0000000000313255

AUTHOR

Martin Lindner

showing 3 related works from this author

Newborn screening and disease variants predict neurological outcome in isovaleric aciduria.

2021

Isovaleric aciduria (IVA), a metabolic disease with severe (classic IVA) or attenuated phenotype (mild IVA), is included in newborn screening (NBS) programs worldwide. The long-term clinical benefit of screened individuals, however, is still rarely investigated. A national, prospective, observational, multi-center study of individuals with confirmed IVA identified by NBS between 1998 and 2018 was conducted. Long-term clinical outcomes of 94 individuals with IVA were evaluated, representing 73.4% (for classic IVA: 92.3%) of the German NBS cohort. In classic IVA (N = 24), NBS prevented untimely death except in one individual with lethal neonatal sepsis (3.8%) but did not completely prevent si…

MalePediatricsmedicine.medical_specialtyAdolescentNeurocognitive DisordersDisease03 medical and health sciencesYoung AdultCognitionNeonatal ScreeningMaintenance therapyGermanyGeneticsmedicineHumansProspective StudiesMetabolic diseaseChildAmino Acid Metabolism Inborn ErrorsGenetics (clinical)030304 developmental biology0303 health sciencesNewborn screeningNeonatal sepsisIsovaleryl-CoA Dehydrogenasebusiness.industry030305 genetics & heredityInfant NewbornInfantmedicine.diseasePrognosisIsovaleric AcidemiaPhenotypeChild PreschoolCohortFemalesense organsbusinessNeurocognitiveJournal of inherited metabolic diseaseREFERENCES
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Issues with European guidelines for phenylketonuria

2017

medicine.medical_specialtybusiness.industryPhenylketonuriasEndocrinology Diabetes and MetabolismMEDLINE610 Medicine & health1310 Endocrinology03 medical and health sciences2712 Endocrinology Diabetes and Metabolism0302 clinical medicineEndocrinology10036 Medical Clinic2724 Internal MedicineFamily medicinePhenylketonuriasInternal MedicineMedicineHumans030212 general & internal medicinebusiness030217 neurology & neurosurgery
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Quantitative Acylcarnitine Profiling in Peripheral Blood Mononuclear Cells Using In Vitro Loading With Palmitic and 2-Oxoadipic Acids: Biochemical Co…

2005

Organic acid (OAD) and fatty acid oxidation disorders (FAOD) are inborn errors of metabolism often presenting with life-threatening metabolic decompensation followed by (irreversible) organ failure, and even death during catabolic state. Most of these diseases are considered as treatable, and metabolic decompensations can be avoided by early diagnosis and start of therapy. Confirmation of suspected diagnosis currently relies on enzymatic and mutation analyses and in vitro loading of palmitic acid in human skin fibroblast cultures. Furthermore, in some cases potentially life-threatening in vivo loading or fasting tests are still performed. In this study, we established a standardized in vitr…

MaleAdipatesPalmitic AcidPeripheral blood mononuclear cellMass SpectrometryMonocytesPalmitic acidBlood cellchemistry.chemical_compoundIn vivoCarnitinemedicineHumansChildBeta oxidationGlutaric aciduriaInfantMetabolismVenous bloodmedicine.anatomical_structurechemistryBiochemistryChild PreschoolPediatrics Perinatology and Child HealthFemaleMetabolism Inborn ErrorsPediatric Research
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