Genetics of Prader-Willi syndrome
Prader-Willi syndrome (PWS) is a complex genomic imprinting disorder associated with a spectrum of medical, cognitive, behavioural, and psychiatric problems and is also the most common cause of life-threatening obesity that can be effectively treated with hormone therapy and restricted diet, if dete...
| Otros Autores: | , |
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| Formato: | Libro electrónico |
| Idioma: | Inglés |
| Publicado: |
Basel :
MDPI - Multidisciplinary Digital Publishing Institute
2022.
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| Materias: | |
| Ver en Biblioteca Universitat Ramon Llull: | https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009746858806719 |
Tabla de Contenidos:
- About the Editors
- Special Issue: Genetics of Prader-Willi Syndrome
- Single-Case Study of Appetite Control in Prader-Willi Syndrome, Over 12-Years by the Indian Extract Caralluma fimbriata
- Venous Thromboembolism in Prader-Willi Syndrome: A Questionnaire Survey
- The Global Prader-Willi Syndrome Registry: Development, Launch, and Early Demographics
- Early Diagnosis in Prader-Willi Syndrome Reduces Obesity and Associated Co-Morbidities
- Defining Mental and Behavioural Disorders in Genetically Determined Neurodevelopmental Syndromes with Particular Reference to Prader-Willi Syndrome
- Age Distribution, Comorbidities and Risk Factors for Thrombosis in Prader-Willi Syndrome
- Prader-Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion
- Food and Non-Food-Related Behavior across Settings in Children with Prader-Willi Syndrome
- Clinical Observations and Treatment Approaches for Scoliosis in Prader-Willi Syndrome
- The Potential Role of Activating the ATP-Sensitive Potassium Channel in the Treatment of Hyperphagic Obesity
- Growth Trajectories in Genetic Subtypes of Prader-Willi Syndrome
- The Gut Microbiota Profile in Children with Prader-Willi Syndrome
- A 24-Week Physical Activity Intervention Increases Bone Mineral Content without Changes in Bone Markers in Youth with PWS
- Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome
- Pharmacogenetic Testing of Cytochrome P450 Drug Metabolizing Enzymes in a Case Series of Patients with Prader-Willi Syndrome.
