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Monique Piraud

Showing results (1-10 of 32) with videos related to

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JAMA Neurology|November 13, 2013
Severe axial myopathy in McArdle diseaseNanna Witting, Morten Duno, Monique Piraud, et al.
Orphanet Journal of Rare Diseases|February 8, 2014
Fast urinary screening of oligosaccharidoses by MALDI-TOF/TOF mass spectrometryLaurent Bonesso, Monique Piraud, Céline Caruba, et al.
Rapid Communications in Mass Spectrometry : RCM|May 26, 2005
Ion-pairing reversed-phase liquid chromatography/electrospray ionization mass spectrometric analysis of 76 underivatized amino acids of biological interest: a new tool for the diagnosis of inherited disorders of amino acid metabolismMonique Piraud, Christine Vianey-Saban, Konstantinos Petritis, et al.
Journal of Inherited Metabolic Disease|March 20, 2019
Phosphoglycerate kinase deficiency: A nationwide multicenter retrospective studyAndoni Echaniz-Laguna, Yann Nadjar, Anthony Béhin, et al.
Rapid Communications in Mass Spectrometry : RCM|April 4, 2017
Development of a new tandem mass spectrometry method for urine and amniotic fluid screening of oligosaccharidosesMonique Piraud, Magali Pettazzoni, Louise Menegaut, et al.
The FEBS Journal|June 16, 2010
Glycan profiling of urine, amniotic fluid and ascitic fluid from galactosialidosis patients reveals novel oligosaccharides with reducing end hexose and aldohexonic acid residuesCees Bruggink, Ben J H M Poorthuis, Monique Piraud, et al.
Rapid Communications in Mass Spectrometry : RCM|June 18, 2003
ESI-MS/MS analysis of underivatised amino acids: a new tool for the diagnosis of inherited disorders of amino acid metabolism. Fragmentation study of 79 molecules of biological interest in positive and negative ionisation modeMonique Piraud, Christine Vianey-Saban, Konstantinos Petritis, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 6, 2011
Amino acid profiling for the diagnosis of inborn errors of metabolismMonique Piraud, Séverine Ruet, Sylvie Boyer, et al.
Journal of the Neurological Sciences|February 28, 2012
Juvenile-onset permanent weakness in muscle phosphofructokinase deficiencyEdoardo Malfatti, Nazha Birouk, Norma B Romero, et al.
Plos One|March 17, 2011
Cerebral changes occurring in arginase and dimethylarginine dimethylaminohydrolase (DDAH) in a rat model of sleeping sicknessDonia Amrouni, Anne Meiller, Sabine Gautier-Sauvigné, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
JAMA Neurology|November 13, 2013
Severe axial myopathy in McArdle diseaseNanna Witting, Morten Duno, Monique Piraud, et al.
Orphanet Journal of Rare Diseases|February 8, 2014
Fast urinary screening of oligosaccharidoses by MALDI-TOF/TOF mass spectrometryLaurent Bonesso, Monique Piraud, Céline Caruba, et al.
Rapid Communications in Mass Spectrometry : RCM|May 26, 2005
Ion-pairing reversed-phase liquid chromatography/electrospray ionization mass spectrometric analysis of 76 underivatized amino acids of biological interest: a new tool for the diagnosis of inherited disorders of amino acid metabolismMonique Piraud, Christine Vianey-Saban, Konstantinos Petritis, et al.
Journal of Inherited Metabolic Disease|March 20, 2019
Phosphoglycerate kinase deficiency: A nationwide multicenter retrospective studyAndoni Echaniz-Laguna, Yann Nadjar, Anthony Béhin, et al.
Rapid Communications in Mass Spectrometry : RCM|April 4, 2017
Development of a new tandem mass spectrometry method for urine and amniotic fluid screening of oligosaccharidosesMonique Piraud, Magali Pettazzoni, Louise Menegaut, et al.
The FEBS Journal|June 16, 2010
Glycan profiling of urine, amniotic fluid and ascitic fluid from galactosialidosis patients reveals novel oligosaccharides with reducing end hexose and aldohexonic acid residuesCees Bruggink, Ben J H M Poorthuis, Monique Piraud, et al.
Rapid Communications in Mass Spectrometry : RCM|June 18, 2003
ESI-MS/MS analysis of underivatised amino acids: a new tool for the diagnosis of inherited disorders of amino acid metabolism. Fragmentation study of 79 molecules of biological interest in positive and negative ionisation modeMonique Piraud, Christine Vianey-Saban, Konstantinos Petritis, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 6, 2011
Amino acid profiling for the diagnosis of inborn errors of metabolismMonique Piraud, Séverine Ruet, Sylvie Boyer, et al.
Journal of the Neurological Sciences|February 28, 2012
Juvenile-onset permanent weakness in muscle phosphofructokinase deficiencyEdoardo Malfatti, Nazha Birouk, Norma B Romero, et al.
Plos One|March 17, 2011
Cerebral changes occurring in arginase and dimethylarginine dimethylaminohydrolase (DDAH) in a rat model of sleeping sicknessDonia Amrouni, Anne Meiller, Sabine Gautier-Sauvigné, et al.
Pageof 4