X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (52) 52
index medicus (45) 45
female (41) 41
hematology (39) 39
male (35) 35
pediatrics (33) 33
child (26) 26
child, preschool (24) 24
children (24) 24
oncology (24) 24
article (23) 23
adolescent (22) 22
infant (20) 20
sickle cell anemia (17) 17
adult (11) 11
hydroxyurea (11) 11
anemia (10) 10
anemia, sickle cell - complications (10) 10
disease (10) 10
infant, newborn (10) 10
analysis (9) 9
anemia, sickle cell - drug therapy (9) 9
antisickling agents - therapeutic use (9) 9
care and treatment (9) 9
hydroxyurea - therapeutic use (9) 9
infants (9) 9
retrospective studies (9) 9
sickle cell disease (9) 9
abridged index medicus (8) 8
health aspects (8) 8
thrombosis (8) 8
follow-up studies (7) 7
hemophilia (7) 7
risk (7) 7
sickle-cell-disease (7) 7
treatment outcome (7) 7
anemia, sickle cell - blood (6) 6
diseases (6) 6
prophylaxis (6) 6
research (6) 6
risk factors (6) 6
therapy (6) 6
young adult (6) 6
young-children (6) 6
age factors (5) 5
childhood (5) 5
management (5) 5
medicine, general & internal (5) 5
peripheral vascular disease (5) 5
prevention (5) 5
risk-factors (5) 5
severity of illness index (5) 5
trial (5) 5
anemia, sickle cell - surgery (4) 4
cancer (4) 4
hematology, oncology and palliative medicine (4) 4
hemoglobins - metabolism (4) 4
patient compliance (4) 4
public, environmental & occupational health (4) 4
quality of life (4) 4
splenectomy - methods (4) 4
surgery (4) 4
thalassemia (4) 4
united-states (4) 4
venous thromboembolism (4) 4
adult patients (3) 3
adults (3) 3
anemia, sickle cell - physiopathology (3) 3
anemia, sickle cell - therapy (3) 3
antisickling agents - administration & dosage (3) 3
antisickling agents - adverse effects (3) 3
bleeding (3) 3
blood transfusion (3) 3
children & youth (3) 3
clinical trials, phase iii as topic (3) 3
cohort studies (3) 3
complications and side effects (3) 3
congenital hemolytic anemia (3) 3
double-blind method (3) 3
efficacy (3) 3
experience (3) 3
factor-viii (3) 3
follow-up (3) 3
health risk assessment (3) 3
health-related quality of life (3) 3
hemic and lymphatic diseases (3) 3
hemoglobinopathy (3) 3
hereditary spherocytosis (3) 3
hospitalization - statistics & numerical data (3) 3
hydroxyurea - administration & dosage (3) 3
hydroxyurea - adverse effects (3) 3
malaria (3) 3
medicine (3) 3
middle aged (3) 3
mortality (3) 3
mutation (3) 3
obstetrics & gynecology (3) 3
partial splenectomy (3) 3
pilot projects (3) 3
pregnancy (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Pediatric Blood & Cancer, ISSN 1545-5009, 12/2018, Volume 65, Issue 12, pp. e27466 - n/a
Previously untreated patients with severe hemophilia A are a vulnerable population at risk for severe bleeding which is currently managed with exogenous... 
factor replacement | hemophilia | inhibitor | prophylaxis | genotyping | IMMUNOLOGICAL DANGER SIGNALS | MANAGEMENT | TOLERANCE | FACTOR-VIII | PREVENTION | THERAPY | ONCOLOGY | PEDIATRICS | INHIBITOR DEVELOPMENT | EMICIZUMAB PROPHYLAXIS | OUTCOMES | HEMATOLOGY | LIFE | Analysis | Blood coagulation factor VIII | Hemophilia | Inhibitors | Decision making | Patients | Bleeding | Clotting
Journal Article
BLOOD, ISSN 0006-4971, 05/2019, Volume 133, Issue 19, pp. 2010 - 2011
In this issue of Blood, De Franceschi et al summarize the recent refugee crisis affecting southern Europe, from the standpoint of providing care for refugees... 
HEMATOLOGY
Journal Article
Pediatric blood & cancer, ISSN 1545-5009, 09/2019, p. e27982
Unique expertise is required for the care of children, adolescents, and young adults with bleeding and clotting disorders. A number of Hemophilia Treatment... 
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 06/2018, Volume 65, Issue 6, pp. e27000 - n/a
Sickle cell disease (SCD) is an inherited red blood cell disorder that occurs worldwide and results in significant morbidity and mortality. In addition to... 
migrant health | immigration | international adoption | sickle cell disease | CANADA | HYDROXYUREA | TRANSPLANTATION | ONCOLOGY | PEDIATRIC-PATIENTS | MALARIA | PEDIATRICS | EXPERIENCE | ANEMIA | HEMATOLOGY | PROGRAM | REFUGEES | PARADIGM | Emigration and immigration | Intercountry adoption | Sickle cell anemia
Journal Article
Lancet, The, ISSN 0140-6736, 2011, Volume 377, Issue 9778, pp. 1663 - 1672
Journal Article
American Journal of Physiology-Cell Physiology, ISSN 0363-6143, 12/2013, Volume 305, Issue 12, pp. C1209 - C1210
Journal Article
Haemophilia, ISSN 1351-8216, 01/2019, Volume 25, Issue 1, pp. e48 - e50
Journal Article
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 22, pp. 4304 - 4310
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 06/2016, Volume 63, Issue 6, pp. 1031 - 1037
The Patient Reported Outcomes Measurement Information System (PROMIS®) has developed pediatric self-report scales measuring several unidimensional health... 
health‐related quality of life | PROMIS | sickle cell disease | Sickle cell disease | Health-related quality of life | Anemia, Sickle Cell - complications | Humans | Self Report | Adolescent | Quality of Life | Female | Male | Surveys and Questionnaires | Patient Outcome Assessment | Child | Pediatrics | Sickle cell anemia | Children | Health aspects | Analysis | Data entry
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2013, Volume 110, Issue 2, pp. 588 - 593
Journal Article
Journal Article
Journal Article