Canlyniadau Chwilio - Ansar, Muhammad

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

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

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Hashimoto Encephalopathy With Status Epilepticus gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan Pedurupillay, Christeen Ramane J., Landsend, Erlend Christoffer Sommer, Vigeland, Magnus Dehli, Ansar, Muhammad, Frengen, Eirik, Misceo, Doriana, Strømme, Petter

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