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Publications by Jean-Baptiste Arnoux
Hyperprolinemia in Type 2 Glutaric Aciduria and MADD-Like Profiles
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Related publications
Prevention of Cerebral Palsy in Glutaric Aciduria Type 1 by Dietary Management
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Subdural Hematomas: Glutaric Aciduria Type 1 or Abusive Head Trauma? A Systematic Review
Forensic Science, Medicine, and Pathology
Medicine
Forensic Medicine
Pathology
Clinical Features and Course of Glutaric Aciduria-Report of Six Cases
Journal of Neurosciences in Rural Practice
Neuroscience
Neurology
Mild Phenotype of Glutaric Aciduria Type 1 in Polish Patients – Novel Data From a Group of 13 Cases
Metabolic Brain Disease
Biochemistry
Molecular Neuroscience
Neurology
Cellular
Clinical and Laboratory Analysis of Late-Onset Glutaric Aciduria Type I (GA-I) in Uighur: A Report of Two Cases
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Newborn Screening for Glutaric Aciduria-Ii: The New England Experience
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
GP225 Better Outcomes of ‘High-Risk’ Screened Glutaric Aciduria Type 1 Patients Give Optimism to Future Cases Diagnosed Through Newborn Screening in Ireland
The Three-Dimensional Structural Basis of Type II Hyperprolinemia
Journal of Molecular Biology
Structural Biology
Molecular Biology
Biophysics
RadioHPLC Profiles of Acyl-Camitines Improve Detection of Mild Glutaric Acidemia Type II and Short Chain Acyl-CoA Dehydrogenase Deficiency
Genetics in Medicine
Medicine
Genetics