Sven F.  Garbade
Sven F. Garbade
Statistical Coordinator at Division for Neuropediatrics and Metabolic Medicine
Verified email at - Homepage
Cited by
Cited by
The relationship between self‐compassion and well‐being: A meta‐analysis
U Zessin, O Dickhäuser, S Garbade
Applied Psychology: Health and Well‐Being 7 (3), 340-364, 2015
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency
S Kölker, SF Garbade, CR Greenberg, JV Leonard, JM Saudubray, ...
Pediatric research 59 (6), 840-847, 2006
Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut−, cblA, cblB)
F Hörster, MR Baumgartner, C Viardot, T Suormala, P Burgard, B Fowler, ...
Pediatric research 62 (2), 225-230, 2007
The genetic landscape and epidemiology of phenylketonuria
A Hillert, Y Anikster, A Belanger-Quintana, A Burlina, BK Burton, ...
The American Journal of Human Genetics 107 (2), 234-250, 2020
Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I
I Harting, E Neumaier-Probst, A Seitz, EM Maier, B Assmann, I Baric, ...
Brain 132 (7), 1764-1782, 2009
Prevalence of SARS-CoV-2 infection in children and their parents in Southwest Germany
B Tönshoff, B Müller, R Elling, H Renk, P Meissner, H Hengel, ...
JAMA pediatrics 175 (6), 586-593, 2021
Neuropsychological speed tests and blood phenylalanine levels in patients with phenylketonuria: a meta-analysis
J Albrecht, SF Garbade, P Burgard
Neuroscience & Biobehavioral Reviews 33 (3), 414-421, 2009
Relationships Between Transformational Leadership and Health: The Mediating Role of Perceived Job Demands and Occupational Self-Efficacy
S Hentrich, A Zimber, SF Garbade, S Gregersen, A Nienhaus, ...
International Journal of Stress Management, 2016
Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany
S Kölker, SF Garbade, N Boy, EM Maier, T Meissner, C Mühlhausen, ...
Pediatric research 62 (3), 357-363, 2007
Newborn screening: a disease‐changing intervention for glutaric aciduria type 1
N Boy, K Mengler, E Thimm, KA Schiergens, T Marquardt, N Weinhold, ...
Annals of neurology 83 (5), 970-979, 2018
Effects of cholesterol and simvastatin treatment in patients with Smith–Lemli–Opitz syndrome (SLOS)
D Haas, SF Garbade, C Vohwinkel, N Muschol, FK Trefz, JM Penzien, ...
Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2007
Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters
F Hörster, SF Garbade, T Zwickler, HI Aydin, OA Bodamer, AB Burlina, ...
Journal of inherited metabolic disease 32, 630-639, 2009
Comprehensive detection of disorders of purine and pyrimidine metabolism by HPLC with electrospray ionization tandem mass spectrometry
S Hartmann, JG Okun, C Schmidt, CD Langhans, SF Garbade, P Burgard, ...
Clinical chemistry 52 (6), 1127-1137, 2006
Gene replacement therapy with onasemnogene abeparvovec in children with spinal muscular atrophy aged 24 months or younger and bodyweight up to 15 kg: an observational cohort study
C Weiß, A Ziegler, LL Becker, J Johannsen, H Brennenstuhl, G Schreiber, ...
The Lancet Child & Adolescent Health 6 (1), 17-27, 2022
Allelic phenotype values: a model for genotype-based phenotype prediction in phenylketonuria
SF Garbade, N Shen, N Himmelreich, D Haas, FK Trefz, GF Hoffmann, ...
Genetics in Medicine 21 (3), 580-590, 2019
Defining clinical subgroups and genotype–phenotype correlations in NBAS-associated disease across 110 patients
C Staufner, B Peters, M Wagner, S Alameer, I Barić, P Broué, D Bulut, ...
Genetics in Medicine 22 (3), 610-621, 2020
Incidence, disease onset and short-term outcome in urea cycle disorders–cross-border surveillance in Germany, Austria and Switzerland
S Nettesheim, S Kölker, D Karall, J Häberle, R Posset, GF Hoffmann, ...
Orphanet journal of rare diseases 12, 1-8, 2017
Quantitative clinical characteristics of 53 patients with MPS VII: a cross-sectional analysis
M Zielonka, SF Garbade, S Kölker, GF Hoffmann, M Ries
Genetics in Medicine 19 (9), 983-988, 2017
Impact of diagnosis and therapy on cognitive function in urea cycle disorders
R Posset, AL Gropman, SCS Nagamani, LC Burrage, JK Bedoyan, ...
Annals of neurology 86 (1), 116-128, 2019
Long-term outcomes of individuals with metabolic diseases identified through newborn screening
U Mütze, SF Garbade, G Gramer, M Lindner, P Freisinger, SC Grünert, ...
Pediatrics 146 (5), 2020
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