Shariati GR - Search Results

1

Novel Homozygous Missense Mutation in RYR1 Leads to Severe Congenital Ptosis, Ophthalmoplegia, and Scoliosis in the Absence of Myopathy.

Dilaver N, Mazaheri N, Maroofian R, Zeighami J, Seifi T, Zamani M, Sedaghat A, Shariati GR, Galehdari H. Dilaver N, et al. Among authors: shariati gr. Mol Syndromol. 2017 Dec;9(1):25-29. doi: 10.1159/000481897. Epub 2017 Nov 15. Mol Syndromol. 2017. PMID: 29456480 Free PMC article.

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. 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. 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. 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. 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. 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. 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

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. 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.

9

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. 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.

10

Effect of the herbal mixture composed of Aloe Vera, Henna, Adiantum capillus-veneris, and Myrrha on wound healing in streptozotocin-induced diabetic rats.

Galehdari H, Negahdari S, Kesmati M, Rezaie A, Shariati G. Galehdari H, et al. BMC Complement Altern Med. 2016 Oct 6;16(1):386. doi: 10.1186/s12906-016-1359-7. BMC Complement Altern Med. 2016. PMID: 27716154 Free PMC article.

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