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Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|December 11, 2012
A liquid chromatography mass spectrometry method for the measurement of cystathionine β-synthase activity in cell extractsDesirée E C Smith, Marisa I S Mendes, Leo A J Kluijtmans, et al.Disability and Rehabilitation|June 2, 2018
The need for additional care in patients with classical galactosaemiaLindsey Welling, Anke Meester-Delver, Terry G Derks, et al.Journal of Inherited Metabolic Disease|June 17, 2022
Pregnancy in cystinosis patients with chronic kidney disease: A European case seriesAude Servais, Mirian C H Janssen, Hannah Blakey, et al.Clinics and Research in Hepatology and Gastroenterology|December 3, 2014
The quality of hereditary haemochromatosis guidelines: a comparative analysisAnnick Vanclooster, David Cassiman, Werner Van Steenbergen, et al.JIMD Reports|February 23, 2013
Inheritance of the m.3243A>G mutationPaul de Laat, Saskia Koene, Lambert P W J Vd Heuvel, et al.Journal of Neuromuscular Diseases|July 24, 2023
Indications for Tube Feeding in Adults with Muscular Disorders: A Scoping ReviewMarloes Middelink, Nicol C Voermans, Baziel G M van Engelen, et al.Nederlands Tijdschrift Voor Geneeskunde|July 13, 2010
[New causes of microcytic anaemia: hereditary disorders of iron homeostasis]Karlijn L van Rooijen, Reinier A P Raymakers, Marloes L H Cuijpers, et al.Pediatrics|July 2, 2014
Successful liver transplantation and long-term follow-up in a patient with MPI-CDGMirian C H Janssen, Ruben H de Kleine, Arie P van den Berg, et al.Hypertension (Dallas, Tex. : 1979)|September 16, 2015
Low Plasma Volume in Normotensive Formerly Preeclamptic Women Predisposes to HypertensionRalph R Scholten, Fred K Lotgering, Maria T Hopman, et al.Molecular Genetics and Metabolism|June 6, 2022
Screening and prevalence of cardiac abnormalities on electro- and echocardiography in a large cohort of patients with mitochondrial diseaseConstant L F Hendrix, Frederik M A van den Heuvel, Laura Rodwell, et al.Pageof 12