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Syed Irfan

Showing results (61-70 of 104) with videos related to

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RSC Advances|April 1, 2025
Improved thermoelectric properties of α-phase Cu<sub>2</sub>Se thin films through multiphase nanostructuringMuhammad Faizan Masoud, Sajid Butt, Muhammad Waseem Akram, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 11, 2021
Precise Warfarin Management through Personalized Modeling and Control with Limited Clinical DataSyed Irfan Ali Meerza, Affan Affan, Hossein Mirinejad, et al.
Plos One|August 15, 2014
In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosisSyed Irfan Raza, Dost Muhammad, Abid Jan, et al.
Computational and Mathematical Methods in Medicine|December 23, 2021
Some Study of Semigroups of <b>h</b>-Bi-Ideals of SemiringsRukhshanda Anjum, Fairouz Tchier, Zeeshan Saleem Mufti, et al.
Pakistan Journal of Medical Sciences|February 13, 2016
Emergency contraception: Awareness, attitudes and barriers of Saudi Arabian WomenSyed Irfan Karim, Farhana Irfan, Norah Al Rowais, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|May 17, 2019
What Are We Doing For Injuries? The Burden And Level Of Preparedness For Mass Emergencies In Khyber Pakhtunkhwa Province Of PakistanFayaz Ahmad, Zia Ul Haq, Dildar Muhammad, et al.
BMC Public Health|July 7, 2026
Assessing the knowledge, attitude, and practices of reproductive health schemes among tribal women in Jharkhand: A cross-sectional studyRohit Raj, Jarina Begum, Syed Irfan Ali, et al.
Immunobiology|April 14, 2020
β2 Integrin Gene (ITGB2) mutation spectra in Pakistani families with leukocyte adhesion deficiency type 1 (LAD1)Hamid Nawaz Tipu, Rubab Raza, Sadaf Jaffar, et al.
Immunogenetics|September 17, 2024
Sequence variants underlying severe combined immunodeficiency and leukocyte adhesion deficiency type 1 in six consanguineous familiesHajra Fayyaz, Atteaya Zaman, Nighat Haider, et al.
BMC Medical Genetics|February 28, 2014
A novel recessive mutation in the gene ELOVL4 causes a neuro-ichthyotic disorder with variable expressivityHina Mir, Syed Irfan Raza, Muhammad Touseef, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
RSC Advances|April 1, 2025
Improved thermoelectric properties of α-phase Cu<sub>2</sub>Se thin films through multiphase nanostructuringMuhammad Faizan Masoud, Sajid Butt, Muhammad Waseem Akram, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 11, 2021
Precise Warfarin Management through Personalized Modeling and Control with Limited Clinical DataSyed Irfan Ali Meerza, Affan Affan, Hossein Mirinejad, et al.
Plos One|August 15, 2014
In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosisSyed Irfan Raza, Dost Muhammad, Abid Jan, et al.
Computational and Mathematical Methods in Medicine|December 23, 2021
Some Study of Semigroups of <b>h</b>-Bi-Ideals of SemiringsRukhshanda Anjum, Fairouz Tchier, Zeeshan Saleem Mufti, et al.
Pakistan Journal of Medical Sciences|February 13, 2016
Emergency contraception: Awareness, attitudes and barriers of Saudi Arabian WomenSyed Irfan Karim, Farhana Irfan, Norah Al Rowais, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|May 17, 2019
What Are We Doing For Injuries? The Burden And Level Of Preparedness For Mass Emergencies In Khyber Pakhtunkhwa Province Of PakistanFayaz Ahmad, Zia Ul Haq, Dildar Muhammad, et al.
BMC Public Health|July 7, 2026
Assessing the knowledge, attitude, and practices of reproductive health schemes among tribal women in Jharkhand: A cross-sectional studyRohit Raj, Jarina Begum, Syed Irfan Ali, et al.
Immunobiology|April 14, 2020
β2 Integrin Gene (ITGB2) mutation spectra in Pakistani families with leukocyte adhesion deficiency type 1 (LAD1)Hamid Nawaz Tipu, Rubab Raza, Sadaf Jaffar, et al.
Immunogenetics|September 17, 2024
Sequence variants underlying severe combined immunodeficiency and leukocyte adhesion deficiency type 1 in six consanguineous familiesHajra Fayyaz, Atteaya Zaman, Nighat Haider, et al.
BMC Medical Genetics|February 28, 2014
A novel recessive mutation in the gene ELOVL4 causes a neuro-ichthyotic disorder with variable expressivityHina Mir, Syed Irfan Raza, Muhammad Touseef, et al.
Pageof 11