Detalles de la búsqueda
1.
Long-term immunogenicity, efficacy and tolerability of simoctocog alfa in patients with severe haemophilia A who had completed the NuProtect study in previously untreated patients.
Haemophilia
; 29(4): 1005-1012, 2023 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-37335546
2.
Simoctocog alfa (Nuwiq®) in previously untreated patients with severe haemophilia A-Final efficacy and safety results from the NuProtect study.
Eur J Haematol
; 111(4): 544-552, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37439123
3.
Patterns of joint damage in severe haemophilia A treated with prophylaxis.
Haemophilia
; 27(4): 666-673, 2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-34015166
4.
Positive effects of ultrasound-guided peripheral IV insertion on pediatric sickle cell anemia/thalassemia patients receiving automated red cell exchange procedures or chronic transfusion therapy.
J Clin Apher
; 36(1): 143-148, 2021 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-33247605
5.
Outcomes indicators and processes in transitional care in adolescents with haemophilia: A Delphi survey of Canadian haemophilia care providers.
Haemophilia
; 25(2): 296-305, 2019 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-30817086
6.
Generation and optimization of the self-administered pediatric bleeding questionnaire and its validation as a screening tool for von Willebrand disease.
Pediatr Blood Cancer
; 64(10)2017 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-28453185
7.
Intra-arterial methylprednisolone for severe steroid refractory gastrointestinal graft-versus-host disease.
Pediatr Blood Cancer
; 61(12): 2321-3, 2014 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-25053422
8.
Congenital thrombotic thrombocytopenic purpura (cTTP) with two novel mutations.
Pediatr Blood Cancer
; 59(7): 1296-8, 2012 Dec 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-22488907
9.
In Utero diagnosis and management of a fetus with homozygous α-Thalassemia in the second trimester: a case report and literature review.
J Pediatr Hematol Oncol
; 33(8): e358-60, 2011 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-22042285
10.
Detectable Unmetabolized Folic Acid and Elevated Folate Concentrations in Folic Acid-Supplemented Canadian Children With Sickle Cell Disease.
Front Nutr
; 8: 642306, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33968971
11.
Magnetic resonance imaging in boys with severe hemophilia A: Serial and end-of-study findings from the Canadian Hemophilia Primary Prophylaxis Study.
Res Pract Thromb Haemost
; 5(7): e12565, 2021 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-34703973
12.
Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect Study.
Thromb Haemost
; 121(11): 1400-1408, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-33581698
13.
Folic acid supplementation in children with sickle cell disease: study protocol for a double-blind randomized cross-over trial.
Trials
; 21(1): 593, 2020 Jun 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-32600389
14.
Hemophilia prophylaxis adherence and bleeding using a tailored, frequency-escalated approach: The Canadian Hemophilia Primary Prophylaxis Study.
Res Pract Thromb Haemost
; 4(2): 318-325, 2020 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-32110763
15.
Prevalence of Vitamin D Deficiency Varies Widely by Season in Canadian Children and Adolescents with Sickle Cell Disease.
J Clin Med
; 7(2)2018 Jan 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-29385701
16.
Tailored frequency-escalated primary prophylaxis for severe haemophilia A: results of the 16-year Canadian Hemophilia Prophylaxis Study longitudinal cohort.
Lancet Haematol
; 5(6): e252-e260, 2018 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-29731369
17.
Diagnosing platelet delta-storage pool disease in children by flow cytometry.
Am J Clin Pathol
; 127(4): 626-32, 2007 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-17369140
18.
The clinical impact of copy number variants in inherited bone marrow failure syndromes.
NPJ Genom Med
; 22017 May 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-28690869
19.
Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy.
Child Neurol Open
; 3: 2329048X16669912, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-28503617
20.
Hyperuricemia and reticulocytopenia in association with autoimmune hemolytic anemia in two children.
Am J Clin Pathol
; 122(6): 849-54, 2004 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-15539377