Ghaemi N - Search Results

1

Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis.

Hashemian S, Eshraghi P, Dilaver N, Galehdari H, Shalbafan B, Vakili R, Ghaemi N, Ahangari N, Rezazadeh Varaghchi J, Zeighami J, Sedaghat A, Aminzadeh M, Hamid M, Saberi A, Ashtari F, Ghayoor Karimiani E, Shariati G. Hashemian S, et al. Among authors: ghaemi n. Iran J Child Neurol. 2019 Spring;13(2):155-162. Iran J Child Neurol. 2019. PMID: 31037088 Free PMC article.

2

Molecular analysis of the CYP21 gene and prenatal diagnosis in families with 21-hydroxylase deficiency in northeastern Iran.

Vakili R, Baradaran-Heravi A, Barid-Fatehi B, Gholamin M, Ghaemi N, Abbaszadegan MR. Vakili R, et al. Among authors: ghaemi n. Horm Res. 2005;63(3):119-24. doi: 10.1159/000084570. Epub 2005 Mar 17. Horm Res. 2005. PMID: 15775714

3

Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran.

Baradaran-Heravi A, Vakili R, Robins T, Carlsson J, Ghaemi N, A'rabi A, Abbaszadegan MR. Baradaran-Heravi A, et al. Among authors: ghaemi n. Clin Endocrinol (Oxf). 2007 Sep;67(3):335-41. doi: 10.1111/j.1365-2265.2007.02886.x. Epub 2007 Jun 15. Clin Endocrinol (Oxf). 2007. PMID: 17573904

4

Novel mutation in the SLC19A2 gene in an Iranian family with thiamine-responsive megaloblastic anemia: a series of three cases.

Ghaemi N, Ghahraman M, Abbaszadegan MR, Baradaran-Heravi A, Vakili R. Ghaemi N, et al. J Clin Res Pediatr Endocrinol. 2013 Sep 10;5(3):199-201. doi: 10.4274/Jcrpe.969. J Clin Res Pediatr Endocrinol. 2013. PMID: 24072090 Free PMC article.

5

Identification of four novel mutations of the WFS1 gene in Iranian Wolfram syndrome pedigrees.

Ghahraman M, Abbaszadegan MR, Vakili R, Hosseini S, Fardi Golyan F, Ghaemi N, Forghanifard MM. Ghahraman M, et al. Among authors: ghaemi n. Acta Diabetol. 2016 Dec;53(6):899-904. doi: 10.1007/s00592-016-0884-7. Epub 2016 Jul 13. Acta Diabetol. 2016. PMID: 27412528

6

The Report of Three Rare Cases of the Niemann-pick Disease in Birjand, South Khorasan, Eastern Iran.

Noroozi Asl S, Vakili R, Ghaemi N, Eshraghi P. Noroozi Asl S, et al. Among authors: ghaemi n. Iran J Child Neurol. 2017 Summer;11(3):53-56. Iran J Child Neurol. 2017. PMID: 28883878 Free PMC article.

7

Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus.

Ghaemi N, Hasanabadi H, Ashrafzadeh F, Sarvari S, Rahimi H, Hashemian S. Ghaemi N, et al. Iran J Child Neurol. 2018 Spring;12(2):83-90. Iran J Child Neurol. 2018. PMID: 29696049 Free PMC article.

8

Novel DNA variation of GPR54 gene in familial central precocious puberty.

Ghaemi N, Ghahraman M, Noroozi Asl S, Vakili R, Fardi Golyan F, Moghbeli M, Abbaszadegan MR. Ghaemi N, et al. Ital J Pediatr. 2019 Jan 11;45(1):10. doi: 10.1186/s13052-019-0601-6. Ital J Pediatr. 2019. PMID: 30635063 Free PMC article.

9

Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of <5 years in the Iranian population.

Yaghootkar H, Abbasi F, Ghaemi N, Rabbani A, Wakeling MN, Eshraghi P, Enayati S, Vakili S, Heidari S, Patel K, Sayarifard F, Borhan-Dayani S, McDonald TJ, Ellard S, Hattersley AT, Amoli MM, Vakili R, Colclough K. Yaghootkar H, et al. Among authors: ghaemi n. Diabet Med. 2019 Dec;36(12):1694-1702. doi: 10.1111/dme.14071. Epub 2019 Jul 25. Diabet Med. 2019. PMID: 31276222 Free PMC article.

10

Novel mutation in AIRE gene with autoimmune polyendocrine syndrome type 1.

Fardi Golyan F, Ghaemi N, Abbaszadegan MR, Dehghan Manshadi SH, Vakili R, Druley TE, Rahimi HR, Ghahraman M. Fardi Golyan F, et al. Among authors: ghaemi n. Immunobiology. 2019 Nov;224(6):728-733. doi: 10.1016/j.imbio.2019.09.004. Epub 2019 Sep 6. Immunobiology. 2019. PMID: 31526676

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