Search research articles
Contact Us
Filters
Showing results (21-30 of 64) with videos related to
Page
of 7
Sort By:
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 21, 2007
Can early subclinical gait changes in children with haemophilia be identified using the GAITRite walkway
M Bladen, L Alderson, K Khair, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
March 29, 2013
Factors affecting the Haemophilia Joint Health Score in children with severe haemophilia
M Bladen, E Main, N Hubert, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 16, 2015
Novel, human cell line-derived recombinant factor VIII (Human-cl rhFVIII, Nuwiq<sup>®</sup> ) in children with severe haemophilia A: efficacy, safety and pharmacokinetics
A Klukowska, T Szczepański, V Vdovin, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 20, 2016
The incidence, risk and functional outcomes of intracranial haemorrhage in children with inherited bleeding disorders at one haemophilia center
M Bladen, E Main, K Khair, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 5, 2014
Similar bleeding phenotype in young children with haemophilia A or B: a cohort study
N Clausen, P Petrini, S Claeyssens-Donadel, et al.
Archives of Disease in Childhood
|
March 29, 2002
Hermansky-Pudlak syndrome: infrequent bleeding and first report of Turkish and Pakistani kindreds
C Harrison, K Khair, B Baxter, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 15, 1998
Inherited prothrombotic states and ischaemic stroke in childhood
V Ganesan, M A McShane, R Liesner, et al.
Blood
|
October 25, 2001
Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease
P J Ancliff, R E Gale, R Liesner, et al.
British Journal of Haematology
|
January 22, 2008
Stem cell transplantation for children with Glanzmann thrombasthenia
P Connor, K Khair, R Liesner, et al.
British Journal of Haematology
|
May 18, 2006
The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation
Charles R M Hay, S Brown, P W Collins, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 64) with videos related to
Sort By:
Page
of 7
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 21, 2007
Can early subclinical gait changes in children with haemophilia be identified using the GAITRite walkway
M Bladen, L Alderson, K Khair, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
March 29, 2013
Factors affecting the Haemophilia Joint Health Score in children with severe haemophilia
M Bladen, E Main, N Hubert, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 16, 2015
Novel, human cell line-derived recombinant factor VIII (Human-cl rhFVIII, Nuwiq<sup>®</sup> ) in children with severe haemophilia A: efficacy, safety and pharmacokinetics
A Klukowska, T Szczepański, V Vdovin, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 20, 2016
The incidence, risk and functional outcomes of intracranial haemorrhage in children with inherited bleeding disorders at one haemophilia center
M Bladen, E Main, K Khair, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 5, 2014
Similar bleeding phenotype in young children with haemophilia A or B: a cohort study
N Clausen, P Petrini, S Claeyssens-Donadel, et al.
Archives of Disease in Childhood
|
March 29, 2002
Hermansky-Pudlak syndrome: infrequent bleeding and first report of Turkish and Pakistani kindreds
C Harrison, K Khair, B Baxter, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 15, 1998
Inherited prothrombotic states and ischaemic stroke in childhood
V Ganesan, M A McShane, R Liesner, et al.
Blood
|
October 25, 2001
Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease
P J Ancliff, R E Gale, R Liesner, et al.
British Journal of Haematology
|
January 22, 2008
Stem cell transplantation for children with Glanzmann thrombasthenia
P Connor, K Khair, R Liesner, et al.
British Journal of Haematology
|
May 18, 2006
The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation
Charles R M Hay, S Brown, P W Collins, et al.
Page
of 7