Resultados da busca - Melissa Nel

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  1. 1
    Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group

    Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group por Aimé Lumaka, Nadia Carstens, Koenraad Devriendt, Amanda Krause, Benard Kulohoma, Judit Kumuthini, Gerrye Mubungu, John Mukisa, Melissa Nel, Timothy O. Olanrewaju, Zané Lombard, Guida Landouré

    Publicado em 2022
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  2. 2
    Clinical testing panels for ALS: global distribution, consistency, and challenges

    Clinical testing panels for ALS: global distribution, consistency, and challenges por Allison A. Dilliott, Ahmad Al Nasser, Marwa Elnageeb, Jennifer A. Fifita, Lyndal Henden, Ingrid M. Keseler, Steven Lenz, Heather Marriott, Emily P. McCann, Maysen Mesaros, Sarah Opie-Martin, Emma Owens, Brooke Palus, Justyne Ross, Zhanjun Wang, Hannah L. White, Ammar Al‐Chalabi, Peter M. Andersen, Michael Benatar, Ian P. Blair, Johnathan Cooper‐Knock, Luke Drury, Elizabeth A. Harrington, Jeannine M. Heckmann, John E. Landers, Cristiane Araújo Martins Moreno, Melissa Nel, Evadnie Rampersaud, Jennifer Roggenbuck, Guy A. Rouleau, Bryan J. Traynor, Marka van Blitterswijk, Wouter van Rheenen, Jan H. Veldink, Jochen H. Weishaupt, Matthew Harms, Sali M.K. Farhan

    Publicado em 2022
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  3. 3
    Clinical testing panels for ALS: global distribution, consistency, and challenges

    Clinical testing panels for ALS: global distribution, consistency, and challenges por Allison A. Dilliott, Ahmad Al Nasser, Marwa Elnagheeb, Jennifer A. Fifita, Lyndal Henden, Ingrid M. Keseler, Steven Lenz, Heather Marriott, Emily P. McCann, Maysen Mesaros, Sarah Opie-Martin, Emma Owens, Brooke Palus, Justyne Ross, Zhanjun Wang, Hannah L. White, Ammar Al‐Chalabi, Peter M. Andersen, Michael Benatar, Ian P. Blair, Johnathan Cooper‐Knock, Elizabeth A. Harrington, Jeannine M. Heckmann, John E. Landers, Cristiane Araújo Martins Moreno, Melissa Nel, Evadnie Rampersaud, Jennifer Roggenbuck, Guy A. Rouleau, Bryan J. Traynor, Marka van Blitterswijk, Wouter van Rheenen, Jan H. Veldink, Jochen H. Weishaupt, Luke Drury, Matthew B. Harms, Sali M.K. Farhan

    Publicado em 2023
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  4. 4
    Neuromuscular disease genetics in under-represented populations: increasing data diversity

    Neuromuscular disease genetics in under-represented populations: increasing data diversity por Lindsay A. Wilson, William L. Macken, Luke Perry, Christopher J. Record, Katherine Schon, Rodrigo Siqueira Soares Frezatti, Sharika Raga, K. Satyam Naidu, Özlem Yayıcı Köken, İpek Polat, Musambo M Kapapa, Natalia Dominik, Stéphanie Efthymiou, Heba Morsy, Melissa Nel, Mahmoud R. Fassad, Fei Gao, Krutik Patel, Maryke Schoonen, Michelle Bisschoff, Armand Vorster, Hallgeir Jonvik, Ronel Human, Elsa Lubbe, Malebo Nonyane, Seena Vengalil, Saraswati Nashi, Kosha Srivastava, Richard J.L.F. Lemmers, Alisha Reyaz, Rinkle Mishra, Ana Töpf, Christina Trainor, Elizabeth Steyn, Amokelani C. Mahungu, Patrick J. van der Vliet, Ahmet Cevdet Ceylan, Semra Hız Kurul, Büşranur Çavdarlı, Cavidan Nur Semerci Gündüz, Gülay Güleç Ceylan, Madhu Nagappa, Karthik Bharadwaj Tallapaka, Periyasamy Govindaraj, Silvère M. van der Maarel, Narayanappa Gayathri, Bevinahalli N. Nandeesh, Somwe Wa Somwe, David Bearden, Michelle Kvalsund, Gita Ramdharry, Yavuz Oktay, Uluç Yiş, Haluk Topaloğlu, Anna Sárközy, Enrico Bugiardini, Franclo Henning, Jo M. Wilmshurst, Jeannine M. Heckmann, Robert McFarland, Robert W. Taylor, Izelle Smuts, Francois H. van der Westhuizen, Cláudia Ferreira da Rosa Sobreira, Pedro José Tomaselli, Wilson Marques, Rohit Bhatia, Ashwin Dalal, M.V. Padma Srivastava, Sireesha Yareeda, Atchayaram Nalini, Venugopalan Y. Vishnu, Kumarasamy Thangaraj, Volker Straub, Rita Horváth, Patrick F. Chinnery, Robert D. S. Pitceathly, Francesco Muntoni, Henry Houlden, Jana Vandrovcová, Mary M. Reilly, Michael G. Hanna

    Publicado em 2023
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