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American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults

Blood advances, 2020-04, Vol.4 (8), p.1554-1588

2020

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5610107 LIVE OUTCOMES AND BIOMETRIC MONITORING: POTENTIAL IMPLICATIONS FOR PATIENT QUALITY OF LIFE IN SICKLE CELL DISEASE

HemaSphere, 2023-04, Vol.7 (S1), p.54-54

2023

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5609968 REAL‐WORLD PATIENT‐REPORTED OUTCOMES AND WEARABLE METRIC CORRELATIONS: REMOTE DAILY MONITORING FOR EXPLORATION OF QUALITY OF LIFE IN SICKLE CELL DISEASE

HemaSphere, 2023-04, Vol.7 (S1), p.8-9

2023

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5613396 DIFFERENCE IN HOSPITALIZATIONS AND ANNUAL BED DAYS FOR PATIENTS WITH SICKLE CELL DISEASE BY VARYING LEVELS OF ANEMIA: A RETROSPECTIVE ANALYSIS OF LINKED PRIMARY AND SECONDARY CARE DATABASES IN ENGLAND

HemaSphere, 2023-04, Vol.7 (S1), p.32-33

2023

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P‐037: EXPLORATION OF THE REAL‐WORLD IMPACTS OF SLEEP UPON QUALITY OF LIFE IN PATIENTS WITH SICKLE CELL DISEASE

HemaSphere, 2022-08, Vol.6 (Suppl), p.35-35

2022

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Hepatic iron concentration combined with long‐term monitoring of serum ferritin to predict complications of iron overload in thalassaemia major

British journal of haematology, 2000-09, Vol.110 (4), p.971-977

2000

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5613294 BASELINE PATIENT CHARACTERISTICS FROM A UK EARLY ACCESS TO MEDICINES SCHEME (EAMS) WITH VOXELOTOR, A HBS POLYMERIZATION INHIBITOR, FOR THE TREATMENT OF HEMOLYTIC ANEMIA DUE TO SICKLE CELL DISEASE

HemaSphere, 2023-04, Vol.7 (S1), p.16-17

2023

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Quality of Life in Thalassemia

Annals of the New York Academy of Sciences, 2005-01, Vol.1054 (1), p.273-282

2005

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P131: REAL‐TIME VACCINATION IMPACTS IN SICKLE CELL DISEASE: A REAL‐WORLD PATIENT CASE STUDY FOR INFLUENZA AND COVID‐19 VACCINATION

HemaSphere, 2022-01, Vol.6 (Suppl), p.32-33

2022

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A Serological Survey of Ebola Virus Infection in Central African Nonhuman Primates

The Journal of infectious diseases, 2004-12, Vol.190 (11), p.1895-1899

2004

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P1488: ASSOCIATION BETWEEN HEMOGLOBIN LEVELS AND END‐ORGAN DAMAGE IN SICKLE CELL DISEASE: A RETROSPECTIVE LINKED PRIMARY AND SECONDARY CARE DATABASE ANALYSIS IN ENGLAND

HemaSphere, 2022-06, Vol.6 (Suppl), p.1370-1371

2022

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P1493: CHRONIC COMPLICATIONS IN THE EAST LONDON SICKLE NEWBORN COHORT STUDY (ELSNCS)

HemaSphere, 2022-06, Vol.6 (Suppl), p.1375-1376

2022

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Intranasal diamorphine for acute sickle cell pain

Archives of disease in childhood, 2009-12, Vol.94 (12), p.979-980

2009

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Guidelines for the management of the acute painful crisis in sickle cell disease

British journal of haematology, 2003-03, Vol.120 (5), p.744-752

2003

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Deferasirox for the treatment of iron overload associated with regular blood transfusions (transfusional haemosiderosis) in patients suffering with chronic anaemia: a systematic review and economic evaluation

Health technology assessment (Winchester, England), 2009-01, Vol.13 (1), p.iii

2009

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Molecular evidence for deep phylogenetic divergence in Mandrillus sphinx

Molecular ecology, 2003-07, Vol.12 (7), p.2019-2024

2003

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S110: ACUTE AND CHRONIC PAIN MANAGEMENT IN SICKLE CELL DISEASE: OUTCOMES OF AN ENGLISH NATIONAL AUDIT

HemaSphere, 2022-01, Vol.6 (Suppl), p.6-6

2022

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S118: LONG‐TERM SAFETY AND EFFICACY OF VOXELOTOR FOR PATIENTS WITH SICKLE CELL DISEASE: RESULTS FROM AN OPEN‐LABEL EXTENSION OF THE PHASE 3 HOPE TRIAL

HemaSphere, 2022-01, Vol.6 (Suppl), p.9-10

2022

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Wild Mandrillus sphinx Are Carriers of Two Types of Lentivirus

Journal of Virology, 2001-08, Vol.75 (15), p.7086-7096

2001

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5613396 DIFFERENCE IN HOSPITALIZATIONS AND ANNUAL BED DAYS FOR PATIENTS WITH SICKLE CELL DISEASE BY VARYING LEVELS OF ANEMIA: A RETROSPECTIVE ANALYSIS OF LINKED PRIMARY AND SECONDARY CARE DATABASES IN ENGLAND

HemaSphere, 2023-04, Vol.7, p.32-33

2023

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Exagamglogene Autotemcel for Severe Sickle Cell Disease

The New England journal of medicine, 2024-05, Vol.390 (18), p.1649-1662

2024

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The progression of HCV‐associated liver disease in a cohort of haemophilic patients

British journal of haematology, 1994-07, Vol.87 (3), p.555-561

1994

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molecular diagnostic for identifying central African forest artiodactyls from faecal pellets

Animal conservation, 2010, Vol.13 (1), p.80-93

2010

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Sickle cell disease pain in London and the Caribbean

Archives of disease in childhood, 2004-03, Vol.89 (3), p.272-273

2004

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Human immunodeficiency virus type 2 (HIV-2) seroprevalence and characterization of a distinct HIV-2 genetic subtype from the natural range of simian immunodeficiency virus-infected sooty mangabeys

Journal of Virology, 1997-05, Vol.71 (5), p.3953-3960

1997

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American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults

5610107 LIVE OUTCOMES AND BIOMETRIC MONITORING: POTENTIAL IMPLICATIONS FOR PATIENT QUALITY OF LIFE IN SICKLE CELL DISEASE

5609968 REAL‐WORLD PATIENT‐REPORTED OUTCOMES AND WEARABLE METRIC CORRELATIONS: REMOTE DAILY MONITORING FOR EXPLORATION OF QUALITY OF LIFE IN SICKLE CELL DISEASE

5613396 DIFFERENCE IN HOSPITALIZATIONS AND ANNUAL BED DAYS FOR PATIENTS WITH SICKLE CELL DISEASE BY VARYING LEVELS OF ANEMIA: A RETROSPECTIVE ANALYSIS OF LINKED PRIMARY AND SECONDARY CARE DATABASES IN ENGLAND

P‐037: EXPLORATION OF THE REAL‐WORLD IMPACTS OF SLEEP UPON QUALITY OF LIFE IN PATIENTS WITH SICKLE CELL DISEASE

Hepatic iron concentration combined with long‐term monitoring of serum ferritin to predict complications of iron overload in thalassaemia major

5613294 BASELINE PATIENT CHARACTERISTICS FROM A UK EARLY ACCESS TO MEDICINES SCHEME (EAMS) WITH VOXELOTOR, A HBS POLYMERIZATION INHIBITOR, FOR THE TREATMENT OF HEMOLYTIC ANEMIA DUE TO SICKLE CELL DISEASE

Quality of Life in Thalassemia

P131: REAL‐TIME VACCINATION IMPACTS IN SICKLE CELL DISEASE: A REAL‐WORLD PATIENT CASE STUDY FOR INFLUENZA AND COVID‐19 VACCINATION

A Serological Survey of Ebola Virus Infection in Central African Nonhuman Primates

P1488: ASSOCIATION BETWEEN HEMOGLOBIN LEVELS AND END‐ORGAN DAMAGE IN SICKLE CELL DISEASE: A RETROSPECTIVE LINKED PRIMARY AND SECONDARY CARE DATABASE ANALYSIS IN ENGLAND

P1493: CHRONIC COMPLICATIONS IN THE EAST LONDON SICKLE NEWBORN COHORT STUDY (ELSNCS)

Intranasal diamorphine for acute sickle cell pain

Guidelines for the management of the acute painful crisis in sickle cell disease

Deferasirox for the treatment of iron overload associated with regular blood transfusions (transfusional haemosiderosis) in patients suffering with chronic anaemia: a systematic review and economic evaluation

Molecular evidence for deep phylogenetic divergence in Mandrillus sphinx

S110: ACUTE AND CHRONIC PAIN MANAGEMENT IN SICKLE CELL DISEASE: OUTCOMES OF AN ENGLISH NATIONAL AUDIT

S118: LONG‐TERM SAFETY AND EFFICACY OF VOXELOTOR FOR PATIENTS WITH SICKLE CELL DISEASE: RESULTS FROM AN OPEN‐LABEL EXTENSION OF THE PHASE 3 HOPE TRIAL

Wild Mandrillus sphinx Are Carriers of Two Types of Lentivirus

5613396 DIFFERENCE IN HOSPITALIZATIONS AND ANNUAL BED DAYS FOR PATIENTS WITH SICKLE CELL DISEASE BY VARYING LEVELS OF ANEMIA: A RETROSPECTIVE ANALYSIS OF LINKED PRIMARY AND SECONDARY CARE DATABASES IN ENGLAND

Exagamglogene Autotemcel for Severe Sickle Cell Disease

The progression of HCV‐associated liver disease in a cohort of haemophilic patients

molecular diagnostic for identifying central African forest artiodactyls from faecal pellets

Sickle cell disease pain in London and the Caribbean

Human immunodeficiency virus type 2 (HIV-2) seroprevalence and characterization of a distinct HIV-2 genetic subtype from the natural range of simian immunodeficiency virus-infected sooty mangabeys

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