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Journal of Inherited Metabolic Disease|September 10, 2005
Successful pregnancy outcome in a patient with Fabry disease receiving enzyme replacement therapy with agalsidase alfaS Wendt, C Whybra, C Kampmann, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|October 21, 2016
[Female Preterm Monozygotic Twins Discordant for Fetal Megacystis due to Cloacal Dysgenesis After Conception by Intracytoplasmatic Sperm Injection - Case Report and Review of Literature]M Schneider, I Schmeh, A Fruth, et al.
Journal of Inherited Metabolic Disease|January 7, 2004
Enzyme replacement therapy in heterozygous females with Fabry disease: results of a phase IIIB studyF Baehner, C Kampmann, C Whybra, et al.
Journal of Inherited Metabolic Disease|January 4, 2008
Correlation between interleukin-6 promoter and C-reactive protein (CRP) polymorphisms and CRP levels with the Mainz Severity Score Index for Fabry diseaseG Altarescu, G Chicco, C Whybra, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|February 8, 2003
Electrocardiographic signs of hypertrophy in fabry disease-associated hypertrophic cardiomyopathyC Kampmann, C M Wiethoff, C Martin, et al.
Der Pathologe|November 8, 2003
[Fabry's disease, glomerulonephritis with crescentic and granulomatous interstitial nephritis. Case of one family]J Kriegsmann, M Otto, E Wandel, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Cumulative incidence rates of the mucopolysaccharidoses in GermanyF Baehner, C Schmiedeskamp, F Krummenauer, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 26, 2006
Enzyme replacement therapy with agalsidase alfa in children with Fabry diseaseU Ramaswami, S Wendt, G Pintos-Morell, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
The right ventricle in Fabry diseaseC Kampmann, F A Baehner, C Whybra, et al.
Journal of Inherited Metabolic Disease|January 24, 2002
Anderson-Fabry disease: clinical manifestations of disease in female heterozygotesC Whybra, C Kampmann, I Willers, et al.
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