Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII
Kaya, Namik, Aldhalaan, Hesham, Al-Younes, Banan, Colak, Dilek, Shuaib, Taghreed, Al-Mohaileb, Fahad, Al-Sugair, Abdulaziz, Nester, Michael, Al-Yamani, Suad, Al-Bakheet, Albandary, Al-Hashmi, Nadia, Al-Sayed, Moeen, Meyer, Brian, Jungbluth, Heinz, Al-Owain, Mohammed
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2011)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2011)
Get full text
Journal Article
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis
Wakil, Salma M, Murad, Hatem N, Baz, Batoul M, Hagos, Samiya T, Al-Amr, Rana A, Al-Yamani, Suad A, Al-Wadaee, Salem M, Meyer, Brian F, Bohlega, Saeed A
Published in Neurosciences (Riyadh, Saudi Arabia) (01.01.2012)
Get full text
Published in Neurosciences (Riyadh, Saudi Arabia) (01.01.2012)
Journal Article
Autozygome and high throughput confirmation of disease genes candidacy
Maddirevula, Sateesh, Alzahrani, Fatema, Al-Owain, Mohammed, Al Muhaizea, Mohammad A, Kayyali, Husam R, AlHashem, Amal, Rahbeeni, Zuhair, Al-Otaibi, Maha, Alzaidan, Hamad I, Balobaid, Ameera, El Khashab, Heba Y, Bubshait, Dalal K, Faden, Maha, Yamani, Suad Al, Dabbagh, Omar, Al-Mureikhi, Mariam, Jasser, Abdulla Al, Alsaif, Hessa S, Alluhaydan, Iram, Seidahmed, Mohammed Zain, Alabbasi, Bashair Hamza, Almogarri, Ibrahim, Kurdi, Wesam, Akleh, Hana, Qari, Alya, Al Tala, Saeed M, Alhomaidi, Suzan, Kentab, Amal Y, Salih, Mustafa A, Chedrawi, Aziza, Alameer, Seham, Tabarki, Brahim, Shamseldin, Hanan E, Patel, Nisha, Ibrahim, Niema, Abdulwahab, Firdous, Samira, Menasria, Goljan, Ewa, Abouelhoda, Mohamed, Meyer, Brian F, Hashem, Mais, Shaheen, Ranad, AlShahwan, Saad, Alfadhel, Majid, Ben-Omran, Tawfeg, Al-Qattan, Mohammad M, Monies, Dorota, Alkuraya, Fowzan S
Published in Genetics in medicine (01.03.2019)
Published in Genetics in medicine (01.03.2019)
Get full text
Journal Article
Developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep in Saudi Arabia: Electroclinical, etiologic, genetic, and outcome multicenter study
Alsini, Hanin, Alghamdi, Abdulaziz, Alshafi, Shatha, Hundallah, Khalid, Almehmadi, Sameer, Alsowat, Daad, Al-Yamani, Suad, Almuzaini, Hanin, Alwadie, Ali, Al-Otaibi, Ali, Jad, Lamyaa, Almadhi, Asma, Bashiri, Fahad, Kentab, Amal, Hamad, Muddathir H, Baarmah, Duaa, Alrifaie, Mohammed, Almuqbel, Mohammed, Baradie, Raidah Al, Mir, Ali, Jan, Mohammed, Muthaffar, Osama, Aljabri, Mohammed, Ali, Elsayed, Saeed, Mohammed, Matar, Abeer, Tabarki, Brahim
Published in Seizure (London, England) (01.04.2023)
Published in Seizure (London, England) (01.04.2023)
Get full text
Journal Article
Phenotypical Spectrum of Cerebellar Ataxic Associated With a Novel Mutation the CA8 Gene, Encoding Carbonic Anhydrase (CA) VIII
KAYA, Namik, ALDHALAAN, Hesham, AL-HASHMI, Nadia, AL-SAYED, Moeen, MEYER, Brian, JUNGBLUTH, Heinz, AL-OWAIN, Mohammed, AL-YOUNES, Banan, COLAK, Dilek, SHUAIB, Taghreed, AL-MOHAILEB, Fahad, AL-SUGAIR, Abdulaziz, NESTER, Michael, AL-YAMANI, Suad, AL-BAKHEET, Albandary
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (2011)
Get full text
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (2011)
Journal Article