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W Ahmad

Showing results (141-150 of 193) with videos related to

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International Journal of Environmental Research and Public Health|July 28, 2022
A Randomized Controlled Trial Evaluating the Levels of the Biomarkers hs-CRP, IL-6, and IL-8 in Patients with Temporomandibular Disorder Treated with LLLT, Traditional Conservative Treatment, and a Combination of BothAbdalwhab Ma Zwiri, Wan Muhamad Amir W Ahmad, Jawaad Ahmed Asif, et al.
Clinical Genetics|July 16, 2004
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Journal of Pharmacy & Bioallied Sciences|January 12, 2022
A Comprehensive Cross-Tabulation Analysis of Oral Carcinoma Patients: A Retrospective Study of Recent 7 YearsWan Muhamad Amir W Ahmad, Farah Muna Mohamad Ghazali, Muhammad Azeem Yaqoob, et al.
BMC Oral Health|November 2, 2024
Assessing the impact of systemic conditions on periodontal health in Malaysian population: a retrospective studySohaib Arshad, Raja Azman Awang, Normastura Abd Rahman, et al.
Biomarkers in Medicine|April 30, 2026
Association of peripheral blood brain-derived neurotrophic factor (BDNF) levels with the use of technology-assisted stroke rehabilitation: a systematic review and meta-analysisRabiatul Adawiyah Mohamad Noor, Hanim Afzan Ibrahim, Wan Muhamad Amir W Ahmad, et al.
Clinical Genetics|July 18, 2002
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Clinical Genetics|May 4, 2011
Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairmentK Lee, S Khan, A Islam, et al.
Genomics|March 3, 1999
Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian familyW Ahmad, A Zlotogorski, A A Panteleyev, et al.
American Journal of Medical Genetics|August 26, 1998
Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindredM Ahmad, M Faiyaz Ul Haque, W Ahmad, et al.
Work (Reading, Mass.)|June 7, 2024
Knowledge and attitude regarding obstructive sleep apnoea among medical and dental practitioners working in North-Eastern Peninsular Malaysia: A comparative cross-sectional studySumaiya Zabin Eusufzai, Bernard Ying Kang Then, Nafij Bin Jamayet, et al.
Pageof 20

Showing results (141-150 of 193) with videos related to

Sort By:
Pageof 20
International Journal of Environmental Research and Public Health|July 28, 2022
A Randomized Controlled Trial Evaluating the Levels of the Biomarkers hs-CRP, IL-6, and IL-8 in Patients with Temporomandibular Disorder Treated with LLLT, Traditional Conservative Treatment, and a Combination of BothAbdalwhab Ma Zwiri, Wan Muhamad Amir W Ahmad, Jawaad Ahmed Asif, et al.
Clinical Genetics|July 16, 2004
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Journal of Pharmacy & Bioallied Sciences|January 12, 2022
A Comprehensive Cross-Tabulation Analysis of Oral Carcinoma Patients: A Retrospective Study of Recent 7 YearsWan Muhamad Amir W Ahmad, Farah Muna Mohamad Ghazali, Muhammad Azeem Yaqoob, et al.
BMC Oral Health|November 2, 2024
Assessing the impact of systemic conditions on periodontal health in Malaysian population: a retrospective studySohaib Arshad, Raja Azman Awang, Normastura Abd Rahman, et al.
Biomarkers in Medicine|April 30, 2026
Association of peripheral blood brain-derived neurotrophic factor (BDNF) levels with the use of technology-assisted stroke rehabilitation: a systematic review and meta-analysisRabiatul Adawiyah Mohamad Noor, Hanim Afzan Ibrahim, Wan Muhamad Amir W Ahmad, et al.
Clinical Genetics|July 18, 2002
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Clinical Genetics|May 4, 2011
Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairmentK Lee, S Khan, A Islam, et al.
Genomics|March 3, 1999
Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian familyW Ahmad, A Zlotogorski, A A Panteleyev, et al.
American Journal of Medical Genetics|August 26, 1998
Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindredM Ahmad, M Faiyaz Ul Haque, W Ahmad, et al.
Work (Reading, Mass.)|June 7, 2024
Knowledge and attitude regarding obstructive sleep apnoea among medical and dental practitioners working in North-Eastern Peninsular Malaysia: A comparative cross-sectional studySumaiya Zabin Eusufzai, Bernard Ying Kang Then, Nafij Bin Jamayet, et al.
Pageof 20