Saberi A - Search Results

1

Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders.

Ortigoza-Escobar JD, Zamani M, Dorison N, Sadeghian S, Azizimalamiri R, Alvi JR, Sultan T, Galehdari H, Shariati G, Saberi A, Leeuwen L, Zifarelli G, Bauer P, d'Hardemare V, Doummar D, Roze E, Travaglini L, Nicita F, Ojea Ponce N, Zahraei SM, Alabdi L, Tamim A, Hashem MO, Ababneh F, Morrow MM, Curry C, Tam A, Ruedy J, Bhambhani V, Veith R, Strømme P, Efthymiou S, Alkuraya FS, Moreno-De-Luca A, Burglen L, Houlden H, Maroofian R. Ortigoza-Escobar JD, et al. Among authors: saberi a. Mov Disord. 2024 Sep;39(9):1624-1630. doi: 10.1002/mds.29883. Epub 2024 Jun 20. Mov Disord. 2024. PMID: 38899514

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: saberi a. 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: saberi a. 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: saberi ah. 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: saberi ah. 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. Among authors: saberi a. 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. Among authors: saberi a. 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

Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran.

Hamid M, Ershadi Oskouei S, Shariati G, Babaei E, Galehdari H, Saberi A, Sedaghat A. Hamid M, et al. Among authors: saberi a. J Pediatr Hematol Oncol. 2018 Apr;40(3):192-195. doi: 10.1097/MPH.0000000000001093. J Pediatr Hematol Oncol. 2018. PMID: 29420372

10

Prenatal diagnosis of a rare de novo 1q22-q25.1 chromosomal deletion syndrome using oligo array CGH.

Shariati G, Saberi A, Hamid M, Galehdari H, Sedaghat A, Abdorasuli N. Shariati G, et al. Among authors: saberi a. Clin Case Rep. 2018 Jun 13;6(8):1464-1469. doi: 10.1002/ccr3.1604. eCollection 2018 Aug. Clin Case Rep. 2018. PMID: 30147883 Free PMC article.

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