Author: "Shaiq, P.A." / Publication Year Range: Last 50 years - Searchworks@Jio Institute Digital Library Search Results

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Your search keyword '"Shaiq, P.A."' showing total 8 results

Start Over Author "Shaiq, P.A." Publication Year Range Last 50 years

8 results on '"Shaiq, P.A."'

1. Association of non alcoholic fatty liver disease (NAFLD) with coronary artery disease in Pakistani subjects

Author: Noorulamin, M., primary, Ali, A.M., additional, Zafar, M.M., additional, Raja, A.M., additional, Raja, G.K., additional, and Shaiq, P.A., additional
Published: 2021
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2. 176 Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide

Author: Stuart, P.E., primary, Tsoi, L., additional, Nair, R.P., additional, Ghosh, M., additional, Kabra, M., additional, Shaiq, P.A., additional, Qamar, R., additional, Tejasvi, T., additional, Voorhees, J.J., additional, Franke, A., additional, Sharma, V.K., additional, and Elder, J.T., additional
Published: 2021
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3. Frequency of endocarditis in pediatric patients admitted in a tertiary care cardiac hospital of Pakistan

Author: Ul Amin, M. Noor, primary, Raja, A.M., additional, and Shaiq, P.A., additional
Published: 2020
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4. Estimation of serum electrolytes dysfunction in acute MI patients presented at tertiary care hospital in Pakistan

Author: Ul Amin, M. Noor, primary, Ali, A.M., additional, Hussain, A.B., additional, Raja, A.M., additional, and Shaiq, P.A., additional
Published: 2020
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5. Assessment of pre & post serum creatinine levels in CABG patients of northern Pakistan

Author: Ul Amin, M. Noor, primary, Hussain, A.B., additional, Ali, A.M., additional, Raja, A.M., additional, and Shaiq, P.A., additional
Published: 2020
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6. Compound heterozygous mutations p.Q1530X and 6103delG in COL7A1 causing recessive dystrophic epidermolysis bullosa in a Pakistani family

Author: Shaiq, P.A., Klausegger, A., Bauer, J.W., Azam, M., Raja, G.K., and Qamar, R.
Subjects: Genetics and epigenetic pathways of disease [NCMLS 6]
Abstract: Item does not contain fulltext
Published: 2012

7. Founder mutation c.676insC in three unrelated Kindler syndrome families belonging to a particular clan from Pakistan

Author: Shaiq, P.A., Klausegger, A., Muzaffar, F., Bauer, J.W., Khan, M.I., Khanum, A., Qamar, R., and Raja, G.K.
Subjects: Genetics and epigenetic pathways of disease [NCMLS 6]
Abstract: Item does not contain fulltext
Published: 2012
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8. Genetic associations of psoriasis in a Pakistani population

Author: Shaiq, P.A., primary, Stuart, P.E., additional, Latif, A., additional, Schmotzer, C., additional, Kazmi, A.H., additional, Khan, M.S., additional, Azam, M., additional, Tejasvi, T., additional, Voorhees, J.J., additional, Raja, G.K., additional, Elder, J.T., additional, Qamar, R., additional, and Nair, R.P., additional
Published: 2013
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