Author/Creator: Fuller, Maria - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Fuller, Maria

1. 014 The diagnostic odyssey for fabry disease: ten years experience in testing. Issue 6 (24th May 2018)

Authors:: Dobbins, Julia; Fuller, Maria; Pyragius, Tim; Brion, Kristian; Chin, Sharon; Gurner, Melissa; Pacyna, Janina; Stark, Samantha; Fletcher, Janice M
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 89:Issue 6(2018)
Page Start:: A7
Record Type:: Journal Article
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2. Autologous, lentivirus‐modified, T‐rapa cell "micropharmacies" for lysosomal storage disorders. Issue 4 (17th March 2022)

Authors:: Nagree, Murtaza S; Felizardo, Tania C; Faber, Mary L; Rybova, Jitka; Rupar, C Anthony; Foley, S Ronan; Fuller, Maria; Fowler, Daniel H; Medin, Jeffrey A
Journal:: EMBO molecular medicine
Issue:: Volume 14:Issue 4(2022)
Page Start:: n/a
Record Type:: Journal Article
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3. Chondroitin sulfate disaccharide is a specific and sensitive biomarker for mucopolysaccharidosis type IVA. Issue 1 (30th June 2020)

Authors:: Chin, Sharon J.; Saville, Jennifer T.; McDermott, Belinda K.; Zankl, Andreas; Fletcher, Janice M.; Fuller, Maria
Journal:: JIMD reports
Issue:: Volume 55:Issue 1(2020)
Page Start:: 68
Record Type:: Journal Article
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4. Education, children’s social care and offending : multi-level modelling.: multi-level modelling. (2023)

Other Names:: Fuller, Maria; McNally, Jenny; Great Britain., Department for Education (2010- ).
Record Type:: Book
Extent:: 1 online resource

5. Expanding the clinical utility of glucosylsphingosine for Gaucher disease. Issue 3 (26th November 2019)

Authors:: Saville, Jennifer T.; McDermott, Belinda K.; Chin, Sharon J.; Fletcher, Janice M.; Fuller, Maria
Journal:: Journal of inherited metabolic disease
Issue:: Volume 43:Issue 3(2020)
Page Start:: 558
Record Type:: Journal Article
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6. Fabry cardiomyopathy: missing links from genotype to phenotype. Issue 8 (16th January 2020)

Authors:: Fuller, Maria; Mehta, Atul
Journal:: Heart
Issue:: Volume 106:Issue 8(2020)
Page Start:: 553
Record Type:: Journal Article
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7. Functional assessment of the genetic findings indicating mucopolysaccharidosis type II in the prenatal setting. Issue 1 (26th March 2021)

Authors:: Fuller, Maria; Ketteridge, David
Journal:: JIMD reports
Issue:: Volume 60:Issue 1(2021)
Page Start:: 10
Record Type:: Journal Article
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8. Gaucher's disease in the lipidomics era. (August 2012)

Authors:: Fuller, Maria
Journal:: Clinical lipidology
Issue:: Volume 7:Number 4(2012)
Page Start:: 431
Record Type:: Journal Article
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9. Globoid cell leukodystrophy (Krabbe disease) in a Merino sheep. (January 2019)

Authors:: Lee, Effie; Fuller, Maria; Carr, Mandi; Manavis, Jim; Finnie, John
Journal:: Journal of veterinary diagnostic investigation
Issue:: Volume 31:Number 1(2019:Jan.)
Page Start:: 118
Record Type:: Journal Article
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10. Increased monohexosylceramide levels in the serum of established rheumatoid arthritis patients. (6th December 2019)

Authors:: Miltenberger-Miltenyi, Gabriel; Cruz-Machado, Ana Rita; Saville, Jennifer; Conceição, Vasco A; Calado, Ângelo; Lopes, Inês; Fuller, Maria; Fonseca, João Eurico
Journal:: Rheumatology
Issue:: Volume 59:Number 8(2020)
Page Start:: 2085
Record Type:: Journal Article
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