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Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons

Annals of neurology, 2006-08, Vol.60 (2), p.253-255

2006

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Where are the stars?

Monthly notices of the Royal Astronomical Society, 2005-10, Vol.362 (4), p.1233-1246

2005

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A novel RAB7 mutation associated with ulcero-mutilating neuropathy

Annals of neurology, 2004-10, Vol.56 (4), p.586-590

2004

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High Incidence of Spontaneous Disease in an HLA-DR15 and TCR Transgenic Multiple Sclerosis Model

The Journal of immunology (1950), 2005-02, Vol.174 (4), p.1938-1946

2005

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Sural nerve pathology in diabetic patients with minimal but progressive neuropathy

Diabetologia, 2005-03, Vol.48 (3), p.578-585

2005

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The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy

Neuromuscular disorders : NMD, 2009-04, Vol.19 (4), p.264-269

2009

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Coexistent hereditary and inflammatory neuropathy

Brain (London, England : 1878), 2004-01, Vol.127 (1), p.193-202

2004

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Ndrg1 in development and maintenance of the myelin sheath

Neurobiology of disease, 2011-06, Vol.42 (3), p.368-380

2011

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TlpC, a novel chemotaxis protein in Rhodobacter sphaeroides, localizes to a discrete region in the cytoplasm

Molecular microbiology, 2002-12, Vol.46 (5), p.1211-1221

2002

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The phagocytic capacity of neurones

The European journal of neuroscience, 2007-05, Vol.25 (10), p.2947-2955

2007

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Rapid, Sensitive Bioluminescent Reporter Technology for Naphthalene Exposure and Biodegradation

Science (American Association for the Advancement of Science), 1990-08, Vol.249 (4970), p.778-781

1990

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The extracellular matrix of peripheral nerve in diabetic polyneuropathy

Acta neuropathologica, 2000-05, Vol.99 (5), p.539-546

2000

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Mutations in the 5′ region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin

Brain (London, England : 1878), 2001-05, Vol.124 (5), p.907-915

2001

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Effects of nonenzymatic glycosylation of extracellular matrix components on cell survival and sensory neurite extension in cell culture

Journal of neurology, 2002-04, Vol.249 (4), p.424-431

2002

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Professor P. K. Thomas: clinician, investigator, editor and leader--a retrospective appreciation

Brain (London, England : 1878), 2011-02, Vol.134 (Pt 2), p.618-626

2011

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Development of a tool for rapidly assessing the implementation difficulty and emissions benefits of innovations

Technovation, 2012, Vol.32 (1), p.19-31

2012

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The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5 year retrospective study

Journal of neurology, neurosurgery and psychiatry, 2008-12, Vol.79 (12), p.1376-1381

2008

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Myelin and Axon Pathology in a Long-Term Study of PMP22-Overexpressing Mice

Journal of neuropathology and experimental neurology, 2011-05, Vol.70 (5), p.386-398

2011

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N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom

American journal of human genetics, 2000-07, Vol.67 (1), p.47-58

2000

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Apparent bioaccumulation of Mn derived from paper-mill effluent by the freshwater crayfish Cherax destructor: the role of Mn oxidising bacteria

The Science of the total environment, 1999-02, Vol.226 (2-3), p.261-267

1999

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YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit

Human molecular genetics, 2002-05, Vol.11 (9), p.1075-1094

2002

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Chronic inflammatory demyelinating polyradiculoneuropathy with cholesterol deposits in a dog

Journal of veterinary diagnostic investigation, 2015-11, Vol.27 (6), p.762-766

2015

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Autosomal recessive hereditary sensory neuropathy with spastic paraplegia

Brain (London, England : 1878), 1994-08, Vol.117 (4), p.651-659

1994

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Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve

Human molecular genetics, 2003-07, Vol.12 (14), p.1713-1723

2003

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Peripheral nerve abnormalities in the congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome

Acta neuropathologica, 1999-08, Vol.98 (2), p.165-170

1999

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Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons

Where are the stars?

A novel RAB7 mutation associated with ulcero-mutilating neuropathy

High Incidence of Spontaneous Disease in an HLA-DR15 and TCR Transgenic Multiple Sclerosis Model

Sural nerve pathology in diabetic patients with minimal but progressive neuropathy

The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy

Coexistent hereditary and inflammatory neuropathy

Ndrg1 in development and maintenance of the myelin sheath

TlpC, a novel chemotaxis protein in Rhodobacter sphaeroides, localizes to a discrete region in the cytoplasm

The phagocytic capacity of neurones

Rapid, Sensitive Bioluminescent Reporter Technology for Naphthalene Exposure and Biodegradation

The extracellular matrix of peripheral nerve in diabetic polyneuropathy

Mutations in the 5′ region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin

Effects of nonenzymatic glycosylation of extracellular matrix components on cell survival and sensory neurite extension in cell culture

Professor P. K. Thomas: clinician, investigator, editor and leader--a retrospective appreciation

Development of a tool for rapidly assessing the implementation difficulty and emissions benefits of innovations

The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5 year retrospective study

Myelin and Axon Pathology in a Long-Term Study of PMP22-Overexpressing Mice

N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom

Apparent bioaccumulation of Mn derived from paper-mill effluent by the freshwater crayfish Cherax destructor: the role of Mn oxidising bacteria

YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit

Chronic inflammatory demyelinating polyradiculoneuropathy with cholesterol deposits in a dog

Autosomal recessive hereditary sensory neuropathy with spastic paraplegia

Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve

Peripheral nerve abnormalities in the congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome

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