28 results on '"Butler, Merlin G."'
Search Results
2. Mowat–Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular Interactions
3. The Arduous Path to Drug Approval for the Management of Prader–Willi Syndrome: A Historical Perspective and Call to Action
4. Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader–Willi Syndrome
5. The Autism Spectrum: Behavioral, Psychiatric and Genetic Associations
6. Prader–Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review
7. Clinical Trials in Prader–Willi Syndrome: A Review
8. Chromosomal Microarray Study in Prader-Willi Syndrome
9. Genetics of Obesity in Humans: A Clinical Review
10. Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and Review
11. Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader–Willi Syndrome
12. Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic Testing
13. Hypogonadism in Women with Prader-Willi Syndrome—Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion
14. Hypogonadism in Adult Males with Prader-Willi Syndrome—Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion
15. Special Issue: Genetics of Prader–Willi Syndrome
16. Effects of Transcranial Direct Current Stimulation (tDCS) on Go/NoGo Performance Using Food and Non-Food Stimuli in Patients with Prader–Willi Syndrome
17. Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families
18. Pharmacogenetic Testing of Cytochrome P450 Drug Metabolizing Enzymes in a Case Series of Patients with Prader-Willi Syndrome
19. An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder
20. Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome
21. Clinical Assessment, Genetics, and Treatment Approaches in Autism Spectrum Disorder (ASD)
22. The 15q11.2 BP1-BP2 Microdeletion (Burnside–Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Disorders
23. Clinical Observations and Treatment Approaches for Scoliosis in Prader–Willi Syndrome
24. Age Distribution, Comorbidities and Risk Factors for Thrombosis in Prader–Willi Syndrome
25. Early Diagnosis in Prader–Willi Syndrome Reduces Obesity and Associated Co-Morbidities
26. Venous Thromboembolism in Prader–Willi Syndrome: A Questionnaire Survey
27. High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA Studies
28. Magnesium Supplement and the 15q11.2 BP1–BP2 Microdeletion (Burnside–Butler) Syndrome: A Potential Treatment?
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