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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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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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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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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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Lrrk2 pathogenic substitutions in Parkinson's disease

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

2005

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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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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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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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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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Genomic investigation of α-synuclein multiplication and parkinsonism

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

2008

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Genomewide Association, Parkinson Disease, and PARK10

American journal of human genetics, 2006-06, Vol.78 (6), p.1084-1088

2006

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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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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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Fine-mapping and candidate gene investigation within the PARK10 locus

European journal of human genetics : EJHG, 2009-03, Vol.17 (3), p.336-343

2009

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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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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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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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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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Leucine-rich repeat kinase 1 : a paralog of LRRK2 and a candidate gene for Parkinson's disease

Neurogenetics, 2007-04, Vol.8 (2), p.95-102

2007

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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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Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease

Movement disorders, 2007-02, Vol.22 (3), p.389-392

2007

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

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

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

Public Health Surveillance of Nonmalignant Blood Disorders

Lrrk2 pathogenic substitutions in Parkinson's disease

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

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

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

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

Providers' Perspectives on Treating Patients With Thalassemia

Genomic investigation of α-synuclein multiplication and parkinsonism

Genomewide Association, Parkinson Disease, and PARK10

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

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

Fine-mapping and candidate gene investigation within the PARK10 locus

State-based surveillance for selected hemoglobinopathies

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

Incidence of Sickle Cell Trait — United States, 2010

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

Leucine-rich repeat kinase 1 : a paralog of LRRK2 and a candidate gene for Parkinson's disease

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

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease

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