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Sven Garbade (1971-)

Psychologe

Name	Sven Garbade
Zeit	1971- (Lebensdaten)
Ort	Heidelberg (Wirkungsort) Deutschland
Akademischer Grad bzw. Titel	Prof. Dr. Phil.
Beruf	Psychologe (charakteristischer Beruf)
Variante	Sven Friedrich Garbade Sven F. Garbade S. F. Garbade
Weitere Angaben	Studiengangsverantwortlicher B.Sc. Psychologie, SRH Hochschule Heidelberg
Datensatztyp	Person
GND-Nummer	129234362
Datensatz-ID	129234362
Beteiligt an alle anzeigen Genetic landscape of pediatric acute liver failure of indeterminate origin Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias Psychosocial issues and coping strategies in families affected by long‐chain fatty acid oxidation disorders Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples Isovaleric aciduria identified by newborn screening: strategies to predict disease severity and stratify treatment Live‐virus neutralization of the omicron variant in children and adults 14 months after SARS‐CoV‐2 wild‐type infection Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening Humoral immune response and live-virus neutralization of the SARS-CoV-2 omicron (BA.1) variant after COVID-19 mRNA vaccination in children and young adults with chronic kidney disease Impact of glycogen storage disease type I on adult daily life: a survey Impact of glycogen storage disease type I on adult daily life: a survey Publisher correction: The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathies Clinical characteristics of 248 patients with Krabbe disease: quantitative natural history modeling based on published cases Allelic phenotype values: a model for genotype-based phenotype prediction in phenylketonuria A cross-sectional quantitative analysis of the natural history of free sialic acid storage disease—an ultra-orphan multisystemic lysosomal storage disorder Age-Related Changes and Reference Values of Bicaudate Ratio and Sagittal Brainstem Diameters on MRI Incidence, disease onset and short-term outcome in urea cycle disorders –cross-border surveillance in Germany, Austria and Switzerland Abstracts of the 52nd Workshop for Pediatric Research : Frankfurt, Germany. 27-28 October 2016 Statische Augenfolgebewegungen: Beeinflussung durch Distraktoren und Kopplung mit visueller Aufmerksamkeit

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Sven Garbade (1971-)

Genetic landscape of pediatric acute liver failure of indeterminate origin

Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias

Psychosocial issues and coping strategies in families affected by long‐chain fatty acid oxidation disorders

Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples

Isovaleric aciduria identified by newborn screening: strategies to predict disease severity and stratify treatment

Live‐virus neutralization of the omicron variant in children and adults 14 months after SARS‐CoV‐2 wild‐type infection

Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening

Humoral immune response and live-virus neutralization of the SARS-CoV-2 omicron (BA.1) variant after COVID-19 mRNA vaccination in children and young adults with chronic kidney disease

Impact of glycogen storage disease type I on adult daily life: a survey

Impact of glycogen storage disease type I on adult daily life: a survey

Publisher correction: The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study

The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study

Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathies

Clinical characteristics of 248 patients with Krabbe disease: quantitative natural history modeling based on published cases

Allelic phenotype values: a model for genotype-based phenotype prediction in phenylketonuria

A cross-sectional quantitative analysis of the natural history of free sialic acid storage disease—an ultra-orphan multisystemic lysosomal storage disorder

Age-Related Changes and Reference Values of Bicaudate Ratio and Sagittal Brainstem Diameters on MRI

Incidence, disease onset and short-term outcome in urea cycle disorders –cross-border surveillance in Germany, Austria and Switzerland

Abstracts of the 52nd Workshop for Pediatric Research : Frankfurt, Germany. 27-28 October 2016

Statische Augenfolgebewegungen: Beeinflussung durch Distraktoren und Kopplung mit visueller Aufmerksamkeit