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D22 Artículos: Envíos recientes
Mostrando ítems 481-500 de 1093
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Spinocerebellar ataxia type 15 caused by missense variants in the ITPR1 gene
(Wiley, 2023-05-08) -
Uncovering genetic causes of hypophosphatemia
(Oxford Blackwell Scientific, 2023) -
Machine learning algorithm improves the detection of NASH (NAS-based) and at-risk NASH: A development and validation study
(American Association for the Study of Liver Diseases, 2023) -
Clinical profiles and patterns of kidney disease progression in C3 glomerulopathy
(Wolters Kluwer, 2023) -
A call for the comprehensive diagnosis of viral hepatitis as a key step towards its elimination
(Wiley-Blackwell, 2023) -
Individualizing anaemia therapy
(Oxford University Press, 2010) -
Serum lipids and bone metabolism in Spanish men: the Camargo cohort study
(The Japan Endocrine Society, 2010)