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 | 1589 | 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 | 318 | 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 | 274 | 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 | 244 | 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 | 187 | 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 | 160 | 2021 |
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 | 154 | 2016 |
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 | 153 | 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 | 132 | 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 | 104 | 2018 |
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 | 91 | 2022 |
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 | 89 | 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 | 85 | 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 | 80 | 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 | 71 | 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 | 63 | 2020 |
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 | 62 | 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 | 60 | 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 | 59 | 2019 |
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 | 57 | 2019 |