Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3)

por Khan, Arif O., Shinwari, Jameela, Abu Dhaim, Nada, Khalil, Dania, Al Sharif, Latifa, Al Tassan, Nada
Publicado 2011

Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome

por Khan, Arif O., Shinwari, Jameela, Al Sharif, Latifa, Khalil, Dania, Al-Gehedan, Saeed, Al Tassan, Nada A.
Publicado 2011

Clinical and Molecular Characterization of Ataxia with Oculomotor Apraxia Patients In Saudi Arabia

por Bohlega, Saeed A, Shinwari, Jameela M, Al Sharif, Latifa J, Khalil, Dania S, Alkhairallah, Thamer S, Al Tassan, Nada A
Publicado 2011

Soy protein supplementation does not cause lymphocytopenia in postmenopausal women

por Soung, Do Y, Patade, Anagha, Khalil, Dania A, Lucas, Edralin A, Devareddy, Latha, Greaves, Kathryn A, Arjmandi, Bahram H
Publicado 2006

Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families

por Khan, Arif O., Shinwari, Jameela, Omar, Aisha, Al-Sharif, Latifa, Khalil, Dania S., Alanazi, Mohammed, Al-Amri, Abdullah, Al Tassan, Nada
Publicado 2011

One year soy protein supplementation has positive effects on bone formation markers but not bone density in postmenopausal women

por Arjmandi, Bahram H, Lucas, Edralin A, Khalil, Dania A, Devareddy, Latha, Smith, Brenda J, McDonald, Jennifer, Arquitt, Andrea B, Payton, Mark E, Mason, Claudia
Publicado 2005

Effects of Vitamin E on Bone Biomechanical and Histomorphometric Parameters in Ovariectomized Rats

por Feresin, Rafaela G., Johnson, Sarah A., Elam, Marcus L., Kim, Jeong-Su, Khalil, Dania A., Lucas, Edralin A., Smith, Brenda J., Payton, Mark E., Akhter, Mohammed P., Arjmandi, Bahram H.
Publicado 2013

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

por Bohlega, Saeed A., Al-Mubarak, Bashayer R., Alyemni, Eman A., Abouelhoda, Mohamed, Monies, Dorota, Mustafa, Abeer E., Khalil, Dania S., Al Haibi, Sara, Abou Al-Shaar, Hussam, Faquih, Tariq, El-Kalioby, Mohamed, Tahir, Asma I., Al Tassan, Nada A.
Publicado 2016

Parkinson’s Disease in Saudi Patients: A Genetic Study

por Al-Mubarak, Bashayer R., Bohlega, Saeed A., Alkhairallah, Thamer S., Magrashi, Amna I., AlTurki, Maha I., Khalil, Dania S., AlAbdulaziz, Basma S., Abou Al-Shaar, Hussam, Mustafa, Abeer E., Alyemni, Eman A., Alsaffar, Bashayer A., Tahir, Asma I., Al Tassan, Nada A.
Publicado 2015

Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel

por Al-Hamed, Mohamed H, Kurdi, Wesam, Alsahan, Nada, Alabdullah, Zainab, Abudraz, Rania, Tulbah, Maha, Alnemer, Maha, Khan, Rubina, Al-Jurayb, Haya, Alahmed, Ahmed, Tahir, Asma I, Khalil, Dania, Edwards, Noel, Al Abdulaziz, Basma, Binhumaid, Faisal S, Majid, Salma, Faquih, Tariq, El-Kalioby, Mohamed, Abouelhoda, Mohamed, Altassan, Nada, Monies, Dorota, Meyer, Brian, Sayer, John A, Albaqumi, Mamdouh
Publicado 2016