BACKGROUND: Alström syndrome (ALMS) is a rare autosomal recessive monogenic disease associated with obesity, hyperinsulinemia, and alterations of glucose metabolism that often lead to the development of type 2 diabetes at a young age. OBJECTIVE: To study the relationship between weight and metabolism in a group of ALMS patients and matched controls. RESEARCH DESIGN AND METHODS: Fifteen ALMS patients (eight males, seven females; aged 3-51) were compared in a cross-sectional study with an age- and weight-matched control population. Anthropometric parameters, fat mass, glucose and insulin secretion in basal and dynamic oral glucose tolerance test (OGTT) conditions were measured. Furthermore, anthropometric and body composition data were obtain...
Context: Young-onset obesity is strongly associated with the early development of type 2 diabetes (T...
Context: Young-onset obesity is strongly associated with the early development of type 2 diabetes (T...
Purpose: Alström syndrome (AS) is a rare genetic disease caused by ALMS1 mutations, characterized b...
The progression from obesity to type 2 diabetes in Alström syndrome. Background: Alström syndrome ...
Context: Alstr\uf6m syndrome (AS) is a monogenic form of infancy-onset obesity and insulin resistanc...
CONTEXT: Alström syndrome (AS) is a monogenic form of infancy-onset obesity and insulin resistance, ...
Background: Alström syndrome (AS), a monogenic form of obesity, is caused by recessive mutations in ...
BACKGROUND: Alstr\uf6m syndrome (ALMS) is a rare recessively inherited progressive disease (OMIM 203...
Obesity is a major risk factor for insulin resistance (IR) and its attendant complications. The path...
Alström syndrome is a rare disorder typified by early childhood obesity, neurosensory deficits, card...
Alström syndrome is a rare autosomal recessive genetic disorder characterized by cone-rod dystrophy,...
BACKGROUND AND AIM: We evaluated the relationship between insulin resistance (IR) and insulin secret...
none17Abstract Background and Aim: We evaluated the relationship between insulin resistance (IR) and...
BACKGROUND AND AIM: We evaluated the relationship between insulin resistance (IR) and insulin secret...
Background and Aim We evaluated the relationship between insulin resistance (IR) and insulin secret...
Context: Young-onset obesity is strongly associated with the early development of type 2 diabetes (T...
Context: Young-onset obesity is strongly associated with the early development of type 2 diabetes (T...
Purpose: Alström syndrome (AS) is a rare genetic disease caused by ALMS1 mutations, characterized b...
The progression from obesity to type 2 diabetes in Alström syndrome. Background: Alström syndrome ...
Context: Alstr\uf6m syndrome (AS) is a monogenic form of infancy-onset obesity and insulin resistanc...
CONTEXT: Alström syndrome (AS) is a monogenic form of infancy-onset obesity and insulin resistance, ...
Background: Alström syndrome (AS), a monogenic form of obesity, is caused by recessive mutations in ...
BACKGROUND: Alstr\uf6m syndrome (ALMS) is a rare recessively inherited progressive disease (OMIM 203...
Obesity is a major risk factor for insulin resistance (IR) and its attendant complications. The path...
Alström syndrome is a rare disorder typified by early childhood obesity, neurosensory deficits, card...
Alström syndrome is a rare autosomal recessive genetic disorder characterized by cone-rod dystrophy,...
BACKGROUND AND AIM: We evaluated the relationship between insulin resistance (IR) and insulin secret...
none17Abstract Background and Aim: We evaluated the relationship between insulin resistance (IR) and...
BACKGROUND AND AIM: We evaluated the relationship between insulin resistance (IR) and insulin secret...
Background and Aim We evaluated the relationship between insulin resistance (IR) and insulin secret...
Context: Young-onset obesity is strongly associated with the early development of type 2 diabetes (T...
Context: Young-onset obesity is strongly associated with the early development of type 2 diabetes (T...
Purpose: Alström syndrome (AS) is a rare genetic disease caused by ALMS1 mutations, characterized b...