Author

Christine Lavery

Observed names: C. A. Lavery, C. Lavery, Christine A Lavery, Lavery C. Christine, Lavery, C., Lavery, Christine

OpenAlex ID: A5108271632

Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document

2015 · Marieke Biegstraaten, Reynir Arngrímsson, et al. · Orphanet Journal of Rare Diseases · 353

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Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

2011 · Maurizio Scarpa, Zsuzsanna Almássy, et al. · Orphanet Journal of Rare Diseases · 245

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The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK

2008 · David Moore, Martin J Connock, et al. · Orphanet Journal of Rare Diseases · 153

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Mortality in Patients with Morquio Syndrome A

2014 · Christine Lavery, Chris Hendriksz · JIMD Reports · 120

Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey

2014 · Christian J Hendriksz, Christine Lavery, et al. · Orphanet Journal of Rare Diseases · 99

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Mortality in patients with Sanfilippo syndrome

2017 · Christine Lavery, Chris J. Hendriksz, et al. · Orphanet Journal of Rare Diseases · 78

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The patient’s view on rare disease trial design – a qualitative study

2019 · C. M. W. Gaasterland, M. C. Jansen – van der Weide, et al. · Orphanet Journal of Rare Diseases · 71

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Recommendations on clinical trial design for treatment of Mucopolysaccharidosis Type III

2017 · Arunabha Ghosh, Elsa Shapiro, et al. · Orphanet Journal of Rare Diseases · 45

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Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell Transplantation

2015 · A. S. Kunin-Batson, E. G. Shapiro, et al. · JIMD Reports · 40

The diagnostic journey of patients with mucopolysaccharidosis I: A real-world survey of patient and physician experiences

2016 · Stefano Bruni, Christine Lavery, et al. · Molecular Genetics and Metabolism Reports · 38

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The Burden Endured by Caregivers of Patients With Morquio A Syndrome

2014 · Christian J. Hendriksz, Christine Lavery, et al. · Journal of Inborn Errors of Metabolism and Screening · 12

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Psychosocial outcomes of bone marrow transplant for individuals affected by Mucopolysaccharidosis I Hurler Disease: patient social competency

2009 · C. Pitt, C. Lavery, et al. · Child Care Health and Development · 12

Mucopolysaccharidosis and Adulthood: Genetics, Inheritance, and Reproductive Options

2018 · Alison Wilson, Christine Lavery, et al. · Journal of Child Science · 4

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Multi-stakeholder engagement leading to access to treatment for MPS IVA (Morquio syndrome type A), a model for the ultra rare disease community

2017 · Charlotte Roberts, Christine Lavery, et al. · Molecular Genetics and Metabolism · 3

32. International patient survey demonstrates treatment satisfaction for mucopolysaccharidosis I

2009 · Gerald F. Cox, Walter Harris, et al. · Molecular Genetics and Metabolism · 3

Impact of elosulfase alfa treatment on patient-reported outcomes in Morquio syndrome type A: Results from the first year of a managed access agreement in England

2018 · Christine Lavery, Simon A. Jones, et al. · Molecular Genetics and Metabolism · 2

Burden of disease suffered by patients with Morquio syndrome type A: results from a patient-reported outcomes survey

2014 · Christian J. Hendriksz, Christine Lavery, et al. · Molecular Genetics and Metabolism · 2

From testimonials to qualitative research embedded in an MPS IIIA observational study

2017 · Samantha Parker, Soraya Bekkali, et al. · Molecular Genetics and Metabolism · 1

Pedigree analysis in patients with Fabry disease: evaluating changes in referral and diagnosis over successive generations

2014 · Christine Lavery, Derralynn Hughes, et al. · Molecular Genetics and Metabolism · 1

On the receiving end of genetic medicine

2020 · Christine Lavery · Garland Science eBooks

A consensus conference for cognitive endpoints for clinical trials and natural history studies in MPS diseases

2018 · Elsa G. Shapiro, Jennifer L. Greenberg, et al. · Molecular Genetics and Metabolism

Patient organisations working in partnership to research the patient experience of rare diseases: The MPS III survey

2018 · Alex Morrison, Michaela Weigl, et al. · Molecular Genetics and Metabolism

Clinical outcomes in Morquio syndrome type A treated with elosulfase alfa: results from the managed access agreement in England

2018 · Derralynn Hughes, Maureen Cleary, et al. · Molecular Genetics and Metabolism

Collaborative working to advance standards of care and the well-being of lysosomal disorder patients and families in the UK

2018 · Tanya Collin-Histed, Christine Lavery, et al. · Molecular Genetics and Metabolism

Raising awareness of lysosomal diseases amongst British medical students

2015 · Christine Lavery, Debra Fine, et al. · Molecular Genetics and Metabolism

Works count: 35

Citation count: 1,282

H-index: 12

I10-index: 12