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

Results by year

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

Year Number of Results
2010 1
2011 1
2012 5
2013 8
2014 10
2015 5
2016 5
2017 5
2018 7
2019 8
2020 5
2021 2
2022 6
2023 4
2024 9
2025 7
2026 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

83 results

Results by year

Filters applied: . Clear all
Page 1
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
Abolhassani A, Fattahi Z, Beheshtian M, Fadaee M, Vazehan R, Ahangari F, Dehdahsi S, Faraji Zonooz M, Parsimehr E, Kalhor Z, Peymani F, Mozaffarpour Nouri M, Babanejad M, Noudehi K, Fatehi F, Zamanian Najafabadi S, Afroozan F, Yazdan H, Bozorgmehr B, Azarkeivan A, Sadat Mahdavi S, Nikuei P, Fatehi F, Jamali P, Ashrafi MR, Karimzadeh P, Habibi H, Kahrizi K, Nafissi S, Kariminejad A, Najmabadi H. Abolhassani A, et al. Among authors: karimzadeh p. NPJ Genom Med. 2024 Feb 19;9(1):12. doi: 10.1038/s41525-024-00393-0. NPJ Genom Med. 2024. PMID: 38374194 Free PMC article.
Bilirubin Induced Encephalopathy.
Karimzadeh P, Fallahi M, Kazemian M, Taslimi Taleghani N, Nouripour S, Radfar M. Karimzadeh P, et al. Iran J Child Neurol. 2020 Winter;14(1):7-19. Iran J Child Neurol. 2020. PMID: 32021624 Free PMC article. Review.
Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review.
Ghasemi MR, Tehrani Fateh S, Moeinafshar A, Sadeghi H, Karimzadeh P, Mirfakhraie R, Rezaei M, Hashemi-Gorji F, Rezvani Kashani M, Fazeli Bavandpour F, Bagheri S, Moghimi P, Rostami M, Madannejad R, Roudgari H, Miryounesi M. Ghasemi MR, et al. Among authors: karimzadeh p. BMC Med Genomics. 2024 Feb 13;17(1):51. doi: 10.1186/s12920-024-01810-0. BMC Med Genomics. 2024. PMID: 38347586 Free PMC article.
Hyperkinetic Movement Disorders in Children: A Brief Review.
Nikkhah A, Karimzadeh P, Taghdiri MM, Nasehi MM, Javadzadeh M, Khari E. Nikkhah A, et al. Among authors: karimzadeh p. Iran J Child Neurol. 2019 Spring;13(2):7-16. Iran J Child Neurol. 2019. PMID: 31037073 Free PMC article. Review.
Moyamoya Syndrome Associated with Henoch-Schönlein Purpura.
Shiari R, Tabatabaei Nodushan SM, Mohebbi MM, Karimzadeh P, Javadzadeh M. Shiari R, et al. Among authors: karimzadeh p. Iran J Child Neurol. 2016 Fall;10(4):71-74. Iran J Child Neurol. 2016. PMID: 27843469 Free PMC article.
Novel TECPR2 variant in two cases of hereditary sensory and autonomic neuropathy type 9: insights from genetic characterization and comprehensive literature review.
Moeinafshar A, Tehrani Fateh S, Hashemi-Gorji F, Karimzadeh P, Gholibeglou E, Rostami M, Sadeghi H, Miryounesi M, Ghasemi MR. Moeinafshar A, et al. Among authors: karimzadeh p. BMC Neurol. 2024 Nov 20;24(1):455. doi: 10.1186/s12883-024-03963-y. BMC Neurol. 2024. PMID: 39567938 Free PMC article. Review.
83 results