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Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in England

Molecular genetics and metabolism, 2020-02, Vol.129 (2), p.98-105

2020

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The evolution of pulmonary function in childhood onset Mucopolysaccharidosis type I

Molecular genetics and metabolism, 2021-02, Vol.132 (2), p.94-99

2021

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Molecular testing of 163 patients with Morquio A (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutations

Molecular genetics and metabolism, 2014-06, Vol.112 (2), p.160-170

2014

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Mucopolysaccharidosis type II: Identification of 30 novel mutations among Latin American patients

Molecular genetics and metabolism, 2014-02, Vol.111 (2), p.133-138

2014

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Hematopoietic stem cell transplantation improves the high incidence of neutralizing allo-antibodies observed in Hurler’s syndrome after pharmacological enzyme replacement therapy

Haematologica (Roma), 2012-09, Vol.97 (9), p.1320-1328

2012

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Attenuated mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) due to homozygosity for the p.Y210C mutation in the ARSB gene

Molecular genetics and metabolism, 2011-07, Vol.103 (3), p.300-302

2011

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Biochemical monitoring after haemopoietic stem cell transplant for Hurler syndrome (MPSIH): implications for functional outcome after transplant in metabolic disease

Bone marrow transplantation (Basingstoke), 2007-02, Vol.39 (4), p.207-210

2007

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Juvenile mucopolysaccharidosis plus disease caused by a missense mutation in VPS33A

Human mutation, 2022-12, Vol.43 (12), p.2265-2278

2022

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Enzyme replacement therapy in 12 patients with MPS I-H/S with homozygous p.Leu490Pro mutation

Journal of inherited metabolic disease, 2007-10, Vol.30 (5), p.821-821

2007

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Corrigendum to “Molecular testing of 163 patients with Morquio A (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutations” [Mol. Genet. Metab. 112 (2014) 160–170]

Molecular genetics and metabolism, 2014-11, Vol.113 (3), p.237-237

2014

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Lithogeochemical and Stratigraphic Controls on Gold Mineralization within the Metavolcanic Rocks of the Hoyle Pond Mine, Timmins, Ontario

Economic geology and the bulletin of the Society of Economic Geologists, 2008-09, Vol.103 (6), p.1341-1363

2008

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Clinical procedures step-by-step

The Veterinary Record, 2017, Vol.180 (10), p.254-254

Dower-Tylee, Olivia K. L.

2017

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A pragmatic randomised controlled trial to compare antidepressants with a community-based psychosocial intervention for the treatment of women with postnatal depression: the RESPOND trial

Health technology assessment (Winchester, England), 2010-09, Vol.14 (43), p.iii-iv

2010

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Evidence-based guidelines for treating depressive disorders with antidepressants: A revision of the 2000 British Association for Psychopharmacology guidelines

Journal of psychopharmacology (Oxford), 2008-06, Vol.22 (4), p.343-396

2008

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Genetically regulated multi-omics study for symptom clusters of posttraumatic stress disorder highlights pleiotropy with hematologic and cardio-metabolic traits

Molecular psychiatry, 2022-03, Vol.27 (3), p.1394-1404

2022

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Differential outcomes of patients with thyroid FNA diagnoses of AUS/FLUS with and without nuclear atypia: The potential need for separation in the Bethesda System

Diagnostic cytopathology, 2020-07, Vol.48 (7), p.610-617

2020

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Cost-effectiveness of computerised cognitive-behavioural therapy for anxiety and depression in primary care: Randomised controlled trial

British journal of psychiatry, 2004-07, Vol.185 (1), p.55-62

2004

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Presence and predictors of pain in depression: Results from the FINDER study

Journal of affective disorders, 2010-09, Vol.125 (1), p.53-60

2010

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Anesthesiologist to Patient Communication: A Systematic Review

JAMA network open, 2020-11, Vol.3 (11), p.e2023503-e2023503

2020

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World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for Biological Treatment of Unipolar Depressive Disorders, Part 1: Update 2013 on the acute and continuation treatment of unipolar depressive disorders

The world journal of biological psychiatry, 2013-07, Vol.14 (5), p.334-385

2013

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Male microchimerism in healthy women and women with scleroderma: cells or circulating DNA? A quantitative answer

Blood, 2002-10, Vol.100 (8), p.2845-2851

2002

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Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways

Human molecular genetics, 2022-08, Vol.31 (16), p.2810-2819

2022

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Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes: A Mendelian Randomization Study

Circulation. Genomic and precision medicine, 2020-06, Vol.13 (3), p.e002872-e002872

2020

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RNA sequencing of transformed lymphoblastoid cells from siblings discordant for autism spectrum disorders reveals transcriptomic and functional alterations: Evidence for sex‐specific effects

Autism research, 2017-03, Vol.10 (3), p.439-455

2017

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Male DNA in female donor apheresis and CD34-enriched products

Blood, 2003-11, Vol.102 (10), p.3845-3847

2003

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Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in England

The evolution of pulmonary function in childhood onset Mucopolysaccharidosis type I

Molecular testing of 163 patients with Morquio A (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutations

Mucopolysaccharidosis type II: Identification of 30 novel mutations among Latin American patients

Hematopoietic stem cell transplantation improves the high incidence of neutralizing allo-antibodies observed in Hurler’s syndrome after pharmacological enzyme replacement therapy

Attenuated mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) due to homozygosity for the p.Y210C mutation in the ARSB gene

Biochemical monitoring after haemopoietic stem cell transplant for Hurler syndrome (MPSIH): implications for functional outcome after transplant in metabolic disease

Juvenile mucopolysaccharidosis plus disease caused by a missense mutation in VPS33A

Enzyme replacement therapy in 12 patients with MPS I-H/S with homozygous p.Leu490Pro mutation

Corrigendum to “Molecular testing of 163 patients with Morquio A (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutations” [Mol. Genet. Metab. 112 (2014) 160–170]

Lithogeochemical and Stratigraphic Controls on Gold Mineralization within the Metavolcanic Rocks of the Hoyle Pond Mine, Timmins, Ontario

Clinical procedures step-by-step

A pragmatic randomised controlled trial to compare antidepressants with a community-based psychosocial intervention for the treatment of women with postnatal depression: the RESPOND trial

Evidence-based guidelines for treating depressive disorders with antidepressants: A revision of the 2000 British Association for Psychopharmacology guidelines

Genetically regulated multi-omics study for symptom clusters of posttraumatic stress disorder highlights pleiotropy with hematologic and cardio-metabolic traits

Differential outcomes of patients with thyroid FNA diagnoses of AUS/FLUS with and without nuclear atypia: The potential need for separation in the Bethesda System

Cost-effectiveness of computerised cognitive-behavioural therapy for anxiety and depression in primary care: Randomised controlled trial

Presence and predictors of pain in depression: Results from the FINDER study

Anesthesiologist to Patient Communication: A Systematic Review

World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for Biological Treatment of Unipolar Depressive Disorders, Part 1: Update 2013 on the acute and continuation treatment of unipolar depressive disorders

Male microchimerism in healthy women and women with scleroderma: cells or circulating DNA? A quantitative answer

Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways

Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes: A Mendelian Randomization Study

RNA sequencing of transformed lymphoblastoid cells from siblings discordant for autism spectrum disorders reveals transcriptomic and functional alterations: Evidence for sex‐specific effects

Male DNA in female donor apheresis and CD34-enriched products

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