Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Walid Dridi"'
Autor:
Walid Dridi, Solaf Kanfar, Patrick M. A. Sleiman, Yichuan Liu, Hakon Hakonarson, Hayaal Rammah, Alia Matrouk
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 6, Pp n/a-n/a (2022)
Abstract Background The vast majority of chronic myeloid leukemia (CML) patients have a single translocation t(9;22)(q34;q11), BCR/ABL1 fusion genes, which is regarded as the hallmark of CML. However, around 5 to 10% of CML patients exhibit the invol
Externí odkaz:
https://doaj.org/article/47cfbb22d1994674b0f8e653180e22eb
Autor:
Salma Bessalah, Samira Jebahi, Asim Faraz, Amel Raoufi, Cem Tırınk, Walid Dridi, Mahmoud Daouad, Hassib Keskes, Touhami Khorchani, Khaled Farah, Abdul Waheed, Mohamed Hammadi
Publikováno v:
Pakistan Journal of Zoology. 55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a77fc667d2561b461cfa8d8dade8b09d
https://doi.org/10.17582/journal.pjz/20220218020207
https://doi.org/10.17582/journal.pjz/20220218020207
Autor:
Naif Al-Zahrani, Walid Dridi, Hakon Hakonarson, Patrick M. A. Sleiman, Talal Al-Harbi, Haya Al-Rammah, Yichuan Liu
Publikováno v:
American Journal of Medical Genetics Part A. 188:618-623
We report a 38-year-old Saudi male with Ehlers-Danlos Syndrome (EDS). The patient presented with rare and unusual neurological manifestations, including but not limited to ophthalmoplegia and myopathic pattern on his electromyography. In addition to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::603f4b100a2871c4efe9656427b09f97
https://doi.org/10.1002/ajmg.a.62539
https://doi.org/10.1002/ajmg.a.62539
Autor:
Amel Raouafi, Samira Jbahi, Salma Bessalah, Mahmoud Daoudi, Walid Dridi, Ahmed Hichem Hamzaoui, Sergey V. Dorohzkin, Faouzi Hosni, Mustapha Hidouri
Publikováno v:
Journal of the Indian Chemical Society. 99:100722
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec2b75135952c71b9e6300daae71205e
https://doi.org/10.1016/j.jics.2022.100722
https://doi.org/10.1016/j.jics.2022.100722
Autor:
Patrick M. A. Sleiman, Michael E. March, Mohamed Sager, Cuiping Hou, Lifeng Tian, Renata Pellegrino, Kenny Nguyen, Hakon Hakonarson, Yousef Housawi, Walid Dridi
Publikováno v:
Human Mutation. 38:507-510
Braddock-Carey Syndrome (BCS) is characterized by microcephaly, congenital thrombocytopenia, Pierre-Robin sequence (PRS), and agenesis of the corpus callosum. BCS has been shown to be caused by a 21q22.11 microdeletion that encompasses multiple genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9abd60090452f986c530cca0802f638d
https://doi.org/10.1002/humu.23188
https://doi.org/10.1002/humu.23188
Publikováno v:
Journal of clinical neuromuscular disease. 21(1)
Hereditary axonal motor and sensory neuropathy or Charcot-Marie-Tooth type 2 (CMT2) is a common inherited peripheral neuropathy. Major symptomatologic signs vary from minimal to significant weakness and loss of sensation, feet usually affected more t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28364f86a90b65ccbe4c8aaffc80d3ee
https://pubmed.ncbi.nlm.nih.gov/31453851
https://pubmed.ncbi.nlm.nih.gov/31453851
Identification of a novel MEN1 gene mutation in Saudi Arabian patient with multiple endocrine tumors
Publikováno v:
Endocrinology&Metabolism International Journal. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a15687c94118cb1444c6192e58a6a1d
https://doi.org/10.15406/emij.2018.06.00179
https://doi.org/10.15406/emij.2018.06.00179
Publikováno v:
Journal of clinical neuromuscular disease. 18(2)
More than 300 mutations were identified in Calpainopathy (CAPN3) gene in limb-girdle muscular dystrophy type 2A (LGMD2A) patients. LGMD2A type is also known as Calpainopathy, which is characterized by selective atrophy and weakness of proximal limb m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d463189ba617ea1bfd454a3d97d0a37
https://pubmed.ncbi.nlm.nih.gov/27861222
https://pubmed.ncbi.nlm.nih.gov/27861222
Publikováno v:
Comptes Rendus Mécanique. 337:238-244
Resume Nous etudions l'influence de l'acoustic streaming (et plus precisement de l'Eckart streaming) sur la stabilite de l'ecoulement cree par le chauffage lateral d'une couche fluide entre deux plaques planes horizontales infinies (ecoulement de Had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::557d8c35c16f8478e9139d1399588f5f
https://doi.org/10.1016/j.crme.2009.04.006
https://doi.org/10.1016/j.crme.2009.04.006
Publikováno v:
Comptes Rendus Mécanique. 335:175-180
Resume Nous etudions la stabilite lineaire d'un ecoulement cree par des ondes ultrasons (Eckart streaming) dans une couche fluide entre deux plaques planes horizontales infinies, dans le cas d'un fluide isotherme ainsi que dans le cas d'un fluide cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d0564c1a1d0798a81dc012a9ae7ca84
https://doi.org/10.1016/j.crme.2007.02.002
https://doi.org/10.1016/j.crme.2007.02.002