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Renal glycosuria
Leading Article the Molecular and Genetic Base of Congenital Transport
Inherited Renal Tubulopathies—Challenges and Controversies
Distribution of Glucose Transporters in Renal Diseases Leszek Szablewski
Cartilage-Hair Hypoplasia
Genetic Disorder
The Genetic Mechanism of Galactosaemia*
Hypoglycemia Charles Wolf
Renal Tubular Disorders
Renal Sodium–Glucose Transport: Role in Diabetes Mellitus and Potential Clinical Implications George L
Glycosuria: Mechanism and Evaluation
Inherited Tubulopathies of the Kidney Insights from Genetics
The Utilization of Carbohydrates in a Case of Chronic Pentosuria
Tubular Disorders and Tubulointerstitial Diseases
An Unusual Cause of Glycosuria in a 5-Year-Old Child
Pentosuria : Chronic Congenital Pentosuria :A Harmless Metabolic Anomaly
Familial Renal Glucosuria and SGLT2: from a Mendelian Trait to a Therapeutic Target
Hypoglycaemia Withwilms' Tumour*
Appendix I: Reference Intervals
Top View
Galactose Malabsorption
Diabetes Mellitus Is Defined As Condition That Occurs Due To
Statistical Analysis Plan
GLYCOSURIA by STELLA INSTONE, M.D., M.R.C.P
Biochemical Examination of Diabetes Mellitus
Genetic Aspects of Renal Tubular Transport: Diversity and Topology of Carriers
Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function
Descriptions of Phenotypes
Molecular Diagnosis of Maturity Onset Diabetes of the Young in India
Glucose and Amino-Acids
Severe Oxalosis Secondary to Acute Kidney Disease Contributes to Delayed Early Recovery of Renal Function
Supplementum 208 the European Journal of Medical Sciences Ad Swiss Med Wkly 2014;144 November 19, 2014
Common Variants in Mendelian Kidney Disorder Genes and Their Association with Renal Function And
Clinical Practice Guidelines
Abnormalities of Carbohydrate Metabolism in Idiopathic Fanconi Syndrome
Neutropenia Associated with Proximal Renal Tubular Dysfunction and Mild Bilateral Cataract
Regulated by Metabolic Pathway • 3 Types: Anabolic Pathways- Synthesis of Compound – E.G
Tm Glucose in a Case of Congenital Intestinal and Renal Malabsorption of Monosaccharides
Hexose Monophosphate Pathway (HMP) (Or, Pentose Shunt)
SGLT2 Mediates Glucose Reabsorption in the Early Proximal Tubule
Aminoaciduria and Glycosuria in Children
Hypoglycemic Reactions Following Glucose Ingestion
Clinical Aspects of Renal Tubular Disorders*
HNF4A-Related Fanconi Syndrome in a Chinese Patient: a Case Report and Review of the Literature Jiaojiao Liu, Qian Shen, Guomin Li and Hong Xu*
The Fanconi Syndrome and Mechanisms of Tubular Transport Dysfunction KARL S
The Molecular Basis of Glucose Galactose Malabsorption in a Large
A Study of the Genetics of Chronic Kidney Disease