Publications by authors named "Aysha Azhar"

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High frequency of simultaneous presence of ESBL and carbapenemase producers among nosocomial coliform isolates in Faisalabad, Pakistan.
Sofia Irfan, Aysha Azhar, Asad Bashir, Salman Ahmed, Abdul Haque

Pak J Med Sci· January 2021

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Venetoclax in the Treatment of Chronic Lymphocytic Leukemia: Evidence, Expectations, and Future Prospects.
Saba Tariq, Sundus Tariq, Maliha Khan, Aysha Azhar, Mukhtiar Baig

Cureus· June 2020

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Detection of high levels of resistance to linezolid and vancomycin in Staphylococcus aureus.
Aysha Azhar, Samreen Rasool, Asma Haque, Sidra Shan, Muhammad Saeed

J Med Microbiol· September 2017

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Rapid screening of pyogenic for confirmation of genus and species, methicillin resistance and virulence factors by using two novel multiplex PCR.
Abdul Haque, Asma Haque, Muhammad Saeed, Aysha Azhar, Samreen Rasool

Pak J Med Sci· January 2017

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Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis.
Doroteya Raykova, Joakim Klar, Aysha Azhar, Tahir Naeem Khan, Naveed Altaf Malik

PLoS One· November 2014

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A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair.
Muhammad Tariq, Aysha Azhar, Shahid Mahmood Baig, Niklas Dahl, Joakim Klar

Sci Rep· March 2013

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A novel mutation in lysophosphatidic acid receptor 6 gene in autosomal recessive hypotrichosis and evidence for a founder effect.
Aysha Azhar, Muhammad Tariq, Shahid Mahmood Baig, Niklas Dahl, Joakim Klar

Eur J Dermatol· February 2013

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β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan.
Shahid Mahmood Baig, Dure Sabih, Muhammad Kashif Rahim, Aysha Azhar, Muhammad Tariq

J Pediatr Hematol Oncol· March 2012

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Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation.
Mahmood Rasool, Sadia Nawaz, Aysha Azhar, Muhammad Wajid, Per Westermark

Eur J Dermatol· September 2010

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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.
Muhammad Farooq, Jesper T Troelsen, Mette Boyd, Hans Eiberg, Lars Hansen, Aysha Azhar

Eur J Hum Genet· June 2010

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