खोज परिणाम - Alrifai, Muhammad T.

  • प्रदर्शित 1 - 17 परिणाम 17
परिणाम को परिष्कृत करें
  1. 1
    Pseudotumor cerebri in a child receiving peritoneal dialysis: recovery of vision after lumbo-pleural shunt

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

    प्रकाशित 2011
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  2. 2
    Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings

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

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  3. 3
    Further Delineation of the Clinical Phenotype of Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4

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

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  4. 4
    The comorbidity of headaches in pediatric epilepsy patients: How common and what types?

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

    प्रकाशित 2019
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  5. 5
    Pediatrics COVID-19 and neurological manifestations: Single tertiary centre experience

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

    प्रकाशित 2021
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  6. 6
    X-linked ichthyosis associated with psychosis and behavioral abnormalities: a case report

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

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  7. 7
    Prevalence and outcomes of Guillain-Barré syndrome among pediatrics in Saudi Arabia: a 10-year retrospective study

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

    प्रकाशित 2019
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  8. 8
    Retrospective review of pediatric status epilepticus in 116 Saudi patients: predictors of outcome

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

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  9. 9
    The response patterns of infantile spasms to treatments in 156 patients: Hormonal therapy with intravenous synthetic ACTH appears promising

    The response patterns of infantile spasms to treatments in 156 patients: Hormonal therapy with intravenous synthetic ACTH appears promising द्वारा 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.

    प्रकाशित 2022
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  10. 10
    Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism

    Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism द्वारा 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

    प्रकाशित 2015
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  11. 11
    Clinical Presentation and outcome of acute disseminated encephalomyelitis in Saudi Arabia: Tertiary Center Experience

    Clinical Presentation and outcome of acute disseminated encephalomyelitis in Saudi Arabia: Tertiary Center Experience द्वारा 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

    प्रकाशित 2019
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  12. 12
    Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans

    Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans द्वारा 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

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  13. 13
    EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay

    EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay द्वारा 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

    प्रकाशित 2020
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  14. 14
    Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening

    Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening द्वारा 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

    प्रकाशित 2019
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  15. 15
    Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia

    Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia द्वारा 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

    प्रकाशित 2020
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  16. 16
    ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies

    ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies द्वारा 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.

    प्रकाशित 2013
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:
  17. 17
    The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic Data

    The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic Data द्वारा 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

    प्रकाशित 2021
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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    में बचाया:

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