Item does not contain fulltextWe assessed bone mineral density (BMD) and body composition in children with Noonan's syndrome (NS) before and during growth hormone (GH) treatment. Sixteen children (12 boys, 4 girls) with NS aged 5.8-14.2 (mean 10.0) years were studied for 2 years. Anthropometry, BMD measurements by radiographic absorptiometry and bioimpedance measurements (Akern-BIA 101/S) were performed at baseline and after 3, 6, 12 and 24 months. Daily GH dosage was 0.05 mg/kg. Trabecular volumetric BMD was normal; cortical BMD was in the lower normal range at baseline and slightly increased over the 2 years. Fat free mass and total body water were below normal at the start and increased significantly over the first 3 months, with a sligh...
Background/Aims: The aim of the present study was to evaluate bone mineral density (BMD) and body co...
BACKGROUND: Bone mineral density (BMD) is unknown in children with Prader-Willi syndrome (PWS), but ...
BackgroundDespite different genetic background, Noonan syndrome (NS) shares similar phenotype featur...
We assessed bone mineral density (BMD) and body composition in children with Noonan's syndrome (NS) ...
We assessed bone mineral density (BMD) and body composition in children with Noonan's syndrome (NS) ...
Item does not contain fulltextThe aim of the study was to evaluate the effect of continuous and disc...
Item does not contain fulltextThe role of GH insufficiency in the pathogenesis of short stature in N...
International audienceAlthough musculoskeletal abnormalities have long been described in patients wi...
Noonan syndrome (NS) is an autosomal dominant disorder that involves multiple organ systems, with sh...
Item does not contain fulltextBACKGROUND: Bone mineral density (BMD) is unknown in children with Pra...
Item does not contain fulltextShort stature is one of the major features of Noonan's syndrome (NS). ...
Objectives: Growth impairment is a common manifestation in Noonan syndrome (NS). Recombinant human G...
Background: Noonan syndrome (NS) is a genetic disorder characterized by phenotypic features, includi...
Objective: Noonan syndrome (NS) is a multisystem disorder, and short stature is its most striking ma...
Background: Bone mineral density (BMD) is unknown in children with Prader-Willi syndrome (PWS), but ...
Background/Aims: The aim of the present study was to evaluate bone mineral density (BMD) and body co...
BACKGROUND: Bone mineral density (BMD) is unknown in children with Prader-Willi syndrome (PWS), but ...
BackgroundDespite different genetic background, Noonan syndrome (NS) shares similar phenotype featur...
We assessed bone mineral density (BMD) and body composition in children with Noonan's syndrome (NS) ...
We assessed bone mineral density (BMD) and body composition in children with Noonan's syndrome (NS) ...
Item does not contain fulltextThe aim of the study was to evaluate the effect of continuous and disc...
Item does not contain fulltextThe role of GH insufficiency in the pathogenesis of short stature in N...
International audienceAlthough musculoskeletal abnormalities have long been described in patients wi...
Noonan syndrome (NS) is an autosomal dominant disorder that involves multiple organ systems, with sh...
Item does not contain fulltextBACKGROUND: Bone mineral density (BMD) is unknown in children with Pra...
Item does not contain fulltextShort stature is one of the major features of Noonan's syndrome (NS). ...
Objectives: Growth impairment is a common manifestation in Noonan syndrome (NS). Recombinant human G...
Background: Noonan syndrome (NS) is a genetic disorder characterized by phenotypic features, includi...
Objective: Noonan syndrome (NS) is a multisystem disorder, and short stature is its most striking ma...
Background: Bone mineral density (BMD) is unknown in children with Prader-Willi syndrome (PWS), but ...
Background/Aims: The aim of the present study was to evaluate bone mineral density (BMD) and body co...
BACKGROUND: Bone mineral density (BMD) is unknown in children with Prader-Willi syndrome (PWS), but ...
BackgroundDespite different genetic background, Noonan syndrome (NS) shares similar phenotype featur...