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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

104 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR).
Rahmani F, Rayzan E, Rahmani MR, Shahkarami S, Zoghi S, Rezaei A, Aryan Z, Najafi M, Rohlfs M, Jeske T, Aflatoonian M, Chavoshzadeh Z, Farahmand F, Motamed F, Rohani P, Alimadadi H, Mahdaviani A, Mansouri M, Tavakol M, Vanderberg M, Kotlarz D, Klein C, Rezaei N. Rahmani F, et al. Among authors: aflatoonian m. Immunol Invest. 2021 May;50(4):445-459. doi: 10.1080/08820139.2020.1776725. Epub 2020 Jul 7. Immunol Invest. 2021. PMID: 32633164
Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder.
Alves MM, Halim D, Maroofian R, de Graaf BM, Rooman R, van der Werf CS, Van de Vijver E, Mehrjardi MY, Aflatoonian M, Chioza BA, Baple EL, Dehghani M, Crosby AH, Hofstra RM. Alves MM, et al. Among authors: aflatoonian m. Eur J Hum Genet. 2016 Nov;24(11):1627-1629. doi: 10.1038/ejhg.2016.58. Epub 2016 Jun 29. Eur J Hum Genet. 2016. PMID: 27352967 Free PMC article.
Association of REarranged during Transfection (RET) c.73 + 9277T > C and c.135G > a Polymorphisms with Susceptibility to Hirschsprung Disease: A Systematic Review and Meta-Analysis.
Bahrami R, Shajari A, Aflatoonian M, Noorishadkam M, Akbarian-Bafghi MJ, Morovati-Sharifabad M, Heiranizadeh N, Neamatzadeh H. Bahrami R, et al. Among authors: aflatoonian m. Fetal Pediatr Pathol. 2020 Dec;39(6):476-490. doi: 10.1080/15513815.2019.1672225. Epub 2019 Oct 7. Fetal Pediatr Pathol. 2020. PMID: 31590591
Association of Neuregulin 1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C Polymorphisms with Susceptibility to Non-Syndromic Hirschsprung's Disease.
Hosseini-Jangjou SH, Dastgheib SA, Aflatoonian M, Amooee A, Bahrami R, Salehi E, Sadeghizadeh-Yazdi J, Neamatzadeh H. Hosseini-Jangjou SH, et al. Among authors: aflatoonian m. Fetal Pediatr Pathol. 2021 Jun;40(3):198-205. doi: 10.1080/15513815.2019.1692113. Epub 2019 Nov 18. Fetal Pediatr Pathol. 2021. PMID: 31738640
104 results