Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2012 1
2014 2
2015 3
2016 6
2017 2
2018 1
2019 4
2020 2
2021 4
2022 2
2023 3
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

26 results

Results by year

Filters applied: . Clear all
Page 1
Immunological Evaluation of Pediatric Patients with Polyautoimmunity.
Mahdavi FS, Tavakol M, Aghamahdi F, Sadri H, Chavoshzadeh Z, Jamee M, Noorian S, Alaei MR, Ashkevari P, Anaya JM, Abolhassani H, Ochs HD, Azizi G. Mahdavi FS, et al. Among authors: alaei mr. Endocr Metab Immune Disord Drug Targets. 2024;24(7):798-807. doi: 10.2174/1871530323666230912124951. Endocr Metab Immune Disord Drug Targets. 2024. PMID: 37702233
Clinical and Paraclinical Characteristics of Non-Classic Phenylketonuria.
Shakiba M, Saneifard H, Alaei MR, Mosallanejad A, Lotfi M, Yasaei M, Alizade Naderi E. Shakiba M, et al. Among authors: alaei mr. Iran J Child Neurol. 2021 Summer;15(3):131-138. doi: 10.22037/ijcn.v15i3.30519. Iran J Child Neurol. 2021. PMID: 34282370 Free PMC article.
A Case Series: Congenital Hyperinsulinism.
Alaei MR, Akbaroghli S, Keramatipour M, Alaei A. Alaei MR, et al. Int J Endocrinol Metab. 2016 Sep 10;14(4):e37311. doi: 10.5812/ijem.37311. eCollection 2016 Oct. Int J Endocrinol Metab. 2016. PMID: 28123437 Free PMC article.
Inborn Errors of Metabolism Associated With Autism Among Children: A Multicenter Study from Iran.
Moravej H, Inaloo S, Nahid S, Mazloumi S, Nemati H, Moosavian T, Nasiri J, Ghasemi F, Alaei MR, Dalili S, Aminzadeh M, Katibeh P, Amirhakimi A, Yazdani N, Ilkhanipoor H, Afshar Z, Hadipour F, Hadipour Z. Moravej H, et al. Among authors: alaei mr. Indian Pediatr. 2023 Mar 15;60(3):193-196. Epub 2023 Jan 2. Indian Pediatr. 2023. PMID: 36604934 Free article.
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
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families.
Akbaroghli S, Kooshavar D, Golchehre Z, Karamzade A, Saberi M, Alaei MR, Abbasi Sadegh M, Asadollahi M, Keramatipour M. Akbaroghli S, et al. Among authors: alaei mr. Iran J Child Neurol. 2022 Winter;16(1):123-133. doi: 10.22037/ijcn.v16i1.31650. Epub 2022 Jan 1. Iran J Child Neurol. 2022. PMID: 35222663 Free PMC article.
26 results