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Elke Miebach

Cumulative incidence rates of the mucopolysaccharidoses in Germany
2005 · F. Baehner, C. Schmiedeskamp, et al. · Journal of Inherited Metabolic Disease · 395
The Mainz Severity Score Index: a new instrument for quantifying the Anderson–Fabry disease phenotype, and the response of patients to enzyme replacement therapy
2004 · C Whybra, C Kampmann, et al. · Clinical Genetics · 266
Onset and progression of the Anderson–Fabry disease related cardiomyopathy
2008 · Christoph Kampmann, Ales Linhart, et al. · International Journal of Cardiology · 173
Enzyme replacement therapy in heterozygous females with Fabry disease: Results of a phase IIIB study
2003 · F. Baehner, C. Kampmann, et al. · Journal of Inherited Metabolic Disease · 126
A 4-year study of the efficacy and tolerability of enzyme replacement therapy with agalsidase alfa in 36 women with Fabry disease
2009 · Catharina Whybra, Elke Miebach, et al. · Genetics in Medicine · 95
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Enzyme replacement therapy in mucopolysaccharidosis type I
2005 · E Miebach · Acta Paediatrica · 52
Clinical characteristics of adults with slowly progressing mucopolysaccharidosis VI: a case series
2012 · Anke Thümler, Elke Miebach, et al. · Journal of Inherited Metabolic Disease · 50
Does enzyme replacement therapy influence the ocular changes in type VI mucopolysaccharidosis?
2009 · Susanne Pitz, Olufunmilola Ogun, et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 46
Mucopolysaccharidosis VI: cardiac involvement and the impact of enzyme replacement therapy
2013 · Christoph Kampmann, Christina Lampe, et al. · Journal of Inherited Metabolic Disease · 44
Abnormal Somatosensory Evoked Potentials Indicate Compressive Cervical Myelopathy in Mucopolysaccharidoses
2000 · R. Boor, E. Miebach, et al. · Neuropediatrics · 36
Electrocardiographic signs of hypertrophy in Fabry disease-associated hypertrophic cardiomyopathy
2002 · C Kampmann, C.M Wiethoff, et al. · Acta Paediatrica · 30
Management of infusion-related reactions to enzyme replacement therapy in a cohort of patients with mucopolysaccharidosis disorders
2009 · E. Miebach · International Journal of Clinical Pharmacology and Therapeutics · 27
The craniocervical junction following successful haematopoietic stem cell transplantation for mucopolysaccharidosis type I H (Hurler syndrome)
2011 · Elke Miebach, Heather Church, et al. · Journal of Inherited Metabolic Disease · 22
Mukopolysaccharidosen
2007 · B. Link, E. Miebach, et al. · Der Orthopäde · 10
Lysosomale Speichererkrankungen - Update und neue therapeutische Optionen
2010 · K. Schöpfer, E. Miebach, et al. · Klinische Monatsblätter für Augenheilkunde · 3
Differential diagnosis of Gaucher and Niemann‐Pick disease in early childhood
2002 · E Mengel, E Miebach, et al. · Acta Paediatrica
Clinical variability in sphingomyelinase deficiency
2002 · E Miebach, E Mengel, et al. · Acta Paediatrica
Works count: 17
Citation count: 1,375
H-index: 13
I10-index: 14
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