotype, demonstrated by array CGH (aCGH).

Saberi A, Shariati G, Hamid M, Galehdari H, Abdorasouli N. Saberi A, et al. Among authors: galehdari h. Arch Iran Med. 2014 Sep;17(9):642-4. Arch Iran Med. 2014. PMID: 25204484

7

Molecular prenatal diagnosis of megalencephalic leukoencephalopathy with subcortical cysts in a child from southwest of Iran.

Shariati G, Hamid M, Saberi A, Andashti B, Galehdari H. Shariati G, et al. Among authors: galehdari h. Clin Case Rep. 2015 Feb;3(2):114-7. doi: 10.1002/ccr3.168. Epub 2014 Nov 26. Clin Case Rep. 2015. PMID: 25767710 Free PMC article.

8

Association Study of rs1333040 and rs1004638 Polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran.

Golabgir Khademi K, Foroughmand AM, Galehdari H, Yazdankhah S, Pourmahdi Borujeni M, Shahbazi Z, Dinarvand P. Golabgir Khademi K, et al. Among authors: galehdari h. Iran Biomed J. 2016;20(2):122-7. doi: 10.7508/ibj.2016.02.008. Epub 2015 Nov 24. Iran Biomed J. 2016. PMID: 26597055 Free PMC article.

9

The First Report of a 290-bp Deletion in β-Globin Gene in the South of Iran.

Hamid M, Dawoody Nejad L, Shariati G, Galehdari H, Saberi A, Mohammadi-Anaei M. Hamid M, et al. Among authors: galehdari h. Iran Biomed J. 2017 Mar;21(2):126-8. doi: 10.18869/acadpub.ibj.21.2.126. Epub 2016 Mar 8. Iran Biomed J. 2017. PMID: 26948378 Free PMC article.

10

Novel Mutation in the ATP-Binding Cassette Transporter A3 (ABCA3) Encoding Gene Causes Respiratory Distress Syndrome in A Term Newborn in Southwest Iran.

Rezaei F, Shafiei M, Shariati G, Dehdashtian A, Mohebbi M, Galehdari H. Rezaei F, et al. Among authors: galehdari h. Iran J Pediatr. 2016 Mar 5;26(2):e2493. doi: 10.5812/ijp.2493. eCollection 2016 Apr. Iran J Pediatr. 2016. PMID: 27437095 Free PMC article.

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