Resultados de procura - Alrifai, Muhammad T.

Pseudotumor cerebri in a child receiving peritoneal dialysis: recovery of vision after lumbo-pleural shunt por Alrifai, Muhammad Talal, Al Naji, Foad, Alamir, Abdulrahman, Russell, Neville

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Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings por Al-Rakan, Maha A., Abothnain, Manal D., Alrifai, Muhammad T., Alfadhel, Majid

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Further Delineation of the Clinical Phenotype of Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4 por Alsahli, Saud, Alrifai, Muhammad Talal, Al Tala, Saeed, Mutairi, Fuad Al, Alfadhel, Majid

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The comorbidity of headaches in pediatric epilepsy patients: How common and what types? por Al-Gethami, Hanin, Alrifai Muhammad, Talal, AlRumayyan, Ahmed, AlTuwaijri, Waleed, Baarmah, Duaa

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Pediatrics COVID-19 and neurological manifestations: Single tertiary centre experience por Aljomah, Lama, Almedlej, Sara, Baarmah, Duaa, Altwaijri, Waleed, Alrumayyan, Ahmad, Alrifai, Muhammad Talal, Almuqbil, Mohammed, Alshalaan, Mohammad

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X-linked ichthyosis associated with psychosis and behavioral abnormalities: a case report por Malik, Amna, Amer, Ahmed Bait, Salama, Mohammed, Haddad, Bander, Alrifai, Muhammad T., Balwi, Mohammed Al, Davies, William, Eyaid, Wafaa

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Prevalence and outcomes of Guillain-Barré syndrome among pediatrics in Saudi Arabia: a 10-year retrospective study por Asiri, Safiyyah, Altwaijri, Waleed A, Ba-Armah, Duaa, Al Rumayyan, Ahmed, Alrifai, Muhammad T, Salam, Mahmoud, Almutairi, Adel F

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Retrospective review of pediatric status epilepticus in 116 Saudi patients: predictors of outcome por Hommady, Raid Harb, Alrifai, Muhammad Talal, Mubayrik, Osama Khaled, Alayed, Ruba Salem, Alsemari, Muhannad Abdulrahman, Arumayyan, Ahmed, Altuwaijri, Waleed, Baarmah, Duaa

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The response patterns of infantile spasms to treatments in 156 patients: Hormonal therapy with intravenous synthetic ACTH appears promising por Alrifai, Muhammad T., Al-Rumayyan, Ahmad R., Al-Tuwaijri, Waleed A., Baarmah, Duaa M., Asiri, Safiyyah A., Bali, Ahmad H., Alsadhan, Muatassem A., Alsugheir, Shaden H.

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Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism por Alfadhel, Majid, Alrifai, Muhammad Talal, Trujillano, Daniel, Alshaalan, Hesham, Al Othaim, Ali, Al Rasheed, Shatha, Assiri, Hussam, Alqahtani, Abdulrhman A., Alaamery, Manal, Rolfs, Arndt, Eyaid, Wafaa

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Clinical Presentation and outcome of acute disseminated encephalomyelitis in Saudi Arabia: Tertiary Center Experience por Aldamkh, Bander Ali, Alamer, Abdalaziz F., Altuwaijri, Mohammed M., Alrumayyan, Mohammed A., Alhaqbani, Abdulaziz H., Alharthi, Nawaf A., Aldamkh, Saeed A., Aldrees, Amjad S., Alrifai, Muhammad T., Altuwaijri, Waleed, Alrumayyan, Ahmed

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Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans por Alfadhel, Majid, Nashabat, Marwan, Qahtani, Hanan Al, Alfares, Ahmed, Mutairi, Fuad Al, Shaalan, Hesham Al, Douglas, Ganka V., Wierenga, Klaas, Juusola, Jane, Alrifai, Muhammad Talal, Arold, Stefan T., Alkuraya, Fowzan, Ali, Qais Abu

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EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay por Umair, Muhammad, Ballow, Mariam, Asiri, Abdulaziz, Alyafee, Yusra, al Tuwaijri, Abeer, Alhamoudi, Kheloud M., Aloraini, Taghrid, Abdelhakim, Marwa, Althagafi, Azza Thamer, Kafkas, Senay, Alsubaie, Lamia, Alrifai, Muhammad Talal, Hoehndorf, Robert, Alfares, Ahmed, Alfadhel, Majid

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Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening por Alfadhel, Majid, Umair, Muhammad, Almuzzaini, Bader, Alsaif, Saif, AlMohaimeed, Sulaiman A., Almashary, Maher A., Alharbi, Wardah, Alayyar, Latifah, Alasiri, Abdulrahman, Ballow, Mariam, AlAbdulrahman, Abdulkareem, Alaujan, Monira, Nashabat, Marwan, Al‐Odaib, Ali, Altwaijri, Waleed, Al‐Rumayyan, Ahmed, Alrifai, Muhammad T., Alfares, Ahmed, AlBalwi, Mohammed, Tabarki, Brahim

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Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia por Bashiri, Fahad A., Al Johani, Sultan, Hamad, Muddathir H., Kentab, Amal Y., Alwadei, Ali H., Hundallah, Khalid, Hasan, Hamdi H., Alshuaibi, Walaa, Jad, Lamyaa, Alrifai, Muhammad Talal, Hudairi, Abrar, Al Sheikh, Rana, Alenizi, Asma'a, Alharthi, Nawaf A., Abdelmagid, Tayseer A., Ba-Armah, Duaa, Salih, Mustafa A., Tabarki, Brahim

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ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies por Webb, Emma A., AlMutair, Angham, Kelberman, Daniel, Bacchelli, Chiara, Chanudet, Estelle, Lescai, Francesco, Andoniadou, Cynthia L., Banyan, Abdul, Alsawaid, Al, Alrifai, Muhammad T., Alahmesh, Mohammed A., Balwi, M., Mousavy-Gharavy, Seyedeh N., Lukovic, Biljana, Burke, Derek, McCabe, Mark J., Kasia, Tessa, Kleta, Robert, Stupka, Elia, Beales, Philip L., Thompson, Dorothy A., Chong, W. Kling, Alkuraya, Fowzan S., Martinez-Barbera, Juan-Pedro, Sowden, Jane C., Dattani, Mehul T.

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The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic Data por Alfadhel, Majid, Almuqbil, Mohammed, Al Mutairi, Fuad, Umair, Muhammad, Almannai, Mohammed, Alghamdi, Malak, Althiyab, Hamad, Albarakati, Rayyan, Bashiri, Fahad A., Alshuaibi, Walaa, Ba-Armah, Duaa, Saleh, Mohammed A., Al-Asmari, Ali, Faqeih, Eissa, Altuwaijri, Waleed, Al-Rumayyan, Ahmed, Balwi, Mohammed Ali, Ababneh, Faroug, Alswaid, Abdulrahman Faiz, Eyaid, Wafaa M., Almontashiri, Naif A. M., Alhashem, Amal, Hundallah, Khalid, Bertoli-Avella, Aida, Bauer, Peter, Beetz, Christian, Alrifai, Muhammad Talal, Alfares, Ahmed, Tabarki, Brahim

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