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Muhammad Zaman

Showing results (171-180 of 183) with videos related to

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Saudi Pharmaceutical Journal : SPJ : the Official Publication of the Saudi Pharmaceutical Society|February 5, 2024
Response Surface Methodology (RSM) approach to formulate and optimize the bilayer combination tablet of Tamsulosin and FinasterideMuneeba Akhtar, Muhammad Zaman, Ahsan Zamir Siddiqi, et al.
Pharmaceutics|June 2, 2021
Synthesis and Evaluation of Thiol-Conjugated Poloxamer and Its Pharmaceutical ApplicationsMuhammad Zaman, Sadaf Saeed, Rabia Imtiaz Bajwa, et al.
Pharmaceutics|May 25, 2024
Correction: Zaman et al. Synthesis and Evaluation of Thiol-Conjugated Poloxamer and Its Pharmaceutical Applications. <i>Pharmaceutics</i> 2021, <i>13</i>, 693Muhammad Zaman, Sadaf Saeed, Rabia Imtiaz Bajwa, et al.
BMJ Open|July 16, 2024
Access to and utilisation of antimicrobials among forcibly displaced persons in Uganda, Yemen and Colombia: a pilot cross-sectional surveyDavid Kamiab Hesari, Saleh Aljadeeah, Petra Brhlikova, et al.
Cureus|November 10, 2018
Cardiovascular Autonomic Neuropathy and its Association with Cardiovascular and All-cause Mortality in Patients with End-stage Renal DiseaseSyed Rizwan A Bokhari, Faisal Inayat, Ali Jawa, et al.
American Journal of Human Genetics|October 1, 2019
Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and MicrocephalyElodie M Richard, Daniel L Polla, Muhammad Zaman Assir, et al.
Investigative Ophthalmology & Visual Science|April 19, 2017
Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity ScreeningJianjun Chen, Qiwei Wang, Patricia E Cabrera, et al.
Annals of Biomedical Engineering|February 7, 2020
Core Competencies for Undergraduates in Bioengineering and Biomedical Engineering: Findings, Consequences, and RecommendationsJohn A White, Donald P Gaver, Robert J Butera, et al.
American Journal of Human Genetics|August 22, 2017
Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical DevelopmentEkaterina L Ivanova, Frédéric Tran Mau-Them, Saima Riazuddin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2017
Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delayMuhammad Ansar, Saima Riazuddin, Muhammad Tahir Sarwar, et al.
Pageof 19

Showing results (171-180 of 183) with videos related to

Sort By:
Pageof 19
Saudi Pharmaceutical Journal : SPJ : the Official Publication of the Saudi Pharmaceutical Society|February 5, 2024
Response Surface Methodology (RSM) approach to formulate and optimize the bilayer combination tablet of Tamsulosin and FinasterideMuneeba Akhtar, Muhammad Zaman, Ahsan Zamir Siddiqi, et al.
Pharmaceutics|June 2, 2021
Synthesis and Evaluation of Thiol-Conjugated Poloxamer and Its Pharmaceutical ApplicationsMuhammad Zaman, Sadaf Saeed, Rabia Imtiaz Bajwa, et al.
Pharmaceutics|May 25, 2024
Correction: Zaman et al. Synthesis and Evaluation of Thiol-Conjugated Poloxamer and Its Pharmaceutical Applications. <i>Pharmaceutics</i> 2021, <i>13</i>, 693Muhammad Zaman, Sadaf Saeed, Rabia Imtiaz Bajwa, et al.
BMJ Open|July 16, 2024
Access to and utilisation of antimicrobials among forcibly displaced persons in Uganda, Yemen and Colombia: a pilot cross-sectional surveyDavid Kamiab Hesari, Saleh Aljadeeah, Petra Brhlikova, et al.
Cureus|November 10, 2018
Cardiovascular Autonomic Neuropathy and its Association with Cardiovascular and All-cause Mortality in Patients with End-stage Renal DiseaseSyed Rizwan A Bokhari, Faisal Inayat, Ali Jawa, et al.
American Journal of Human Genetics|October 1, 2019
Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and MicrocephalyElodie M Richard, Daniel L Polla, Muhammad Zaman Assir, et al.
Investigative Ophthalmology & Visual Science|April 19, 2017
Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity ScreeningJianjun Chen, Qiwei Wang, Patricia E Cabrera, et al.
Annals of Biomedical Engineering|February 7, 2020
Core Competencies for Undergraduates in Bioengineering and Biomedical Engineering: Findings, Consequences, and RecommendationsJohn A White, Donald P Gaver, Robert J Butera, et al.
American Journal of Human Genetics|August 22, 2017
Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical DevelopmentEkaterina L Ivanova, Frédéric Tran Mau-Them, Saima Riazuddin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2017
Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delayMuhammad Ansar, Saima Riazuddin, Muhammad Tahir Sarwar, et al.
Pageof 19