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The impact of chelation therapy on survival in transfusional iron overload: a meta‐analysis of myelodysplastic syndrome

British journal of haematology, 2014-12, Vol.167 (5), p.720-723

2014

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Defining Sickle Cell Disease Mortality Using a Population-Based Surveillance System, 2004 through 2008

Public health reports (1974), 2016-03, Vol.131 (2), p.367-375

2016

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Providers' Perspectives on Treating Patients With Thalassemia

Journal of pediatric hematology/oncology, 2019-10, Vol.41 (7), p.e421-e426

2019

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Concordance with comprehensive iron assessment, hepatitis A vaccination, and hepatitis B vaccination recommendations among patients with sickle cell disease and thalassaemia receiving chronic transfusions: an analysis from the Centers for Disease Control haemoglobinopathy blood safety project

British journal of haematology, 2021-12, Vol.195 (5), p.e160-e164

2021

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LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study

Lancet neurology, 2008-07, Vol.7 (7), p.591-594

2008

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Genomic investigation of α-synuclein multiplication and parkinsonism

Annals of neurology, 2008-06, Vol.63 (6), p.743-750

2008

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DCTN1 mutations in Perry syndrome

Nature genetics, 2009-02, Vol.41 (2), p.163-165

2009

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Emergency department utilization by Californians with sickle cell disease, 2005–2014

Pediatric blood & cancer, 2017-06, Vol.64 (6), p.np-n/a

2017

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The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia

Genetics in medicine, 2014-01, Vol.16 (1), p.33-39

2014

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Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease

JAMA : the journal of the American Medical Association, 2006-08, Vol.296 (6), p.661

2006

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Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

American journal of human genetics, 2005-04, Vol.76 (4), p.672-680

2005

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Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

Parkinsonism & related disorders, 2007-03, Vol.13 (2), p.89-92

2007

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Using surveillance to determine the number of individuals with sickle cell disease in California and Georgia, 2005-2016

Pediatric hematology and oncology, 2020-11, Vol.37 (8), p.747-751

2020

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Public Health Surveillance of Nonmalignant Blood Disorders

American journal of preventive medicine, 2014-11, Vol.47 (5), p.664-668

2014

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Newborn Screening Practices for Beta-Thalassemia in the United States

International journal of neonatal screening, 2021-12, Vol.7 (4), p.83

2021

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Effectiveness of Clinical Decision Support Based Intervention in the Improvement of Care for Adult Sickle Cell Disease Patients in Primary Care

Journal of the American Board of Family Medicine, 2018-09, Vol.31 (5), p.812-816

2018

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State-based surveillance for selected hemoglobinopathies

Genetics in medicine, 2015-02, Vol.17 (2), p.125-130

2015

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Lrrk2 pathogenic substitutions in Parkinson's disease

Neurogenetics, 2005-12, Vol.6 (4), p.171-177

2005

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Incidence of Sickle Cell Trait — United States, 2010

MMWR. Morbidity and mortality weekly report, 2014-12, Vol.63 (49), p.1155-1158

2014

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Attitudes toward Management of Sickle Cell Disease and Its Complications: A National Survey of Academic Family Physicians

Anemia, 2015-01, Vol.2015 (2015), p.1-6

2015

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Public health implications of sickle cell trait: a report of the CDC meeting

American journal of preventive medicine, 2011-12, Vol.41 (6 Suppl 4), p.S435-S439

2011

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Transferrin Saturation and Hospital Length of Stay and Mortality in Medicare Beneficiaries

Journal of the American Geriatrics Society (JAGS), 2013-01, Vol.61 (1), p.132-136

2013

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Elevated transferrin saturation, health-related quality of life and telomere length

Biometals, 2014-02, Vol.27 (1), p.135-141

2014

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Telomere length and elevated iron: The influence of phenotype and HFE genotype

American journal of hematology, 2013-06, Vol.88 (6), p.492-496

2013

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Iron overload: what is the role of public health?

American journal of preventive medicine, 2011-12, Vol.41 (6 Suppl 4), p.S422-S427

2011

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The impact of chelation therapy on survival in transfusional iron overload: a meta‐analysis of myelodysplastic syndrome

Defining Sickle Cell Disease Mortality Using a Population-Based Surveillance System, 2004 through 2008

Providers' Perspectives on Treating Patients With Thalassemia

Concordance with comprehensive iron assessment, hepatitis A vaccination, and hepatitis B vaccination recommendations among patients with sickle cell disease and thalassaemia receiving chronic transfusions: an analysis from the Centers for Disease Control haemoglobinopathy blood safety project

LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study

Genomic investigation of α-synuclein multiplication and parkinsonism

DCTN1 mutations in Perry syndrome

Emergency department utilization by Californians with sickle cell disease, 2005–2014

The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia

Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease

Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

Using surveillance to determine the number of individuals with sickle cell disease in California and Georgia, 2005-2016

Public Health Surveillance of Nonmalignant Blood Disorders

Newborn Screening Practices for Beta-Thalassemia in the United States

Effectiveness of Clinical Decision Support Based Intervention in the Improvement of Care for Adult Sickle Cell Disease Patients in Primary Care

State-based surveillance for selected hemoglobinopathies

Lrrk2 pathogenic substitutions in Parkinson's disease

Incidence of Sickle Cell Trait — United States, 2010

Attitudes toward Management of Sickle Cell Disease and Its Complications: A National Survey of Academic Family Physicians

Public health implications of sickle cell trait: a report of the CDC meeting

Transferrin Saturation and Hospital Length of Stay and Mortality in Medicare Beneficiaries

Elevated transferrin saturation, health-related quality of life and telomere length

Telomere length and elevated iron: The influence of phenotype and HFE genotype

Iron overload: what is the role of public health?

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