Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Inaam Mohamed"'
Autor:
Giovanni Stevanin, Ahlam Hamed, Inaam Mohamed, Maha Elseed, Mustafa Salih, Sarah Elsadig, Hassab Elrasoul Siddig, Ali Nasreldien, Mohamed Ahmed Abdullah, Maha Elzubair, Farouk Omer, Aisha BAKHIET, Rayan Abubaker, Fatima Abozar, Rawaa Adil, Sara Emad, Mhammed Alhassan Musallam, Isra Eltazi, Zulfa Omer, Hiba Malik, Mayada Mohamed, Ali Elhassan, Eman Mohamed, Ahmed Ahmed, Elhami Ahmed, Esraa Eltaraifee, Bidour Hussein, Amal Abd Allah, Lina Mohamed, Mohamed Nimir, Omnia Tag Elseed, Tasneem Elhassan, Abubakr Elbashier, Esraa Alfadul, Moneeb Fadul, Khalil Ali, Shaimaa Taha, Elfatih Bushara, Mutaz Amin, Mahmoud koko, Muntaser Ibrahim, Ammar Ahmed, Liena Elsayed, Ashraf Yahia
Hereditary spinocerebellar degenerative disorders (SCDs) is an umbrella term that covers a group of monogenic conditions that share common pathogenic mechanisms and include spastic paraplegia, spastic ataxia, cerebellar ataxia, and spinocerebellar at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94ad8c371f6701cff359a196fe67fa45
https://doi.org/10.21203/rs.3.rs-2219015/v1
https://doi.org/10.21203/rs.3.rs-2219015/v1
Autor:
Tamara Dangouloff, Eva Vrščaj, Laurent Servais, Damjan Osredkar, Thierry Adoukonou, Omid Aryani, Nina Barisic, Fahad Bashiri, Laila Bastaki, Afaf Benitto, Tawfeg Ben Omran, Guenther Bernert, Enrico Bertini, Patricia Borde, Peter Born, Rose-Mary Boustani, Nina Butoianu, Claudia Castiglioni, Feriha Catibusic, Sophelia Chan, Yin Hsiu Chien, Kyproula Christodoulou, Donniphat Dejsuphong, Michelle Farrar, Duma Filip, Nathalie Goemans, Kokou Guinhouya, Jana Haberlova, Kinga Hadzsiev, Kristine Hovhannesyan, Pirjo Isohanni, Nelica Ivanovic Radovic, David Jacquier, Alusine Jalloh, Maria Jedrzejowska, Gwen Kandawasvika, Celestin Kaputu, Nfwama Kawatu, Kristin Kernohan, Jan Kirschner, Barbara Klink, Sherry Kodsy, Ange-Eric Kouame-Assouan, Ruzica Kravljanac, Madara Kreile, Ivan Litvinenko, Hugh McMillan, Sandra Mesa, Inaam Mohamed, Liljana Muaremoska Kanzoska, Yoram Nevo, Seraphin Nguefack, Kafula Nkole, Gina O'Grady, Declan O'Rourke, Maryam Oskoui, Flavia Piazzon, Dimitri Poddighe, Audrone Prasauskiene, Juan Prieto, Magnhild Rasmussen, Santara Razafindrasata, Narayan Saha, Kayoko Saito, Foksouna Sakadi, Modibo Sangare, Mary Schroth, Leanid Shalkevich, Andriy Shatillo, Renu Suthar, Lena Szabo, Nana Tatishvili, Meriem Tazir, Eduardo Tizzano, Haluk Topaloglu, Mar Tulinius, Ludo van der Pol, Gabriel Vazquez, Dimitry Vlodavets, Jithangi Wanigasinghe, Jo Wilmshurst, Hui Xiong, Dimitrios Zafeiriou, Eleni Zamba
Publikováno v:
Neuromuscular Disorders. 31:574-582
Spinal muscular atrophy (SMA) is a rare and devastating disease. New disease-modifying treatments have recently been approved and early treatment has been related to a better outcome. In this context, several newborn screening (NBS) programs have bee
Autor:
Inaam Mohamed
Publikováno v:
Journal of medical science and clinical research. 5