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VASCULAR SMOOTH MUSCLE CELL PROLIFERATION IN SHR AND WKY RATS: EVIDENCE FOR SPECIFIC DIFFERENCES IN GROWTH INHIBITORY REGULATORY MECHANISMS.
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- Clinical & Experimental Pharmacology & Physiology, 1993, v. 20, n. 5, p. 327, doi. 10.1111/j.1440-1681.1993.tb01696.x
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- Article
Erratum to: Development and validation of the Charcot-Marie-Tooth Disease Infant Scale.
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- 2019
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- journal article
Development and validation of the Charcot-Marie-Tooth Disease Infant Scale.
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- 2018
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- journal article
Health status of boys with Duchenne muscular dystrophy: A parent's perspective.
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- Journal of Paediatrics & Child Health, 2011, v. 47, n. 8, p. 557, doi. 10.1111/j.1440-1754.2011.02022.x
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- Article
L‐carnitine supplementation for muscle weakness and fatigue in children with neurofibromatosis type 1: A Phase 2a clinical trial.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 10, p. 2976, doi. 10.1002/ajmg.a.62392
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- Article
Pilot study of a virtual weight management program for Duchenne muscular dystrophy.
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- Muscle & Nerve, 2024, v. 69, n. 4, p. 459, doi. 10.1002/mus.28065
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- Article
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy.
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- Muscle & Nerve, 2024, v. 69, n. 4, p. 448, doi. 10.1002/mus.28062
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- Article
Hand Impairment and Function in Children and Adolescents With Heritable Disorders of Connective Tissue.
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- American Journal of Occupational Therapy, 2022, v. 76, n. 6, p. 1, doi. 10.5014/ajot.2022.049282
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- Article
Balance impairment in pediatric charcot-marie-tooth disease.
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- 2019
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- journal article
Magnetic resonance imaging of the anterior compartment of the lower leg is a biomarker for weakness, disability, and impaired gait in childhood Charcot-Marie-Tooth disease.
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- 2019
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- journal article
Impact of heritable disorders of connective tissue on daily life of children: Parent perspectives.
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- 2021
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- journal article
An exploratory study into an adapted use of the Alert Program for tic disorder in children.
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- 2019
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- journal article
Phenotypic Variability of Childhood Charcot-Marie-Tooth Disease.
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- JAMA Neurology, 2016, v. 73, n. 6, p. 645, doi. 10.1001/jamaneurol.2016.0171
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- Article
Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedS.
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- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 9, p. 1713, doi. 10.1002/acn3.51145
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- Article
Comparison of 3D scanning versus traditional methods of capturing foot and ankle morphology for the fabrication of orthoses: a systematic review.
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- Journal of Foot & Ankle Research, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13047-020-00442-8
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- Article
Natural history of Charcot-Marie-Tooth disease during childhood.
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- 2017
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- journal article
Proxy‐reported sensory measures for children and adolescents with neurodevelopmental disorders: A systematic review.
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- Developmental Medicine & Child Neurology, 2023, v. 65, n. 2, p. 185, doi. 10.1111/dmcn.15367
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- Article
Providing Australian children and adolescents with equitable access to new and emerging therapies through clinical trials: a call to action.
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- Medical Journal of Australia, 2024, v. 220, n. 3, p. 121, doi. 10.5694/mja2.52191
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- Article
COVID-19 in New South Wales children during 2021: severity and clinical spectrum.
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- Medical Journal of Australia, 2022, v. 217, n. 6, p. 303, doi. 10.5694/mja2.51661
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- Article
Sensory dysregulation in tic disorders is associated with executive dysfunction and comorbidities.
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- 2019
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- journal article
Health-related Quality of Life in Boys With Duchenne Muscular Dystrophy: Agreement Between Parents and Their Sons.
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- Journal of Child Neurology, 2010, v. 25, n. 10, p. 1188, doi. 10.1177/0883073809357624
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Can in-the-moment diary methods measure health-related quality of life in Duchenne muscular dystrophy?
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- 2017
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- journal article
Toll-like receptors in the brain and their potential roles in neuropathology.
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- Immunology & Cell Biology, 2007, v. 85, n. 6, p. 476, doi. 10.1038/sj.icb.7100103
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- Article
Clinical applications of machine learning in predicting 3D shapes of the human body: a systematic review.
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- BMC Bioinformatics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12859-022-04979-2
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- Article
Variations of the human glucocorticoid receptor gene (NR3C1): Pathological and in vitro mutations and polymorphisms(Communicated by Edward G.D. Tuddenham).
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- Human Mutation, 2003, v. 21, n. 6, p. 557, doi. 10.1002/humu.10213
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DNA 2000: International Symposium on the State-of-the-Art in Genetic Analysis, June 1-3, 2000, Boston, U.S.A.
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- Human Mutation, 2000, v. 16, n. 4, p. 364, doi. 10.1002/1098-1004(200010)16:4<364::AID-HUMU9>3.0.CO;2-P
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- Article
Reliability of the Charcot‐Marie‐Tooth functional outcome measure.
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- Journal of the Peripheral Nervous System, 2020, v. 25, n. 3, p. 288, doi. 10.1111/jns.12406
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- Article
Established and novel measures of upper limb impairment in children with Charcot<bold>‐</bold>Marie<bold>‐</bold>tooth disease type 1A and riboflavin transporter deficiency type 2.
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- Journal of the Peripheral Nervous System, 2018, v. 23, n. 1, p. 29, doi. 10.1111/jns.12245
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Handwriting difficulties of children with Charcot-Marie-Tooth disease type 1A.
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- Journal of the Peripheral Nervous System, 2017, v. 22, n. 1, p. 34, doi. 10.1111/jns.12198
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- Article