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Associations between birth weight and adult apolipoproteins: The LifeGene cohort

PloS one, 2024-03, Vol.19 (3), p.e0299725-e0299725

2024

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P‐017: POINT‐OF‐CARE DIAGNOSTIC FOR QUANTIFICATION OF FOETAL HAEMOGLOBIN (HB F) LEVELS IN MONITORING HYDROXYUREA THERAPY FOR CHILDREN WITH SICKLE CELL DISEASE (SCD) IN GHANA

HemaSphere, 2022-08, Vol.6 (Suppl), p.25-25

2022

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Risk of disability among adult leprosy cases and determinants of delay in diagnosis in five states of India: A case-control study

PLoS neglected tropical diseases, 2019-06, Vol.13 (6), p.e0007495-e0007495

2019

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Synthesis of findings from the literature and a qualitative research study on the impacts of gender, disability, and ethnicity in Neglected Tropical Diseases programs

PLoS neglected tropical diseases, 2023-12, Vol.17 (12), p.e0011782-e0011782

2023

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5612992 SICKLE CELL HEALTH AWARENESS, PERSPECTIVES, AND EXPERIENCES (SHAPE) SURVEY: FINDINGS ON THE BURDEN OF SICKLE CELL DISEASE AND IMPACT ON THE QUALITY OF LIFE OF PATIENTS AND CAREGIVERS IN THE UK

HemaSphere, 2023-04, Vol.7 (S1), p.10-11

2023

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S129: IMPLEMENTATION OF HYDROXYUREA THERAPY FOR SICKLE CELL DISEASE ON A LARGE SCALE IN GHANA

HemaSphere, 2022-01, Vol.6 (Suppl), p.16-16

2022

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Active case detection methods for crusted scabies and leprosy: A systematic review

PLoS neglected tropical diseases, 2021-07, Vol.15 (7), p.e0009577-e0009577

2021

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P1487: SICKLE CELL HEALTH AWARENESS, PERSPECTIVES AND EXPERIENCES (SHAPE) SURVEY: FINDINGS ON THE BURDEN OF SICKLE CELL DISEASE ON PATIENTS AND THEIR UNMET NEEDS AS REPORTED BY HEALTHCARE PROFESSIONALS

HemaSphere, 2022-06, Vol.6 (Suppl), p.1369-1370

2022

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Altered composition and functional profile of high-density lipoprotein in leprosy patients

PLoS neglected tropical diseases, 2020-03, Vol.14 (3), p.e0008138-e0008138

2020

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Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations

Journal of medical genetics, 2011-09, Vol.48 (9), p.618-628

2011

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O‐10: SICKLE CELL HEALTH AWARENESS, PERSPECTIVES AND EXPERIENCES (SHAPE) SURVEY: FINDINGS ON THE BURDEN OF SICKLE CELL DISEASE AND UNMET NEEDS AS REPORTED BY PATIENTS AND CAREGIVERS

HemaSphere, 2022-08, Vol.6 (Suppl), p.06-07

2022

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P‐002: MULTISPECTRAL IMAGING FOR MICROCHIP ELECTROPHORESIS ENABLES POINT‐OF‐CARE NEWBORN HEMOGLOBIN VARIANT SCREENING

HemaSphere, 2022-08, Vol.6 (Suppl), p.16-17

2022

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S122: SAFETY AND EFFICACY OF CRIZANLIZUMAB IN ADOLESCENTS WITH SICKLE CELL DISEASE (SCD): INITIAL DATA FROM THE PHASE II, MULTICENTER, OPEN‐LABEL SOLACE‐KIDS TRIAL

HemaSphere, 2022-01, Vol.6 (Suppl), p.12-12

2022

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Molecular, immunological and neurophysiological evaluations for early diagnosis of neural impairment in seropositive leprosy household contacts

PLoS neglected tropical diseases, 2018-05, Vol.12 (5), p.e0006494-e0006494

2018

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Global practices in regard to implementation of preventive measures for leprosy

PLoS neglected tropical diseases, 2017-05, Vol.11 (5), p.e0005399

2017

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Triple oral beta-lactam containing therapy for Buruli ulcer treatment shortening

PLoS neglected tropical diseases, 2019-01, Vol.13 (1), p.e0007126

2019

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Assessing and managing wounds of Buruli ulcer patients at the primary and secondary health care levels in Ghana

PLoS neglected tropical diseases, 2017-02, Vol.11 (2), p.e0005331

2017

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Complement C1q expression in Erythema nodosum leprosum

PLoS neglected tropical diseases, 2018-03, Vol.12 (3), p.e0006321-e0006321

2018

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Defeating re-emerging Alkhurma hemorrhagic fever virus outbreak in Saudi Arabia and worldwide

PLoS neglected tropical diseases, 2018-09, Vol.12 (9), p.e0006707-e0006707

2018

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Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer

PLoS neglected tropical diseases, 2018-04, Vol.12 (4), p.e0006429-e0006429

2018

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Implementing active community-based surveillance-response system for Buruli ulcer early case detection and management in Ghana

PLoS neglected tropical diseases, 2018-09, Vol.12 (9), p.e0006776-e0006776

2018

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Understanding perceptions on 'Buruli' in northwestern Uganda: A biosocial investigation

PLoS neglected tropical diseases, 2018-07, Vol.12 (7), p.e0006689-e0006689

2018

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Report of a series of 82 cases of Buruli ulcer from Nigeria treated in Benin, from 2006 to 2016

PLoS neglected tropical diseases, 2018-03, Vol.12 (3), p.e0006358-e0006358

2018

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Mycolactone cytotoxicity in Schwann cells could explain nerve damage in Buruli ulcer

PLoS neglected tropical diseases, 2017-08, Vol.11 (8), p.e0005834-e0005834

2017

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Epidemiological survey of central nervous system germ cell tumors in Canadian children

Journal of neuro-oncology, 2007-05, Vol.82 (3), p.289-295

2007

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Associations between birth weight and adult apolipoproteins: The LifeGene cohort

P‐017: POINT‐OF‐CARE DIAGNOSTIC FOR QUANTIFICATION OF FOETAL HAEMOGLOBIN (HB F) LEVELS IN MONITORING HYDROXYUREA THERAPY FOR CHILDREN WITH SICKLE CELL DISEASE (SCD) IN GHANA

Risk of disability among adult leprosy cases and determinants of delay in diagnosis in five states of India: A case-control study

Synthesis of findings from the literature and a qualitative research study on the impacts of gender, disability, and ethnicity in Neglected Tropical Diseases programs

5612992 SICKLE CELL HEALTH AWARENESS, PERSPECTIVES, AND EXPERIENCES (SHAPE) SURVEY: FINDINGS ON THE BURDEN OF SICKLE CELL DISEASE AND IMPACT ON THE QUALITY OF LIFE OF PATIENTS AND CAREGIVERS IN THE UK

S129: IMPLEMENTATION OF HYDROXYUREA THERAPY FOR SICKLE CELL DISEASE ON A LARGE SCALE IN GHANA

Active case detection methods for crusted scabies and leprosy: A systematic review

P1487: SICKLE CELL HEALTH AWARENESS, PERSPECTIVES AND EXPERIENCES (SHAPE) SURVEY: FINDINGS ON THE BURDEN OF SICKLE CELL DISEASE ON PATIENTS AND THEIR UNMET NEEDS AS REPORTED BY HEALTHCARE PROFESSIONALS

Altered composition and functional profile of high-density lipoprotein in leprosy patients

Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations

O‐10: SICKLE CELL HEALTH AWARENESS, PERSPECTIVES AND EXPERIENCES (SHAPE) SURVEY: FINDINGS ON THE BURDEN OF SICKLE CELL DISEASE AND UNMET NEEDS AS REPORTED BY PATIENTS AND CAREGIVERS

P‐002: MULTISPECTRAL IMAGING FOR MICROCHIP ELECTROPHORESIS ENABLES POINT‐OF‐CARE NEWBORN HEMOGLOBIN VARIANT SCREENING

S122: SAFETY AND EFFICACY OF CRIZANLIZUMAB IN ADOLESCENTS WITH SICKLE CELL DISEASE (SCD): INITIAL DATA FROM THE PHASE II, MULTICENTER, OPEN‐LABEL SOLACE‐KIDS TRIAL

Molecular, immunological and neurophysiological evaluations for early diagnosis of neural impairment in seropositive leprosy household contacts

Global practices in regard to implementation of preventive measures for leprosy

Triple oral beta-lactam containing therapy for Buruli ulcer treatment shortening

Assessing and managing wounds of Buruli ulcer patients at the primary and secondary health care levels in Ghana

Complement C1q expression in Erythema nodosum leprosum

Defeating re-emerging Alkhurma hemorrhagic fever virus outbreak in Saudi Arabia and worldwide

Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer

Implementing active community-based surveillance-response system for Buruli ulcer early case detection and management in Ghana

Understanding perceptions on 'Buruli' in northwestern Uganda: A biosocial investigation

Report of a series of 82 cases of Buruli ulcer from Nigeria treated in Benin, from 2006 to 2016

Mycolactone cytotoxicity in Schwann cells could explain nerve damage in Buruli ulcer

Epidemiological survey of central nervous system germ cell tumors in Canadian children

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