Rohani F - Search Results

1

Molecular Characterization of QDPR Gene in Iranian Families with BH4 Deficiency: Reporting Novel and Recurrent Mutations.

Foroozani H, Abiri M, Salehpour S, Bagherian H, Sharifi Z, Alaei MR, Khatami S, Azadmeh S, Setoodeh A, Rejali L, Rohani F, Zeinali S. Foroozani H, et al. Among authors: rohani f. JIMD Rep. 2015;21:123-8. doi: 10.1007/8904_2015_441. Epub 2015 May 26. JIMD Rep. 2015. PMID: 26006720 Free PMC article.

2

Motor development skills of 1- to 4-year-old Iranian children with early treated phenylketonuria.

Nazi S, Rohani F, Sajedi F, Biglarian A, Setoodeh A. Nazi S, et al. Among authors: rohani f. JIMD Rep. 2014;12:85-9. doi: 10.1007/8904_2013_248. Epub 2013 Aug 6. JIMD Rep. 2014. PMID: 23918467 Free PMC article.

3

Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients.

Khatami S, Dehnabeh SR, Zeinali S, Thöny B, Alaei M, Salehpour S, Setoodeh A, Rohani F, Hajivalizadeh F, Samavat A. Khatami S, et al. Among authors: rohani f. JIMD Rep. 2017;32:7-14. doi: 10.1007/8904_2016_572. Epub 2016 Jun 1. JIMD Rep. 2017. PMID: 27246466 Free PMC article.

4

Relationship Between Obesity and Liver Enzymes Levels in Turner's Syndrome.

Rohani F, Golgiri F, Alaei MR, Karimi M, Nikraftar P, Bozorgmehr R. Rohani F, et al. Gastroenterology Res. 2017 Feb;10(1):28-32. doi: 10.14740/gr778w. Epub 2017 Feb 21. Gastroenterology Res. 2017. PMID: 28270874 Free PMC article.

5

The treatment and clinical follow-up outcome in Iranian patients with tetrahydrobiopterin deficiency.

Khani S, Barzegari M, Esmaeilizadeh Z, Farsian P, Alaei M, Salehpour S, Setoodeh A, Rohani F, Samavat A, Zekri A, Mirzazadeh R, Sadeghi S, Khatami S. Khani S, et al. Among authors: rohani f. J Pediatr Endocrinol Metab. 2021 Jul 2;34(9):1157-1167. doi: 10.1515/jpem-2021-0155. Print 2021 Sep 27. J Pediatr Endocrinol Metab. 2021. PMID: 34214291

6

Identification of Novel Mutations in the MMAA and MUT Genes among Methylmalonic Aciduria Families.

Jafari M, Karami F, Setoodeh A, Rahmanifar A, Bagherian H, Alaei MR, Rohani F, Zeinali S. Jafari M, et al. Among authors: rohani f. Iran Biomed J. 2023 Feb 12;27(6):397-403. doi: 10.61186/ibj.3782. Online ahead of print. Iran Biomed J. 2023. PMID: 38158783 Free PMC article.

7

Mutation analysis of Phenylalanine hydroxylase gene in Iranian patients with Phenylketonuria.

Rastegar Moghadam M, Shojaei A, Babaei V, Rohani F, Ghazi F. Rastegar Moghadam M, et al. Among authors: rohani f. Med J Islam Repub Iran. 2018 Mar 11;32:21. doi: 10.14196/mjiri.32.21. eCollection 2018. Med J Islam Repub Iran. 2018. PMID: 30159272 Free PMC article.

8

Association between diabetes complications and leukocyte counts in Iranian patients.

Moradi S, Kerman SR, Rohani F, Salari F. Moradi S, et al. Among authors: rohani f. J Inflamm Res. 2012;5:7-11. doi: 10.2147/JIR.S26917. Epub 2012 Jan 24. J Inflamm Res. 2012. PMID: 22334791 Free PMC article.

9

Are There Neurological Symptoms in Type 1 of Gaucher Disease?

Alaei M, Jafari N, Rohani F, Ahmadabadi F, Azadi R. Alaei M, et al. Among authors: rohani f. Iran J Child Neurol. 2018 Spring;12(2):99-106. Iran J Child Neurol. 2018. PMID: 29696051 Free PMC article.

10

The Nomogram of Clitoral Length and Width in Iranian Term and Preterm Neonates.

Alaei M, Rohani F, Norouzi E, Hematian Boroujeni N, Tafreshi RI, Salehiniya H, Soheilipour F. Alaei M, et al. Among authors: rohani f. Front Endocrinol (Lausanne). 2020 Jun 3;11:297. doi: 10.3389/fendo.2020.00297. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32582020 Free PMC article.

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