Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2012 | 1 |
2013 | 1 |
2014 | 1 |
2018 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Identification of Novel Mutations in the MMAA and MUT Genes among Methylmalonic Aciduria Families.
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.
Clinical, laboratory data and outcomes of 17 Iranian citrullinemia type 1 patients: Identification of five novel ASS1 gene mutations.
Moarefian S, Zamani M, Rahmanifar A, Behnam B, Zaman T.
Moarefian S, et al. Among authors: rahmanifar a.
JIMD Rep. 2022 Mar 9;63(3):231-239. doi: 10.1002/jmd2.12277. eCollection 2022 May.
JIMD Rep. 2022.
PMID: 35433176
Free PMC article.
Item in Clipboard
Effects of miglustat on stabilization of neurological disorder in niemann-pick disease type C: Iranian pediatric case series.
Karimzadeh P, Tonekaboni SH, Ashrafi MR, Shafeghati Y, Rezayi A, Salehpour S, Ghofrani M, Taghdiri MM, Rahmanifar A, Zaman T, Aryani O, Shoar BN, Shiva F, Tavasoli A, Houshmand M.
Karimzadeh P, et al. Among authors: rahmanifar a.
J Child Neurol. 2013 Dec;28(12):1599-606. doi: 10.1177/0883073812464526. Epub 2012 Nov 8.
J Child Neurol. 2013.
PMID: 23143717
Item in Clipboard
Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort.
Shafaat M, Alaee MR, Rahmanifar A, Setoodeh A, Razzaghy-Azar M, Bagherian H, Bagheri SD, Zafarghandi Motlagh F, Hashemi M, Abiri M, Zeinali S.
Shafaat M, et al. Among authors: rahmanifar a.
Metab Brain Dis. 2018 Oct;33(5):1689-1697. doi: 10.1007/s11011-018-0277-4. Epub 2018 Jul 18.
Metab Brain Dis. 2018.
PMID: 30022420
Item in Clipboard
Mild reduction of plasmalogens causes rhizomelic chondrodysplasia punctata: functional characterization of a novel mutation.
Noguchi M, Honsho M, Abe Y, Toyama R, Niwa H, Sato Y, Ghaedi K, Rahmanifar A, Shafeghati Y, Fujiki Y.
Noguchi M, et al. Among authors: rahmanifar a.
J Hum Genet. 2014 Jul;59(7):387-92. doi: 10.1038/jhg.2014.39. Epub 2014 May 22.
J Hum Genet. 2014.
PMID: 24849933
Item in Clipboard
Cite
Cite