Galehdari H - Search Results

1

Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome.

De Nittis P, Efthymiou S, Sarre A, Guex N, Chrast J, Putoux A, Sultan T, Raza Alvi J, Ur Rahman Z, Zafar F, Rana N, Rahman F, Anwar N, Maqbool S, Zaki MS, Gleeson JG, Murphy D, Galehdari H, Shariati G, Mazaheri N, Sedaghat A; SYNAPS Study Group; Lesca G, Chatron N, Salpietro V, Christoforou M, Houlden H, Simonds WF, Pedrazzini T, Maroofian R, Reymond A. De Nittis P, et al. Among authors: galehdari h. J Med Genet. 2021 Dec;58(12):815-831. doi: 10.1136/jmedgenet-2020-107015. Epub 2020 Nov 10. J Med Genet. 2021. PMID: 33172956 Free PMC article.

2

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

3

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.

4

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

5

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.

6

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.

7

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.

8

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.

9

Identification of a Novel HADHB Gene Mutation in an Iranian Patient with Mitochondrial Trifunctional Protein Deficiency.

Shahrokhi M, Shafiei M, Galehdari H, Shariati G. Shahrokhi M, et al. Among authors: galehdari h. Arch Iran Med. 2017 Jan;20(1):22-27. Arch Iran Med. 2017. PMID: 28112527

10

Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy.

Osborn DPS, Pond HL, Mazaheri N, Dejardin J, Munn CJ, Mushref K, Cauley ES, Moroni I, Pasanisi MB, Sellars EA, Hill RS, Partlow JN, Willaert RK, Bharj J, Malamiri RA, Galehdari H, Shariati G, Maroofian R, Mora M, Swan LE, Voit T, Conti FJ, Jamshidi Y, Manzini MC. Osborn DPS, et al. Among authors: galehdari h. Am J Hum Genet. 2017 Mar 2;100(3):537-545. doi: 10.1016/j.ajhg.2017.01.019. Epub 2017 Feb 9. Am J Hum Genet. 2017. PMID: 28190459 Free PMC article.

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