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The Journal of Rheumatology|November 7, 2006
Bone involvement in generalized crystal-storing histiocytosisVictoire de Lastours, Thomas Papo, Dominique Cazals-Hatem, et al.Journal of Molecular Medicine (Berlin, Germany)|December 31, 2024
Deciphering metabolic shifts in Gaucher disease type 1: a multi-omics studyFranklin Ducatez, Marc G Berger, Carine Pilon, et al.Seminars in Arthritis and Rheumatism|August 4, 2006
Spinal tuberculosis: a longitudinal study with clinical, laboratory, and imaging outcomesLaurence Le Page, Antoine Feydy, Ludovic Rillardon, et al.JIMD Reports|January 21, 2021
Pregnancy outcome in women with Gaucher disease type 1 who had unplanned pregnancies during eliglustat clinical trialsElena Lukina, Manisha Balwani, Nadia Belmatoug, et al.Stem Cells and Development|August 27, 2011
Bone marrow microenvironment in an in vitro model of Gaucher disease: consequences of glucocerebrosidase deficiencySéverine Lecourt, Valérie Vanneaux, Audrey Cras, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 25, 2019
Gaucher Disease in Bone: From Pathophysiology to PracticeDerralynn Hughes, Peter Mikosch, Nadia Belmatoug, et al.Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|October 20, 2005
Is idiopathic chronic pancreatitis an autoimmune disease?Karine Nahon Uzan, Philippe Lévy, Dermot O'Toole, et al.Journal of Chromatography. A|October 25, 2017
Optimization of ultra-high pressure liquid chromatography - tandem mass spectrometry determination in plasma and red blood cells of four sphingolipids and their evaluation as biomarker candidates of Gaucher's diseaseCaroline Chipeaux, Marine de Person, Nathalie Burguet, et al.Blood Cells, Molecules & Diseases|May 21, 2013
Miglustat therapy in type 1 Gaucher disease: clinical and safety outcomes in a multicenter retrospective cohort studyDavid J Kuter, Atul Mehta, Carla E M Hollak, et al.Molecular Genetics and Metabolism|January 2, 2017
Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher RegistryAmal El-Beshlawy, Anna Tylki-Szymanska, Ashok Vellodi, et al.Pageof 8