Niamh Finnegan

Allogeneic hematopoietic SCT for alpha-mannosidosis: an analysis of 17 patients

Martin Mynarek, Jakub Tolar, Michael H. Albert et al. · Bone Marrow Transplantation · 2011 · 92 citations

Life Sciences, Hematology, Immunology +8

Response of 33 UK patients with infantile‐onset Pompe disease to enzyme replacement therapy

Alexander Broomfield, Joan Fletcher, James Davison et al. · Journal of Inherited Metabolic Disease · 2015 · 70 citations

Medicine, Neurology, Pediatrics +4

Urine analysis of glucose tetrasaccharide by HPLC; a useful marker for the investigation of patients with Pompe and other glycogen storage diseases

Victoria Manwaring, Helen Prunty, Katie Bainbridge et al. · Journal of Inherited Metabolic Disease · 2011 · 46 citations · Full text

Life Sciences, Biochemistry, Endocrinology +14

Discovery of a new biomarker for the mucopolysaccharidoses (MPS), dipeptidyl peptidase IV (DPP-IV; CD26), by SELDI-TOF mass spectrometry

Clare Beesley, Elisabeth Young, Niamh Finnegan et al. · Molecular Genetics and Metabolism · 2009 · 30 citations

Life Sciences, Biochemistry, Molecular Biology +15

Treatment of mucopolysaccharidosis type II (Hunter syndrome) with idursulfase: the relevance of clinical trial end points

Emma Glamuzina, Emma Fettes, Katie Bainbridge et al. · Journal of Inherited Metabolic Disease · 2011 · 29 citations

Life Sciences, Pathobiology, Molecular Pathology +4