57 results on '"Butler, Merlin G."'
Search Results
2. Prader–Willi syndrome and early‐onset morbid obesity NIH rare disease consortium: A review of natural history study
3. Rare FMR1 gene mutations causing fragile X syndrome: A review
4. Effects of MetAP2 inhibition on hyperphagia and body weight in Prader–Willi syndrome: A randomized, double‐blind, placebo‐controlled trial
5. Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome
6. Benefits and limitations of prenatal screening for Prader–Willi syndrome
7. Transcranial Direct Current Stimulation Reduces Food-Craving and Measures of Hyperphagia Behavior in Participants With Prader-Willi Syndrome
8. Currently Recognized Genes for Schizophrenia: High-Resolution Chromosome Ideogram Representation
9. Elevated plasma oxytocin levels in children with Prader–Willi syndrome compared with healthy unrelated siblings
10. Metabolic profiling in Prader–Willi syndrome and nonsyndromic obesity: sex differences and the role of growth hormone
11. High Plasma Neurotensin Levels in Children with Prader–Willi Syndrome
12. Increased Plasma Chemokine Levels in Children with Prader–Willi Syndrome
13. Exon Microarray Analysis of Human Dorsolateral Prefrontal Cortex in Alcoholism
14. Growth hormone receptor (GHR) gene polymorphism and prader–willi syndrome
15. Growth Hormone Research Society Workshop Summary: Consensus Guidelines for Recombinant Human Growth Hormone Therapy in Prader-Willi Syndrome
16. Comparison of biological specimens and DNA collection methods for PCR amplification and microarray analysis
17. Development and Implementation of Electronic Growth Charts for Infants With Prader–Willi Syndrome
18. X Chromosome Inactivation in Women with Alcoholism
19. Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele
20. The neuroanatomy of genetic subtype differences in Prader–Willi syndrome
21. Umbilical cord blood banking: an update
22. TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome
23. Nutritional phases in Prader-Willi syndrome
24. An interstitial 15q11-q14 deletion: Expanded Prader-Willi syndrome phenotype
25. An 18-year follow-up report on an infant with a duplication of 9q34
26. Genomic imprinting disorders in humans: a mini-review
27. Is gestation in Prader-Willi syndrome affected by the genetic subtype?
28. Morning melatonin levels in Prader–Willi syndrome
29. “Efficacy of Laparoscopic Sleeve Gastrectomy as a Stand-alone Technique for Children with Morbid Obesity” and “BioEnterics® Intragastric Balloon for Treatment of Morbid Obesity in Prader-Willi Syndrome: Specific Risks and Benefits”
30. Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndrome
31. Follicle stimulating and leutinizing hormones, estradiol and testosterone in Prader–Willi syndrome
32. Autistic and dysmorphic features associated with a submicroscopic 2q33.3–q34 interstitial deletion detected by array comparative genomic hybridization
33. Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts
34. Neuroimaging findings in macrocephaly–capillary malformation: A longitudinal study of 17 patients
35. Deaths due to choking in Prader–Willi syndrome
36. Thyroid function studies in Prader–Willi syndrome
37. X-chromosome inactivation patterns in females with Prader–Willi syndrome
38. Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader–Willi syndrome
39. Whole genome microarray analysis of gene expression in Prader–Willi syndrome
40. Energy expenditure and physical activity in Prader–Willi syndrome: Comparison with obese subjects
41. Plasma obestatin and ghrelin levels in subjects with Prader–Willi syndrome
42. Management of obesity in Prader-Willi syndrome
43. Expression-Based T2D Profiling Reveals a Shared, Putative Transcription Factor Binding Site: 1055-P
44. A 9-year-old male with a duplication of chromosome 3p25.3p26.2: Clinical report and gene expression analysis
45. Deletion of and Novel Missense Mutation in POU3F4 in 2 Families Segregating X-Linked Nonsyndromic Deafness
46. Maladaptive behaviors and risk factors among the genetic subtypes of Prader–Willi syndrome
47. DO KNOWN MUTATIONS IN NEUROLIGIN GENES (NLGN3 AND NLGN4) CAUSE AUTISM?
48. Specific Genetic Diseases at Risk for Sedation/Anesthesia Complications
49. Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy
50. Plasma leptin concentrations in lean and obese human subjects and Prader-Willi syndrome: Comparison of RIA and ELISA methods
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