Publications by authors named "Kate Craig"

16Publications

POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonism.

Ann Clin Transl Neurol 2017 01 16;4(1):4-14. Epub 2016 Nov 16.

Department of Molecular and Human Genetics Baylor College of Medicine Houston Texas.

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January 2017

Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure.

Authors:

Patrick McKiernan Sarah Ball Saikat Santra Katherine Foster Carl Fratter Joanna Poulton Kate Craig Robert McFarland Shamima Rahman Iain Hargreaves Girish Gupte Khalid Sharif Robert W Taylor

J Pediatr Gastroenterol Nutr 2016 12;63(6):592-597

*Liver Unit, Birmingham Children's Hospital †University of Birmingham ‡Department of Clinical IMD §Department of Radiology, Birmingham Children's Hospital, Birmingham ||Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust ¶Nuffield Department of Obstetrics and Gynaecology, University of Oxford #Wellcome Trust Centre for Mitochondrial Research and Highly Specialised Rare Mitochondrial Disease Service, Newcastle University **Genetics and Genomic Medicine, UCL Institute of Child Health, London, United Kingdom.

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December 2016

Ultrasonography in the Assessment of Lateral Ankle Ligament Injury, Instability, and Anterior Ankle Impingement: A Diagnostic Case Report.

Authors:

Patrick J Battaglia Kate Craig Norman W Kettner

J Chiropr Med 2015 Dec 14;14(4):265-9. Epub 2015 Nov 14.

Chair, Department of Radiology, Logan University, Chesterfield, MO.

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December 2015

Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failure.

Authors:

Abdulrahman Al-Hussaini Eissa Faqeih Ayman W El-Hattab Majid Alfadhel Ali Asery Badr Alsaleem Eman Bakhsh Ashraf Ali Ali Alasmari Khurram Lone Ahmed Nahari Wafaa Eyaid Mohammed Al Balwi Kate Craig Anna Butterworth Langping He Robert W Taylor

J Pediatr 2014 Mar 8;164(3):553-9.e1-2. Epub 2013 Dec 8.

Newcastle Mitochondrial Highly Specialized Services Diagnostic Laboratory, Wellcome Trust Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne, United Kingdom.

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March 2014

Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions.

Authors:

Charlotte L Alston Andrew M Schaefer Pravrutha Raman Nicola Solaroli Kim J Krishnan Emma L Blakely Langping He Kate Craig Mark Roberts Aashish Vyas John Nixon Rita Horvath Douglass M Turnbull Anna Karlsson Grainne S Gorman Robert W Taylor

Neurology 2013 Dec 6;81(23):2051-3. Epub 2013 Nov 6.

From Newcastle University (C.L.A., A.M.S., P.R., K.J.K., E.L.B., L.H., K.C., R.H., D.M.T., G.S.G., R.W.T.), Newcastle upon Tyne, UK; Karolinska Institute (N.S., A.K.), Stockholm, Sweden; Hope Hospital (M.R.), Salford; and Royal Preston Hospital (A.V., J.N.), Preston, UK.

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December 2013

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene.

Eur J Hum Genet 2014 Feb 29;22(2):184-91. Epub 2013 May 29.

Nuffield Department of Obstetrics and Gynaecology, University of Oxford The Women's Centre, Oxford, UK.

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February 2014

Pathogenic mitochondrial tRNA point mutations: nine novel mutations affirm their importance as a cause of mitochondrial disease.

Authors:

Emma L Blakely John W Yarham Charlotte L Alston Kate Craig Joanna Poulton Charlotte Brierley Soo-Mi Park Andrew Dean John H Xuereb Kirstie N Anderson Alistair Compston Chris Allen Saba Sharif Peter Enevoldson Martin Wilson Simon R Hammans Douglass M Turnbull Robert McFarland Robert W Taylor

Hum Mutat 2013 Sep;34(9):1260-8

Wellcome Trust Centre for Mitochondrial Research, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, UK.

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September 2013

Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics.

Brain 2012 Nov 29;135(Pt 11):3392-403. Epub 2012 Oct 29.

MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.

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November 2012

Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction?

Authors:

Saskia B Wortmann Michael P Champion Lambert van den Heuvel H Barth B Trutnau Kate Craig Martin Lammens Michiel F Schreuder Robert W Taylor Jan A M Smeitink Ron A Wevers Richard J Rodenburg Eva Morava

Eur J Med Genet 2012 Oct 7;55(10):552-6. Epub 2012 Jul 7.

Nijmegen Centre for Mitochondrial Disorders at the Department of Pediatrics and the Institute of Genetic and Metabolic Disease, Radboud University Medical Centre, PO Box 9101, Huispost 804, Postbus 9101, 6500 HB Nijmegen, The Netherlands.

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October 2012

A p.R369G POLG2 mutation associated with adPEO and multiple mtDNA deletions causes decreased affinity between polymerase γ subunits.

Authors:

Kate Craig Matthew J Young Emma L Blakely Matthew J Longley Douglass M Turnbull William C Copeland Robert W Taylor

Mitochondrion 2012 Mar 4;12(2):313-9. Epub 2011 Dec 4.

Mitochondrial Research Group, Institute for Ageing and Health, The Medical School, Framlington Place, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.

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March 2012

Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome?

Authors:

Kate Craig Yoshihisa Takiyama Bing-Wen Soong Laura B Jardim Maria Luiza Saraiva-Pereira Kieren Lythgow Hiroyuki Morino Hirofumi Maruyama Hideshi Kawakami Patrick F Chinnery

Eur J Hum Genet 2008 Jul 20;16(7):841-7. Epub 2008 Feb 20.

Medical School,University of Newcastle upon Tyne, Newcastle upon Tyne, UK.

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July 2008

The A467T and W748S POLG substitutions are a rare cause of adult-onset ataxia in Europe.

Authors:

Kate Craig Gianfrancesco Ferrari Watcharee Tiangyou Gavin Hudson Cinzia Gellera Massimo Zeviani Patrick F Chinnery

Brain 2007 Apr;130(Pt 4):E69; author reply E70

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April 2007

Differential selection of acridine resistance mutations in human DNA topoisomerase IIbeta is dependent on the acridine structure.

Authors:

Chrysoula Leontiou Gary P Watters Kathryn L Gilroy Pauline Heslop Ian G Cowell Kate Craig Robert N Lightowlers Jeremy H Lakey Caroline A Austin

Mol Pharmacol 2007 Apr 5;71(4):1006-14. Epub 2007 Jan 5.

The Institute for Cell and Molecular Biosciences, The Medical School, Newcastle University, Framlington Place, Newcastle Upon Tyne, NE2 4HH, United Kingdom.

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April 2007

Patterning lines by capillary flows.

Authors:

Saurabh Vyawahare Kate M Craig Axel Scherer

Nano Lett 2006 Feb;6(2):271-6

Thomas J. Watson, Sr. Laboratories of Applied Physics, California Institute of Technology, Pasadena, California 91125, USA.

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February 2006

Minimum prevalence of spinocerebellar ataxia 17 in the north east of England.

Authors:

Kate Craig Sharon M Keers Timothy J Walls Anne Curtis Patrick F Chinnery

J Neurol Sci 2005 Dec 11;239(1):105-9. Epub 2005 Oct 11.

Neurology, The University of Newcastle upon Tyne, United Kingdom.

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December 2005

Molecular epidemiology of spinocerebellar ataxia type 6.

Authors:

Kate Craig Sharon M Keers Kate Archibald Ann Curtis Patrick F Chinnery

Ann Neurol 2004 May;55(5):752-5

Neurology, University Newcastle upon Tyne, United Kingdom.

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May 2004