Jim McGill

Jim McGill

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Jim McGill

Jim McGill

Publications by authors named "Jim McGill"

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25Publications

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Nutrition process improvements for adult inpatients with inborn errors of metabolism using the i-PARIHS framework.

Nutr Diet 2019 Apr 7;76(2):141-149. Epub 2019 Mar 7.

Department of Dietetics and Food Services, Mater Health, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1111/1747-0080.12517DOI Listing
April 2019

Immunoassay interference secondary to therapeutic high-dose biotin: A paediatric case report.

J Paediatr Child Health 2018 May 6;54(5):572-575. Epub 2018 Feb 6.

Department of Chemical Pathology, Pathology Queensland, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1111/jpc.13857DOI Listing
May 2018

GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS.

J Neurol Neurosurg Psychiatry 2018 02 1;89(2):221-222. Epub 2017 Jul 1.

Department of Neuroscience, Rehabilitation and Metabolic Medicine, Lady Cilento Children's Hospital, South Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1136/jnnp-2017-315653DOI Listing
February 2018

Lysosomal storage disorders: A review of the musculoskeletal features.

J Paediatr Child Health 2016 Mar;52(3):262-71

Queensland Paediatric Rheumatology Services, Wesley Hospital, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1111/jpc.13122DOI Listing
March 2016

Executive functioning of 4 children with hyperphenylalaninemia from childhood to adolescence.

Pediatrics 2015 Apr;135(4):e1072-4

Neurometabolic Department, Lady Cilento Children's Hospital, South Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1542/peds.2013-4200DOI Listing
April 2015

Depression, anxiety, and stress in young adults with phenylketonuria: associations with biochemistry.

J Dev Behav Pediatr 2014 Jul-Aug;35(6):388-91

*School of Social Sciences, University of the Sunshine Coast, Maroochydore, Australia; and †Department of Metabolic Medicine, Royal Children's Hospital, Brisbane, Australia.

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http://dx.doi.org/10.1097/DBP.0000000000000072DOI Listing
March 2015

Rare presentation of a treatable disorder: glutaric aciduria type 1.

N Z Med J 2015 Feb 20;128(1409):61-4. Epub 2015 Feb 20.

Gold Coast University Hospital, Level 5, A-Block, 1 Hospital Boulevard, Southport, QLD 4215, Australia.

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February 2015

Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region.

Mol Genet Metab 2012 Sep 20;107(1-2):136-44. Epub 2012 Jul 20.

Department of Pediatrics and Medical Genetics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei 100, Taiwan.

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http://dx.doi.org/10.1016/j.ymgme.2012.07.019DOI Listing
September 2012

Depressive symptoms in adolescents with early and continuously treated phenylketonuria: associations with phenylalanine and tyrosine levels.

Gene 2012 Aug 15;504(2):288-91. Epub 2012 May 15.

School of Social Sciences, University of the Sunshine Coast, QLD 4558, Australia.

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http://dx.doi.org/10.1016/j.gene.2012.05.007DOI Listing
August 2012

Enzyme replacement therapy "drug holiday": results from an unexpected shortage of an orphan drug supply in Australia.

Blood Cells Mol Dis 2011 Jan 1;46(1):107-10. Epub 2010 Jun 1.

School of Paediatrics and Child Health, University of Western Australia, Australia.

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http://dx.doi.org/10.1016/j.bcmd.2010.05.002DOI Listing
January 2011

A preliminary investigation of the role of the phenylalanine:tyrosine ratio in children with early and continuously treated phenylketonuria: toward identification of "safe" levels.

Dev Neuropsychol 2010 ;35(1):57-65

Queensland University of Technology, School of Psychology and Counselling, and Institute of Health and Biomedical Innovation, Brisbane, Australia.

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https://www.tandfonline.com/doi/full/10.1080/875656409033257
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http://dx.doi.org/10.1080/87565640903325725DOI Listing
July 2010

The natural history and osteodystrophy of mucolipidosis types II and III.

J Paediatr Child Health 2010 Jun 29;46(6):316-22. Epub 2010 Mar 29.

Department of Clinical Genetics, The Children's Hospital at Westmead, New South Wales, Australia.

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http://dx.doi.org/10.1111/j.1440-1754.2010.01715.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188554PMC
June 2010

Acute hyperammonemic encephalopathy in adult onset ornithine transcarbamylase deficiency.

Intensive Care Med 2008 Oct 24;34(10):1922-4. Epub 2008 Jul 24.

Intensive Care Unit, Logan Hospital, Cnr Armstrong and Loganlea Rds, Meadowbrook, QLD 4131, Australia.

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http://dx.doi.org/10.1007/s00134-008-1217-2DOI Listing
October 2008

Fourier transform infrared reflectance spectra of latent fingerprints: a biometric gauge for the age of an individual.

J Forensic Sci 2008 Mar 19;53(2):369-76. Epub 2008 Feb 19.

Southeast Missouri Hospital College of Nursing and Health Sciences, Cape Girardeau, MO 63701, USA.

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http://doi.wiley.com/10.1111/j.1556-4029.2007.00649.x
Publisher Site
http://dx.doi.org/10.1111/j.1556-4029.2007.00649.xDOI Listing
March 2008

Congenital disorder of glycosylation type Ia presenting as early-onset cerebellar ataxia in an adult.

Mov Disord 2006 Jun;21(6):869-72

Department of Neurology, Royal Brisbane and Women's Hospital, Brisbane, Australia.

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http://dx.doi.org/10.1002/mds.20804DOI Listing
June 2006

The molecular basis of cystathionine beta-synthase deficiency in Australian patients: genotype-phenotype correlations and response to treatment.

Hum Mutat 2002 Aug;20(2):117-26

Cardiovascular Genetics Laboratory, Prince of Wales Hospital, Randwick, New South Wales, Australia.

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http://dx.doi.org/10.1002/humu.10104DOI Listing
August 2002