Zobrazeno 1 - 10
of 295
pro vyhledávání: '"S, Garrel"'
Autor:
Brown, Teresa E.1,2 (AUTHOR) teresa.brown@health.qld.gov.au, Byrnes, Angela1,2 (AUTHOR), Chan, Aaron C.2 (AUTHOR), Dwyer, Kathleen3 (AUTHOR), Edwards, Anna2,4 (AUTHOR), Blake, Claire L.1 (AUTHOR), Banks, Merrilyn D.1,2 (AUTHOR), Hughes, Brett G. M.5,6 (AUTHOR), Lin, Charles Y.5,6 (AUTHOR), Kenny, Lizbeth M.5,6 (AUTHOR), Spurgin, Ann-Louise7 (AUTHOR), Bauer, Judith D.2,8 (AUTHOR)
Publikováno v:
Current Oncology. Nov2024, Vol. 31 Issue 11, p6938-6955. 18p.
Autor:
A.L. Benabid, Minotti L, S. Garrel, A. Joannard, Benoît Polack, C. Barro, I. Wrobleski, P. Kahn, A. Koudsie, F. Blanc-Jouvan, G. Pernod, B. Arnutti
Publikováno v:
Haemophilia. 9:121-124
Summary. Factor XIII (FXIII) deficiency is a rare autosomal recessive congenital disorder of haemostasis, associated with a high risk of intracranial haemorrhage. Intracranial haemorrhage can result in neurological sequelae including seizure disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56c95d1fb041f63503370f92f221aeb7
https://doi.org/10.1046/j.1365-2516.2003.00700.x
https://doi.org/10.1046/j.1365-2516.2003.00700.x
Autor:
Guruvaiah, Praveen1 (AUTHOR), Gupta, Romi1,2 (AUTHOR) romigup@uab.edu
Publikováno v:
Journal of Translational Medicine. 7/9/2024, Vol. 22 Issue 1, p1-14. 14p.
Autor:
G, Pernod, C, Barro, B, Arnutti, F, Blanc-Jouvan, S, Garrel, P, Kahn, L, Minotti, A, Koudsie, A L, Benabid, I, Wrobleski, A, Joannard, B, Polack
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 9(1)
Factor XIII (FXIII) deficiency is a rare autosomal recessive congenital disorder of haemostasis, associated with a high risk of intracranial haemorrhage. Intracranial haemorrhage can result in neurological sequelae including seizure disorders. In som
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b96eb5a0d2d03403525d8f1831fd594c
https://pubmed.ncbi.nlm.nih.gov/12558790
https://pubmed.ncbi.nlm.nih.gov/12558790
Autor:
S Garrel
Publikováno v:
Neurophysiologie Clinique/Clinical Neurophysiology. 22:198-200
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e55dbf6889aae4da5659489d4f16da8d
https://doi.org/10.1016/s0987-7053(05)80757-9
https://doi.org/10.1016/s0987-7053(05)80757-9
Autor:
Pace-Loscos, Tanguy1 (AUTHOR) tanguy.pace-loscos@nice.unicancer.fr, Gal, Jocelyn1 (AUTHOR), Contu, Sara1 (AUTHOR), Schiappa, Renaud1 (AUTHOR), Chamorey, Emmanuel1 (AUTHOR), Culié, Dorian2 (AUTHOR)
Publikováno v:
BMC Bioinformatics. 6/12/2024, Vol. 25 Issue 1, p1-11. 11p.
Akademický článek
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Publikováno v:
Archives de Pédiatrie. 2:909-910
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a14f1d00c18bbd4a8f5a0bcdbf3e093d
https://doi.org/10.1016/0929-693x(95)90462-c
https://doi.org/10.1016/0929-693x(95)90462-c
Autor:
S Garrel
Publikováno v:
Neurophysiologie Clinique/Clinical Neurophysiology. 21:142-143
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44fa5418c453e80c10121a13e9f20f70
https://doi.org/10.1016/s0987-7053(05)80072-3
https://doi.org/10.1016/s0987-7053(05)80072-3
Publikováno v:
Archives de Pédiatrie. 3:933
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4577072f018492f3a20c2b75b79e3bc8
https://doi.org/10.1016/0929-693x(96)87636-6
https://doi.org/10.1016/0929-693x(96)87636-6