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Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 1(4)
Summary. To evaluate the frequency and potency of inhibitor formation based on the product used, we retrospectively reviewed the records of 99 children with various types and severity of haemophilia (haemophilia A 82, severe 46; haemophilia B 10, sev
Publikováno v:
Acta Paediatrica. 91:87-91
Aim: To investigate whether the factor V Leiden mutation (FVL), the prothrombin gene G20210A variant or the methylenetetrahydrofolate reductase (MTHFR) C677T genotype are risk factors for central nervous system (CNS) thrombosis or intraventricular he
Autor:
Maria Moschovi, A. Kattamis, S Aronis, Helen Platokouki, H. Pergantou, A. Komitopoulou, Z. Kapsimali
Publikováno v:
Pathophysiology of Haemostasis and Thrombosis. 35:392-397
The distribution of mutations/polymorphisms in genes affecting haemostasis [factor V Leiden (FVL), FV H1298R (FVR2), FII 20210A, b-Fib 455G→A, FXIII V34L, PAI-1 4G, HPA-1b] among 141 children with thrombosis at various sites and 103 controls was co
Autor:
Fotini Tzortzatou-Stathopoulou, Maria Moschovi, H. Platokouki, K Salavoura, S Aronis, Georgios Trimis
Publikováno v:
Haemophilia. 12:95-99
The development of antibodies to factor VIII (FVIII) in severely affected haemophilia A patients is a serious complication associated with increased morbidity and mortality. Bypassing agents are used to treat acute bleeding episodes; however, elimina
Publikováno v:
Acta Paediatrica. 93:638-642
Aim: To review the long-term efficacy and safety of splenectomy in children with chronic idiopathic thrombocytopenic purpura (cITP). Patients and methods: Data from 33 splenectomized children were retrospectively analysed (median follow up period: 18
Autor:
K. Kurnik-Auberger, Ségolène Claeyssens, A. Glomstein, C. Van Geet, Owen P. Smith, Wolfgang Muntean, F. Hill, L. Rosado, E Scheibel, M. Siimes, Ian Hann, P Petrini, W. Kreuz, Hervé Chambost, Rolf Ljung, G. Mancuso, J. M. Tusell, Rainer Kobelt, S. Aronis-Vournas, M. van den Berg
Publikováno v:
Haemophilia. 6:619-624
A survey was made of the current status of treatment of haemophilic boys at 20 centres in 16 European countries and includes approximately 1500 of the estimated 6500 haemophiliacs in the participating countries. Many mild haemophiliacs are not seen,
Publikováno v:
Pediatrics International. 40:381-384
The case of a 7-year-old girl with a 2 year history of easy bruising associated with thrombocytopenia is reported. On admission she presented with ecchymoses, abdominal distention and splenomegaly. Hemostasis investigation revealed a consumption coag
Publikováno v:
Thrombosis Research. 86:73-78
Lupus anticoagulant (LA) is an acquired inhibitor usually associated with thrombotic tendency and rarely with hemorrhagic manifestations, except in cases of LA with hypoprothrombinemia. In vitro LA is manifested with a prolongation in the activated p
Autor:
H Platokouki, Evangelos D. Papakonstantinou, E Adamtziki, A. Bargeliotis, Kleopatra H. Schulpis, S Aronis
Publikováno v:
Journal of Inherited Metabolic Disease. 19:603-609
Classical phenylketonuria (PKU) (McKusick 261600) is an inborn error of metabolism treated by a controlled low-phenylalanine (Phe) diet started as soon as possible in the first days of life. Such a diet can be achieved with vegetable protein and can