Výsledky vyhledávání

Spectrum of F8 gene mutations in haemophilia A patients from a region of Italy: identification of 23 new mutations

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

Zobrazit plný text záznamu

A web-based registry of inherited bleeding disorders in the region of Emilia-Romagna: results at three and a half years

Autor: Gianna Franca Rivolta, P. Albertini, G. Rodorigo, S. Moratelli, C. Pattacini, Chiara Biasoli, Lelia Valdrè, M. C. Arbasi, Annarita Tagliaferri, M. D'Incà, M. Marietta, D. Vincenzi

Publikováno v: Haemophilia. 14:343-354

A Registry of inherited bleeding disorders was set up in the Region of Emilia-Romagna (RER) to collect information about these diseases and to improve the quality of care. From January 2003, the eight Haemophilia Centres (HC) in the RER began to use

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c63e88be3e37c13d4ff747d9e484f660
https://doi.org/10.1111/j.1365-2516.2007.01623.x

Zobrazit plný text záznamu

Growing up with a chronic disease: identity, autonomy and compliance in adolescents and young adults affected by hemophilia

Autor: POTI', SILVIA, EMILIANI, FRANCESCA, PALARETI, LAURA, L. Valdre, L. Piscitelli, G. Rodorigo

Introduction: An extensive medical literature (Petrini & Seuser, 2009) regarding adolescents with chronic illness shows that during adolescence there is an abandonment of treatment regimens and a reduced adherence to medical prescriptions. The aim of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4094::edbb4029a8fac59871a885b15d115aed
http://hdl.handle.net/11585/381440

Zobrazit plný text záznamu

SOCIAL REPRESENTATIONS OF HAEMOPHILIA IN ADOLESCENTS AND YOUNG ADULTS: A PSYCHOSOCIAL PERPECTIVE ON COMPLIANCE

Autor: S. Potì, L. Piscitelli, G. Rodorigo, L. Valdrè, EMILIANI, FRANCESCA, PALARETI, LAURA

Background. This paper is intended as an exploration of the Social Representations of haemophilia, and the normalization process in adolescents and young adults affected by congenital hemorrhagic diseases. An extensive medical literature (Petrini & S

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4094::46a062e457ada659011a732a5ac94403
http://hdl.handle.net/11585/127574

Zobrazit plný text záznamu

Recurrent 'Migrainelike' Episodes in Patients With HIV Disease

Autor: Rita Rinaldi, Roberto D'Alessandro, G. Azzimondi, G. Rodorigo, V. De Rosa, Roberto Manfredi, Francesco Chiodo, Caterina Tonon, A. Mastroianni, O. Coronado, C Legnani

Publikováno v: Headache: The Journal of Head and Face Pain. 37:443-448

Recurrent transient neurological deficits have been described in human immunodeficiency virus (HIV)-infected subjects, but their frequency, pathogenesis, and outcome are still unsettled. We describe 10 HIV-infected patients with transient neurologica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59177c6fad8e1d791e359f46252b6b44
https://doi.org/10.1046/j.1526-4610.1997.3707443.x

Zobrazit plný text záznamu

Spectrum of F8 gene mutations in haemophilia A patients from a region of Italy: identification of 23 new mutations

Autor: F, Riccardi, A, Tagliaferri, D, Martorana, G F, Rivolta, L, Valdrè, G, Rodorigo, C, Biasoli, M, D'Incà, M L, Serino, S, Macchi, D, Vincenzi, M, Arbasi, P, Pedrazzi, M, Volta, C, DI Perna, L, Ippolito, M, Savi, T M, Neri

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 16(5)

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 the F8 g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3bfb2ff786e84e589f41b647b6c61503
https://pubmed.ncbi.nlm.nih.gov/20331761

Zobrazit plný text záznamu

[Deep venous thrombosis. Evaluation of a non-invasive diagnostic procedure based on compression ultrasonography and measurement of D-dimer plasma levels]

Autor: G, Guazzaloca, G, Palareti, C, Legnani, G, Fortunato, F, Grauso, G, Rodorigo, V, De Rosa, R, Golfieri, E, Gianpalma, D, Marri, M, Pazzaglia, R, Franchi, S, Coccheri

Publikováno v: Minerva cardioangiologica. 45(6)

Clinical diagnosis of deep venous thrombosis (DVT) of the leg is unreliable. An accurate diagnosis is important for therapeutic decision since anticoagulant treatment, though potentially dangerous, is useless in case of a false positive diagnosis, wh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c9b7fe565a7623cce3101579cbfbee58
https://pubmed.ncbi.nlm.nih.gov/9432566

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání