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

Text availability

Article attribute

Article type

Publication date

Search Results

69 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
X-linked SCID with a rare mutation.
Mahdavi FS, Keramatipour M, Ansari S, Sharafian S, Karamzade A, Tavakol M. Mahdavi FS, et al. Among authors: keramatipour m. Allergy Asthma Clin Immunol. 2021 Oct 11;17(1):107. doi: 10.1186/s13223-021-00605-7. Allergy Asthma Clin Immunol. 2021. PMID: 34635152 Free PMC article.
Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome.
Latour BL, Van De Weghe JC, Rusterholz TD, Letteboer SJ, Gomez A, Shaheen R, Gesemann M, Karamzade A, Asadollahi M, Barroso-Gil M, Chitre M, Grout ME, van Reeuwijk J, van Beersum SE, Miller CV, Dempsey JC, Morsy H; University of Washington Center for Mendelian Genomics; Bamshad MJ; Genomics England Research Consortium; Nickerson DA, Neuhauss SC, Boldt K, Ueffing M, Keramatipour M, Sayer JA, Alkuraya FS, Bachmann-Gagescu R, Roepman R, Doherty D. Latour BL, et al. Among authors: keramatipour m. J Clin Invest. 2020 Aug 3;130(8):4423-4439. doi: 10.1172/JCI131656. J Clin Invest. 2020. PMID: 32453716 Free PMC article.
Whole-Exome Sequencing Identified a Novel Variant (C.405_422+39del) in DSP Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy.
Eshaghkhani Y, Mohamadifar A, Asadollahi M, Taghizadeh M, Karamzade A, Saberi M, Nourmohammadi P, Golchehre Z, Amin A, Keramatipour M. Eshaghkhani Y, et al. Among authors: keramatipour m. Rep Biochem Mol Biol. 2021 Jul;10(2):280-287. doi: 10.52547/rbmb.10.2.280. Rep Biochem Mol Biol. 2021. PMID: 34604417 Free PMC article.
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: keramatipour m. 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.
Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature.
Fallahi M, Jamee M, Enayat J, Abdollahimajd F, Mesdaghi M, Khoddami M, Segarra-Roca A, Frohne A, Dmytrus J, Keramatipour M, Mansouri M, Eslamian G, Fallah S, Boztug K, Chavoshzadeh Z. Fallahi M, et al. Among authors: keramatipour m. Allergy Asthma Clin Immunol. 2022 Dec 24;18(1):111. doi: 10.1186/s13223-022-00749-0. Allergy Asthma Clin Immunol. 2022. PMID: 36566211 Free PMC article.
New Presentation of CD27 Deficiency; Coronary Ectasia and COVID-19.
Golchehre Z, Sharafian S, Momtazmanesh N, Chavoshzadeh Z, Karimi A, Abolhassani H, Kazemi Aghdam M, Vahidshahi K, Hashemimoghaddam S, Kosari F, Khafafpour Z, Shamsian BS, Keramatipour M. Golchehre Z, et al. Among authors: keramatipour m. Iran J Allergy Asthma Immunol. 2023 Feb 20;22(1):110-118. doi: 10.18502/ijaai.v22i1.12013. Iran J Allergy Asthma Immunol. 2023. PMID: 37002625 Free article.
69 results