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Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALS

Scientific reports, 2017-12, Vol.7 (1), p.17652-10, Article 17652

2017

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Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration

Molecular neurobiology, 2018-08, Vol.55 (8), p.6480-6499

2018

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Biological follow-up in amyotrophic lateral sclerosis: decrease in creatinine levels and increase in ferritin levels predict poor prognosis

European journal of neurology, 2015-10, Vol.22 (10), p.1385-1390

2015

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ABCB4 gene mutations and single-nucleotide polymorphisms in women with intrahepatic cholestasis of pregnancy

Journal of medical genetics, 2009-10, Vol.46 (10), p.711-715

2009

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Amyotrophic Lateral Sclerosis, 2016: existing therapies and the ongoing search for neuroprotection

Expert opinion on pharmacotherapy, 2016-08, Vol.17 (12), p.1669-1682

2016

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The specific metabolome profiling of patients infected by SARS-COV-2 supports the key role of tryptophan-nicotinamide pathway and cytosine metabolism

Scientific reports, 2020-10, Vol.10 (1), p.16824-16824, Article 16824

2020

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SMN1 gene, but not SMN2, is a risk factor for sporadic ALS

Neurology, 2006-10, Vol.67 (7), p.1147

2006

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Roles of LIM kinases in central nervous system function and dysfunction

FEBS letters, 2015-12, Vol.589 (24), p.3795-3806

2015

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A Multiplatform Metabolomics Approach to Characterize Plasma Levels of Phenylalanine and Tyrosine in Phenylketonuria

JIMD Reports, Volume 32, 2017-01, Vol.32, p.69-79

2017

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Comparative analysis of targeted metabolomics: Dominance-based rough set approach versus orthogonal partial least square-discriminant analysis

Journal of biomedical informatics, 2015-02, Vol.53, p.291-299

2015

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Low IDL-B and high LDL-1 subfraction levels in serum of ALS patients

Journal of the neurological sciences, 2017-09, Vol.380, p.124-127

2017

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Genetics of amyotrophic lateral sclerosis

Revue neurologique, 2017-05, Vol.173 (5), p.254-262

2017

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The combination of four analytical methods to explore skeletal muscle metabolomics: Better coverage of metabolic pathways or a marketing argument?

Journal of pharmaceutical and biomedical analysis, 2018-01, Vol.148, p.273-279

2018

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Validation of plasma amino acid profile using UHPLC-mass spectrometer (QDa) as a screening method in a metabolic disorders reference centre: Performance and accreditation concerns

Clinical biochemistry, 2021-06, Vol.92, p.34-45

2021

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Behavioral, Hormonal, Inflammatory, and Metabolic Effects Associated with FGF21-Pathway Activation in an ALS Mouse Model

Neurotherapeutics, 2021-01, Vol.18 (1), p.297-308

2021

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GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability

Molecular psychiatry, 2016-03, Vol.21 (3), p.411-418

2016

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Metabolomics in amyotrophic lateral sclerosis: how far can it take us?

European journal of neurology, 2016-03, Vol.23 (3), p.447-454

2016

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Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma

Journal of the neurological sciences, 2011-10, Vol.309 (1), p.16-17

2011

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A decrease in blood cholesterol after gastrostomy could impact survival in ALS

European journal of clinical nutrition, 2017-09, Vol.71 (9), p.1133-1135

2017

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Typical bulbar ALS can be linked to GARS mutation

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-04, Vol.20 (3-4), p.275-277

2019

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Maladie de Tay-Sachs révélée par un tableau d’amyotrophie spinale

Revue neurologique, 2011-06, Vol.167 (6), p.549-550

2011

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Biomarkers in amyotrophic lateral sclerosis: combining metabolomic and clinical parameters to define disease progression

European journal of neurology, 2016-02, Vol.23 (2), p.346-353

2016

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Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management

Clinical biochemistry, 2016-09, Vol.49 (13-14), p.1047-1050

2016

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Further development of biomarkers in amyotrophic lateral sclerosis

Expert review of molecular diagnostics, 2016-08, Vol.16 (8), p.853-868

2016

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Erratum to “Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management” [Clin. Biochem. 49 (2016) 1047–1050]

Clinical biochemistry, 2017-06, Vol.50 (9), p.546-546

2017

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Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALS

Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration

Biological follow-up in amyotrophic lateral sclerosis: decrease in creatinine levels and increase in ferritin levels predict poor prognosis

ABCB4 gene mutations and single-nucleotide polymorphisms in women with intrahepatic cholestasis of pregnancy

Amyotrophic Lateral Sclerosis, 2016: existing therapies and the ongoing search for neuroprotection

The specific metabolome profiling of patients infected by SARS-COV-2 supports the key role of tryptophan-nicotinamide pathway and cytosine metabolism

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS

Roles of LIM kinases in central nervous system function and dysfunction

A Multiplatform Metabolomics Approach to Characterize Plasma Levels of Phenylalanine and Tyrosine in Phenylketonuria

Comparative analysis of targeted metabolomics: Dominance-based rough set approach versus orthogonal partial least square-discriminant analysis

Low IDL-B and high LDL-1 subfraction levels in serum of ALS patients

Genetics of amyotrophic lateral sclerosis

The combination of four analytical methods to explore skeletal muscle metabolomics: Better coverage of metabolic pathways or a marketing argument?

Validation of plasma amino acid profile using UHPLC-mass spectrometer (QDa) as a screening method in a metabolic disorders reference centre: Performance and accreditation concerns

Behavioral, Hormonal, Inflammatory, and Metabolic Effects Associated with FGF21-Pathway Activation in an ALS Mouse Model

GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability

Metabolomics in amyotrophic lateral sclerosis: how far can it take us?

Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma

A decrease in blood cholesterol after gastrostomy could impact survival in ALS

Typical bulbar ALS can be linked to GARS mutation

Maladie de Tay-Sachs révélée par un tableau d’amyotrophie spinale

Biomarkers in amyotrophic lateral sclerosis: combining metabolomic and clinical parameters to define disease progression

Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management

Further development of biomarkers in amyotrophic lateral sclerosis

Erratum to “Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management” [Clin. Biochem. 49 (2016) 1047–1050]

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