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Frontiers in Cellular Neuroscience
|
April 27, 2026
Cynanchum bungei Decne-derived extracellular vesicles alleviate cognitive impairment and pathological damage in Alzheimer's disease
Rui Hong, Jingjing Han, Fuxing Dong, et al.
BMC Health Services Research
|
June 17, 2026
Management of COPD and comorbidities in COPD patients by dispensing pharmaceutical care following Global Initiative for Chronic Obstructive Lung Disease-guidelines (GOLD guidelines 2020): a prospective randomized clinical trial
Hafsa Kanwal, Gaber E Eldesoky, Umm-E- Kalsoom, et al.
JPMA. the Journal of the Pakistan Medical Association
|
August 2, 2013
FDG-PET scan in assessing lymphomas and the application of Deauville Criteria
Umm-e-kalsoom Awan, Neelam Siddiqui, Mohammad SaadUllah, et al.
Clinical Dysmorphology
|
February 6, 2026
Identification of a novel mutation in metabotropic glutamate receptor 1 causing autosomal recessive spinocerebellar ataxia-13 in a Pakistani family
Shafeeq Ahmad, Bushra Khan, Hamza Shams, et al.
Neurogenetics
|
May 19, 2025
Identification of mutations in five Pakistani families with Epilepsy
Nayab Ahsan, Arsalan Ahmad, Shahnawaz Hussain, et al.
Plos One
|
February 4, 2026
Implementation of guideline-directed medical treatment for ischemic heart disease management: A knowledge, attitude and practice based cross-sectional survey
Umm-E- Kalsoom, Amjad Khan, Syed Sikandar Shah, et al.
Journal of Medical Genetics
|
November 20, 2012
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A
Umm-e- Kalsoom, Eva Klopocki, Naveed Wasif, et al.
Neurology Asia
|
November 4, 2021
A novel deletion mutation in <i>EPM2A</i> underlies progressive myoclonic epilepsy (Lafora body disease) in a Pakistani family
Fizza Orooj, Umm-E-Kalsoom, XiaoChu Zhao, et al.
Cureus
|
January 30, 2023
Baseline Characteristics, Prognostic Factors, and Treatment Outcomes for Adult Patients With Rhabdomyosarcoma (RMS)
Saif Ur Rab, Sameen Bin Naeem, Naqib Ullah Baloch, et al.
Genetic Testing and Molecular Biomarkers
|
December 3, 2025
Expanding the Phenotypic and Genotypic Spectrum of Postaxial Polydactyly: A Study of Four Consanguineous Pakistani Families
Tayyaba Saeed, Bushra Khan, Muhammad Haris Khan, et al.
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Search research articles
Search
Showing results (21-30 of 38) with videos related to
Sort By:
Page
of 4
Frontiers in Cellular Neuroscience
|
April 27, 2026
Cynanchum bungei Decne-derived extracellular vesicles alleviate cognitive impairment and pathological damage in Alzheimer's disease
Rui Hong, Jingjing Han, Fuxing Dong, et al.
BMC Health Services Research
|
June 17, 2026
Management of COPD and comorbidities in COPD patients by dispensing pharmaceutical care following Global Initiative for Chronic Obstructive Lung Disease-guidelines (GOLD guidelines 2020): a prospective randomized clinical trial
Hafsa Kanwal, Gaber E Eldesoky, Umm-E- Kalsoom, et al.
JPMA. the Journal of the Pakistan Medical Association
|
August 2, 2013
FDG-PET scan in assessing lymphomas and the application of Deauville Criteria
Umm-e-kalsoom Awan, Neelam Siddiqui, Mohammad SaadUllah, et al.
Clinical Dysmorphology
|
February 6, 2026
Identification of a novel mutation in metabotropic glutamate receptor 1 causing autosomal recessive spinocerebellar ataxia-13 in a Pakistani family
Shafeeq Ahmad, Bushra Khan, Hamza Shams, et al.
Neurogenetics
|
May 19, 2025
Identification of mutations in five Pakistani families with Epilepsy
Nayab Ahsan, Arsalan Ahmad, Shahnawaz Hussain, et al.
Plos One
|
February 4, 2026
Implementation of guideline-directed medical treatment for ischemic heart disease management: A knowledge, attitude and practice based cross-sectional survey
Umm-E- Kalsoom, Amjad Khan, Syed Sikandar Shah, et al.
Journal of Medical Genetics
|
November 20, 2012
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A
Umm-e- Kalsoom, Eva Klopocki, Naveed Wasif, et al.
Neurology Asia
|
November 4, 2021
A novel deletion mutation in <i>EPM2A</i> underlies progressive myoclonic epilepsy (Lafora body disease) in a Pakistani family
Fizza Orooj, Umm-E-Kalsoom, XiaoChu Zhao, et al.
Cureus
|
January 30, 2023
Baseline Characteristics, Prognostic Factors, and Treatment Outcomes for Adult Patients With Rhabdomyosarcoma (RMS)
Saif Ur Rab, Sameen Bin Naeem, Naqib Ullah Baloch, et al.
Genetic Testing and Molecular Biomarkers
|
December 3, 2025
Expanding the Phenotypic and Genotypic Spectrum of Postaxial Polydactyly: A Study of Four Consanguineous Pakistani Families
Tayyaba Saeed, Bushra Khan, Muhammad Haris Khan, et al.
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of 4