Zobrazeno 1 - 8
of 8
pro vyhledávání: '"T A, Younes"'
Autor:
M. Akkari, I. Kraoua, H. Klaa, H. Benrhouma, T. Ben Younes, A. Rouissi, M. Chaabouni, I. Ben Youssef‐Turki
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 12, Pp n/a-n/a (2020)
Abstract Background Mutations in SQSTM1 gene have been recently identified as a rare cause of progressive childhood neurodegenerative disorder. So far, only 25 patients from 10 unrelated families were reported. Methods and results We report on the fi
Externí odkaz:
https://doaj.org/article/0182cf0826954ad1b4be5ec314547efe
Autor:
S. Tlili, L. Ben Fatma, H. Boudabous, I. Kraoua, A. Ben Chahida, H. Ghabi, L. Rais, T. Ben Younes, I. Mami, M.K. Zouaghi
Publikováno v:
Néphrologie & Thérapeutique. 18:392
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a655e52c6281e6ecd87b5e2b8932d5c
https://doi.org/10.1016/j.nephro.2022.07.319
https://doi.org/10.1016/j.nephro.2022.07.319
Autor:
Manel Akkari, Ichraf Kraoua, Myriam Chaabouni, I. Ben Youssef-Turki, Hanene Benrhouma, T. Ben Younes, Aida Rouissi, Hedia Klaa
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Mutations in SQSTM1 gene have been recently identified as a rare cause of progressive childhood neurodegenerative disorder. So far, only 25 patients from 10 unrelated families were reported. Methods and results We report on the first Tunis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0305299d2f472a1fac12808c17bc8098
https://doi.org/10.1002/mgg3.1543
https://doi.org/10.1002/mgg3.1543
Publikováno v:
Surface and Coatings Technology. 220:36-39
The interaction of CMAS (an acronym for a mixture of oxides including CaO, MgO, Al2O3, SiO2) with aerospace materials has been studied as part of the degradation of protective coatings on turbine blades, since the presence of these mixture oxides can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::278e396a541b43dbc040b36f8c2bcec6
https://doi.org/10.1016/j.surfcoat.2012.04.066
https://doi.org/10.1016/j.surfcoat.2012.04.066
Autor:
T. Ben Younes, H. Benrhouma, J.-F. Benoist, N. Ben Achour, H. Klaa, A. Hassen-Rouissi, I. Kraoua, F. Nasrallah, C. Drissi, I. Ben Youssef-Turki
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 24(3)
Pyridoxine-dependent epilepsy (PDE) is a rare autosomal recessive metabolic disease characterized by seizures in neonates or infants, which is unresponsive to antiepileptic drugs but controlled by pyridoxine. Without prompt treatment, continued seizu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e0544d5fe9ecb936316e0391b4fbd90
https://pubmed.ncbi.nlm.nih.gov/28131559
https://pubmed.ncbi.nlm.nih.gov/28131559
Autor:
Y. Sidhom, Riadh Gouider, A. Nasri, T. Ben Younes, Imen Kacem, M. Ben Djebara, Amina Gargouri
Publikováno v:
Journal of the Neurological Sciences. 381:737-738
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b41284f298d68faf42a1ea6c3b3d9f9a
https://doi.org/10.1016/j.jns.2017.08.2080
https://doi.org/10.1016/j.jns.2017.08.2080
Publikováno v:
Journal of the Egyptian Society of Parasitology. 26(3)
Sixty patients with chronic liver disease complaining of persistent or recurrent diarrhoea where studied. The stools were examined by direct smear, formol ether concentration method and modified Ziehl Neelsen technique for Cryptosporidium in addition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6c504a50cbf3b38acd3e8122798c2e76
https://pubmed.ncbi.nlm.nih.gov/8918043
https://pubmed.ncbi.nlm.nih.gov/8918043
Publikováno v:
Journal of the Egyptian Society of Parasitology. 21(1)
This study was done on 110 patients with different types of malignant diseases and 20 healthy controls. Cases were divided into four groups according to parasitological and serological examination. The first group included 37 patients without any par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a1ed018c52103c2e4b3c03d351fb44ed
https://pubmed.ncbi.nlm.nih.gov/2033284
https://pubmed.ncbi.nlm.nih.gov/2033284