Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mhammed Alhassan Musallam"'
Autor:
Ashraf Yahia, Liena E. O. Elsayed, Remi Valter, Ahlam A. A. Hamed, Inaam N. Mohammed, Maha A. Elseed, Mustafa A. Salih, Typhaine Esteves, Nicolas Auger, Rayan Abubaker, Mahmoud Koko, Fatima Abozar, Hiba Malik, Rawaa Adil, Sara Emad, Mhammed Alhassan Musallam, Razaz Idris, Isra Z. M. Eltazi, Arwa Babai, Elhami A. A. Ahmed, Amal S. I. Abd Allah, Mathilde Mairey, Ahmed K. M. A. Ahmed, Mustafa I. Elbashir, Alexis Brice, Muntaser E. Ibrahim, Ammar E. Ahmed, Foudil Lamari, Giovanni Stevanin
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Introduction: Hereditary spastic paraplegia is a clinically and genetically heterogeneous neurological entity that includes more than 80 disorders which share lower limb spasticity as a common feature. Abnormalities in multiple cellular processes are
Externí odkaz:
https://doaj.org/article/9a848f054ed841349194e7fb29f2f808
Autor:
Ashraf Yahia, Ahlam A. A. Hamed, Inaam N. Mohamed, Maha A. Elseed, Mustafa A. Salih, Sarah M. El-sadig, Hassab Elrasoul Siddig, Ali Elsir Musa Nasreldien, Mohamed Ahmed Abdullah, Maha Elzubair, Farouk Yassen Omer, Aisha Motwakil Bakhiet, Rayan Abubaker, Fatima Abozar, Rawaa Adil, Sara Emad, Mhammed Alhassan Musallam, Isra Z. M. Eltazi, Zulfa Omer, Hiba Malik, Mayada O. E. Mohamed, Ali A. Elhassan, Eman O. E. Mohamed, Ahmed K. M. A. Ahmed, Elhami A. A. Ahmed, Esraa Eltaraifee, Bidour K. Hussein, Amal S. I. Abd Allah, Lina Salah, Mohamed Nimir, Omnia M. Tag Elseed, Tasneem E. A. Elhassan, Abubakr Elbashier, Esraa S. A. Alfadul, Moneeb Fadul, Khalil F. Ali, Shaimaa Omer M. A. Taha, Elfatih E. Bushara, Mutaz Amin, Mahmoud Koko, Muntaser E. Ibrahim, Ammar E. Ahmed, Liena E. O. Elsayed, Giovanni Stevanin
Publikováno v:
European Journal of Human Genetics.
Hereditary spinocerebellar degenerations (SCDs) is an umbrella term that covers a group of monogenic conditions that share common pathogenic mechanisms and include hereditary spastic paraplegia (HSP), cerebellar ataxia, and spinocerebellar ataxia. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6065f2626112aa0df0ad52e9f622cc64
https://doi.org/10.1038/s41431-023-01344-6
https://doi.org/10.1038/s41431-023-01344-6
Autor:
Ashraf Yahia, Ikhlas Ben Ayed, Ahlam A. Hamed, Inaam N. Mohammed, Maha A. Elseed, Aisha M. Bakhiet, Lena Guillot‐Noel, Fatima Abozar, Rawaa Adil, Sara Emad, Rayan Abubaker, Mhammed Alhassan Musallam, Isra Z. M. Eltazi, Zulfa Omer, Omer M. Maaroof, Amal Soussi, Amal Bouzid, Sana Kmiha, Hassen Kamoun, Mustafa A. Salih, Ammar E. Ahmed, Liena Elsayed, Saber Masmoudi, Giovanni Stevanin
Publikováno v:
Ann Hum Genet
Intellectual disability is a form of neurodevelopmental disorders that begin in childhood and is characterized by substantial intellectual difficulties as well as difficulties in conceptual, social, and practical areas of living. Several genetic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c75559be6f2a2579ad557a5fdb097aaf
https://doi.org/10.1111/ahg.12460
https://doi.org/10.1111/ahg.12460
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:
Ashraf Yahia, Aisha M. Bakhiet, Ahlam A. Hamed, Fatima Abozar, Rawaa Adil, Sara Emad, Mhammed Alhassan Musallam, Isra Z. M. Eltazi, Omer M. Maaroof, Ammar E. Ahmed, Liena E. Elsayed, Giovanni Stevanin
BackgroundAutosomal recessive intellectual disabilities, syndromic and non-syndromic, are of specific importance in consanguineous communities. High throughput sequencing technologies have enhanced diagnosing the Mendelian forms of intellectual disab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a25d0bb00c16a0adc5b3c7d97489616e
https://doi.org/10.21203/rs.3.rs-46782/v1
https://doi.org/10.21203/rs.3.rs-46782/v1