المؤلفون: Mahmoud, Ranim, Kimonis, Virginia, Butler, Merlin G

المصدر: International Journal of Molecular Sciences. 24(3)

مصطلحات موضوعية: Biological Sciences, Genetics, Brain Disorders, Congenital Structural Anomalies, Clinical Research, Pediatric, Behavioral and Social Science, Nutrition, Intellectual and Developmental Disabilities (IDD), Rare Diseases, Obesity, Metabolic and endocrine, Mental health, Female, Humans, Prader-Willi Syndrome, Transcranial Direct Current Stimulation, Hyperphagia, Anxiety, Mothers, Prader-Willi syndrome, obesity, hyperphagia, clinical trials, genetics, Prader–Willi syndrome, Other Chemical Sciences, Other Biological Sciences, Chemical Physics, Biochemistry and cell biology, Microbiology, Medicinal and biomolecular chemistry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/8g31502g

المؤلفون: Huang, Yue, Grand, Katheryn, Kimonis, Virginia, Butler, Merlin G, Jain, Suparna, Huang, Alden Yen-Wen, Martinez-Agosto, Julian A, Nelson, Stanley F, Sanchez-Lara, Pedro A

المصدر: Journal of Medical Genetics. 59(7)

مصطلحات موضوعية: Biological Sciences, Bioinformatics and Computational Biology, Biomedical and Clinical Sciences, Genetics, Rare Diseases, Congenital Structural Anomalies, Obesity, Clinical Research, Human Genome, Pediatric, Brain Disorders, Intellectual and Developmental Disabilities (IDD), 2.1 Biological and endogenous factors, Aetiology, Child, Female, Humans, Chromosomes, Human, Pair 15, DNA, DNA Methylation, Genomic Imprinting, Mouth Mucosa, Prader-Willi Syndrome, snRNP Core Proteins, Polymorphism, Single Nucleotide, imprinting, point mutation, Medical and Health Sciences, Genetics & Heredity, Clinical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/2k99x00b

المؤلفون: Mahmoud, Ranim, Kimonis, Virginia, Butler, Merlin G

المصدر: International Journal of Molecular Sciences. 23(19)

مصطلحات موضوعية: Biological Sciences, Genetics, Pediatric, Rare Diseases, Obesity, Nutrition, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Stroke, Cancer, Cardiovascular, Metabolic and endocrine, Brain-Derived Neurotrophic Factor, Genome-Wide Association Study, Humans, Leptin, Pro-Opiomelanocortin, Proprotein Convertase 1, Receptor, Melanocortin, Type 4, Receptor, trkB, Receptors, Leptin, obesity, genetics, monogenic, polygenic, Prader-Willi, syndrome, Other Chemical Sciences, Other Biological Sciences, Chemical Physics, Biochemistry and cell biology, Microbiology, Medicinal and biomolecular chemistry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/7b914599

المؤلفون: Mahmoud, Ranim, Swanson, Heidi D, Butler, Merlin G, Flodman, Pamela, Gold, June-Anne, Miller, Jennifer L, Roof, Elizabeth, Osann, Kathryn, Dykens, Elisabeth, Driscoll, Daniel J, Kimonis, Virginia

المصدر: Journal of Clinical Medicine. 11(9)

مصطلحات موضوعية: Paediatrics, Biomedical and Clinical Sciences, Behavioral and Social Science, Violence Research, Brain Disorders, Pediatric, Clinical Research, Mental Health, Basic Behavioral and Social Science, Obesity, Rare Diseases, Prader-Willi syndrome, behavior, genetic subtypes, growth hormone, Prader–Willi syndrome, Clinical Sciences, Biomedical and clinical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/1s27w3bw

المؤلفون: Butler, Merlin G.^{Aff1, IDs10286022009097_cor1}, Victor, A. Kaitlyn^{Aff2, Aff3}, Reiter, Lawrence T.^{Aff2, Aff4}

المصدر: Clinical Autonomic Research: Official journal of the American Autonomic Society and the European Federation of Autonomic Societies. 33(3):281-286

المؤلفون: Veatch, Olivia J, Malow, Beth A, Lee, Hye-Seung, Knight, Aryn, Barrish, Judy O, Neul, Jeffrey L, Lane, Jane B, Skinner, Steven A, Kaufmann, Walter E, Miller, Jennifer L, Driscoll, Daniel J, Bird, Lynne M, Butler, Merlin G, Dykens, Elisabeth M, Gold, June-Anne, Kimonis, Virginia, Bacino, Carlos A, Tan, Wen-Hann, Kothare, Sanjeev V, Peters, Sarika U, Percy, Alan K, Glaze, Daniel G

مصطلحات موضوعية: Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Neurosciences, Lung, Pediatric, Rare Diseases, Behavioral and Social Science, Intellectual and Developmental Disabilities (IDD), Genetics, Mental Health, Clinical Research, Sleep Research, Neurodegenerative, Brain Disorders, Adolescent, Angelman Syndrome, Child, Child, Preschool, Humans, Neurodevelopmental Disorders, Prader-Willi Syndrome, Rett Syndrome, Sleep Wake Disorders, Pediatric sleep, Rare disease, Genetic syndromes, Neurodevelopment, Paediatrics and Reproductive Medicine, Neurology & Neurosurgery, Paediatrics

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6zx0t3dr

المؤلفون: Mahmoud, Ranim, Leonenko, Anna, Butler, Merlin G, Flodman, Pamela, Gold, June‐Anne, Miller, Jennifer L, Roof, Elizabeth, Dykens, Elisabeth, Driscoll, Daniel J, Kimonis, Virginia

المصدر: Clinical Genetics. 100(1)

مصطلحات موضوعية: Congenital Structural Anomalies, Clinical Research, Pediatric, Adolescent, Adult, Body Height, Child, Child, Preschool, Female, Growth Hormone, Humans, Infant, Male, Middle Aged, Phenotype, Prader-Willi Syndrome, Young Adult, dysmorphology, genetic subtypes, genotype–, phenotype, growth, growth hormone treatment, Prader‐, Willi syndrome, Prader-Willi syndrome, genotype-phenotype, Genetics, Clinical Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/96s8x853

المؤلفون: Butler, Merlin G.^Aff4

المساهمون: Butler, Merlin G., editor^Aff1, Lee, Phillip D. K., editor^Aff2, Whitman, Barbara Y., editor^Aff3

المصدر: Management of Prader-Willi Syndrome. :499-527

المؤلفون: Duis, Jessica^Aff4, Butler, Merlin G.^Aff5

المساهمون: Butler, Merlin G., editor^Aff1, Lee, Phillip D. K., editor^Aff2, Whitman, Barbara Y., editor^Aff3

المصدر: Management of Prader-Willi Syndrome. :93-120

المؤلفون: Butler, Merlin G.^Aff4, Thompson, Travis^Aff5

المساهمون: Butler, Merlin G., editor^Aff1, Lee, Phillip D. K., editor^Aff2, Whitman, Barbara Y., editor^Aff3

المصدر: Management of Prader-Willi Syndrome. :3-50