Showing results (161-170 of 246) with videos related to

Sort By:
Pageof 25
Clinical Kidney Journal|October 27, 2025
Growth hormone treatment associates with improved circulating anti-aging protein Klotho and reduced arterial stiffness in children with CKDStella Stabouli, Maren Leifheit-Nestler, Michael Föller, et al.
Clinical Journal of the American Society of Nephrology : CJASN|December 18, 2012
Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndromeJohannes Hofer, Andreas R Janecke, L B Zimmerhackl, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 23, 2020
Relationship between GFR, intact PTH, oxidized PTH, non-oxidized PTH as well as FGF23 in patients with CKDShufei Zeng, Uwe Querfeld, Martina Feger, et al.
Human Molecular Genetics|November 17, 2018
SPINT2 (HAI-2) missense variants identified in congenital sodium diarrhea/tufting enteropathy affect the ability of HAI-2 to inhibit prostasin but not matriptaseLasse Holt-Danborg, Julia Vodopiutz, Annika W Nonboe, et al.
The American Journal of Pathology|April 26, 2011
Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and functionRobert Gruber, Peter M Elias, Debra Crumrine, et al.
Traffic (Copenhagen, Denmark)|April 14, 2017
Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion diseaseGeorg F Vogel, Andreas R Janecke, Iris M Krainer, et al.
Brain : a Journal of Neurology|March 25, 2016
De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth diseaseWilliam W Motley, Paulius Palaima, Sabrina W Yum, et al.
Clinical Journal of the American Society of Nephrology : CJASN|June 26, 2010
The Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) study: objectives, design, and methodologyUwe Querfeld, Ali Anarat, Aysun K Bayazit, et al.
The Journal of Investigative Dermatology|December 27, 2016
Autosomal Recessive Keratoderma-Ichthyosis-Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen ModificationRobert Gruber, Clare Rogerson, Christian Windpassinger, et al.
Brain : a Journal of Neurology|May 18, 2011
Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skinMichaela Auer-Grumbach, Martin Weger, Regina Fink-Puches, et al.
Pageof 25