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
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
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
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
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
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
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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