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Drug Discovery Today|February 19, 2013
Cysteamine: an old drug with new potentialMartine Besouw, Rosalinde Masereeuw, Lambert van den Heuvel, et al.Molecular Genetics and Metabolism|July 27, 2012
Halitosis in cystinosis patients after administration of immediate-release cysteamine bitartrate compared to delayed-release cysteamine bitartrateMartine Besouw, Albert Tangerman, Elisabeth Cornelissen, et al.Ultrasound (Leeds, England)|February 16, 2023
OHVIRA syndrome: Early recognition prevents genitourinary complicationsAnne Sijmons, Suzanne Broekhuizen, Karin van der Tuuk, et al.Molecular Genetics and Metabolism|May 22, 2007
The origin of halitosis in cystinotic patients due to cysteamine treatmentMartine Besouw, Henk Blom, Albert Tangerman, et al.Plos One|August 23, 2012
Stem cell microvesicles transfer cystinosin to human cystinotic cells and reduce cystine accumulation in vitroDiana M Iglesias, Reyhan El-Kares, Anna Taranta, et al.Journal of Inherited Metabolic Disease|September 18, 2022
Outcome of infantile nephropathic cystinosis depends on early intervention, not genotype: A multicenter sibling cohort studyKoenraad Veys, Ward Zadora, Katharina Hohenfellner, et al.Journal of Inherited Metabolic Disease|September 8, 2021
Human and animal fertility studies in cystinosis reveal signs of obstructive azoospermia, an altered blood-testis barrier and a subtherapeutic effect of cysteamine in testisAhmed Reda, Koenraad Veys, Prashant Kadam, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 28, 2022
Clinical and genetic characteristics of Dent's disease type 1 in EuropeCarla Burballa, Gerard Cantero-Recasens, Larisa Prikhodina, et al.Kidney International|October 26, 2024
Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2cMax Brunkhorst, Lena Brunkhorst, Helge Martens, et al.Pageof 2