Torthaí cuardaigh - Ansar, Muhammad

MON-345 Recovery of Adrenal Function Following Bilateral Adrenal Hemorrhage: Two Case Reports de réir Ansar, Muhammad, Morselli, Lisa, Shibli-Rahhal, Amal

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SAT-613 Heterophile Antibody Interference Causing Elevated TSH Levels: A Challenging Diagnosis de réir Ansar, Muhammad, O’Neill, Brian, Halvorson, Tracy

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Hashimoto Encephalopathy With Status Epilepticus de réir Sliwinska, Aleksandra, Fumuso, Perry, Stringer, Bryan, Ansar, Muhammad, Baldwin, Jennifer

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Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort de réir Khan, Amjad, Han, Shirui, Wang, Rongrong, Ansar, Muhammad, Ahmad, Wasim, Zhang, Xue

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Post-transcriptional inhibition of hepatitis C virus replication through small interference RNA de réir Ali Ashfaq, Usman, Ansar, Muhammad, Sarwar, Muhammad Tahir, Javed, Tariq, Rehman, Sidra, Riazuddin, Sheikh

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A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family de réir Basit, Sulman, Naqvi, Syed Kamran-ul-Hassan, Wasif, Naveed, Ali, Ghazanfar, Ansar, Muhammad, Ahmad, Wasim

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A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31 de réir Habib, Rabia, Ansar, Muhammad, Mattheisen, Manuel, Shahid, Muhammad, Ali, Ghazanfar, Ahmad, Wasim, Betz, Regina C.

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Lapachol-Induced Upregulation of Sirt1/Sirt3 is linked with Improved Skin Wound Healing in Alloxan-induced Diabetic Mice de réir Bibi, Shaheen, Ahmad, Fayyaz, Alam, Muhammad Rizwan, Ansar, Muhammad, Yeou, Kim Sun, Wahedi, Hussain Mustatab

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A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families de réir Lee, Kwanghyuk, Khan, Saadullah, Ansar, Muhammad, Santos-Cortez, Regie Lyn P., Ahmad, Wasim, Leal, Suzanne M.

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A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability de réir Khan, Muzammil Ahmad, Rafiq, Muhammad Arshad, Noor, Abdul, Ali, Nadir, Ali, Ghazanfar, Vincent, John B, Ansar, Muhammad

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Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly de réir Kousar, Rizwana, Hassan, Muhammad Jawad, Khan, Bushra, Basit, Sulman, Mahmood, Saqib, Mir, Asif, Ahmad, Wasim, Ansar, Muhammad

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Inhibition of full length Hepatitis C Virus particles of 1a genotype through small interference RNA de réir Ansar, Muhammad, Ashfaq, Usman Ali, shahid, Imran, Sarwar, Muhammad Tahir, Javed, Tariq, Rehman, Sidra, Hassan, Sajida, Riazuddin, Sheikh

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Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene de réir Lee, Kwanghyuk, Amin ud Din, Mohammad, Ansar, Muhammad, Santos-Cortez, Regie Lyn P., Ahmad, Wasim, Leal, Suzanne M.

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A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Three Pakistani Families with Autosomal Recessive Hypotrichosis de réir Rafiq, Muhammad Arshad, Ansar, Muhammad, Mahmood, Saqib, Haque, Sayedul, Faiyaz-ul-Haque, Muhammad, Leal, Suzanne M., Ahmad, Wasim

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Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3 de réir Chishti, Muhammad Salman, Lee, Kwanghyuk, McDonald, Merry-Lynn, Hassan, Muhammad Jawad, Ansar, Muhammad, Ahmad, Wasim, Leal, Suzanne M

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DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22–q21.12 de réir Wajid, Muhammad, Abbasi, Amir Ali, Ansar, Muhammad, Pham, Thanh L, Yan, Kai, Haque, Sayedul, Ahmad, Wasim, Leal, Suzanne M

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Localization of A Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus (DFNB38) to 6q26–q27 in a Consanguineous Kindred from Pakistan de réir Ansar, Muhammad, Ramzan, Mohammad, Pham, Thanh L., Yan, Kai, Jamal, Syed Muhammad, Haque, Sayedul, Ahmad, Wasim, Leal, Suzanne M.

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Novel CLDN14 Mutations in Pakistani Families With Autosomal Recessive Non-Syndromic Hearing Loss de réir Lee, Kwanghyuk, Ansar, Muhammad, Andrade, Paula B., Khan, Bushra, Santos-Cortez, Regie Lyn P., Ahmad, Wasim, Leal, Suzanne M.

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Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree de réir Makrythanasis, Periklis, Guipponi, Michel, Santoni, Federico A., Zaki, Maha, Issa, Mahmoud Y., Ansar, Muhammad, Hamamy, Hanan, Antonarakis, Stylianos E.

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Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan de réir Pedurupillay, Christeen Ramane J., Landsend, Erlend Christoffer Sommer, Vigeland, Magnus Dehli, Ansar, Muhammad, Frengen, Eirik, Misceo, Doriana, Strømme, Petter

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