David Ketteridge

David Ketteridge

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David Ketteridge

David Ketteridge

Publications by authors named "David Ketteridge"

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17Publications

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Tarsal tunnel syndrome in the mucopolysaccharidoses: A case series and literature review.

JIMD Rep 2019 Mar 14;46(1):16-22. Epub 2019 Mar 14.

Department of Genetics and Molecular Pathology Women's and Children's Hospital Adelaide Australia.

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http://dx.doi.org/10.1002/jmd2.12021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498821PMC
March 2019

Presentation of m.3243A>G (MT-TL1; tRNALeu) variant with focal neurology in infancy.

Am J Med Genet A 2015 Nov 20;167A(11):2697-701. Epub 2015 Aug 20.

Department of Paediatrics, School of Paediatrics and Reproductive Health, University of Adelaide, North Adelaide, Australia.

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http://dx.doi.org/10.1002/ajmg.a.37161DOI Listing
November 2015

Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.

Pathology 2014 Jan;46(1):41-5

1Cytogenetics, Department of Genetic Medicine, Directorate of Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, North Adelaide 2Molecular Genetics, Department of Genetic Medicine, Directorate of Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, North Adelaide 3School of Molecular and Biomedical Sciences, The University of Adelaide 4School of Paediatrics and Reproductive Health, The University of Adelaide 5South Australian Clinical Genetics Service, SA Pathology at Women's and Children's Hospital, North Adelaide 6Centre for Disability Health, North East Clinic, Modbury Hospital, Adelaide 7Ashford Medical Centre, Ashford, Adelaide 8Flinders Medical Centre, Bedford Park 9Calvary Hospital, North Adelaide 10Women's and Children's Health Network, North Adelaide 11Parks Community Health Service, Angle Park, South Australia, Australia 12see Acknowledgements for all members.

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http://linkinghub.elsevier.com/retrieve/pii/S003130251630641
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http://dx.doi.org/10.1097/PAT.0000000000000043DOI Listing
January 2014

An overview of intra-articular therapy for mucopolysaccharidosis VI.

J Pediatr Rehabil Med 2010 ;3(1):3-6

Lysosomal Diseases Research Unit, SA Pathology (at Women's and Children's Hospital), North Adelaide, SA, Australia.

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http://dx.doi.org/10.3233/PRM-2010-0101DOI Listing
October 2012

Dietary L-tyrosine supplementation in nemaline myopathy.

J Child Neurol 2008 Jun 13;23(6):609-13. Epub 2007 Dec 13.

Neurosciences Department, The Royal Children's Hospital, Melbourne, Australia.

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http://dx.doi.org/10.1177/0883073807309794DOI Listing
June 2008

Mutational analysis of 105 mucopolysaccharidosis type VI patients.

Hum Mutat 2007 Sep;28(9):897-903

Lysosomal Diseases Research Unit, Department of Genetic Medicine, Children, Youth and Women's Health Service, North Adelaide, South Australia, Australia.

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http://dx.doi.org/10.1002/humu.20534DOI Listing
September 2007

Mutational analysis of mucopolysaccharidosis type VI patients undergoing a phase II trial of enzyme replacement therapy.

Mol Genet Metab 2007 Feb 11;90(2):164-70. Epub 2006 Dec 11.

Lysosomal Diseases Research Unit, Department of Genetic Medicine, Children, Youth and Women's Health Service, North Adelaide, SA 5006, Australia.

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http://linkinghub.elsevier.com/retrieve/pii/S109671920600353
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http://dx.doi.org/10.1016/j.ymgme.2006.10.008DOI Listing
February 2007