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

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URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942017000100704

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

المؤلفون: Abukhaled, Musaad^{Aff1, IDs00431023048865_cor1}, Al Muqbil, Mohammed^{Aff2, Aff3, Aff4}, Alghamdi, Malak Ali, Hundallah, Khalid, Suleiman, Jehan^{Aff7, Aff8, Aff9}, Ben-Omran, Tawfeg^{Aff10, Aff11}, Alfadhel, Majid^{Aff12, Aff13}, Almannai, Mohammed^{Aff12, Aff13}, Alsaleh, Rehab, Tabarki, Brahim

المصدر: European Journal of Pediatrics. 182(6):2535-2545

المؤلفون: Almannai, Mohammed^{Aff1, Aff2, Aff3, IDs00439022025131_cor1}, AlAbdi, Lama^{Aff4, Aff5}, Maddirevula, Sateesh, Alotaibi, Maha, Alsaleem, Badr M., Aljadhai, Yaser I., Alsaif, Hessa S.^{Aff4, Aff9}, Abukhalid, Musaad, Alkuraya, Fowzan S^{Aff4, Aff11, IDs00439022025131_cor9}

المصدر: Human Genetics. 142(3):399-405

المؤلفون: Abukhaled, Musaad^{Aff1, IDs00431023050121_cor1}, Al Muqbil, Mohammed^{Aff2, Aff3, Aff4}, Alghamdi, Malak Ali, Hundallah, Khalid, Suleiman, Jehan^{Aff7, Aff8, Aff9}, Ben-Omran, Tawfeg^{Aff10, Aff11}, Alfadhel, Majid^{Aff12, Aff13}, Almannai, Mohammed^{Aff12, Aff13}, Alsaleh, Rehab, Tabarki, Brahim

المصدر: European Journal of Pediatrics. 182(6):2547-2548

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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

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URL الوصول: https://escholarship.org/uc/item/48w6q46x

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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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