Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ahmed, Elhami A."'
Autor:
Koko, Mahmoud, Elseed, Maha A., Mohammed, Inaam N., Hamed, Ahlam A., Abd Allah, Amal S. I., Yahia, Ashraf, Siddig, Rayan A., Altmüller, Janine, Toliat, Mohammad Reza, Elmahdi, Esra O., Amin, Mutaz, Ahmed, Elhami A., Eltazi, Isra Z. M., Elmugadam, Fatima A., Abdelgadir, Wasma A., Eltaraifee, Esraa, Ibrahim, Mohamed O. M., Ali, Nabila M. H., Malik, Hiba M., Babai, Arwa M., Bakhit, Yousuf H., Nürnberg, Peter, Ibrahim, Muntaser E., Salih, Mustafa A., Schubert, Julian, Elsayed, Liena E. O., Lerche, Holger
Publikováno v:
European Journal of Human Genetics: EJHG; October 2024, Vol. 32 Issue: 10 p1338-1342, 5p
Autor:
Yahia, Ashraf, Hamed, Ahlam A. A., Mohamed, Inaam N., Elseed, Maha A., Salih, Mustafa A., El-sadig, Sarah M., Siddig, Hassab Elrasoul, Nasreldien, Ali Elsir Musa, Abdullah, Mohamed Ahmed, Elzubair, Maha, Omer, Farouk Yassen, Bakhiet, Aisha Motwakil, Abubaker, Rayan, Abozar, Fatima, Adil, Rawaa, Emad, Sara, Musallam, Mhammed Alhassan, Eltazi, Isra Z. M., Omer, Zulfa, Malik, Hiba, Mohamed, Mayada O. E., Elhassan, Ali A., Mohamed, Eman O. E., Ahmed, Ahmed K. M. A., Ahmed, Elhami A. A., Eltaraifee, Esraa, Hussein, Bidour K., Abd Allah, Amal S. I., Salah, Lina, Nimir, Mohamed, Tag Elseed, Omnia M., Elhassan, Tasneem E. A., Elbashier, Abubakr, Alfadul, Esraa S. A., Fadul, Moneeb, Ali, Khalil F., Taha, Shaimaa Omer M. A., Bushara, Elfatih E., Amin, Mutaz, Koko, Mahmoud, Ibrahim, Muntaser E., Ahmed, Ammar E., Elsayed, Liena E. O., Stevanin, Giovanni
Publikováno v:
European Journal of Human Genetics: EJHG; October 2024, Vol. 32 Issue: 10 p1214-1226, 13p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Akademický článek
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Autor:
Yahia, Ashraf, Elsayed, Liena, Valter, Remi, Hamed, Ahlam, Mohammed, Inaam, Elseed, Maha, Salih, Mustafa, Esteves, Typhaine, Auger, Nicolas, Abubaker, Rayan, Koko, Mahmoud, Abozar, Fatima, Malik, Hiba, Adil, Rawaa, Emad, Sara, Musallam, Mhammed Alhassan, Idris, Razaz, Eltazi, Isra, Babai, Arwa, Ahmed, Elhami, Abd Allah, Amal, Mairey, Mathilde, Ahmed, Ahmed, Elbashir, Mustafa, Brice, Alexis, Ibrahim, Muntaser, Ahmed, Ammar, Lamari, Foudil, Stevanin, Giovanni
Publikováno v:
Frontiers in Neurology
Frontiers in Neurology, 2021, 12, ⟨10.3389/fneur.2021.720201⟩
Frontiers in Neurology, Frontiers, 2021, 12, ⟨10.3389/fneur.2021.720201⟩
Frontiers in Neurology, 2021, 12, ⟨10.3389/fneur.2021.720201⟩
Frontiers in Neurology, Frontiers, 2021, 12, ⟨10.3389/fneur.2021.720201⟩
International audience; 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 multipl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::bda1dd87d210dc17b629a5166dca888f
http://europepmc.org/articles/PMC8417901
http://europepmc.org/articles/PMC8417901
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Dahawi M; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS - Hôpital La Pitié-Salpêtrière, Paris, France. mahadahawi11@gmail.com.; Department of Physiology, Faculty of Medicine, University of Khartoum, Khartoum, Sudan. mahadahawi11@gmail.com., de Sainte Agathe JM; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS - Hôpital La Pitié-Salpêtrière, Paris, France.; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France.; Sorbonne Université, Paris, France., Elmagzoub MS; Faculty of Medicine, National Ribat University, Khartoum, Sudan.; Neuroscience Department, College of Applied Medical Sciences, Imam Abdulrahman Bin Faisal University, Jubail, Saudi Arabia., Ahmed EA; Faculty of Dentistry, Shendi University, Shendi, Sudan.; Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Buratti J; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France., Courtin T; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS - Hôpital La Pitié-Salpêtrière, Paris, France.; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France.; Sorbonne Université, Paris, France., Noé E; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS - Hôpital La Pitié-Salpêtrière, Paris, France., Bogoin J; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France., Copin B; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France., Elmugadam FA; Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Abdelgadir WA; Department of Biochemistry and Molecular Biology, Faculty of Science and Technology, Al-Neelain University, Khartoum, Sudan., Ahmed AKMA; Department of Molecular Neuroscience, Graduate School of Medicine, Osaka University, 2-2, Yamadaoka, Suita, Osaka, 565-0871, Japan., Daldoum MA; Faculty of Medicine, University of Khartoum, Khartoum, Sudan.; Division of Neurology, Sudan Medical Council, Khartoum, Sudan., Altayeb RMI; Faculty of Medicine, University of Khartoum, Khartoum, Sudan.; Imperial College London, London, UK., Bashir M; Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Khalid LM; Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Gamil S; Department of Basic Sciences, College of Medicine, Prince Sattam bin Abdulaziz University, AL-Kharj, Saudi Arabia.; Department of Biochemistry, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Baldassari S; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS - Hôpital La Pitié-Salpêtrière, Paris, France., Elsayed L; Department of Basic Sciences, College of Medicine, Princess Nourah Bint Abdulrahman University, P.O.Box 84428, 11671, Riyadh, Saudi Arabia., Keren B; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France., Nuel G; Stochastics and Biology Group (MAV), Probability and Statistics (LPSM, CNRS 8001), Sorbonne Université, Paris, France., Ahmed AE; Department of Physiology, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Leguern E; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS - Hôpital La Pitié-Salpêtrière, Paris, France.; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France.; Sorbonne Université, Paris, France.
Publikováno v:
Human genomics [Hum Genomics] 2024 Nov 21; Vol. 18 (1), pp. 130. Date of Electronic Publication: 2024 Nov 21.
Autor:
Koko M; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany., Elseed MA; Department of Pediatrics, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Mohammed IN; Department of Pediatrics, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Hamed AA; Department of Pediatrics, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Abd Allah ASI; Neurogenetics Research Group, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Yahia A; Department of Biochemistry, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Siddig RA; Neurogenetics Research Group, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Altmüller J; Cologne Center for Genomics, University of Cologne, Cologne, Germany.; Berlin Institute of Health at Charité- Universitätsmedizin Berlin, Berlin, Germany.; Max Delbrück Center for Molecular Medicine, Berlin, Germany., Toliat MR; Cologne Center for Genomics, University of Cologne, Cologne, Germany., Elmahdi EO; Neurogenetics Research Group, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Amin M; Department of Biochemistry, Faculty of Medicine, Al-Neelain University, Khartoum, Sudan., Ahmed EA; UNESCO Chair on Bioethics, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Eltazi IZM; Department of Medicine, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Elmugadam FA; Neurogenetics Research Group, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Abdelgadir WA; Department of Biochemistry and Molecular Biology, Faculty of Sciences and Technology, Al-Neelain University, Khartoum, Sudan., Eltaraifee E; Neurogenetics Research Group, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Ibrahim MOM; Department of Biochemistry, Faculty of Medicine, Sudan University of Science and Technology, Khartoum, Sudan., Ali NMH; Neurogenetics Research Group, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Malik HM; Neurogenetics Research Group, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Babai AM; Neurogenetics Research Group, Faculty of Medicine, University of Khartoum, Khartoum, Sudan., Bakhit YH; Department of Neurology, Neurobiology Division, University Hospital Bonn, Bonn, Germany., Nürnberg P; Cologne Center for Genomics, University of Cologne, Cologne, Germany., Ibrahim ME; Department of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan., Salih MA; Division of Pediatric Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.; Consultant Pediatric Neurologist, Health Sector, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia., Schubert J; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany., Elsayed LEO; Department of Basic Sciences, College of Medicine, Princess Nourah bint Abdulrahman University, P.O.Box 84428, Riyadh, 11671, Saudi Arabia. leelsayed@pnu.edu.sa., Lerche H; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Publikováno v:
European journal of human genetics : EJHG [Eur J Hum Genet] 2024 Oct; Vol. 32 (10), pp. 1338-1342. Date of Electronic Publication: 2024 Feb 05.
Autor:
Elmugadam FM; Institute of Endemic Diseases., Ahmed H; Faculty of Medicine., Karamelghani M; Faculty of Medicine., Ali A; Faculty of Medicine., Ali I; Faculty of Medicine., Ahmed A; Faculty of Medicine., Salman M; Faculty of Medicine., Mohamed W; Faculty of Medicine., Ahmed EA; UNESCO Chair in Bioethics., Abbasher Hussien Mohamed Ahmed K; Faculty of Medicine., Mustafa Ahmed GE; Faculty of Medicine., Elsayed L; Department of Basic Sciences, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia., Musa A; Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan.
Publikováno v:
Annals of medicine and surgery (2012) [Ann Med Surg (Lond)] 2024 May 28; Vol. 86 (7), pp. 3959-3971. Date of Electronic Publication: 2024 May 28 (Print Publication: 2024).