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W Ahmad

Showing results (151-160 of 193) with videos related to

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American Journal of Human Genetics|October 3, 1998
A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellersW Ahmad, A D Irvine, H Lam, et al.
Journal of Medical Internet Research|May 26, 2025
Effectiveness of Digital Health Interventions for Chronic Obstructive Pulmonary Disease: Systematic Review and Meta-AnalysisMiaoqing Zhuang, Intan Idiana Hassan, Wan Muhamad Amir W Ahmad, et al.
Current Diabetes Reviews|April 5, 2026
Evaluation of Alpha-Lipoic Acid and B Vitamins on Quality of Life and Metabolic Parameters Among Diabetic Patients with Symptomatic Distal Symmetric Polyneuropathy: A Randomized Controlled TrialNani Draman, Che Nur Ain Che Abdullah, Noraini Mohamad, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|February 6, 2010
Knowledge, attitudes and practices regarding tuberculosis in two districts of Punjab, PakistanM U Mushtaq, M A Majrooh, W Ahmad, et al.
Biomed Research International|January 3, 2022
The Use of Hall's Technique Preformed Metal Crown (HTPMC) by Pediatric Dentists in MalaysiaFabiha Jesmin, Aimi Kamarudin, Fadzlinda Baharin, et al.
The British Journal of Dermatology|November 17, 2006
Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2M Naeem, M Jelani, K Lee, et al.
BMC Oral Health|July 7, 2023
Evaluation of bacterial leakage and marginal adaptation of the bioceramics pulp dressing materials: an invitro studyNiher Tabassum Siddiqua Snigdha, Aimi Kamarudin, Fadzlinda Baharin, et al.
Acta Virologica|June 25, 2015
Efficiency of live attenuated and inactivated rabies viruses in prophylactic and post exposure vaccination against the street virus strainF Huang, W Ahmad, M Duan, et al.
Clinical Genetics|June 18, 2004
Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3M A Rafiq, M Ansar, T Pham, et al.
Clinical Genetics|November 24, 2012
Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani familiesK Lee, I Chiu, R L P Santos-Cortez, et al.
Pageof 20

Showing results (151-160 of 193) with videos related to

Sort By:
Pageof 20
American Journal of Human Genetics|October 3, 1998
A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellersW Ahmad, A D Irvine, H Lam, et al.
Journal of Medical Internet Research|May 26, 2025
Effectiveness of Digital Health Interventions for Chronic Obstructive Pulmonary Disease: Systematic Review and Meta-AnalysisMiaoqing Zhuang, Intan Idiana Hassan, Wan Muhamad Amir W Ahmad, et al.
Current Diabetes Reviews|April 5, 2026
Evaluation of Alpha-Lipoic Acid and B Vitamins on Quality of Life and Metabolic Parameters Among Diabetic Patients with Symptomatic Distal Symmetric Polyneuropathy: A Randomized Controlled TrialNani Draman, Che Nur Ain Che Abdullah, Noraini Mohamad, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|February 6, 2010
Knowledge, attitudes and practices regarding tuberculosis in two districts of Punjab, PakistanM U Mushtaq, M A Majrooh, W Ahmad, et al.
Biomed Research International|January 3, 2022
The Use of Hall's Technique Preformed Metal Crown (HTPMC) by Pediatric Dentists in MalaysiaFabiha Jesmin, Aimi Kamarudin, Fadzlinda Baharin, et al.
The British Journal of Dermatology|November 17, 2006
Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2M Naeem, M Jelani, K Lee, et al.
BMC Oral Health|July 7, 2023
Evaluation of bacterial leakage and marginal adaptation of the bioceramics pulp dressing materials: an invitro studyNiher Tabassum Siddiqua Snigdha, Aimi Kamarudin, Fadzlinda Baharin, et al.
Acta Virologica|June 25, 2015
Efficiency of live attenuated and inactivated rabies viruses in prophylactic and post exposure vaccination against the street virus strainF Huang, W Ahmad, M Duan, et al.
Clinical Genetics|June 18, 2004
Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3M A Rafiq, M Ansar, T Pham, et al.
Clinical Genetics|November 24, 2012
Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani familiesK Lee, I Chiu, R L P Santos-Cortez, et al.
Pageof 20