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1

The effect of aerobic exercise on serum creatine kinase activities

Garth A. Nicholson, Graeme J. Morgan, Matthew Meerkin, Eric R. Strauss, Dr. James G. McLeod

Journal:

Year:

1986

Language:

english

File:

PDF, 454 KB

english, 1986

2

Charcot-Marie-Tooth disease: Histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and Connexin32 mutations (CMTX1)

Stefanie Sander, Garth A. Nicholson, Robert A. Ouvrier, James G. McLeod, John D. Pollard

Journal:

Year:

1998

Language:

english

File:

PDF, 693 KB

english, 1998

3

The dominantly inherited motor and sensory neuropathies: Clinical and molecular advances

Garth A. Nicholson

Journal:

Year:

2006

Language:

english

File:

PDF, 188 KB

english, 2006

4

Effect of neural activity on skeletal muscle phosphoproteins

Dr. Garth A. Nicholson, Scott Hawkins, James G. McLeod

Journal:

Year:

1990

Language:

english

File:

PDF, 523 KB

english, 1990

5

Copper deficiency in potato dextrose agar causes reduced pigmentation in cultures of various fungi

Garth W. Griffith, Gary L. Easton, Andrew Detheridge, Kevin Roderick, Arwyn Edwards, Hilary J. Worgan, Jean Nicholson, William T. Perkins

Journal:

FEMS Microbiology Letters

Year:

2007

Language:

english

File:

PDF, 1.19 MB

english, 2007

6

A family with 2 X-linked disorders: Charcot-Marie-Tooth disease and hemophilia A

Nortina Shahrizaila, Khean Jin Goh, Azlina Ahmad-Annuar, Rabia Chaudhry, Carolyn Ly, Monique M. Ryan, Garth Nicholson, Marina Kennerson

Journal:

Year:

2012

Language:

english

File:

PDF, 113 KB

english, 2012

7

Correlation between muscle atrophy on MRI and manual strength testing in hereditary neuropathies

Lana A. del Porto, Garth A. Nicholson, Pon Ketheswaren

Journal:

Journal of Clinical Neuroscience

Year:

2010

Language:

english

File:

PDF, 195 KB

english, 2010

8

Charcot–Marie–Tooth – A Practical Guide, 2nd ed. Researched and written by John Isitt for CMT United Kingdom (2006). Available as CD or loose leaf binder from . £6

Garth Nicholson

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 48 KB

english, 2007

9

Is there acetylcholine receptor in human thymus?

Garth A. Nicholson, Stanley H. Appel

Journal:

Journal of the Neurological Sciences

Year:

1977

Language:

english

File:

PDF, 421 KB

english, 1977

10

Controversies and priorities in amyotrophic lateral sclerosis

Turner, Martin R, Hardiman, Orla, Benatar, Michael, Brooks, Benjamin R, Chio, Adriano, de Carvalho, Mamede, Ince, Paul G, Lin, Cindy, Miller, Robert G, Mitsumoto, Hiroshi, Nicholson, Garth, Ravits, Jo

Journal:

The Lancet Neurology

Year:

2013

Language:

english

File:

PDF, 549 KB

english, 2013

11

Re-analysis of an original CMTX3 family using exome sequencing identifies a known BSCL2 mutation

Chaudhry, Rabia, Kidambi, Aditi, Brewer, Megan Hwa, Antonellis, Anthony, Mathews, Katherine, Nicholson, Garth, Kennerson, Marina

Journal:

Year:

2013

Language:

english

File:

PDF, 176 KB

english, 2013

12

Mutation analysis of MATR3 in Australian familial amyotrophic lateral sclerosis

Fifita, Jennifer A., Williams, Kelly L., McCann, Emily P., O'Brien, Aidan, Bauer, Denis C., Nicholson, Garth A., Blair, Ian P.

Journal:

Neurobiology of Aging

Year:

2015

Language:

english

File:

PDF, 171 KB

english, 2015

13

Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathy

Sawyer, Sarah L., Cheuk-Him Ng, Andy, Innes, A. Micheil, Wagner, Justin D., Dyment, David A., Tetreault, Martine, Majewski, Jacek, Boycott, Kym M., Screaton, Robert A., Nicholson, Garth

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 930 KB

english, 2015

14

Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy

Ghaoui, Roula, Cooper, Sandra T., Lek, Monkol, Jones, Kristi, Corbett, Alastair, Reddel, Stephen W., Needham, Merrilee, Liang, Christina, Waddell, Leigh B., Nicholson, Garth, O’Grady, Gina, Kaur, Simr

Journal:

Year:

2015

Language:

english

File:

PDF, 314 KB

english, 2015

15

Histopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated With Mitofusin 2 Mutations

Vallat, Jean-Michel, Ouvrier, Robert A., Pollard, John D., Magdelaine, Corinne, Zhu, Danqing, Nicholson, Garth A., Grew, Simon, Ryan, Monique M., Funalot, Benoît

Journal:

Journal of Neuropathology and Experimental Neurology

Year:

2008

Language:

english

File:

PDF, 540 KB

english, 2008

16

Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing

Drew, Alexander P., Zhu, Danqing, Kidambi, Aditi, Ly, Carolyn, Tey, Shelisa, Brewer, Megan H., Ahmad-Annuar, Azlina, Nicholson, Garth A., Kennerson, Marina L.

Journal:

Molecular Genetics & Genomic Medicine

Year:

2015

Language:

english

File:

PDF, 195 KB

english, 2015

17

The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 Family

Albulym, Obaid M., Zhu, Danqing, Reddel, Stephen, Kennerson, Marina, Nicholson, Garth

Journal:

Journal of Neurodegenerative Diseases

Year:

2013

Language:

english

File:

PDF, 1.71 MB

english, 2013

18

Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetus

Rudnik-Sch�neborn, Sabine, Nicholson, Garth A., Morgan, Graeme, R�hrig, Dorothee, Zerres, Klaus

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 113 KB

english, 1998

19

Clinical and genetic study of Friedreich ataxia in an Australian population

Delatycki, Martin B., Paris, Damien B.B.P., Gardner, R.J. McKinlay, Nicholson, Garth A., Nassif, Najah, Storey, Elsdon, MacMillan, John C., Collins, Veronica, Williamson, Robert, Forrest, Susan M.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 90 KB

english, 1999

20

Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia

Elsdon Storey, Desiree du Sart, Janet H. Shaw, Peter Lorentzos, Louise Kelly, R.J. McKinley Gardner, Susan M. Forrest, Ivan Biros, Garth A. Nicholson

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 263 KB

english, 2000

21

Variable phenotype of Alzheimer's disease with spastic paraparesis

Margaret J. Smith, John B.J. Kwok, Catriona A. McLean, Jillian J. Kril, G. Anthony Broe, Garth A. Nicholson, Roberto Cappai, Marianne Hallupp, Richard G.H. Cotton, Colin L. Masters, Peter R. Schofield

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 6.37 MB

english, 2001

22

Charcot-Marie-Tooth neuropathy type 1A mutation: Apparent crossovers with D17S122 are due to a duplication

Dr. Garth A. Nicholson, Marina L. Kennerson, Bronya J. B. Keats, Nikola Mesterovic, Wayne Churcher, David Barker, David A. Ross

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 510 KB

english, 1992

23

Tau haplotypes regulate transcription and are associated with Parkinson's disease

John B. J. Kwok, Erdahl T. Teber, Clement Loy, Marianne Hallupp, Garth Nicholson, George D. Mellick, Daniel D. Buchanan, Peter A. Silburn, Peter R. Schofield

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 195 KB

english, 2004

24

Clinical and pathological features of a parkinsonian syndrome in a family with an Ala53Thr α-synuclein mutation

Paul J. Spira, David M. Sharpe, Glenda Halliday, Julie Cavanagh, Garth A. Nicholson

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 549 KB

english, 2001

25

Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutation

Linda J. Valentijn, Robert A. Ouvrier, Norbert H. A. Van Den Bosch, Pieter A. Bolhuis, Frank Baas, Garth A. Nicholson

Journal:

Year:

1995

Language:

english

File:

PDF, 588 KB

english, 1995

26

De novo mutation of the myelin Po gene in Déjérine-Sottas disease (hereditary motor and sensory neuropathy type III): Two amino acid insertion after Asp 118

Tohru Ikegami, Garth Nicholson, Hiroyuki Ikeda, Akihiro Ishida, Heather Johnston, Grahame Wise, Robert Ouvrier, Kiyoshi Hayasaka

Journal:

Year:

1998

Language:

english

File:

PDF, 314 KB

english, 1998

27

Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansion

Danqing Zhu, Christopher Burke, Anthony Leslie, Garth A. Nicholson

Journal:

Movement Disorders

Year:

2002

Language:

english

File:

PDF, 194 KB

english, 2002

28

“Dancing feet dyskinesias”: A clue to parkin gene mutations

Florence C.F. Chang, Prachi Mehta, Brianada Koentjoro, Mark Latt, Nick Blair, Garth Nicholson, Carolyn M. Sue, Victor S.C. Fung

Journal:

Movement Disorders

Year:

2012

Language:

english

File:

PDF, 694 KB

english, 2012

29

Proteolysis and invasiveness of brain tumors: Role of urokinase-type plasminogen activator receptor

Sanjeeva Mohanam, Raymond E. Sawaya, Masaaki Yamamoto, Janet M. Bruner, Garth L. Nicholson, Jasti S. Rao

Journal:

Journal of Neuro-Oncology

Year:

1994

Language:

english

File:

PDF, 1.05 MB

english, 1994

30

A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36

Sumana Gopinath, Ian P. Blair, Marina L. Kennerson, Jennifer C. Durnall, Garth A. Nicholson

Journal:

Year:

2007

Language:

english

File:

PDF, 307 KB

english, 2007

31

Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis

Dennis J. Hulme, Ian P. Blair, Jennifer L. Dawkins, Garth A. Nicholson

Journal:

Year:

2000

Language:

english

File:

PDF, 129 KB

english, 2000

32

Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region

Danqing Zhu, Marina Kennerson, John Merory, Roman Chrast, Mark Verheijen, Greg Lemke, Garth Nicholson

Journal:

Year:

2003

Language:

english

File:

PDF, 177 KB

english, 2003

33

Transcript map of the candidate region for HSNI with cough and gastroesophageal reflux on chromosome 3p and exclusion of candidate genes

Cindy Kok, Marina L. Kennerson, Simon J. Myers, Garth A. Nicholson

Journal:

Year:

2004

Language:

english

File:

PDF, 157 KB

english, 2004

34

Evidence of a founder haplotype refines the X-linked Charcot–Marie-Tooth (CMTX3) locus to a 2.5 Mb region

Megan Brewer, Febriani Changi, Anthony Antonellis, Kurt Fischbeck, Patsie Polly, Garth Nicholson, Marina Kennerson

Journal:

Year:

2008

Language:

english

File:

PDF, 208 KB

english, 2008

35

A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated

Thorsten Hornemann, Anke Penno, Stephane Richard, Garth Nicholson, Fleur S. van Dijk, Annelies Rotthier, Vincent Timmerman, Arnold von Eckardstein

Journal:

Year:

2009

Language:

english

File:

PDF, 238 KB

english, 2009

36

X-linked CMT: genes and gene loci in an Australian cohort

Megan Hwa Brewer, Rabia Chaudhry, Keta McDowall, Shannon Chu, Bartosz Kowalski, Patsie Polly, Garth Nicholson, Marina Kennerson

Journal:

Year:

2010

Language:

english

File:

PDF, 83 KB

english, 2010

37

The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in theFRDAgene

S. M. Forrest, Melanie Knight, Martin B. Delatycki, Damien Paris, Robert Williamson, John King, Leone Yeung, Najah Nassif, Garth A. Nicholson

Journal:

Year:

1998

Language:

english

File:

PDF, 1.37 MB

english, 1998

38

K-RAS MUTATION AND LOSS OF HETEROZYGOSITY OF CHROMOSOME 17P AND SURVIVAL IN COLORECTAL CANCER

Caroline Fung, Tara Bragg, Ronald Newland, Owen Dent, Garth Nicholson, Lesley BOKEY, Pierre Chapuis

Journal:

ANZ Journal of Surgery

Year:

1997

Language:

english

File:

PDF, 620 KB

english, 1997

39

Peripheral neuropathies of infancy

Jo M Wilmshurst, John D Pollard, Garth Nicholson, Jayne Antony

Journal:

Developmental Medicine & Child Neurology

Year:

2003

Language:

english

File:

PDF, 1.10 MB

english, 2003

40

Agroindustrialization through institutional innovation Transaction costs, cooperatives and milk-market development in the east-African highlands

Garth Holloway, Charles Nicholson, Chris Delgado, Steve Staal, Simeon Ehui

Journal:

Agricultural Economics

Year:

2000

Language:

english

File:

PDF, 821 KB

english, 2000

41

A revised Tobit procedure for mitigating bias in the presence of non-zero censoring with an application to milk-market participation in the Ethiopian highlands

Garth Holloway, Charles Nicholson, Chris Delgado, Steve Staal, Simeon Ehui

Journal:

Agricultural Economics

Year:

2004

Language:

english

File:

PDF, 825 KB

english, 2004

42

Mutation Testing in Charcot-Marie-Tooth Neuropathy

GARTH A. NICHOLSON

Journal:

Annals of the New York Academy of Sciences

Year:

1999

File:

PDF, 416 KB

1999

43

10.1038/85879

Dawkins, Jennifer L., Hulme, Dennis J., Brahmbhatt, Sonal B., Auer-Grumbach, Michaela, Nicholson, Garth A.

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 100 KB

english, 2001

44

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

Klein, Christopher J, Botuyan, Maria-Victoria, Wu, Yanhong, Ward, Christopher J, Nicholson, Garth A, Hammans, Simon, Hojo, Kaori, Yamanishi, Hiromitch, Karpf, Adam R, Wallace, Douglas C

Journal:

Nature Genetics

Year:

2011

Language:

english

File:

PDF, 1.39 MB

english, 2011

45

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies

Nicholson, Garth A., Valentijn, Linda J., Cherryson, Annia K., Kennerson, Marina L., Bragg, Tara L., DeKroon, Robert M., Ross, David A., Pollard, John D., Mcleod, James G., Bolhuis, Pieter A.

Journal:

Nature Genetics

Year:

1994

File:

PDF, 412 KB

1994

46

The gene for hereditary sensory neuropathy type I (HSN–I) maps to chromosome 9q22.1–q22.3

Nicholson, Garth A., Dawkins, Jennifer L., Blair, Ian P., Kennerson, Marina L., Gordon, Melissa J., Cherryson, Annia K., Nash, Janet, Bananis, Tessy

Journal:

Nature Genetics

Year:

1996

File:

PDF, 422 KB

1996

47

De novo mutation of the myelin Po gene in Dejerine–Sottas disease (hereditary motor and sensory neuropathy type III)

Hayasaka, Kiyoshi, Himoro, Masato, Sawaishi, Yukio, Nanao, Kenji, Takahashi, Tsutomu, Takada, Goro, Nicholson, Garth A., Ouvrier, Robert A., Tachi, Nobutada

Journal:

Nature Genetics

Year:

1993

File:

PDF, 327 KB

1993

48

Intermediate forms of Charcot-Marie-Tooth neuropathy

Garth Nicholson, Simon Myers

Journal:

NeuroMolecular Medicine

Year:

2006

Language:

english

File:

PDF, 139 KB

english, 2006

49

A revised Tobit procedure for mitigating bias in the presence of non-zero censoring with an application to milk-market participation in the Ethiopian highlands

Garth Holloway, Charles Nicholson, Chris Delgado, Steve Staal, Simeon Ehui

Journal:

Agricultural Economics

Year:

2004

Language:

english

File:

PDF, 115 KB

english, 2004

50

Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy

Marina L. Kennerson, Garth A. Nicholson, Stephen G. Kaler, Bartosz Kowalski, Julian F.B. Mercer, Jingrong Tang, Roxana M. Llanos, Shannon Chu, Reinaldo I. Takata, Carlos E. Speck-Martins, Jonathan Bae

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1.37 MB

english, 2010

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