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Anita Inwood

Observed names: A. Inwood, AC Inwood, Inwood, Anita
Observed institutions: Mater Health Services, Royal Children's Hospital, The University of Queensland, Mater Children's Hospital, Mater Adult Hospital, Children's Health Queensland Hospital and Health Service
ORCID: 0000-0002-2558-7456
Observed ORCID: 0000-0002-2558-7456
OpenAlex ID: A5113889349
Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age–a sibling control study
2009 · JJ McGill, AC Inwood, et al. · Clinical Genetics · 174
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations
2016 · Seema R. Lalani, Pengfei Liu, et al. · The American Journal of Human Genetics · 143
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Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis
2018 · David Coman, Lisenka E.L.M. Vissers, et al. · The American Journal of Human Genetics · 42
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The collective burden of childhood dementia: a scoping review
2023 · Kristina L Elvidge, John Christodoulou, et al. · Brain · 33
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Psychosocial functioning in children with phenylketonuria: Relationships between quality of life and parenting indicators
2019 · Alina Morawska, Amy E. Mitchell, et al. · Child Care Health and Development · 33
Overcoming the barriers to diagnosis of Morquio A syndrome
2014 · Kaustuv Bhattacharya, Shanti Balasubramaniam, et al. · Orphanet Journal of Rare Diseases · 28
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Systematic literature review of the somatic comorbidities experienced by adults with phenylketonuria
2024 · Kaleigh B. Whitehall, Sarah Rose, et al. · Orphanet Journal of Rare Diseases · 24
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Undiagnosed Phenylketonuria Can Exist Everywhere: Results From an International Survey
2021 · Annemiek M.J. van Wegberg, Friedrich Trefz, et al. · The Journal of Pediatrics · 20
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Expert Consensus on the Long-Term Effectiveness of Medical Nutrition Therapy and Its Impact on the Outcomes of Adults with Phenylketonuria
2023 · Júlio César Rocha, Kirsten K. Ahring, et al. · Nutrients · 15
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Molecular genetic analysis of candidate genes for glutaric aciduria type II in a cohort of patients from Queensland, Australia
2024 · Kalliope Demetriou, Janelle Nisbet, et al. · Molecular Genetics and Metabolism · 14
Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI)
2015 · Yew Sing Choy, Kaustuv Bhattacharya, et al. · Molecular Genetics and Metabolism · 14
Triple P for Parents of Children with Phenylketonuria: A Nonrandomized Trial
2020 · Amy E Mitchell, Alina Morawska, et al. · Journal of Pediatric Psychology · 11
Effect of long-term sepiapterin treatment on dietary phenylalanine tolerance in patients with phenylketonuria: Interim results from the phase 3 APHENITY Extension Study
2026 · Francjan van Spronsen, Heidi Peters, et al. · Genetics in Medicine · 8
Meta-analysis of bone mineral density in adults with phenylketonuria
2024 · Júlio C. Rocha, Álvaro Hermida, et al. · Orphanet Journal of Rare Diseases · 7
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Efficacy and safety of sepiapterin versus sapropterin in patients with phenylketonuria: Results from the Phase 3, randomized, crossover, open-label, active-controlled AMPLIPHY trial
2026 · Maria Giżewska, Anita Inwood, et al. · Metabolism · 6
Pharmacodynamics, safety, tolerability and pharmacokinetics of a single oral dose of an engineered phenylalanine ammonia-lyase in patients with phenylketonuria
2023 · Timothy Nicholas Fazio, Louise Healy, et al. · Molecular Genetics and Metabolism Reports · 4
N‐acetylglutamate synthase deficiency with associated 3‐methylglutaconic aciduria: A case report
2022 · Arthavan Selvanathan, Kalliope Demetriou, et al. · JIMD Reports · 3
Clinician experience, perceptions, and acceptance of paediatric complex care nurse practitioner roles
2020 · Anita Inwood, Leanne Philips, et al. · Collegian Journal of the Royal College of Nursing Australia · 2
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Abnormal Newborn Screening Resembling Carnitine Palmitoyltransferase 1a Deficiency in Three Patients With COASY Protein Associated Neurodegeneration
2026 · Matthew Lynch, Sophie Manoy, et al. · JIMD Reports · 1
Antenatal and Neonatal Management of Siblings With Carbonic Anhydrase VA Deficiency
2026 · Sophie Manoy, Tahlee Minto, et al. · JIMD Reports · 1
Effects of commencing sapropterin therapy on quality of life for children with phenylketonuria and their families: a qualitative interview study
2024 · Amy Mitchell, Alina Morawska, et al. · Australian journal of advanced nursing · 1
Changes in Child Behaviour Following a Brief Parenting Intervention (Triple P) for Families of Children with Phenylketonuria (PKU): A Case Series
2026 · Grace Kirby, Alina Morawska, et al. · Behavior Modification
Efficacy and safety of sepiapterin versus sapropterin in patients with phenylketonuria
2026 · Giżewska, Maria, Inwood, Anita, et al. · DiRROS repository (University of Maribor)
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A Case Series of Sudden Death in Children Aged 12 Months to 4 Years From LPIN1 Deficiency and PPA2 Deficiency in Queensland
2026 · Sophie Manoy, Sally Smith, et al. · Journal of Paediatrics and Child Health
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Neurocognitive outcomes in phenylketonuria: bridging hemispheres in a first exploratory comparison between Australia and the Netherlands
2026 · S. Haitjema, E.M. van Steenis, et al. · SSRN Electronic Journal
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Works count: 41
Citation count: 584
H-index: 11
I10-index: 12
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