Literature DB >> 27489471

Five-year-old girl with tongue bleeding.

Hande Kızılocak1, Nihal Özdemir1, Fatih Varol2, Begüm Şirin Koç1, Gürcan Dikme1, Halit Çam2, Tiraje Celkan1.   

Abstract

Entities:  

Year:  2016        PMID： 27489471      PMCID： PMC4959741          DOI： 10.5152/TurkPediatriArs.2016.3458

Source DB:  PubMed          Journal:  Turk Pediatri Ars


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  8 in total

1.  Combined factor V and VIII deficiency: a new family and their haemorrhagic manifestations.

Authors:  H Mansouritorghabeh; Z Rezaieyazdi; A A Pourfathollah
Journal:  Haemophilia       Date:  2006-03       Impact factor: 4.287

2.  Factor V and VIII combined deficiency: clinical perioperative management for tonsillectomy in a child.

Authors:  R Lanchon; F Robin; O Brissaud; M Marro; K Nouette-Gaulain
Journal:  Ann Fr Anesth Reanim       Date:  2014-02-21

3.  Factor VIII inhibitory antibody in a patient with combined factor V/factor VIII deficiency.

Authors:  T W Buckner; B I Nielsen; N S Key; A Ma
Journal:  Haemophilia       Date:  2014-12-04       Impact factor: 4.287

4.  Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.

Authors:  Dipika Mohanty; Kanjaksha Ghosh; Shrimati Shetty; Marta Spreafico; Isabella Garagiola; Flora Peyvandi
Journal:  Am J Hematol       Date:  2005-08       Impact factor: 10.047

5.  Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran.

Authors:  Mehran Karimi; Andrea Cairo; Mohammad M Safarpour; Sezaneh Haghpanah; Maryam Ekramzadeh; Abdolreza Afrasiabi; Mahdi Shahriari; Marzia Menegatti
Journal:  Blood Coagul Fibrinolysis       Date:  2014-06       Impact factor: 1.276

Review 6.  Congenital factor V and VIII deficiency in women: a systematic review of literature and report of two new cases.

Authors:  Dimitrios Spiliopoulos; Rezan A Kadir
Journal:  Blood Coagul Fibrinolysis       Date:  2016-04       Impact factor: 1.276

7.  Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders.

Authors:  F Peyvandi; R Palla; M Menegatti; S M Siboni; S Halimeh; B Faeser; H Pergantou; H Platokouki; P Giangrande; K Peerlinck; T Celkan; N Ozdemir; C Bidlingmaier; J Ingerslev; M Giansily-Blaizot; J F Schved; R Gilmore; A Gadisseur; M Benedik-Dolničar; L Kitanovski; D Mikovic; K M Musallam; F R Rosendaal
Journal:  J Thromb Haemost       Date:  2012-04       Impact factor: 5.824

8.  Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India.

Authors:  G Jayandharan; M Spreafico; A Viswabandya; M Chandy; A Srivastava; F Peyvandi
Journal:  Haemophilia       Date:  2007-07       Impact factor: 4.287
  8 in total

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