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Journal of Medical Genetics|October 9, 2014
OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epitheliumAjoy Vincent, Nicole Forster, Jason T Maynes, et al.Rheumatology (Oxford, England)|January 18, 2023
Genetics of osteonecrosis in children and adults with systemic lupus erythematosusDeclan Webber, Jingjing Cao, Daniela Dominguez, et al.Diabetology & Metabolic Syndrome|June 3, 2017
Skin autofluorescence, a non-invasive biomarker for advanced glycation end products, is associated with the metabolic syndrome and its individual componentsRobert P van Waateringe, Sandra N Slagter, Andre P van Beek, et al.The Journal of Clinical Endocrinology and Metabolism|October 21, 2011
Genome-wide scan for loci of adolescent obesity and their relationship with blood pressureMelkaye G Melka, Manon Bernard, Amel Mahboubi, et al.Diabetes Care|March 6, 2019
Risk Factors for Kidney Disease in Type 1 DiabetesBruce A Perkins, Ionut Bebu, Ian H de Boer, et al.Journal of the American Society of Nephrology : JASN|October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKDYork Pei, James Obaji, Annie Dupuis, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 5, 2017
X-Linked Glomerulopathy Due to COL4A5 Founder VariantMoumita Barua, Rohan John, Lorenzo Stella, et al.American Journal of Human Genetics|January 8, 2013
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2Pierre Moffatt, Mouna Ben Amor, Francis H Glorieux, et al.Metabolic Bone Disease & Related Research|January 1, 1981
Biochemical markers of bone turnover in Paget's diseaseR G Russell, D J Beard, E C Cameron, et al.Diabetologia|November 22, 2018
Skin autofluorescence predicts incident type 2 diabetes, cardiovascular disease and mortality in the general populationRobert P van Waateringe, Bernardina T Fokkens, Sandra N Slagter, et al.Pageof 44