Zobrazeno 1 - 4
of 4
pro vyhledávání: '"B. Arnutti"'
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:
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:
Yesim Dargaud, P. Amaranto, Lucia Rugeri, M.C. Trzeciak, Jacques Ninet, B. Arnutti, Claude Negrier, P. Gaucherand, M.C. Vergnes
Publikováno v:
Thrombosis Research. 123:S139-S140
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7990f2ef9051622f6b3971f06b3bd450
https://doi.org/10.1016/s0049-3848(09)70048-9
https://doi.org/10.1016/s0049-3848(09)70048-9
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