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Heidi Peters

Showing results (1-10 of 35) with videos related to

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Journal of Inherited Metabolic Disease|September 20, 2014
Screening for cerebrotendinous xanthomatosisJames J Pitt, Heidi Peters
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 22, 2014
Cobalamin E defect, a rare inborn error of vitamin B12 metabolism: value of early diagnosis and treatmentTejaswi Kandula, Heidi Peters, Michael Fahey
Archives of Disease in Childhood. Education and Practice Edition|February 14, 2018
A critically ill child with dark urineAmir Zayegh, Joy Lee, Heidi Peters, et al.
Cognitive Neuropsychology|December 7, 2017
Cognitive and behaviour profiles of children with mucopolysaccharidosis Type IILouise Crowe, Joy Yaplito-Lee, Vicki Anderson, et al.
Physical & Occupational Therapy in Pediatrics|January 1, 2003
The effect of therapeutic horseback riding on gross motor function and gait speed in children who are developmentally delayedPatricia Winchester, Kyla Kendall, Heidi Peters, et al.
Internal Medicine Journal|November 19, 2020
Treatable lysosomal storage diseases in the advent of disease-specific therapyHeidi Peters, Carolyn Ellaway, Kathleen Nicholls, et al.
Paediatric Anaesthesia|March 3, 2012
A retrospective audit of anesthetic techniques and complications in children with mucopolysaccharidosesGeoff Frawley, Daniella Fuenzalida, Susan Donath, et al.
Pediatric Neurology|October 18, 2011
Alpers syndrome with mutations in POLG: clinical and investigative featuresMatthew F Hunter, Heidi Peters, Renato Salemi, et al.
Molecular Genetics and Metabolism|April 16, 2008
Newborn screening for glutaric aciduria type I in Victoria: treatment and outcomeAvihu Boneh, Miriam Beauchamp, Maureen Humphrey, et al.
JIMD Reports|December 26, 2024
Sleep quality in children with hepatic glycogen storage diseases, a prospective observational pilot studyLucas Agnoletto, Moya Vandeleur, Mary White, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|September 20, 2014
Screening for cerebrotendinous xanthomatosisJames J Pitt, Heidi Peters
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 22, 2014
Cobalamin E defect, a rare inborn error of vitamin B12 metabolism: value of early diagnosis and treatmentTejaswi Kandula, Heidi Peters, Michael Fahey
Archives of Disease in Childhood. Education and Practice Edition|February 14, 2018
A critically ill child with dark urineAmir Zayegh, Joy Lee, Heidi Peters, et al.
Cognitive Neuropsychology|December 7, 2017
Cognitive and behaviour profiles of children with mucopolysaccharidosis Type IILouise Crowe, Joy Yaplito-Lee, Vicki Anderson, et al.
Physical & Occupational Therapy in Pediatrics|January 1, 2003
The effect of therapeutic horseback riding on gross motor function and gait speed in children who are developmentally delayedPatricia Winchester, Kyla Kendall, Heidi Peters, et al.
Internal Medicine Journal|November 19, 2020
Treatable lysosomal storage diseases in the advent of disease-specific therapyHeidi Peters, Carolyn Ellaway, Kathleen Nicholls, et al.
Paediatric Anaesthesia|March 3, 2012
A retrospective audit of anesthetic techniques and complications in children with mucopolysaccharidosesGeoff Frawley, Daniella Fuenzalida, Susan Donath, et al.
Pediatric Neurology|October 18, 2011
Alpers syndrome with mutations in POLG: clinical and investigative featuresMatthew F Hunter, Heidi Peters, Renato Salemi, et al.
Molecular Genetics and Metabolism|April 16, 2008
Newborn screening for glutaric aciduria type I in Victoria: treatment and outcomeAvihu Boneh, Miriam Beauchamp, Maureen Humphrey, et al.
JIMD Reports|December 26, 2024
Sleep quality in children with hepatic glycogen storage diseases, a prospective observational pilot studyLucas Agnoletto, Moya Vandeleur, Mary White, et al.
Pageof 4