Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Lelia Valdrè"'
Publikováno v:
International Journal of Adolescence and Youth, Vol 23, Iss 2, Pp 133-144 (2018)
The main aim of the research is to study how youths affected by haemophilia, a congenital hemorrhagic chronic disease, make sense of their condition, with particular reference to the transition from early adolescence to early adulthood. We administer
Externí odkaz:
https://doaj.org/article/f4f620b616d4449ba5d3397f392c25af
Autor:
Benedetti, Danilo Donati, Paolo Spinnato, Lelia Valdrè, Lydia Piscitelli, Giuseppina Mariagrazia Farella, Enrico Pagliarulo, Maria Grazia
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 13; Pages: 4513
Background: Hemophilia is a inherited bleeding disorder that is characterized by intra-articular bleeding (hemarthrosis). The aim of the study was to evaluate the state of the satellite tendons of the target joints in the patient with hemophilic arth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::59b540e974411e7309e9cd8d80edf4e3
Autor:
Federica Riccardi, Antonio Coppola, Gianna Franca Rivolta, Annalisa Matichecchia, Gabriele Quintavalle, Chiara Biasoli, Lelia Valdrè, Lydia Piscitelli, Antonio Percesepe, Annarita Tagliaferri
Publikováno v:
Haemophilia : the official journal of the World Federation of HemophiliaREFERENCES. 28(2)
Haemophilias are X-linked inherited bleeding disorders, due to de novo F8/F9 gene variants in 30-50% of cases. The identification of causative variant in index cases (IC) is crucial for genetic counselling in related women. Over the last 20 years the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62eadebdd8e5c5bd0547228a190bc497
https://pubmed.ncbi.nlm.nih.gov/35060226
https://pubmed.ncbi.nlm.nih.gov/35060226
Autor:
Emily Oliovecchio, Pier Mannuccio Mannucci, Antonio Coppola, Elena Santagostino, Cosimo Ettorre, Giovanni Barillari, Alfonso Iorio, Annarita Tagliaferri, Lelia Valdrè, Teresa Maria Caimi, Gianluca Sottilotta, Giancarlo Castaman, Emanuela Marchesini, Isabella Cantori, Cristina Santoro, Silvia Riva, Ezio Zanon, Paolo Radossi
Publikováno v:
Haemophilia. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f1841b8e54023c5467403c103529985
https://doi.org/10.1111/hae.14268
https://doi.org/10.1111/hae.14268
Autor:
Antonio Coppola, Laura Cortesi, Cristina Santoro, Elena Santagostino, Gianluca Sottilotta, Emanuela Marchesini, Teresa Maria Caimi, Alessandro Nobili, Lelia Valdrè, Emily Oliovecchio, Pier Mannuccio Mannucci, Alfonso Iorio, Annarita Tagliaferri, Isabella Cantori, Giovanni Barillari, Paolo Radossi, Flora Peyvandi, Giancarlo Castaman, Ezio Zanon, Cosimo Ettorre
Publikováno v:
Haemophilia. 24:726-732
BACKGROUND In older people, multiple chronic ailments lead to the intake of multiple medications (polypharmacy) that carry a number of negative consequences (adverse events, prescription and intake errors, poor adherence, higher mortality). Because a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::febbd34947ed1abea6db81077d1570a1
https://doi.org/10.1111/hae.13595
https://doi.org/10.1111/hae.13595
Publikováno v:
International Journal of Adolescence and Youth, Vol 23, Iss 2, Pp 133-144 (2018)
The main aim of the research is to study how youths affected by haemophilia, a congenital hemorrhagic chronic disease, make sense of their condition, with particular reference to the transition from early adolescence to early adulthood. We administer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96ea22f37c8a633a23556682c0a5adae
https://doaj.org/article/f4f620b616d4449ba5d3397f392c25af
https://doaj.org/article/f4f620b616d4449ba5d3397f392c25af
Autor:
Paolo Radossi, P. M. Mannucci, Isabella Cantori, A. Coppola, Cristina Santoro, Giovanni Barillari, Teresa Maria Caimi, Elena Santagostino, Emily Oliovecchio, Cosimo Ettorre, Ezio Zanon, Lelia Valdrè, Giancarlo Castaman, Alfonso Iorio, Annarita Tagliaferri, Gianluca Sottilotta, Emanuela Marchesini
Publikováno v:
Haemophilia. 24:e6-e10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86624f66ba0bbcd63cf0c600f3d1053b
https://doi.org/10.1111/hae.13379
https://doi.org/10.1111/hae.13379
Autor:
Giuseppina Rodorigo, Cristina Legnani, Claudia Pancani, Costanza Cappelli, Benilde Cosmi, Lelia Valdrè, Mirella Frascaro, Michela Cini
Background:Laboratory investigation with specific factor XIII (FXIII) assays plays a crucial role in diagnosis of FXIII deficiency. According to the International Society on Thrombosis and Hemostasis (ISTH), it is necessary a blank sample with iodoac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c5bee0610a3aafd8b17c3b45ac8d7c
http://hdl.handle.net/11585/545693
http://hdl.handle.net/11585/545693
Autor:
G. Rodorigo, M. L. Serino, L. Ippolito, S. Macchi, Lelia Valdrè, Chiara Biasoli, P. Pedrazzi, D. Vincenzi, Annarita Tagliaferri, Davide Martorana, M. Savi, M. Volta, M. D'Incà, C. Di Perna, Tauro Maria Neri, Gianna Franca Rivolta, Federica Riccardi, M. C. Arbasi
Publikováno v:
Haemophilia. 16:791-800
Summary. Haemophilia A (HA) is an X-linked recessive bleeding disorder caused by a lack or decrease of coagulation factor VIII activity. The molecular diagnosis of HA is challenging and a variety of different mutations have been identified throughout
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcce42e336738034042a343f90f7223b
https://doi.org/10.1111/j.1365-2516.2010.02228.x
https://doi.org/10.1111/j.1365-2516.2010.02228.x
Autor:
Lucio Catalano, Michele Cavo, Patrizia Tosi, Francesca Patriarca, Lelia Valdrè, Cristina Legnani, Michela Cini, Elena Zamagni, Alessandro Gozzetti, Paola Tacchetti, Gualtiero Palareti, Luciano Masini
Publikováno v:
European Journal of Haematology. 84:484-492
Background: Venous thromboembolism (VTE) is a major complication of myeloma therapy recently observed with the increasing use of up-front thalidomide and dexamethasone (thal–dex). The pathogenesis of thal-induced VTE is not well recognized, and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebea03d6b59b473829dcc8bf9793bd06
https://doi.org/10.1111/j.1600-0609.2010.01434.x
https://doi.org/10.1111/j.1600-0609.2010.01434.x