Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lulwa A Aljeryan"'
Autor:
Sara A Alefasi, Hanns Lochmüller, Lulwa A Aljeryan, Abdullah Al-Ajmi, Laila Bastaki, Hadil Alrohaif, Nuwayer H Alrashidi, Andoni Urtizberea, Oksana Pogoryelova
Publikováno v:
Muscle & Nerve. 58:700-707
Introduction GNE myopathy is a rare recessive myopathy caused by mutations in the GNE gene. It is mainly a distal myopathy with relative sparing of the quadriceps muscle. Methods Patients with distal myopathies from Kuwait were examined and tested fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7277c7044cadf5472bacd6edbd0bb4ae
https://doi.org/10.1002/mus.26337
https://doi.org/10.1002/mus.26337
Autor:
Hadil, Alrohaif, Oksana, Pogoryelova, Abdullah, Al-Ajmi, Lulwa A, Aljeryan, Nuwayer H, Alrashidi, Sara A, Alefasi, Andoni, Urtizberea, Hanns, Lochmüller, Laila, Bastaki
Publikováno v:
Musclenerve. 58(5)
GNE myopathy is a rare recessive myopathy caused by mutations in the GNE gene. It is mainly a distal myopathy with relative sparing of the quadriceps muscle.Patients with distal myopathies from Kuwait were examined and tested for the Middle Eastern G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a738c44a6ee58eaa643a32d91a980fa9
https://pubmed.ncbi.nlm.nih.gov/30192030
https://pubmed.ncbi.nlm.nih.gov/30192030
Autor:
R. A. Wahba, S. Al‐Hijji, Talaat I. Farag, E. A. Qurban, Lulwa A Aljeryan, Makia J. Marafie, B. Kasrawi, G. Yadav, I S al-Sulaiman, S. A. Al-Awadi, N. Al‐Hashash, M. Y. El-Khalifa, H. Al‐Aboud, F. M. Mohammed, D. S. Krishna Murthy, M. A. Redha, S. Abul Hassan, Laila Bastaki, M. H. El‐Badramary, A. A. Redha, M. A. Aref, H. Al‐Khorafi, D. Al‐Dighashem
Publikováno v:
Clinical Genetics. 44:329-334
Farag TI, Al-Awadi SA, El-Badramary MH, Aref MA, Kasrawi B, Krishna Murthy DS, El-Khalifa MY, Yadav G, Marafie MJ, Bastaki L, Wahba RA, Mohammed FM, Abul Hasan S, Redha AA, Redha MA, Al-aboud H, Al-Hijji S, Al-Dighashem D, Al-Hashash N, Al-Jeeryan L,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d528176dfb6bc2ec83d424ed6bc4b788
https://doi.org/10.1111/j.1399-0004.1993.tb03910.x
https://doi.org/10.1111/j.1399-0004.1993.tb03910.x
Autor:
Sulaiman A. Al‐Othman, Talaat I. Farag, Nawal Al‐Hashash, Laila Bastaki, Makia J. Marafie, Amira A. Reda, R. Uma, Lulwa A Aljeryan, Hutham Al‐Khorafi, Sawsan J. Abul Hasan, Mohammed M. Al-Ghanem, Fawziyah M. Mohamed, Iman A. Q. Haji, Mariam A. Reda, D. S. Krishna Murthy, R. Usha, Sadika A. Al-Awadi, Kadr Al‐Nagdi, S.A. Mady, Ibrahim Al-Suliman
Publikováno v:
American Journal of Medical Genetics. 46:347-348
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8855ac852e5bdda4a93dc4312013eeb9
https://doi.org/10.1002/ajmg.1320460323
https://doi.org/10.1002/ajmg.1320460323