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Journal of Molecular Medicine (Berlin, Germany)|February 23, 2010
Insights into lysosomal cobalamin trafficking: lessons learned from cblF diseaseSusann Gailus, Wolfgang Höhne, Bruno Gasnier, et al.Bone|July 12, 2021
Autosomal recessive hypophosphatemic rickets type 2 (ARHR2) due to ENPP1-deficiencyJakob Höppner, Uwe Kornak, Kathrin Sinningen, et al.European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|March 11, 2020
Reversion of arterial calcification by elastin-targeted DTPA-HSA nanoparticlesJacqueline Keuth, Yvonne Nitschke, Dennis Mulac, et al.Experimental & Molecular Medicine|October 30, 2018
ENPP1-Fc prevents neointima formation in generalized arterial calcification of infancy through the generation of AMPYvonne Nitschke, Yan Yan, Insa Buers, et al.Connective Tissue Research|August 27, 2014
Establishment of Singleton-Merten syndrome pulp cells: evidence of mineralization dysregulationChangming Lu, Olga A Mamaeva, Chun Cui, et al.Nature Clinical Practice. Endocrinology & Metabolism|February 21, 2009
Generalized arterial calcification of infancy: treatment with bisphosphonatesKim A Ramjan, Tony Roscioli, Frank Rutsch, et al.Acta Paediatrica (Oslo, Norway : 1992)|November 9, 2024
Neurocognitive functioning remained unchanged in adults with phenylketonuria: Report of a 15-year follow-upReinhold Feldmann, Eva Philippa Leberer, Juliane Fromm, et al.Journal of Cellular and Molecular Medicine|April 11, 2016
Lmbrd1 expression is essential for the initiation of gastrulationInsa Buers, Petra Pennekamp, Yvonne Nitschke, et al.American Journal of Medical Genetics. Part A|June 9, 2005
Generalized arterial calcification of infancy: different clinical courses in two affected siblingsKun-Shan Cheng, Ming-Ren Chen, Nico Ruf, et al.Current Opinion in Pharmacology|March 2, 2016
New perspectives on rare connective tissue calcifying diseasesNabil A Rashdan, Frank Rutsch, Hervé Kempf, et al.Pageof 12