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O06 Heat shock proteins and protein homeostasis in hereditary neuropathies

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S2-S2

Timmerman, V

2014

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Developing 3D SEM in a broad biological context

Journal of microscopy (Oxford), 2015-08, Vol.259 (2), p.80-96

2015

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S.I.3 Molecular genetics of Charcot–Marie–Tooth neuropathies: From mutations to gene interaction networks

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.680-680

Timmerman, V

2011

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MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets

Molecular psychiatry, 2015-04, Vol.20 (4), p.472-481

2015

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O04 New molecular targets in hereditary neuropathies

Neuromuscular disorders : NMD, 2011, Vol.21, p.S2-S2

Timmerman, V

2011

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Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation

Annals of human genetics, 2008-05, Vol.72 (3), p.416-441

2008

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Multimorbidity, control and treatment of non- communicable diseases among primary healthcare attenders in the Western Cape, South Africa

South African Medical Journal, 2015-09, Vol.105 (8), p.642-647

2015

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The effect of social media use on work-related learning

Journal of computer assisted learning, 2014-04, Vol.30 (2), p.159-172

2014

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Dominant GDAP1 mutations cause predominantly mild CMT phenotypes

Neurology, 2011-08, Vol.77 (6), p.540-548

2011

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Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot–Marie–Tooth disease

Brain (London, England : 1878), 2003-03, Vol.126 (3), p.590-597

2003

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Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency

Neurology, 2011-12, Vol.77 (24), p.2105-2114

2011

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Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy

Brain (London, England : 1878), 2009-07, Vol.132 (7), p.1741-1752

2009

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Animal models of Charcot-Marie-Tooth disease and their relevance for understanding the disease in humans

Revue neurologique, 2013-12, Vol.169 (12), p.971-977

2013

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Modèles animaux dans la maladie de Charcot-Marie-Tooth et applications de la compréhension de la maladie chez l’homme

Revue neurologique, 2013-12, Vol.169 (12), p.971-977

2013

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Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy

Neurology, 2002-12, Vol.59 (12), p.1865-1872

2002

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Socioeconomic and modifiable predictors of blood pressure control for hypertension in primary care attenders in the Western Cape, South Africa

SAMJ: South African Medical Journal, 2016-12, Vol.106 (12), p.1241-1246

2016

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Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H

Neurology, 2009-03, Vol.72 (13), p.1160-1164

2009

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Understanding the pathomechanisms of inherited peripheral neuropathies

Journal of the neurological sciences, 2013-10, Vol.333, p.e435-e435

Timmerman, V.

2013

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Next generation sequencing identifies a novel ATP7A mutation in two brothers with distal hereditary motor neuropathy and autonomic dysfunction

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S224-S225

2015

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NeurOmics: EU-funded-omics research for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S298-S299

2015

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Socioeconomic and modifiable predictors of blood pressure control for hypertension in primary care attenders in the Western Cape, South Africa

South African Medical Journal, 2016-12, Vol.106 (12), p.1241

2016

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Consistent Relationships Among Productivity Rate Methods in the NE Subarctic Pacific

Global biogeochemical cycles, 2021-02, Vol.35 (2), p.n/a

2021

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Ocean Ventilation Controls the Contrasting Anthropogenic CO2 Uptake Rates Between the Western and Eastern South Atlantic Ocean Basins

Global biogeochemical cycles, 2022-06, Vol.36 (6), p.n/a

2022

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The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype

Brain (London, England : 1878), 1999-02, Vol.122 (2), p.281-290

1999

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G.P.237

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.888-888

2014

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O06 Heat shock proteins and protein homeostasis in hereditary neuropathies

Developing 3D SEM in a broad biological context

S.I.3 Molecular genetics of Charcot–Marie–Tooth neuropathies: From mutations to gene interaction networks

MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets

O04 New molecular targets in hereditary neuropathies

Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation

Multimorbidity, control and treatment of non- communicable diseases among primary healthcare attenders in the Western Cape, South Africa

The effect of social media use on work-related learning

Dominant GDAP1 mutations cause predominantly mild CMT phenotypes

Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot–Marie–Tooth disease

Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency

Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy

Animal models of Charcot-Marie-Tooth disease and their relevance for understanding the disease in humans

Modèles animaux dans la maladie de Charcot-Marie-Tooth et applications de la compréhension de la maladie chez l’homme

Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy

Socioeconomic and modifiable predictors of blood pressure control for hypertension in primary care attenders in the Western Cape, South Africa

Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H

Understanding the pathomechanisms of inherited peripheral neuropathies

Next generation sequencing identifies a novel ATP7A mutation in two brothers with distal hereditary motor neuropathy and autonomic dysfunction

NeurOmics: EU-funded-omics research for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases

Socioeconomic and modifiable predictors of blood pressure control for hypertension in primary care attenders in the Western Cape, South Africa

Consistent Relationships Among Productivity Rate Methods in the NE Subarctic Pacific

Ocean Ventilation Controls the Contrasting Anthropogenic CO2 Uptake Rates Between the Western and Eastern South Atlantic Ocean Basins

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype

G.P.237

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