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1دورية أكاديمية
المؤلفون: El-Hattab, Ayman W., Almannai, Mohammed, Scaglia, Fernando
المصدر: Journal of Inborn Errors of Metabolism and Screening. January 2017 5
مصطلحات موضوعية: stroke-like episodes, nitric oxide (NO), mitochondrial diseases, stable isotope, encephalomyopathy, lactic acidosis
وصف الملف: text/html
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2دورية أكاديمية
المؤلفون: Kentab, Amal, Muddathir, H.H., Salih, M.A., Mushiba, Aziza M., Zada, A.P., Bamajboor, Mohammed S., Zameer, Sadique, AlBassam, Fahad, Mahmoud, Adel, Alnawfal, A.A., AlAmr, Mushari, Bawazir, Maryam, Al Rumayyan, Ahmed, Al-Twaijri, Waleed, Alrifai, Muhammed Talal, Al Hajjaj, Sumayah, Saleh, Mohammed M., Hamhom, Abdulrahim M., Al-Otaibi, Ali, AlGhamdi, Malak, Housawi, Yousef, Aljadhai, Yaser I., Alameer, Seham, Almannai, Mohammed, Jad, Lamyaa A., Alwadei, Ali H., Tabassum, Sadia, Alsaman, Abdulaziz, AlAsmari, Ali, Al Mutairi, Fuad, Althiyab, Hamad, Bashiri, Fahad A., AlHumaidi, Suzan, Alfadhel, Majid, Mink, Jonathan W., AlHashim, Aqeela, Faqeih, Eissa A.
المصدر: In Pediatric Neurology June 2024 155:149-155
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3دورية أكاديمية
المؤلفون: Abukhaled, MusaadAff1, IDs00431023048865_cor1, Al Muqbil, MohammedAff2, Aff3, Aff4, Alghamdi, Malak Ali, Hundallah, Khalid, Suleiman, JehanAff7, Aff8, Aff9, Ben-Omran, TawfegAff10, Aff11, Alfadhel, MajidAff12, Aff13, Almannai, MohammedAff12, Aff13, Alsaleh, Rehab, Tabarki, Brahim
المصدر: European Journal of Pediatrics. 182(6):2535-2545
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4دورية أكاديمية
المؤلفون: Almannai, MohammedAff1, Aff2, Aff3, IDs00439022025131_cor1, AlAbdi, LamaAff4, Aff5, Maddirevula, Sateesh, Alotaibi, Maha, Alsaleem, Badr M., Aljadhai, Yaser I., Alsaif, Hessa S.Aff4, Aff9, Abukhalid, Musaad, Alkuraya, Fowzan SAff4, Aff11, IDs00439022025131_cor9
المصدر: Human Genetics. 142(3):399-405
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5دورية أكاديمية
المؤلفون: Abukhaled, MusaadAff1, IDs00431023050121_cor1, Al Muqbil, MohammedAff2, Aff3, Aff4, Alghamdi, Malak Ali, Hundallah, Khalid, Suleiman, JehanAff7, Aff8, Aff9, Ben-Omran, TawfegAff10, Aff11, Alfadhel, MajidAff12, Aff13, Almannai, MohammedAff12, Aff13, Alsaleh, Rehab, Tabarki, Brahim
المصدر: European Journal of Pediatrics. 182(6):2547-2548
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6دورية أكاديمية
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7دورية أكاديمية
المؤلفون: Ng, Bobby G, Sosicka, Paulina, Agadi, Satish, Almannai, Mohammed, Bacino, Carlos A, Barone, Rita, Botto, Lorenzo D, Burton, Jennifer E, Carlston, Colleen, Chung, Brian Hon‐Yin, Cohen, Julie S, Coman, David, Dipple, Katrina M, Dorrani, Naghmeh, Dobyns, William B, Elias, Abdallah F, Epstein, Leon, Gahl, William A, Garozzo, Domenico, Hammer, Trine Bjørg, Haven, Jaclyn, Héron, Delphine, Herzog, Matthew, Hoganson, George E, Hunter, Jesse M, Jain, Mahim, Juusola, Jane, Lakhani, Shenela, Lee, Hane, Lee, Joy, Lewis, Katherine, Longo, Nicola, Lourenço, Charles Marques, Mak, Christopher CY, McKnight, Dianalee, Mendelsohn, Bryce A, Mignot, Cyril, Mirzaa, Ghayda, Mitchell, Wendy, Muhle, Hiltrud, Nelson, Stanley F, Olczak, Mariusz, Palmer, Christina GS, Partikian, Arthur, Patterson, Marc C, Pierson, Tyler M, Quinonez, Shane C, Regan, Brigid M, Ross, M Elizabeth, Sacoto, Maria J Guillen, Scaglia, Fernando, Scheffer, Ingrid E, Segal, Devorah, Singhal, Nilika Shah, Striano, Pasquale, Sturiale, Luisa, Symonds, Joseph D, Tang, Sha, Vilain, Eric, Willis, Mary, Wolfe, Lynne A, Yang, Hui, Yano, Shoji, Powis, Zöe, Suchy, Sharon F, Rosenfeld, Jill A, Edmondson, Andrew C, Grunewald, Stephanie, Freeze, Hudson H
المصدر: Human Mutation. 40(7)
مصطلحات موضوعية: Clinical Research, Pediatric, Genetics, Aetiology, 2.1 Biological and endogenous factors, Animals, Biopsy, CHO Cells, Cells, Cultured, Congenital Disorders of Glycosylation, Cricetulus, Female, Humans, Male, Monosaccharide Transport Proteins, Mutation, Uridine Diphosphate Galactose, congenital disorders of glycosylation, glycoside, nucleotide sugar transporter, UDP-galactose, Clinical Sciences, Genetics & Heredity
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/48w6q46x
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8دورية أكاديمية
المؤلفون: Almannai, Mohammed, Marafi, Dana, Zaki, Maha S., Maroofian, Reza, Efthymiou, Stephanie, Saadi, Nebal Waill, Filimban, Bilal, Dafsari, Hormos Salimi, Rahman, Fatima, Maqbool, Shazia, Faqeih, Eissa, Al Mutairi, Fuad, Alsharhan, Hind, Abdelaty, Omar, Bin‐Hasan, Saadoun, Duan, Ruizhi, Noureldeen, Mahmoud M., Alqattan, Alaa, Houlden, Henry, Hunter, Jill V.
المصدر: Clinical Genetics; Jun2024, Vol. 105 Issue 6, p620-629, 10p
مصطلحات موضوعية: NEURAL development, PHENOTYPES, DEVELOPMENTAL delay, INTELLECTUAL disabilities, BRAIN imaging
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9دورية أكاديمية
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10دورية أكاديمية
المؤلفون: del Caño-Ochoa, Francisco, Ng, Bobby G., Abedalthagafi, Malak, Almannai, Mohammed, Cohn, Ronald D., Costain, Gregory, Elpeleg, Orly, Houlden, Henry, Karimiani, Ehsan Ghayoor, Liu, Pengfei, Manzini, M. Chiara, Maroofian, Reza, Muriello, Michael, Al-Otaibi, Ali, Patel, Hema, Shimon, Edvardson, Sutton, V. Reid, Toosi, Mehran Beiraghi, Wolfe, Lynne A., Rosenfeld, Jill A., Freeze, Hudson H., Ramón-Maiques, Santiago
المصدر: In Genetics in Medicine October 2020 22(10):1598-1605