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Journal of Cardiovascular Electrophysiology
|
September 16, 2025
Catheter Ablation for Ventricular Tachycardia in Ischemic Cardiomyopathy: A Meta-Analysis With Reconstructed Time-to-Event and Trial Sequential Analysis
Hossam Elbenawi, Youmna Ayman, Ahmed Hashim, et al.
Genome Medicine
|
August 26, 2024
Genome Tunisia Project: paving the way for precision medicine in North Africa
Yosr Hamdi, Mediha Trabelsi, Kais Ghedira, et al.
Human Mutation
|
September 25, 2009
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation
Soumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker, et al.
La Clinica Terapeutica
|
June 24, 2026
CAR-T Cell Therapy Versus Salvage Chemotherapy in Relapsed/Refractory DLBCL: A Systematic Review and Meta-Analysis Integrating Radiologic, Laboratory, and Histopathologic Correlates
Fatma M Elsayed, Juman Baban, Heba Yahia Elkholy, et al.
Frontiers in Medicine
|
September 19, 2025
Development and implementation of the International AIDA Network Castleman's disease registry
Antonio Vitale, Jessica Sbalchiero, Valeria Caggiano, et al.
Cell
|
September 24, 2016
Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation
Franklin L Zhong, Ons Mamaï, Lorenzo Sborgi, et al.
Annals of Neurology
|
February 12, 2014
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa
Modibo Sangaré, Brant Hendrickson, Hammadoun Ali Sango, et al.
Molecular Cytogenetics
|
February 14, 2026
Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights
Rim Khelifi, Houcemeddine Othmane, Houda Ajmi, et al.
Nature Genetics
|
October 16, 2012
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma
Elizabeth Pohler, Ons Mamai, Jennifer Hirst, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 24, 2017
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Ahmed Khattab, Shozeb Haider, Ameet Kumar, et al.
Page
of 36
Search research articles
Search
Showing results (341-350 of 359) with videos related to
Sort By:
Page
of 36
Journal of Cardiovascular Electrophysiology
|
September 16, 2025
Catheter Ablation for Ventricular Tachycardia in Ischemic Cardiomyopathy: A Meta-Analysis With Reconstructed Time-to-Event and Trial Sequential Analysis
Hossam Elbenawi, Youmna Ayman, Ahmed Hashim, et al.
Genome Medicine
|
August 26, 2024
Genome Tunisia Project: paving the way for precision medicine in North Africa
Yosr Hamdi, Mediha Trabelsi, Kais Ghedira, et al.
Human Mutation
|
September 25, 2009
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation
Soumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker, et al.
La Clinica Terapeutica
|
June 24, 2026
CAR-T Cell Therapy Versus Salvage Chemotherapy in Relapsed/Refractory DLBCL: A Systematic Review and Meta-Analysis Integrating Radiologic, Laboratory, and Histopathologic Correlates
Fatma M Elsayed, Juman Baban, Heba Yahia Elkholy, et al.
Frontiers in Medicine
|
September 19, 2025
Development and implementation of the International AIDA Network Castleman's disease registry
Antonio Vitale, Jessica Sbalchiero, Valeria Caggiano, et al.
Cell
|
September 24, 2016
Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation
Franklin L Zhong, Ons Mamaï, Lorenzo Sborgi, et al.
Annals of Neurology
|
February 12, 2014
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa
Modibo Sangaré, Brant Hendrickson, Hammadoun Ali Sango, et al.
Molecular Cytogenetics
|
February 14, 2026
Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights
Rim Khelifi, Houcemeddine Othmane, Houda Ajmi, et al.
Nature Genetics
|
October 16, 2012
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma
Elizabeth Pohler, Ons Mamai, Jennifer Hirst, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 24, 2017
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Ahmed Khattab, Shozeb Haider, Ameet Kumar, et al.
Page
of 36