Klippel-Trenaunay and Sturge-Weber overlapping syndrome in a Saudi boy

Por Kentab, Amal Y
Publicado no Sudan J Paediatr (2016)

The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature

Por Kentab, Amal Y, Hassan, Hamdy H, Hamad, Muddathir H A, Alhumidi, Ahmed
Publicado no Sudan J Paediatr (2014)

Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans

Por Shamseldin, Hanan E., Smith, Laura L., Kentab, Amal, Alkhalidi, Hisham, Summers, Brady, Alsedairy, Haifa, Xiong, Yong, Gupta, Vandana A., Alkuraya, Fowzan S.
Publicado no Hum Genet (2015)

Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly

Por Alkuraya, Fowzan S., Cai, Xuyu, Emery, Carina, Mochida, Ganeshwaran H., Al-Dosari, Mohammed S., Felie, Jillian M., Hill, R. Sean, Barry, Brenda J., Partlow, Jennifer N., Gascon, Generoso G., Kentab, Amal, Jan, Mohammad, Shaheen, Ranad, Feng, Yuanyi, Walsh, Christopher A.
Publicado em 2011

Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly

Por Alkuraya, Fowzan S., Cai, Xuyu, Emery, Carina, Mochida, Ganeshwaran H., Al-Dosari, Mohammed S., Felie, Jillian M., Hill, R. Sean, Barry, Brenda J., Partlow, Jennifer N., Gascon, Generoso G., Kentab, Amal, Jan, Mohammad, Shaheen, Ranad, Feng, Yuanyi, Walsh, Christopher A.
Publicado em 2011

New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations

Por Salih, Mustafa A., Mundwiller, Emeline, Khan, Arif O., AlDrees, Abdulmajeed, Elmalik, Salah A., Hassan, Hamdy H., Al-Owain, Mohammed, Alkhalidi, Hisham M. S., Katona, Istvan, Kabiraj, Mohammad M., Chrast, Roman, Kentab, Amal Y., Alzaidan, Hamad, Rodenburg, Richard J., Bosley, Thomas M., Weis, Joachim, Koenig, Michel, Stevanin, Giovanni, Azzedine, Hamid
Publicado em 2013

Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations

Por Salih, Mustafa A., Mundwiller, Emeline, Khan, Arif O., AlDrees, Abdulmajeed, Elmalik, Salah A., Hassan, Hamdy H., Al-Owain, Mohammed, Alkhalidi, Hisham M. S., Katona, Istvan, Kabiraj, Mohammad M., Chrast, Roman, Kentab, Amal Y., Alzaidan, Hamad, Rodenburg, Richard J., Bosley, Thomas M., Weis, Joachim, Koenig, Michel, Stevanin, Giovanni, Azzedine, Hamid
Publicado em 2013

Management of convulsive status epilepticus in children: an adapted clinical practice guideline for pediatricians in Saudi Arabia

Por Bashiri, Fahad A., Hamad, Muddathir H., Amer, Yasser S., Abouelkheir, Manal M., Mohamed, Sarar, Kentab, Amal Y., Salih, Mustafa A., Nasser, Mohammad N. Al, Al-Eyadhy, Ayman A., Othman, Mohammed A. Al, Al-Ahmadi, Tahani, Iqbal, Shaikh M., Somily, Ali M., Wahabi, Hayfaa A., Hundallah, Khalid J., Alwadei, Ali H., Albaradie, Raidah S., Al-Twaijri, Waleed A., Jan, Mohammed M., Al-Otaibi, Faisal, Alnemri, Abdulrahman M., Al-Ansary, Lubna A.
Publicado no Neurosciences (Riyadh) (2017)