Alaei M - Search Results

1

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: alaei m. 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

2

Validation of Urinary Glycosaminoglycans in Iranian patients with Mucopolysaccharidase type I: The effect of urine sedimentation characteristics.

Abdi M, Hakhamaneshi MS, Alaei MR, Azadi NA, Vakili R, Zamanfar D, Taghikhani M, Khatami S. Abdi M, et al. Among authors: alaei mr. Iran J Child Neurol. 2014 Fall;8(4):39-45. Iran J Child Neurol. 2014. PMID: 25657769 Free PMC article.

3

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: alaei mr. JIMD Rep. 2015;21:123-8. doi: 10.1007/8904_2015_441. Epub 2015 May 26. JIMD Rep. 2015. PMID: 26006720 Free PMC article.

4

Determination of Biological Variance and Validation of a Fluorometric Assay for Measurement of α-l-Iduronidase Activity in Dried Blood Spots Samples: The First Experience in Iran.

Abdi M, Hakhamaneshi MS, Alaei MR, Azadi NA, Vakili R, Zamanfar D, Taghikhani M, Khatami S. Abdi M, et al. Among authors: alaei mr. Indian J Clin Biochem. 2015 Jul;30(3):318-22. doi: 10.1007/s12291-014-0444-2. Epub 2014 Jul 30. Indian J Clin Biochem. 2015. PMID: 26089619 Free PMC article.

5

Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysis.

Abiri M, Karamzadeh R, Karimipoor M, Ghadami S, Alaei MR, Bagheri SD, Bagherian H, Setoodeh A, Noori-Daloii MR, Sirous Zeinali. Abiri M, et al. Among authors: alaei mr. Mutat Res. 2016 Apr;786:34-40. doi: 10.1016/j.mrfmmm.2016.01.005. Epub 2016 Jan 25. Mutat Res. 2016. PMID: 26901124

6

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: alaei m. JIMD Rep. 2017;32:7-14. doi: 10.1007/8904_2016_572. Epub 2016 Jun 1. JIMD Rep. 2017. PMID: 27246466 Free PMC article.

7

Chitotriosidase Activity and Gene Polymorphism in Iranian Patients with Gaucher Disease and Sibling Carriers.

Mozafari H, Taghikhani M, Khatami S, Alaei MR, Vaisi-Raygani A, Rahimi Z. Mozafari H, et al. Among authors: alaei mr. Iran J Child Neurol. 2016 Fall;10(4):62-70. Iran J Child Neurol. 2016. PMID: 27843468 Free PMC article.

8

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. Among authors: alaei mr. Gastroenterology Res. 2017 Feb;10(1):28-32. doi: 10.14740/gr778w. Epub 2017 Feb 21. Gastroenterology Res. 2017. PMID: 28270874 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. Iran J Child Neurol. 2018 Spring;12(2):99-106. Iran J Child Neurol. 2018. PMID: 29696051 Free PMC article.

10

Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.

Shirzadeh T, Saeidian AH, Bagherian H, Salehpour S, Setoodeh A, Alaei MR, Youssefian L, Samavat A, Touati A, Fallah MS, Vahidnezhad H, Karimipoor M, Azadmehr S, Raeisi M, Bandehi Sarhadi A, Zafarghandi Motlagh F, Jamali M, Zeinali Z, Abiri M, Zeinali S; Additional individual contributors. Shirzadeh T, et al. Among authors: alaei mr. J Inherit Metab Dis. 2018 Nov;41(6):1159-1167. doi: 10.1007/s10545-018-0228-6. Epub 2018 Aug 29. J Inherit Metab Dis. 2018. PMID: 30159852

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