Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Adriano Brunetti"'
Autor:
Adriano Brunetti, Sandro Scarpelini
Publikováno v:
Medicina, Vol 40, Iss 3 (2007)
O abdômen agudo pode ser definido como uma dor abdominal de aparecimento súbito, não traumático, que pode necessitar de intervenção cirúrgica ou não. A anamnese detalhada direcionando o exame físico será a base que orientará a condução d
Externí odkaz:
https://doaj.org/article/125eedb89fda4f6db3f86d9a99f3f920
Autor:
Fábio Thuller, Djalma Ernesto Coelho, Manoel Galvao Neto, Almino Ramos, James Skinovsky, Marcus Vinicius Dantas de Campos Martins, Adriano Brunetti, Luiz de Carli, Leandro Totti Cavazolla, José Eduardo Rodrigues, Josemberg Marins Campos
Publikováno v:
Surgical innovation. 16(4)
Background: The advent of endoscopic surgery has radically changed surgery worldwide.The concept of minimally invasive procedures has spread quickly, allowing less pain and more rapid recovery for patients. The authors have developed a device for a n
Publikováno v:
Blut Zeitschrift für die Gesamte Blutforschung. 31:291-298
The behavior of K-test (Trypsin clotting time) has been studied in 38 patients on long-term coumarin therapy and in 19 patients with congenital coagulation disorders of the prothrombin complex. All coumarin treated patients showed a clear prolongatio
Publikováno v:
Blut. 34:363-370
Para-amino-methyl benzoic acid (PAMBA) in a dose of 50 mg/kg body weight was unable to alter the ellagic acid induced hypercoagulable state. No change in the hypercoagulability pattern was observed regardless of the time of administration of the comp
Publikováno v:
Acta Haematologica. 51:40-50
Data are reported pertaining to the 57 subjects so far found to be heterozygotes for the abnormal factor X (factor X Friuli) coagulation disorder. 41 of these subjects were related to the 11 patients
Publikováno v:
Blut Zeitschrift für die Gesamte Blutforschung. 25:77-84
Factor X was assayed in 22 anticoagulated patients, in 9 normal subjects, in 3 patients with severe factor X deficiency, in 4 subjects with mild factor X deficiency and in 4 “plasmas” obtained by mixing factor X deficient plasma with the plasma o
Publikováno v:
Blut. 28(1)
A patient with a congenital deficiency of factor V and factor VIII is described (brother/sister incest). The deficiency of the two factors was accompanied by a life-long bleeding tendency. A peculiar family history is added.
Publikováno v:
American journal of clinical pathology. 67(1)
A Normotest (NT)-Thrombotest (TT) discrepancy is claimed to reflect the presence of coumarin-induced inhibitors or intravascular coagulation, or both. The results of this study indicate, however, that a significant NT-TT discrepancy is also present i
Publikováno v:
Acta haematologica. 50(2)
A case of platelet factor 3 deficiency (thrombocytopathy) is presented. The coagulation study showed a normal plasmatic pattern but a defective prothrombin consumption. The thromboplastin generation w
Publikováno v:
European Journal of Trauma & Emergency Surgery; Feb2014, Vol. 40 Issue 1, p93-103, 11p