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

le Ansar, Muhammad, Morselli, Lisa, Shibli-Rahhal, Amal
Foilsithe in J Endocr Soc (2019)

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

le Ansar, Muhammad, O’Neill, Brian, Halvorson, Tracy
Foilsithe in J Endocr Soc (2019)

Hashimoto Encephalopathy With Status Epilepticus

le Sliwinska, Aleksandra, Fumuso, Perry, Stringer, Bryan, Ansar, Muhammad, Baldwin, Jennifer
Foilsithe in Cureus (2020)

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

le Khan, Amjad, Han, Shirui, Wang, Rongrong, Ansar, Muhammad, Ahmad, Wasim, Zhang, Xue
Foilsithe in Mol Genet Genomic Med (2019)

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

le Ali Ashfaq, Usman, Ansar, Muhammad, Sarwar, Muhammad Tahir, Javed, Tariq, Rehman, Sidra, Riazuddin, Sheikh
Foilsithe 2011

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

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

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

le Habib, Rabia, Ansar, Muhammad, Mattheisen, Manuel, Shahid, Muhammad, Ali, Ghazanfar, Ahmad, Wasim, Betz, Regina C.
Foilsithe in PLoS One (2015)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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