ObjectiveTo estimate the incidence rates of kidney-related clinical outcomes among patients with tuberous sclerosis complex (TSC)-related angiomyolipoma (AML) compared to an age-matched control cohort in the United States.Materials and MethodsThis was a retrospective, observational study. Administrative data from the MarketScan Research Databases were used to select patients with TSC and renal AML. An age-matched group with no TSC or renal AML was identified for comparison. Outcomes were incidence rates per 100 patient-years and number of months to development of hematuria, chronic kidney disease, renal hemorrhage, kidney failure, and inpatient death.ResultsAmong the commercially insured TSC-renal AML patients (N = 605) and matched controls...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
OBJECTIVE:To compare kidney size (used as proxy for total renal angiomyolipoma [rAML] size) and kidn...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...
BackgroundLong-term data from patients with tuberous sclerosis complex (TSC)-associated renal angiom...
BACKGROUND: Long-term data from patients with tuberous sclerosis complex (TSC)-associated renal angi...
Tuberous sclerosis complex is a genetic disorder characterized by hamartomatous lesions in multiple ...
Renal angiomyolipomas are one of the most common renal manifestations in patients with tuberous scle...
Renal angiomyolipomas are one of the most common renal manifestations in patients with tuberous scle...
Abstract Background Tuberous sclerosis complex (TSC) is a rare genetic disorder characterized by ben...
PURPOSE: The purpose of this study is to set guidelines for the management of renal angiomyolipoma (...
Background Renal angiomyolipomas (AMLs) are a major clinical feature in patients wit...
AbstractObjectiveTo deduce recommendations from the literature on the management of kidney damage ca...
International audienceIn patients with tuberous sclerosis complex (TSC), renal complications are not...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
Objectives: To report the frequency of renal symptoms and complications of patients with tuberous sc...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
OBJECTIVE:To compare kidney size (used as proxy for total renal angiomyolipoma [rAML] size) and kidn...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...
BackgroundLong-term data from patients with tuberous sclerosis complex (TSC)-associated renal angiom...
BACKGROUND: Long-term data from patients with tuberous sclerosis complex (TSC)-associated renal angi...
Tuberous sclerosis complex is a genetic disorder characterized by hamartomatous lesions in multiple ...
Renal angiomyolipomas are one of the most common renal manifestations in patients with tuberous scle...
Renal angiomyolipomas are one of the most common renal manifestations in patients with tuberous scle...
Abstract Background Tuberous sclerosis complex (TSC) is a rare genetic disorder characterized by ben...
PURPOSE: The purpose of this study is to set guidelines for the management of renal angiomyolipoma (...
Background Renal angiomyolipomas (AMLs) are a major clinical feature in patients wit...
AbstractObjectiveTo deduce recommendations from the literature on the management of kidney damage ca...
International audienceIn patients with tuberous sclerosis complex (TSC), renal complications are not...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
Objectives: To report the frequency of renal symptoms and complications of patients with tuberous sc...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
OBJECTIVE:To compare kidney size (used as proxy for total renal angiomyolipoma [rAML] size) and kidn...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...