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November 1, 2019
Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome
Shahram Torkamandi, Somaye Rezaei, Reza Mirfakhraei, et al.
Scientific Reports
|
June 10, 2026
Controlled delivery of nilotinib using LDH/Fe<sub>2</sub>O<sub>3</sub>-modified chitosan nanocomposite hydrogel beads for the treatment of chronic myeloid leukemia
Milad Gholami, Hori Ghaneialvar, Somayeh Molaei, et al.
Journal of Biomedical Physics & Engineering
|
June 14, 2023
Investigating Glenohumeral Joint Contact Forces and Kinematics in Different Keyboard and Monitor Setups using Opensim
Milad Gholami, Alireza Choobineh, Mohammad Taghi Karimi, et al.
Basic and Clinical Neuroscience
|
July 1, 2026
Expanding the Phenotype and Genotype Spectrum of a Novel Mutation in Hypomyelinating Leukodystrophy-5 With a Review of the Literature on 42 Cases
Sahar Bayat, Milad Gholami, Hamidreza Khodadadi, et al.
Applied Bionics and Biomechanics
|
May 16, 2022
Investigating the Effect of Keyboard Distance on the Posture and 3D Moments of Wrist and Elbow Joints among Males Using OpenSim
Milad Gholami, Alireza Choobineh, Mohammad Abdoli-Eramaki, et al.
Clinical Case Reports
|
February 9, 2026
Identification of Novel Mutation in the <i>ABCA12</i> Gene Causing Harlequin Ichthyosis
Nadia Soltani, Zahra Bayati, Mohsen Soosanabadi, et al.
Molecular Biology Reports
|
February 18, 2025
Comprehensive review and outline of genotypes and phenotypes of Arboleda-Tham syndrome spectrum: insights from novel variants
Sahar Bayat, Milad Gholami, Hamidreza Khodadadi, et al.
Journal of Clinical Laboratory Analysis
|
May 19, 2020
A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity)
Shahram Torkamandi, Somaye Rezaei, Reza Mirfakhraie, et al.
Advanced Biomedical Research
|
November 17, 2022
A Retrospective Cytogenetic Abnormality in Pediatric Acute Lymphoblastic Leukemia: Report of 11 Years
Kazem Ghaffari, Athena Kouhfar, Ali Ghasemi, et al.
Journal of the Turkish German Gynecological Association
|
December 6, 2021
Differential expression of <i>Hsa-miR-517a/b</i> in placental tissue may contribute to the pathogenesis of preeclampsia
Mona Amin-Beidokhti, Hossein Sadeghi, Reihaneh Pirjani, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 39) with videos related to
Sort By:
Page
of 4
Gene
|
November 1, 2019
Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome
Shahram Torkamandi, Somaye Rezaei, Reza Mirfakhraei, et al.
Scientific Reports
|
June 10, 2026
Controlled delivery of nilotinib using LDH/Fe<sub>2</sub>O<sub>3</sub>-modified chitosan nanocomposite hydrogel beads for the treatment of chronic myeloid leukemia
Milad Gholami, Hori Ghaneialvar, Somayeh Molaei, et al.
Journal of Biomedical Physics & Engineering
|
June 14, 2023
Investigating Glenohumeral Joint Contact Forces and Kinematics in Different Keyboard and Monitor Setups using Opensim
Milad Gholami, Alireza Choobineh, Mohammad Taghi Karimi, et al.
Basic and Clinical Neuroscience
|
July 1, 2026
Expanding the Phenotype and Genotype Spectrum of a Novel Mutation in Hypomyelinating Leukodystrophy-5 With a Review of the Literature on 42 Cases
Sahar Bayat, Milad Gholami, Hamidreza Khodadadi, et al.
Applied Bionics and Biomechanics
|
May 16, 2022
Investigating the Effect of Keyboard Distance on the Posture and 3D Moments of Wrist and Elbow Joints among Males Using OpenSim
Milad Gholami, Alireza Choobineh, Mohammad Abdoli-Eramaki, et al.
Clinical Case Reports
|
February 9, 2026
Identification of Novel Mutation in the <i>ABCA12</i> Gene Causing Harlequin Ichthyosis
Nadia Soltani, Zahra Bayati, Mohsen Soosanabadi, et al.
Molecular Biology Reports
|
February 18, 2025
Comprehensive review and outline of genotypes and phenotypes of Arboleda-Tham syndrome spectrum: insights from novel variants
Sahar Bayat, Milad Gholami, Hamidreza Khodadadi, et al.
Journal of Clinical Laboratory Analysis
|
May 19, 2020
A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity)
Shahram Torkamandi, Somaye Rezaei, Reza Mirfakhraie, et al.
Advanced Biomedical Research
|
November 17, 2022
A Retrospective Cytogenetic Abnormality in Pediatric Acute Lymphoblastic Leukemia: Report of 11 Years
Kazem Ghaffari, Athena Kouhfar, Ali Ghasemi, et al.
Journal of the Turkish German Gynecological Association
|
December 6, 2021
Differential expression of <i>Hsa-miR-517a/b</i> in placental tissue may contribute to the pathogenesis of preeclampsia
Mona Amin-Beidokhti, Hossein Sadeghi, Reihaneh Pirjani, et al.
Page
of 4