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Ali Amar

Showing results (31-40 of 46) with videos related to

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Einstein (Sao Paulo, Brazil)|January 29, 2015
Delayed postoperative radiation therapy in local control of squamous cell carcinoma of the tongue and floor of the mouthAli Amar, Helma Maria Chedid, Otávio Alberto Curioni, et al.
Brazilian Journal of Otorhinolaryngology|August 10, 2013
Epidemiological assessment and therapeutic response in hypopharyngeal cancerAli Amar, Otávio Alberto Curioni, Diógenes Lopes de Paiva, et al.
Hematology, Transfusion and Cell Therapy|January 11, 2026
Association of the ABCB1 gene polymorphism C3435T (rs1045642) with acute myeloid leukemia: A genetic studyRoh Ullah, Nazish Mazari, Ghulam Mustafa, et al.
Brazilian Journal of Otorhinolaryngology|February 1, 2006
Comparative analysis of perceptual evaluation, acoustic analysis and indirect laryngoscopy for vocal assessment of a population with vocal complaintKátia Nemr, Ali Amar, Marcio Abrahão, et al.
Neurogenetics|July 25, 2015
In silico analysis of SIGMAR1 variant (rs4879809) segregating in a consanguineous Pakistani family showing amyotrophic lateral sclerosis without frontotemporal lobar dementiaMuhammad Ikram Ullah, Arsalan Ahmad, Syed Irfan Raza, et al.
Thrombosis and Haemostasis|July 3, 2026
Novel/Recurrent Variants in Pakistani Glanzmann Thrombasthenia and Glanzmann-like bleeding diathesis: Insights from NGS AnalysisMadiha Shakoor, Ali Amar, Saima Farhan, et al.
Revista Da Associacao Medica Brasileira (1992)|February 4, 2003
[Relationship between the outcome and the frequency of micronuclei in cells of patients with oral and oropharyngeal carcinoma]Marcos Brasilino de Carvalho, Andrea Ramirez, Gilka Jorge F Gattás, et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma|December 28, 2023
Exploring the diversity of <i>CFTR</i> gene mutations in cystic fibrosis individuals of South AsiaHassan Rafique, Anum Safdar, Muhammad Usman Ghani, et al.
Genes|March 25, 2022
Delineating Novel and Known Pathogenic Variants in <i>TYR</i>, <i>OCA2</i> and <i>HPS-1</i> Genes in Eight Oculocutaneous Albinism (OCA) Pakistani FamiliesMuhammad Shakil, Abida Akbar, Nazish Mahmood Aisha, et al.
Genes|June 24, 2022
Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand DiseaseMuhammad Asif Naveed, Aiysha Abid, Nadir Ali, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Einstein (Sao Paulo, Brazil)|January 29, 2015
Delayed postoperative radiation therapy in local control of squamous cell carcinoma of the tongue and floor of the mouthAli Amar, Helma Maria Chedid, Otávio Alberto Curioni, et al.
Brazilian Journal of Otorhinolaryngology|August 10, 2013
Epidemiological assessment and therapeutic response in hypopharyngeal cancerAli Amar, Otávio Alberto Curioni, Diógenes Lopes de Paiva, et al.
Hematology, Transfusion and Cell Therapy|January 11, 2026
Association of the ABCB1 gene polymorphism C3435T (rs1045642) with acute myeloid leukemia: A genetic studyRoh Ullah, Nazish Mazari, Ghulam Mustafa, et al.
Brazilian Journal of Otorhinolaryngology|February 1, 2006
Comparative analysis of perceptual evaluation, acoustic analysis and indirect laryngoscopy for vocal assessment of a population with vocal complaintKátia Nemr, Ali Amar, Marcio Abrahão, et al.
Neurogenetics|July 25, 2015
In silico analysis of SIGMAR1 variant (rs4879809) segregating in a consanguineous Pakistani family showing amyotrophic lateral sclerosis without frontotemporal lobar dementiaMuhammad Ikram Ullah, Arsalan Ahmad, Syed Irfan Raza, et al.
Thrombosis and Haemostasis|July 3, 2026
Novel/Recurrent Variants in Pakistani Glanzmann Thrombasthenia and Glanzmann-like bleeding diathesis: Insights from NGS AnalysisMadiha Shakoor, Ali Amar, Saima Farhan, et al.
Revista Da Associacao Medica Brasileira (1992)|February 4, 2003
[Relationship between the outcome and the frequency of micronuclei in cells of patients with oral and oropharyngeal carcinoma]Marcos Brasilino de Carvalho, Andrea Ramirez, Gilka Jorge F Gattás, et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma|December 28, 2023
Exploring the diversity of <i>CFTR</i> gene mutations in cystic fibrosis individuals of South AsiaHassan Rafique, Anum Safdar, Muhammad Usman Ghani, et al.
Genes|March 25, 2022
Delineating Novel and Known Pathogenic Variants in <i>TYR</i>, <i>OCA2</i> and <i>HPS-1</i> Genes in Eight Oculocutaneous Albinism (OCA) Pakistani FamiliesMuhammad Shakil, Abida Akbar, Nazish Mahmood Aisha, et al.
Genes|June 24, 2022
Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand DiseaseMuhammad Asif Naveed, Aiysha Abid, Nadir Ali, et al.
Pageof 5