Related Experiment Videos
Molecular genetics of basement membranes: the paradigm of Alport syndrome
1INSERM U423, Hôpital Necker-Enfants Malades, Paris, France.
Kidney International. Supplement
|June 1, 1995
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).
Journal of medical genetics·2009
Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutation.
European journal of ophthalmology·2008
Effect of kidney disease on glucose handling (including genetic defects).
Kidney international. Supplement·2011
Need for better diabetes treatment for improved renal outcome.
Kidney international. Supplement·2011
Glucose dynamics and mechanistic implications of SGLT2 inhibitors in animals and humans.
Kidney international. Supplement·2011
SGLT2 inhibitors: molecular design and potential differences in effect.
Kidney international. Supplement·2011
Glucose handling by the kidney.
Kidney international. Supplement·2011
Bone: from a reservoir of minerals to a regulator of energy metabolism.
Kidney international. Supplement·2011
Congenital Hyperinsulinism in the Era of Precision Medicine: Genetically Driven Diagnosis and Novel Therapies.
Children (Basel, Switzerland)·2026
Antioxidant Strategies for Inherited Retinal Degenerations in the Era of Gene Therapy.
Antioxidants (Basel, Switzerland)·2026
Genetic Testing in Irritable Bowel Syndrome.
Gastroenterology clinics of North America·2026
Genetics of Inflammatory Bowel Disease-What is Unsought Goes Undetected.
Gastroenterology clinics of North America·2026