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Search Results - Al Yamani, Suad
Search Results - Al Yamani, Suad
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Case report: Aromatic L-amino acid decarboxylase deficiency in three patient cases from the Kingdom of Saudi Arabia
by
Abukhaled, Musaad
,
Alrakaf, Laila
,
Aldhalaan, Hesham
,
Al Yamani, Suad
Published in
Frontiers in pediatrics
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Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII
by
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
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Autozygome and high throughput confirmation of disease genes candidacy
by
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
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Developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep in Saudi Arabia: Electroclinical, etiologic, genetic, and outcome multicenter study
by
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)
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5
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Case report: Aromatic L-amino acid decarboxylase deficiency in three patient cases from the Kingdom of Saudi Arabia
by
Abukhaled, Musaad
,
Alrakaf, Laila
,
Aldhalaan, Hesham
,
Al Yamani, Suad
Published in
Frontiers in pediatrics
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6
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Phenotypical Spectrum of Cerebellar Ataxic Associated With a Novel Mutation the CA8 Gene, Encoding Carbonic Anhydrase (CA) VIII
by
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
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7
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
by
Monies, Dorota
,
Abouelhoda, Mohammed
,
Assoum, Mirna
,
Moghrabi, Nabil
,
Rafiullah, Rafiullah
,
Almontashiri, Naif
,
Alowain, Mohammed
,
Alzaidan, Hamad
,
Alsayed, Moeen
,
Subhani, Shazia
,
Cupler, Edward
,
Faden, Maha
,
Alhashem, Amal
,
Qari, Alya
,
Aldhalaan, Hisham
,
Kurdi, Wesam
,
Khan, Sameena
,
Rahbeeni, Zuhair
,
Goljan, Ewa
,
Elbardisy, Hadeel
,
ElKalioby, Mohamed
,
Shah, Zeeshan
,
Jaafar, Amal
,
Albar, Ranad
,
Akilan, Asma
,
Tayeb, Hamsa
,
Tahir, Asma
,
Fawzy, Mohammed
,
Nasr, Mohammed
,
Makki, Shaza
,
Alfaifi, Abdullah
,
Akleh, Hanna
,
Yamani, Suad
,
Bubshait, Dalal
,
Mahnashi, Mohammed
,
Basha, Talal
,
Alsagheir, Afaf
,
Alsaleem, Khalid
,
Badawi, Manal
,
Bashiri, Fahad
,
Bohlega, Saeed
,
Tous, Ehab
,
Ahmed, Syed
,
Algoufi, Talal
,
Al-Mousa, Hamoud
,
Alaki, Emadia
,
Alhumaidi, Susan
,
Alghamdi, Hadeel
,
Alghamdi, Malak
,
Sahly, Ahmed
,
Al-Ahmari, Ali
,
Alkuraya, Hisham
,
Almehaidib, Ali
,
Abanemai, Mohammed
,
Alsohaibaini, Fahad
,
Arnaout, Rand
,
Abdel-Salam, Ghada M.H.
,
Aldhekri, Hasan
,
AlKhater, Suzan
,
Alqadi, Khalid
,
Alshareef, Turki
,
Banjar, Hanaa
,
Alsahan, Nada
,
Abosoudah, Ibraheem
,
Alashwal, Abdullah
,
Alhajjar, Sami
,
Al-Mayouf, Sulaiman
,
Alsemari, Abdulaziz
,
Alshuaibi, Walaa
,
Altala, Saeed
,
Baz, Salah
,
Hamad, Muddathir
,
Abalkhail, Tariq
,
Alenazi, Badi
,
Alkaff, Alya
,
Almohareb, Fahad
,
Al Mutairi, Fuad
,
Alsaleh, Mona
,
Alzelaye, Somaya
,
Bahzad, Shakir
,
Manee, Abdulaziz Bin
,
Jarrad, Ola
,
Meriki, Neama
,
Albeirouti, Bassem
,
Alqasmi, Amal
,
AlBalwi, Mohammed
,
Makhseed, Nawal
,
Hassan, Saeed
,
Shaheen, Marwan
,
Sermin, Saadeh
,
Shahrukh, Shamsad
,
Hashmi, Shahrukh
,
Shawli, Ayman
,
Tamim, Abdullah
,
Alnahari, Ahmed
,
Ghemlas, Ibrahim
,
Hussein, Maged
,
Wali, Sami
,
Murad, Hatem
,
Alkuraya, Fowzan S.
Published in
American journal of human genetics
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8
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
by
Monies, Dorota
,
Abouelhoda, Mohammed
,
Assoum, Mirna
,
Moghrabi, Nabil
,
Almontashiri, Naif
,
Alowain, Mohammed
,
Alzaidan, Hamad
,
Alsayed, Moeen
,
Subhani, Shazia
,
Cupler, Edward
,
Faden, Maha
,
Alhashem, Amal
,
Qari, Alya
,
Aldhalaan, Hisham
,
Kurdi, Wesam
,
Rahbeeni, Zuhair
,
Alotaibi, Maha
,
Goljan, Ewa
,
Elbardisy, Hadeel
,
ElKalioby, Mohamed
,
Shah, Zeeshan
,
Alruwaili, Hibah
,
Jaafar, Amal
,
Albar, Ranad
,
Tayeb, Hamsa
,
Fawzy, Mohammed
,
Nasr, Mohammed
,
Makki, Shaza
,
Alfaifi, Abdullah
,
Akleh, Hanna
,
Yamani, Suad
,
Bubshait, Dalal
,
Mahnashi, Mohammed
,
Basha, Talal
,
Alsagheir, Afaf
,
Khaled, Musad Abu
,
Almugbel, Maisoon
,
Badawi, Manal
,
Sulaiman, Raashida
,
Algoufi, Talal
,
Alaki, Emadia
,
Alhumaidi, Susan
,
Alghamdi, Hadeel
,
Alghamdi, Malak
,
Sahly, Ahmed
,
Nahrir, Shapar
,
Al-Ahmari, Ali
,
Alkuraya, Hisham
,
Almehaidib, Ali
,
Abanemai, Mohammed
,
Alsohaibaini, Fahad
,
Alsaud, Bandar
,
Arnaout, Rand
,
Abdel-Salam, Ghada M.H.
,
Aldhekri, Hasan
,
AlKhater, Suzan
,
Alqadi, Khalid
,
Alsabban, Essam
,
Alshareef, Turki
,
Awartani, Khalid
,
Banjar, Hanaa
,
Alsahan, Nada
,
Aldekhail, Wajeeh
,
Alhajjar, Sami
,
Al-Mayouf, Sulaiman
,
Alsemari, Abdulaziz
,
Alshuaibi, Walaa
,
Altala, Saeed
,
Altalhi, Abdulhadi
,
Baz, Salah
,
Hamad, Muddathir
,
Abalkhail, Tariq
,
Alenazi, Badi
,
Alkaff, Alya
,
Almohareb, Fahad
,
Alsaleh, Mona
,
Alsonbul, Abdullah
,
Alzelaye, Somaya
,
Bahzad, Shakir
,
Manee, Abdulaziz Bin
,
Jarrad, Ola
,
Meriki, Neama
,
Albeirouti, Bassem
,
AlBalwi, Mohammed
,
Hassan, Saeed
,
Salih, Isam
,
Salih, Mustafa A.
,
Shaheen, Marwan
,
Sermin, Saadeh
,
Shahrukh, Shamsad
,
Hashmi, Shahrukh
,
Tajuddin, Ameen
,
Tamim, Abdullah
,
Alnahari, Ahmed
,
Ghemlas, Ibrahim
,
Hussein, Maged
,
Wali, Sami
,
Murad, Hatem
,
Meyer, Brian F.
,
Alkuraya, Fowzan S.
Published in
American journal of human genetics
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