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Edward Cupler

Universite Paris Cite

23H指数
97论文数
3.0K被引数
收录论文 27
发表时间
A Multidisciplinary Perspective Addressing the Diagnostic Challenges of Late-Onset Pompe Disease in the Arabian Peninsula Region Developed From an Expert Group Meeting
err2022-06-23
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errOAAI
errAl Shehri, Ali; Al-Asmi, Abdullah; Al Salti, Abdullah Mohammed; Almadani, Abubaker; Hassan, Ali; Bamaga, Ahmed K.; Cupler, Edward J.; Al-Hashel, Jasem; Alabdali, Majed M.; Alanazy, Mohammed H.; Noori, Suzan
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SARS-COV-2 Triggers the Development of Class I and Class II HLA Antibodies in Recovered Convalescent Plasma Donors
err2022-04-04
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errOAAI
errDada, Ashraf; Elhassan, Khalid; Bawayan, Rayan Mohammed; Albishi, Ghadeer; Hefni, Lama; Bassi, Sawsan; Sobahy, Turki; Cupler, Edward; AlBaz, Nabeela; Wali, Ghassan; Alraddadi, Basem; Alshukairi, Abeer N.
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Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia
err2022-02-22
err8
errOAAI
errAlharbi, Norah; Matar, Rawan; Cupler, Edward; Al-Hindi, Hindi; Murad, Hatem; Alhomud, Iftteah; Monies, Dorota; Alshehri, Ali; Alyahya, Mossaed; Meyer, Brian; Bohlega, Saeed
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Spectrum analysis of the inherited mutations of BRCA1/-2 genes that associated with high risk breast cancer in Saudi population
err2020-02-15
err0
PREAI
errHawsawi, Yousef MohammedRabaa; Meliti, Abdelrazak; Cupler, Edward; Sobahy, Turki; Zailaie, Samar; Baghdadi, Mohammed; Alardati, Hosam
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Cladribine Tablets and Relapsing-Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know
err2020-02-13
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errAlJumah, Mohamed; Alkhawajah, Mona Marwan; Qureshi, Shireen; Al-Thubaiti, Ibtisam; Ayoub, Omar; Bohlega, Saeed A.; Bushnag, Areej; Cupler, Edward; Daif, Abdulkader; El Boghdady, Ahmed; Hassan, Ahmed; Al Malik, Yaser; Saeedi, Jameelah; Al-Shamrany, Fawzia; Shosha, Eslam; Rieckmann, Peter
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population (vol 104, pg 1182, 2019)
err2019-10-01
err20
errOAAI
errMonies, 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; Chedrawi, Aziza; Aldhalaan, Hisham; Kurdi, Wesam; Khan, Sameena; Rahbeeni, Zuhair; Alotaibi, Maha; Goljan, Ewa; Elbardisy, Hadeel; ElKalioby, Mohamed; Shah, Zeeshan; Alruwaili, Hibah; 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; Abu Khaled, Musad; Alsaleem, Khalid; Almugbel, Maisoon; Badawi, Manal; Bashiri, Fahad; Bohlega, Saeed; Sulaiman, Raashida; Tous, Ehab; Ahmed, Syed; Algoufi, Talal; Al-Mousa, Hamoud; 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; Abosoudah, Ibraheem; Alashwal, Abdullah; 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; Al Mutairi, Fuad; Alsaleh, Mona; Alsonbul, Abdullah; Alzelaye, Somaya; Bahzad, Shakir; Bin Manee, Abdulaziz; Jarrad, Ola; Meriki, Neama; Albeirouti, Bassem; Alqasmi, Amal; AlBalwi, Mohammed; Makhseed, Nawal; Hassan, Saeed; Salih, Isam; Salih, Mustafa A.; Shaheen, Marwan; Sermin, Saadeh; Shahrukh, Shamsad; Hashmi, Shahrukh; Shawli, Ayman; Tajuddin, Ameen; Tamim, Abdullah; Alnahari, Ahmed; Ghemlas, Ibrahim; Hussein, Maged; Wali, Sami; Murad, Hatem; Meyer, Brian F.; Alkuraya, Fowzan S.
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Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders常染色体隐性ADCY5-Related肌张力障碍和肌阵挛: 扩大ADCY5-Related运动障碍的遗传谱
err2019-07-01
err20
PREAI
errBohlega, Saeed A.; Abou-Al-Shaar, Hussam; AlDakheel, Amaal; Alajlan, Huda; Bohlega, Balsam S.; Meyer, Brian F.; Monies, Dorota; Cupler, Edward J.; Al-Saif, Amr M.
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
err2019-06-01
err206
errOAAI
errMonies, 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; Chedrawi, Aziza; Aldhalaan, Hisham; Kurdi, Wesam; Khan, Sameena; Rahbeeni, Zuhair; Alotaibi, Maha; Goljan, Ewa; Elbardisy, Hadeel; ElKalioby, Mohamed; Shah, Zeeshan; Alruwaili, Hibah; 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; Abu Khaled, Musad; Alsaleem, Khalid; Almugbel, Maisoon; Badawi, Manal; Bashiri, Fahad; Bohlega, Saeed; Sulaiman, Raashida; Tous, Ehab; Ahmed, Syed; Algoufi, Talal; Al-Mousa, Hamoud; Alaki, Emadia; Alhumaidi, Susan; Althagafi, Malak; 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; Abosoudah, Ibraheem; Alashwal, Abdullah; 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; Al Mutairi, Fuad; Alsaleh, Mona; Alsonbul, Abdullah; Alzelaye, Somaya; Bahzad, Shakir; Bin Manee, Abdulaziz; Jarrad, Ola; Meriki, Neama; Albeirouti, Bassem; Alqasmi, Amal; AlBalwi, Mohammed; Makhseed, Nawal; Hassan, Saeed; Salih, Isam; Salih, Mustafa A.; Shaheen, Marwan; Sermin, Saadeh; Shahrukh, Shamsad; Hashmi, Shahrukh; Shawli, Ayman; Tajuddin, Ameen; Tamim, Abdullah; Alnahari, Ahmed; Ghemlas, Ibrahim; Hussein, Maged; Wali, Sami; Murad, Hatem; Meyer, Brian F.; Alkuraya, Fowzan S.
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The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
err2017-06-09
err223
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errMonies, Dorota; Abouelhoda, Mohamed; AlSayed, Moeenaldeen; Alhassnan, Zuhair; Alotaibi, Maha; Kayyali, Husam; Al-Owain, Mohammed; Shah, Ayaz; Rahbeeni, Zuhair; Al-Muhaizea, Mohammad A.; Alzaidan, Hamad I.; Cupler, Edward; Bohlega, Saeed; Faqeih, Eissa; Faden, Maha; Alyounes, Banan; Jaroudi, Dyala; Goljan, Ewa; Elbardisy, Hadeel; Akilan, Asma; Albar, Renad; Aldhalaan, Hesham; Gulab, Shamshad; Chedrawi, Aziza; Al Saud, Bandar K.; Kurdi, Wesam; Makhseed, Nawal; Alqasim, Tahani; El Khashab, Heba Y.; Al-Mousa, Hamoud; Alhashem, Amal; Kanaan, Imaduddin; Algoufi, Talal; Alsaleem, Khalid; Basha, Talal A.; Al-Murshedi, Fathiya; Khan, Sameena; Al-Kindy, Adila; Alnemer, Maha; Al-Hajjar, Sami; Alyamani, Suad; Aldhekri, Hasan; Al-Mehaidib, Ali; Arnaout, Rand; Dabbagh, Omar; Shagrani, Mohammad; Broering, Dieter; Tulbah, Maha; Alqassmi, Amal; Almugbel, Maisoon; AlQuaiz, Mohammed; Alsaman, Abdulaziz; Al-Thihli, Khalid; Sulaiman, Raashda A.; Al-Dekhail, Wajeeh; Alsaegh, Abeer; Bashiri, Fahad A.; Qari, Alya; Alhomadi, Suzan; Alkuraya, Hisham; Alsebayel, Mohammed; Hamad, Muddathir H.; Szonyi, Laszlo; Abaalkhail, Faisal; Al-Mayouf, Sulaiman M.; Almojalli, Hamad; Alqadi, Khalid S.; Elsiesy, Hussien; Shuaib, Taghreed M.; Seidahmed, Mohammed Zain; Abosoudah, Ibraheem; Akleh, Hana; AlGhonaium, Abdulaziz; Alkharfy, Turki M.; Al Mutairi, Fuad; Eyaid, Wafa; Alshanbary, Abdullah; Sheikh, Farrukh R.; Alsohaibani, Fahad I.; Alsonbul, Abdullah; Al Tala, Saeed; Balkhy, Soher; Bassiouni, Randa; Alenizi, Ahmed S.; Hussein, Maged H.; Hassan, Saeed; Khalil, Mohamed; Tabarki, Brahim; Alshahwan, Saad; Oshi, Amira; Sabr, Yasser; Alsaadoun, Saad; Salih, Mustafa A.; Mohamed, Sarar; Sultana, Habiba; Tamim, Abdullah; El-Haj, Moayad; Alshahrani, Saif; Bubshait, Dalal K.; Alfadhel, Majid; Faquih, Tariq; El-Kalioby, Mohamed; Subhani, Shazia; Shah, Zeeshan; Moghrabi, Nabil; Meyer, Brian F.; Alkuraya, Fowzan S.
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Neuromyelitis optica (NMO) antibody positive disorder: a case series from Saudi Arabia
err2015-10-01
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errOAAI
errAl-Said, Y.; Hassan, A.; Al-Yaefi, R.; Basndwah, A.; Kurdi, K.; Ali, Q.; Wazzan, O.; Cupler, E.
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Limb girdle muscular dystrophy (lgdm) mutation pattern using next generation sequencing (ngs)
err2015-10-01
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PREAI
errBohlega, S.; Monies, D.; Cupler, E.; Hamoud, E.; Muhaeza, H.; Majed, S.; Meyer, B.
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Focal motor status epilepticus (FMSE) due to reversible CNS ischemia
err2015-10-01
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PREAI
errAl-Said, Y.; Hassan, A.; Basndwah, A.; Kurdi, K.; El-Zeftawy, H.; Cupler, E.
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The Heterogeneity of Pompe Disease: Early Data on Genotype From the Pompe Registry
err2011-06-01
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PREAI
errKishnani, Priya; Byrne, Barry; Case, Laura; Cupler, Edward; Genge, Angela; van der Ploeg, Ans; Prasad, Suyash
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The heterogeneity of pompe disease: Early data on genotype from the Pompe registry
err2011-02-01
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PREAI
errKishnani, Priya; Byrne, Barry; Case, Laura; Cupler, Edward; Genge, Angela; Prasad, Suyash
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