Literature DB >> 27893350

The Bleeding Assessment Tool and laboratory data in the characterisation of a female with inherited haemophilia A.

Viviana Daidone1, Eva Galletta1, Antonella Bertomoro1, Alessandra Casonato1.   

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Year:  2016        PMID: 27893350      PMCID: PMC5770322          DOI: 10.2450/2016.0132-16

Source DB:  PubMed          Journal:  Blood Transfus        ISSN: 1723-2007            Impact factor:   3.443


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  19 in total

1.  Age- and tissue-specific variation of X chromosome inactivation ratios in normal women.

Authors:  A Sharp; D Robinson; P Jacobs
Journal:  Hum Genet       Date:  2000-10       Impact factor: 4.132

2.  Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis.

Authors:  G C White; F Rosendaal; L M Aledort; J M Lusher; C Rothschild; J Ingerslev
Journal:  Thromb Haemost       Date:  2001-03       Impact factor: 5.249

3.  Severe hemophilia A in a Japanese female caused by an F8-intron 22 inversion associated with skewed X chromosome inactivation.

Authors:  Yuhri Miyawaki; Atsuo Suzuki; Yuhta Fujimori; Akira Takagi; Takashi Murate; Nobuaki Suzuki; Akira Katsumi; Tomoki Naoe; Koji Yamamoto; Tadashi Matsushita; Junki Takamatsu; Tetsuhito Kojima
Journal:  Int J Hematol       Date:  2010-08-11       Impact factor: 2.490

4.  ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders.

Authors:  F Rodeghiero; A Tosetto; T Abshire; D M Arnold; B Coller; P James; C Neunert; D Lillicrap
Journal:  J Thromb Haemost       Date:  2010-09       Impact factor: 5.824

5.  Carrier detection in hemophilia A: a cooperative international study. I. The carrier phenotype.

Authors:  J B Graham; C R Rizza; J Chediak; P M Mannucci; E Briët; R Ljung; C K Kasper; E M Essien; P P Green
Journal:  Blood       Date:  1986-06       Impact factor: 22.113

6.  Characterization of the human factor VIII gene.

Authors:  J Gitschier; W I Wood; T M Goralka; K L Wion; E Y Chen; D H Eaton; G A Vehar; D J Capon; R M Lawn
Journal:  Nature       Date:  1984 Nov 22-28       Impact factor: 49.962

7.  Nonrandom X-inactivation patterns in normal females: lyonization ratios vary with age.

Authors:  L Busque; R Mio; J Mattioli; E Brais; N Blais; Y Lalonde; M Maragh; D G Gilliland
Journal:  Blood       Date:  1996-07-01       Impact factor: 22.113

8.  Developing a new generation of tests for genotyping hemophilia-causative rearrangements involving int22h and int1h hotspots in the factor VIII gene.

Authors:  L C Rossetti; C P Radic; I B Larripa; C D De Brasi
Journal:  J Thromb Haemost       Date:  2008-02-12       Impact factor: 5.824

9.  Molecular mechanisms underlying hemophilia A phenotype in seven females.

Authors:  A Pavlova; H Brondke; J Müsebeck; H Pollmann; A Srivastava; J Oldenburg
Journal:  J Thromb Haemost       Date:  2009-03-19       Impact factor: 5.824

10.  Identifying type Vicenza von Willebrand disease.

Authors:  Alessandra Casonato; Elena Pontara; Francesca Sartorello; Maria Grazia Cattini; Lisa Gallinaro; Antonella Bertomoro; Antonio Rosato; Roberto Padrini; Antonio Pagnan
Journal:  J Lab Clin Med       Date:  2006-02
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  1 in total

1.  Mechanistic Insights into Factor VIII Immune Tolerance Induction via Prenatal Cell Therapy in Hemophilia A.

Authors:  Martin Rodriguez; Christopher D Porada; Graҫa Almeida-Porada
Journal:  Curr Stem Cell Rep       Date:  2019-11-20
  1 in total

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