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Showing results for parvaneh karimzadeh
Search for Parvane Karimzadeh instead (1 results)
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.
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.
Genetic spectrum among 2009 Iranian individuals with neuromuscular disorders using next generation sequencing and multiple ligation dependent probe amplification methods.
Molaei N, Alagha P, Khanbazi A, Beheshtian M, Ahangari F, Dehdahsi S, Fadaee M, Ashki M, Ghaderi Z, Elahi Z, Vazehan R, Parsimehr E, Nouri MM, Saei P, Noudehi K, Fatehi F, Najafabadi SZ, Abolhassani A, Afroozan F, Yazdan H, Kelishomi MA, Azad M, Parvini F, Kassaee SM, Ramezani M, Zemorshidi F, Salimipour H, Abdi S, Bakhshandeh M, Fayyazi A, Zamani G, Ashrafi MR, Jamali P, Sarraf P, Okhovat AA, Ashtiani BH, Fatehi F, Karimzadeh P, Nafissi S, Kahrizi K, Kariminejad A, Najmabadi H. Molaei N, et al. Among authors: karimzadeh p. Sci Rep. 2025 Nov 28;15(1):42736. doi: 10.1038/s41598-025-26836-x. Sci Rep. 2025. PMID: 41315541 Free PMC article.
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.
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