MON-345 Recovery of Adrenal Function Following Bilateral Adrenal Hemorrhage: Two Case Reports

由 Ansar, Muhammad, Morselli, Lisa, Shibli-Rahhal, Amal
發表在 J Endocr Soc (2019)

SAT-613 Heterophile Antibody Interference Causing Elevated TSH Levels: A Challenging Diagnosis

由 Ansar, Muhammad, O’Neill, Brian, Halvorson, Tracy
發表在 J Endocr Soc (2019)

Hashimoto Encephalopathy With Status Epilepticus

由 Sliwinska, Aleksandra, Fumuso, Perry, Stringer, Bryan, Ansar, Muhammad, Baldwin, Jennifer
發表在 Cureus (2020)

Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort

由 Khan, Amjad, Han, Shirui, Wang, Rongrong, Ansar, Muhammad, Ahmad, Wasim, Zhang, Xue
發表在 Mol Genet Genomic Med (2019)

Post-transcriptional inhibition of hepatitis C virus replication through small interference RNA

由 Ali Ashfaq, Usman, Ansar, Muhammad, Sarwar, Muhammad Tahir, Javed, Tariq, Rehman, Sidra, Riazuddin, Sheikh
出版 2011

A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family

由 Basit, Sulman, Naqvi, Syed Kamran-ul-Hassan, Wasif, Naveed, Ali, Ghazanfar, Ansar, Muhammad, Ahmad, Wasim
出版 2008

A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31

由 Habib, Rabia, Ansar, Muhammad, Mattheisen, Manuel, Shahid, Muhammad, Ali, Ghazanfar, Ahmad, Wasim, Betz, Regina C.
發表在 PLoS One (2015)

Mutations in <it>WDR62 </it>gene in Pakistani families with autosomal recessive primary microcephaly

由 Mir Asif, Mahmood Saqib, Basit Sulman, Khan Bushra, Hassan Muhammad, Kousar Rizwana, Ahmad Wasim, Ansar Muhammad
出版 2011-10-01

A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families

由 Lee, Kwanghyuk, Khan, Saadullah, Ansar, Muhammad, Santos-Cortez, Regie Lyn P., Ahmad, Wasim, Leal, Suzanne M.
出版 2011

A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability

由 Khan, Muzammil Ahmad, Rafiq, Muhammad Arshad, Noor, Abdul, Ali, Nadir, Ali, Ghazanfar, Vincent, John B, Ansar, Muhammad
出版 2011

Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly

由 Kousar, Rizwana, Hassan, Muhammad Jawad, Khan, Bushra, Basit, Sulman, Mahmood, Saqib, Mir, Asif, Ahmad, Wasim, Ansar, Muhammad
出版 2011

Inhibition of full length Hepatitis C Virus particles of 1a genotype through small interference RNA

由 Ansar, Muhammad, Ashfaq, Usman Ali, shahid, Imran, Sarwar, Muhammad Tahir, Javed, Tariq, Rehman, Sidra, Hassan, Sajida, Riazuddin, Sheikh
出版 2011

Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene

由 Lee, Kwanghyuk, Amin ud Din, Mohammad, Ansar, Muhammad, Santos-Cortez, Regie Lyn P., Ahmad, Wasim, Leal, Suzanne M.
出版 2011

A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Three Pakistani Families with Autosomal Recessive Hypotrichosis

由 Rafiq, Muhammad Arshad, Ansar, Muhammad, Mahmood, Saqib, Haque, Sayedul, Faiyaz-ul-Haque, Muhammad, Leal, Suzanne M., Ahmad, Wasim
發表在 J Invest Dermatol (2004)

Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3

由 Chishti, Muhammad Salman, Lee, Kwanghyuk, McDonald, Merry-Lynn, Hassan, Muhammad Jawad, Ansar, Muhammad, Ahmad, Wasim, Leal, Suzanne M
出版 2009

Localization of A Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus (DFNB38) to 6q26–q27 in a Consanguineous Kindred from Pakistan

由 Ansar, Muhammad, Ramzan, Mohammad, Pham, Thanh L., Yan, Kai, Jamal, Syed Muhammad, Haque, Sayedul, Ahmad, Wasim, Leal, Suzanne M.
出版 2003

DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22–q21.12

由 Wajid, Muhammad, Abbasi, Amir Ali, Ansar, Muhammad, Pham, Thanh L, Yan, Kai, Haque, Sayedul, Ahmad, Wasim, Leal, Suzanne M
出版 2003

Novel CLDN14 Mutations in Pakistani Families With Autosomal Recessive Non-Syndromic Hearing Loss

由 Lee, Kwanghyuk, Ansar, Muhammad, Andrade, Paula B., Khan, Bushra, Santos-Cortez, Regie Lyn P., Ahmad, Wasim, Leal, Suzanne M.
出版 2012

Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree

由 Makrythanasis, Periklis, Guipponi, Michel, Santoni, Federico A., Zaki, Maha, Issa, Mahmoud Y., Ansar, Muhammad, Hamamy, Hanan, Antonarakis, Stylianos E.
發表在 Hum Genomics (2016)

Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan

由 Pedurupillay, Christeen Ramane J., Landsend, Erlend Christoffer Sommer, Vigeland, Magnus Dehli, Ansar, Muhammad, Frengen, Eirik, Misceo, Doriana, Strømme, Petter
發表在 Genes (Basel) (2016)