|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 (mut 0, mut−, cblA, cblB)|
F Hörster, MR Baumgartner, C Viardot, T Suormala, P Burgard, B Fowler, ...
Pediatric research 62 (2), 225-230, 2007
|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
|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
|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
|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
|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
|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
|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 (5), 630-639, 2009
|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
|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, 2021
|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
|Patterns, evolution, and severity of striatal injury in insidious‐vs acute‐onset glutaric aciduria type 1|
N Boy, SF Garbade, J Heringer, A Seitz, S Kölker, I Harting
Journal of inherited metabolic disease 42 (1), 117-127, 2019
|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), 1-8, 2017
|Blood trimethylamine-N-oxide originates from microbiota mediated breakdown of phosphatidylcholine and absorption from small intestine|
W Stremmel, KV Schmidt, V Schuhmann, F Kratzer, SF Garbade, ...
PLoS One 12 (1), e0170742, 2017
|Blood phenylalanine concentrations in patients with PAH-deficient hyperphenylalaninaemia off diet without and with three different single oral doses of tetrahydrobiopterin …|
M Lindner, G Gramer, SF Garbade, P Burgard
Journal of inherited metabolic disease 32 (4), 514-522, 2009
|Unravelling the complex MRI pattern in glutaric aciduria type I using statistical models—a cohort study in 180 patients|
SF Garbade, CR Greenberg, M Demirkol, G Gökçay, A Ribes, J Campistol, ...
Journal of inherited metabolic disease 37 (5), 763-773, 2014
|Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblasts|
D Haas, J Morgenthaler, F Lacbawan, B Long, H Runz, SF Garbade, ...
Journal of medical genetics 44 (5), 298-305, 2007
|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