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Alireza Dostmohammadi

Showing results (1-10 of 7) with videos related to

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NPJ Systems Biology and Applications|November 17, 2025
TrackRefiner a tool for refinement of bacillus cell tracking dataAtiyeh Ahmadi, Alireza Dostmohammadi, Rhyan Mclean, et al.
European Journal of Medical Genetics|December 4, 2025
A novel frameshift CUX2 variant in a patient with epilepsy and global developmental delay: phenotypic and genotypic expansionFerruccio Romano, Mohammad Sadegh Shams Nosrati, Francesca Madia, et al.
Clinical Genetics|January 7, 2026
Biallelic COL4A2 Variants Associated With Brain Small Vessel Disease and Brain MalformationsAnees Muhammad, Mohammad Sadegh Shams Nosrati, Alireza Dostmohammadi, et al.
Epilepsia Open|February 13, 2026
Isolated absence epilepsy associated with a de novo FBXW7 missense variant in the F-box domainAnees Muhammad, Mohammad Sadegh Shams Nosrati, Alireza Dostmohammadi, et al.
Computers in Biology and Medicine|May 28, 2026
namiRa: A comprehensive, manually curated database for MicroRNA expression, function, and deregulation in cancerSaeed Mohebbi, Alireza Dostmohammadi, Sara Amjadian, et al.
European Journal of Medical Genetics|March 25, 2026
Horizontal gaze palsy with progressive scoliosis (HGPPS): expanding ROBO3 molecular spectrum and refining clinical-neuroimaging phenotypesMohammad Sadegh Shams Nosrati, Ferruccio Romano, Alireza Dostmohammadi, et al.
European Journal of Human Genetics : EJHG|March 26, 2025
A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcificationsMarcello Scala, Nancy C P Leong, Thanh Nha Uyen Le, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
NPJ Systems Biology and Applications|November 17, 2025
TrackRefiner a tool for refinement of bacillus cell tracking dataAtiyeh Ahmadi, Alireza Dostmohammadi, Rhyan Mclean, et al.
European Journal of Medical Genetics|December 4, 2025
A novel frameshift CUX2 variant in a patient with epilepsy and global developmental delay: phenotypic and genotypic expansionFerruccio Romano, Mohammad Sadegh Shams Nosrati, Francesca Madia, et al.
Clinical Genetics|January 7, 2026
Biallelic COL4A2 Variants Associated With Brain Small Vessel Disease and Brain MalformationsAnees Muhammad, Mohammad Sadegh Shams Nosrati, Alireza Dostmohammadi, et al.
Epilepsia Open|February 13, 2026
Isolated absence epilepsy associated with a de novo FBXW7 missense variant in the F-box domainAnees Muhammad, Mohammad Sadegh Shams Nosrati, Alireza Dostmohammadi, et al.
Computers in Biology and Medicine|May 28, 2026
namiRa: A comprehensive, manually curated database for MicroRNA expression, function, and deregulation in cancerSaeed Mohebbi, Alireza Dostmohammadi, Sara Amjadian, et al.
European Journal of Medical Genetics|March 25, 2026
Horizontal gaze palsy with progressive scoliosis (HGPPS): expanding ROBO3 molecular spectrum and refining clinical-neuroimaging phenotypesMohammad Sadegh Shams Nosrati, Ferruccio Romano, Alireza Dostmohammadi, et al.
European Journal of Human Genetics : EJHG|March 26, 2025
A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcificationsMarcello Scala, Nancy C P Leong, Thanh Nha Uyen Le, et al.
Pageof 1