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CORONAVIRUS DISEASE 2019 (COVID-19)

Journal of University Medical & Dental College, 2020-09, Vol.11 (3), p.v-vi

Aysha Azhar

2020

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Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis

PloS one, 2014-04, Vol.9 (4), p.e93607

2014

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Rapid screening of pyogenic Staphylococcus aureus for confirmation of genus and species, methicillin resistance and virulence factors by using two novel multiplex PCR

Pakistan Journal of Medical Sciences, 2017-10, Vol.33 (5), p.1095-1100

2017

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Detection of high levels of resistance to linezolid and vancomycin in Staphylococcus aureus

Journal of medical microbiology, 2017-09, Vol.66 (9), p.1328-1331

2017

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MMP-2 levels evaluation and their relationship with breast cancer progression

The professional medical journal, 2020-02, Vol.27 (2), p.424-430

2020

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Venetoclax in the Treatment of Chronic Lymphocytic Leukemia: Evidence, Expectations, and Future Prospects

Curēus (Palo Alto, CA), 2020-06

2020

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High frequency of simultaneous presence of ESBL and carbapenemase producers among nosocomial coliform isolates in Faisalabad, Pakistan

Pakistan journal of medical sciences, 2021-02, Vol.37 (1), p.34-39

2021

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A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair

Scientific reports, 2012-10, Vol.2 (1), p.730-730, Article 730

2012

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Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS

European journal of human genetics : EJHG, 2010-06, Vol.18 (6), p.733-736

2010

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A novel mutation in Lysophosphatidic Acid Receptor 6 gene in autosomal recessive hypotrichosis and evidence for a founder effect

EJD. European journal of dermatology, 2012-07, Vol.22 (4), p.464-466

2012

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Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation

EJD. European journal of dermatology, 2010-07, Vol.20 (4), p.443-446

2010

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β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan

Journal of pediatric hematology/oncology, 2012-03, Vol.34 (2), p.90-92

2012

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Pulmonary Tuberculosis: Atypical Presentation

Dhaka Shishu (Children) Hospital Journal, 2022-12, Vol.37 (2), p.140-142

2022

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Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis: e93607

PloS one, 2014-04, Vol.9 (4)

2014

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Report of a recurrent mutation in ARS (component B) gene with severe Mal de Meleda in a large consanguineous Pakistani family

Pakistan journal of medical sciences, 2011-09, Vol.27 (3), p.686

2011

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Report of a recurrent mutation in ARS (component B) gene with severe Mal de Meleda in a large consanguineous Pakistani family

Pakistan journal of medical sciences, 2011-06, Vol.27 (2)

2011

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"A Lot of Us Have a Very Difficult Time Reconciling What Being Muslim Is": A Phenomenological Study on the Meaning of Being Muslim American

Cultural diversity & ethnic minority psychology, 2020-07, Vol.26 (3), p.338-346

2020

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Identification of Ascorbic Acid and Gallic Acid as Novel Inhibitors of Secreted Frizzled-Related Protein for the Treatment of Obesity-Induced Type 2 Diabetes

Dose-response, 2022-01, Vol.20 (1), p.15593258211069707-15593258211069707

2022

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Secreted frizzled‐related protein 4 and its implication in obesity and type‐2 diabetes

IUBMB life, 2019-11, Vol.71 (11), p.1701-1710

2019

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A RARE CASE OF SPINAL CORD INFARCTION IN A YOUNG PATIENT WITH SICKLE CELL DISEASE

Chest, 2024-10, Vol.166 (4), p.A1927-A1928

2024

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Extraction of dietary fiber and polyphenols from mango peel and its therapeutic potential to improve gut health

Food bioscience, 2023-06, Vol.53, p.102669, Article 102669

2023

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Association of Workplace stress with age among physiotherapists working in public and private sectors of Faisalabad

Journal of Riphah College of Rehabilitation Sciences, 2020-12, Vol.8 (2), p.88

2020

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Indicators of Obesity and Cardiovascular Parameters in Obese and Non-Obese Subjects

Pakistan Journal of Medical and Health Sciences, 2021-10, Vol.15 (10), p.3413-3416

2021

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A narrative review on extraction techniques of phytosterols and their applications in food industry

Biomass conversion and biorefinery, 2023-10

2023

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ASSOCIATION OF CONTRACEPTIVE BARRIERS WITH SOCIO DEMOGRAPHIC VARIABLES

Gomal journal of medical sciences, 2018-09, Vol.16 (3), p.75-78

2018

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CORONAVIRUS DISEASE 2019 (COVID-19)

Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis

Rapid screening of pyogenic Staphylococcus aureus for confirmation of genus and species, methicillin resistance and virulence factors by using two novel multiplex PCR

Detection of high levels of resistance to linezolid and vancomycin in Staphylococcus aureus

MMP-2 levels evaluation and their relationship with breast cancer progression

Venetoclax in the Treatment of Chronic Lymphocytic Leukemia: Evidence, Expectations, and Future Prospects

High frequency of simultaneous presence of ESBL and carbapenemase producers among nosocomial coliform isolates in Faisalabad, Pakistan

A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair

Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS

A novel mutation in Lysophosphatidic Acid Receptor 6 gene in autosomal recessive hypotrichosis and evidence for a founder effect

Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation

β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan

Pulmonary Tuberculosis: Atypical Presentation

Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis: e93607

Report of a recurrent mutation in ARS (component B) gene with severe Mal de Meleda in a large consanguineous Pakistani family

Report of a recurrent mutation in ARS (component B) gene with severe Mal de Meleda in a large consanguineous Pakistani family

"A Lot of Us Have a Very Difficult Time Reconciling What Being Muslim Is": A Phenomenological Study on the Meaning of Being Muslim American

Identification of Ascorbic Acid and Gallic Acid as Novel Inhibitors of Secreted Frizzled-Related Protein for the Treatment of Obesity-Induced Type 2 Diabetes

Secreted frizzled‐related protein 4 and its implication in obesity and type‐2 diabetes

A RARE CASE OF SPINAL CORD INFARCTION IN A YOUNG PATIENT WITH SICKLE CELL DISEASE

Extraction of dietary fiber and polyphenols from mango peel and its therapeutic potential to improve gut health

Association of Workplace stress with age among physiotherapists working in public and private sectors of Faisalabad

Indicators of Obesity and Cardiovascular Parameters in Obese and Non-Obese Subjects

A narrative review on extraction techniques of phytosterols and their applications in food industry

ASSOCIATION OF CONTRACEPTIVE BARRIERS WITH SOCIO DEMOGRAPHIC VARIABLES

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