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Results 1 to 25 of 96

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New therapeutic options for lysosomal storage disorders : enzyme replacement, small molecules and gene therapyBECK, Michael.Human genetics. 2007, Vol 121, Num 1, pp 1-22, issn 0340-6717, 22 p.Article

Reibwertoptimierung zwischen Rad und Schiene - ein nachhaltiger Lösungsansatz für das Schlupfwellenproblem = Optimised friction between wheel and rail - a sustainable solution to the corrugation problemSTOCK, Richard; BECK, Michael.ZEV rail Glasers Annalen. 2014, Vol 138, Num 11-12, pp 470-476, 7 p.Article

Loss, status and trends for coastal marine habitats of EuropeAIROLDI, Laura; BECK, Michael W.Oceanography and Marine Biology. 2007, Vol 45, pp 345-405, issn 0078-3218, 61 p.Article

Fabry disease in children and the effects of enzyme replacement treatmentPINTOS-MORELL, Guillem; BECK, Michael.European journal of pediatrics. 2009, Vol 168, Num 11, pp 1355-1363, issn 0340-6199, 9 p.Article

Biomass allocation to roots and shoots is more sensitive to shade and drought in European beech than in Norway spruce seedlingsSCHALL, Peter; LÖDIGE, Christina; BECK, Michael et al.Forest ecology and management. 2012, Vol 266, pp 246-253, issn 0378-1127, 8 p.Article

Early Treatment With Alglucosidase Alfa Prolongs Long-Term Survival of Infants With Pompe DiseaseKISHNANI, Priya S; CORZO, Deya; JOKIC, Mikael et al.Pediatric research. 2009, Vol 66, Num 3, pp 329-335, issn 0031-3998, 7 p.Article

Identification of a spatially efficient portfolio of priority conservation sites in marine and estuarine areas of FloridaGESELBRACHT, Laura; TORRES, Roberto; CUMMING, Graeme S et al.Aquatic conservation (Print). 2009, Vol 19, Num 4, pp 408-420, issn 1052-7613, 13 p.Article

Onset and progression of the Anderson-Fabry disease related cardiomyopathyKAMPMANN, Christoph; LINHART, Ales; BAEHNER, Frank et al.International journal of cardiology. 2008, Vol 130, Num 3, pp 367-373, issn 0167-5273, 7 p.Article

Metachromatic leukodystrophy: genetics, pathogenesis and therapeutic optionsGIESELMANN, Volkmar.Acta paediatrica. Supplement. 2008, Vol 97, Num 457, pp 15-21, issn 0803-5326, 7 p.Article

Magnetic resonance imaging findings in Hunter syndromeFINN, Chelsea T; VEDOLIN, Leonardo; SCHWARTZ, Ida V et al.Acta paediatrica. Supplement. 2008, Vol 97, Num 457, pp 61-68, issn 0803-5326, 8 p.Article

Dicaprylyl maleate - : an emerging cosmetic allergenLOTERY, Helen; KIRK, Stephen; LOVELL, Christopher et al.Contact dermatitis. 2007, Vol 57, Num 3, pp 169-172, issn 0105-1873, 4 p.Article

An association study of inflammatory cytokine gene polymorphisms in Fabry diseaseSAFYAN, Rachael; WHYBRA, Catharina; BECK, Michael et al.European cytokine network (Montrouge). 2006, Vol 17, Num 4, pp 271-275, issn 1148-5493, 5 p.Article

Hunter Disease Before and During Enzyme Replacement TherapyHOFFMANN, Bjöm; SCHULZE-FRENKING, Gudrun; AL-SAWAF, Sulaiman et al.Pediatric neurology. 2011, Vol 45, Num 3, pp 181-184, issn 0887-8994, 4 p.Article

Fabry disease during childhood: clinical manifestations and treatment with agalsidase alfaRAMASWAMI, Uma.Acta paediatrica. Supplement. 2008, Vol 97, Num 457, issn 0803-5326, 38-40 [3 p.]Article

Enzyme replacement therapy with idursulfase in patients with mucopolysaccharidosis type IIWRAITH, J. Edmond.Acta paediatrica. Supplement. 2008, Vol 97, Num 457, pp 76-78, issn 0803-5326, 3 p.Article

Nature and prevalence of pain in fabry disease and its response to enzyme replacement therapy- : A retrospective analysis from the fabry outcome surveyHOFFMANN, Bjoern; BECK, Michael; SUNDER-PLASSMANN, Gere et al.The Clinical journal of pain. 2007, Vol 23, Num 6, pp 535-542, issn 0749-8047, 8 p.Article

Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with mucopolysaccharidosis VI (Maroteaux-Pamy Syndrome)SWIEDLER, Stuart J; BECK, Michael; GUFFON, Nathalie et al.American journal of medical genetics. 2005, Vol 134A, Num 2, pp 144-150, issn 0148-7299, 7 p.Article

Slider vibration reduction using slider surface textureLIN ZHOU; BECK, Michael; GATZEN, Hans H et al.Microsystem technologies. 2005, Vol 11, Num 8-10, pp 857-866, issn 0946-7076, 10 p.Conference Paper

The relationship between public causal beliefs and social distance toward mentally ill people. CommentaryDIETRICH, Sandra; BECK, Michael; BUJANTUGS, Bujana et al.Australian and New Zealand journal of psychiatry. 2004, Vol 38, Num 5, pp 348-357, issn 0004-8674, 10 p.Article

The stigma of mental illness: Patients' anticipations and experiencesANGERMEYER, Matthias C; BECK, Michael; DIETRICH, Sandra et al.International journal of social psychiatry. 2004, Vol 50, Num 2, pp 153-162, issn 0020-7640, 10 p.Article

Cardiac manifestations of Anderson-Fabry disease in heterozygous femalesKAMPMANN, Christoph; BAEHNER, Frank; WHYBRA, Catharina et al.Journal of the American College of Cardiology. 2002, Vol 40, Num 9, pp 1668-1674, issn 0735-1097, 7 p.Article

Lysosomal storage diseases. Fabry disease: clinical heterogeneity and management challenges. 2nd international symposium, Cannes, April 2002: ProceedingsBECK, Michael; COX, Timothy M; VANIER, Marie T et al.Acta paediatrica. Supplement. 2002, Vol 91, Num 439, issn 0803-5326, 162 p.Conference Proceedings

Novel mutations in lysosomal neuraminidase identify functional domains and determine clinical severity in sialidosisBONTEN, Erik J; ARTS, Willem F; BECK, Michael et al.Human molecular genetics (Print). 2000, Vol 9, Num 18, pp 2715-2725, issn 0964-6906Article

Spinal involvement in mucopolysaccharidosis IVA (Morquio-Brailsford or Morquio A syndrome): presentation, diagnosis and managementSOLANKI, Guirish A; MARTIN, Kenneth W; HARMATZ, Paul R et al.Journal of inherited metabolic disease. 2013, Vol 36, Num 2, pp 339-355, issn 0141-8955, 17 p.Article

Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfataseHARMATZ, Paul; YU, Zi-Fan; SCARPA, Maurizio et al.Journal of inherited metabolic disease. 2010, Vol 33, Num 1, pp 51-60, issn 0141-8955, 10 p.Article

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