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First report of bacterial leaf spot of Hydrangea in retail nurseries in Belgium caused by strains assigned to a new Xanthomonas hortorum clade

New disease reports, 2021-04, Vol.43 (2), p.n/a

2021

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SP0022 Inflammatory Mediators in Inflammatory Myopathies

Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.7-7

De Paepe, B.

2016

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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C

Journal of neurology, neurosurgery and psychiatry, 2010, Vol.81 (1), p.90-93

2010

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Unfiltering of the Geostationary Earth Radiation Budget (GERB) Data. Part I: Shortwave Radiation

Journal of atmospheric and oceanic technology, 2008-07, Vol.25 (7), p.1087-1105

2008

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Unfiltering of the Geostationary Earth Radiation Budget (GERB) Data. Part II: Longwave Radiation

Journal of atmospheric and oceanic technology, 2008-07, Vol.25 (7), p.1106-1117

2008

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Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome

Acta anaesthesiologica Scandinavica, 2012-04, Vol.56 (4), p.520-525

2012

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Mild early epileptic encephalopathy evolving to spastic paraplegia, neurogenic bladder and generalized slow colon transit in an 18-year old patient with pathogenic mutations in FARS2

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S175-S175

2016

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Test performance study for detection of Ralstonia solanacearum and Clavibacter sepedonicus in potato tubers with TaqMan PCR

Bulletin OEPP, 2020-04, Vol.50 (1), p.177-185

2020

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Pathogenic mutations in TMEM126B, a recently discovered complex I assembly factor, identified in four siblings from two Belgian families

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S174-S175

2016

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The Geostationary Earth Radiation Budget Edition 1 data processing algorithms

Advances in space research, 2008, Vol.41 (11), p.1906-1913

2008

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Inflammatory- and NaCl-induced expression of NFAT5 in muscle cells point to common stress response mechanisms

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S252-S253

2015

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G.P.215

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.881-881

2014

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PP03.14 – 2978: Massive early leukoencephalopathy caused by a pathogenic mutation in IBA57: A new clinical presentation for this recently described gene defect

European journal of paediatric neurology, 2015-05, Vol.19, p.S40-S40

2015

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G.P.21 Proteomic analysis of cultured skin fibroblasts from UCMD patients reveals the involvement of two new cellular pathways

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.828-829

2012

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P1.25. Localization of chemokines and their receptors in muscle tissues from Duchenne muscular dystrophy patients

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.649-649

2011

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P3.26 Analysis of the Giant axonal neuropathy fibroblasts proteome

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.689-689

2011

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P5.41 ATP synthase deficiency: A diagnostic strategy for not such an uncommon cause of OXPHOS dysfunction

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.736-736

2011

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Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects

Journal of clinical pathology, 2009-02, Vol.62 (2), p.172-176

2009

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P.10Growth differentiation factor-15 as a novel biomarker for idiopathic inflammatory myopathies

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S44-S44

2019

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205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2015-03, Vol.25 (3), p.268-272

2015

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Role of cytokines and chemokines in idiopathic inflammatory myopathies

Current opinion in rheumatology, 2009-11, Vol.21 (6), p.610-616

2009

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G.P.16.08 Expression of HSP90α and HSP90β in the idiopathic inflammatory myopathies and Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.653-653

2009

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P424 Identify genetic modifiers controlling severity of collagen-6 related dystrophies (COL6-RD)

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S158-S158

2023

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High-dose statins and skeletal muscle metabolism in humans: A randomized, controlled trial

Clinical pharmacology and therapeutics, 2005-07, Vol.78 (1), p.60-68

2005

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First report of bacterial leaf spot of Hydrangea in retail nurseries in Belgium caused by strains assigned to a new Xanthomonas hortorum clade

SP0022 Inflammatory Mediators in Inflammatory Myopathies

Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C

Unfiltering of the Geostationary Earth Radiation Budget (GERB) Data. Part I: Shortwave Radiation

Unfiltering of the Geostationary Earth Radiation Budget (GERB) Data. Part II: Longwave Radiation

Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome

Mild early epileptic encephalopathy evolving to spastic paraplegia, neurogenic bladder and generalized slow colon transit in an 18-year old patient with pathogenic mutations in FARS2

Test performance study for detection of Ralstonia solanacearum and Clavibacter sepedonicus in potato tubers with TaqMan PCR

Pathogenic mutations in TMEM126B, a recently discovered complex I assembly factor, identified in four siblings from two Belgian families

The Geostationary Earth Radiation Budget Edition 1 data processing algorithms

Inflammatory- and NaCl-induced expression of NFAT5 in muscle cells point to common stress response mechanisms

G.P.215

PP03.14 – 2978: Massive early leukoencephalopathy caused by a pathogenic mutation in IBA57: A new clinical presentation for this recently described gene defect

G.P.21 Proteomic analysis of cultured skin fibroblasts from UCMD patients reveals the involvement of two new cellular pathways

P1.25. Localization of chemokines and their receptors in muscle tissues from Duchenne muscular dystrophy patients

P3.26 Analysis of the Giant axonal neuropathy fibroblasts proteome

P5.41 ATP synthase deficiency: A diagnostic strategy for not such an uncommon cause of OXPHOS dysfunction

Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies

Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects

P.10Growth differentiation factor-15 as a novel biomarker for idiopathic inflammatory myopathies

205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands

Role of cytokines and chemokines in idiopathic inflammatory myopathies

G.P.16.08 Expression of HSP90α and HSP90β in the idiopathic inflammatory myopathies and Duchenne muscular dystrophy

P424 Identify genetic modifiers controlling severity of collagen-6 related dystrophies (COL6-RD)

High-dose statins and skeletal muscle metabolism in humans: A randomized, controlled trial

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