Pages that link to "Q68518778"
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The following pages link to Renal disease in type I glycogen storage disease (Q68518778):
Displaying 50 items.
- Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus (Q24671452) (← links)
- Glycogen storage disease type 1a in Israel: Biochemical, clinical, and mutational studies (Q28251413) (← links)
- Glucose-6-phosphatase dependent substrate transport in the glycogen storage disease type-1a mouse (Q28279887) (← links)
- Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy (Q28296663) (← links)
- Advanced glycation end products and the absence of premature atherosclerosis in glycogen storage disease Ia. (Q33563689) (← links)
- Hypoglycemia in infants and children (Q33740556) (← links)
- Liver transplantation for glycogen storage disease types I, III, and IV (Q33797826) (← links)
- Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy. (Q33802779) (← links)
- Hypoglycemia in infancy and childhood (Q33894759) (← links)
- Glycogen storage diseases: new perspectives (Q34098766) (← links)
- Oxidative stress mediates nephropathy in type Ia glycogen storage disease. (Q34807521) (← links)
- AA Amyloidosis in a patient with glycogen storage disorder and progressive chronic kidney disease (Q35453099) (← links)
- Hepatorenal Correction in Murine Glycogen Storage Disease Type I With a Double-stranded Adeno-associated Virus Vector (Q35568513) (← links)
- An overview of renal pathology in insulin-dependent diabetes mellitus in relationship to altered glomerular hemodynamics (Q35589622) (← links)
- Angiotensin mediates renal fibrosis in the nephropathy of glycogen storage disease type Ia (Q36717914) (← links)
- Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease (Q36777763) (← links)
- The molecular basis of the hepatic microsomal glucose-6-phosphatase system (Q37173118) (← links)
- Renal function in glycogen storage disease type I, natural course, and renopreservative effects of ACE inhibition (Q37415732) (← links)
- Type I glycogen storage disease: kidney involvement, pathogenesis and its treatment (Q37711983) (← links)
- Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics (Q38263927) (← links)
- Pathogenesis and significance of nonprimary focal and segmental glomerulosclerosis (Q38639121) (← links)
- Psammomys obesus, a particularly important animal model for the study of the human diabetic nephropathy (Q38738365) (← links)
- Proteinuria in a child with sialidosis: case report and histological studies (Q38790758) (← links)
- The hepatic glycogen storage diseases--problems beyond childhood (Q40379240) (← links)
- Hyperglycaemia associated with lactic acidaemia in a renal allograft recipient with type I glycogen storage disease (Q41973160) (← links)
- Immunohistochemical localisation of glucose-6-phosphatase in developing human kidney (Q42492987) (← links)
- The long-term outcome of patients with glycogen storage diseases (Q43577266) (← links)
- Variability of renal length in type I glycogen storage disease (Q43738637) (← links)
- Effect of ramipril in a patient with glycogen storage disease type I and nephrotic-range proteinuria (Q43840604) (← links)
- Rescue administration of a helper-dependent adenovirus vector with long-term efficacy in dogs with glycogen storage disease type Ia (Q44199828) (← links)
- Gouty tendinitis revealing glycogen storage disease Type Ia in two adolescents (Q44416665) (← links)
- In search of proof-of-concept: gene therapy for glycogen storage disease type Ia. (Q45876893) (← links)
- Activation of glycolysis and apoptosis in glycogen storage disease type Ia. (Q46023432) (← links)
- Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes (Q46210619) (← links)
- Renal sonographic findings of type I glycogen storage disease in infancy and early childhood (Q46500323) (← links)
- Elements of diabetic nephropathy in a patient with GLUT 2 deficiency (Q46804403) (← links)
- Renal function and kidney size in glycogen storage disease type I. (Q47412403) (← links)
- Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy (Q50355525) (← links)
- Tight metabolic control plus ACE inhibitor therapy improves GSD I nephropathy (Q50945731) (← links)
- Glycogenosis type I and diabetes mellitus: a common mechanism for renal dysfunction? (Q51541525) (← links)
- Biochemical evidence for the requirement of continuous glucose therapy in young adults with type 1 glycogen storage disease (Q51597579) (← links)
- The human embryonic-fetal kidney endoplasmic reticulum phosphate-pyrophosphate transport protein. (Q52202654) (← links)
- Diabetes-like renal glomerular disease in Fanconi-Bickel syndrome. (Q52208070) (← links)
- Urolithiasis and psoas abscess in a 2-year-old boy with type 1 glycogen storage disease. (Q53522984) (← links)
- Long-term outcome of liver transplantation in patients with glycogen storage disease type Ia. (Q53542646) (← links)
- Glycogen Storage Disease Type I Presenting with Hypertension During Infancy. (Q53596292) (← links)
- Nephrolithiasis, hypocitraturia, and a distal renal tubular acidification defect in type 1 glycogen storage disease (Q63384428) (← links)
- Echogenic kidneys and medullary calcium deposition in a young child with glycogen storage disease type 1a (Q68137522) (← links)
- Genetic Factors and Susceptibility to Diabetic Nephropathy (Q68420453) (← links)
- Hypertension in a child with type IA glycogen storage disease (Q68520418) (← links)