Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hailee Hunt-Hawkins"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background Prader-Willi syndrome (PWS) is a rare, neurodevelopmental disorder caused by the lack of expression of paternally imprinted genes on chromosome 15q11-13. PWS features a complex behavioral phenotype, including hyperphagia, anxiety,
Externí odkaz:
https://doaj.org/article/86fa6043f60a4851b949d4e7792b7103
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
IntroductionPeople with neurodevelopmental disabilities, including Prader-Willi syndrome (PWS), are at heightened risk for the negative sequalae of loneliness, including depression and anxiety. While societal factors such as stigma or limited social
Externí odkaz:
https://doaj.org/article/ef059e1074024262b293f6e038ab7cb8
Autor:
Elisabeth M. Dykens, Elizabeth Roof, Hailee Hunt-Hawkins, Nathan Dankner, Evon Batey Lee, Carolyn M. Shivers, Christopher Daniell, Soo-Jeong Kim
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 9, Iss 1, Pp 1-12 (2017)
Abstract Background A small percentage of people with autism spectrum disorders (ASD) have alterations in chromosome 15q11.2-q3, the critical region for Prader-Willi syndrome (PWS). Data are limited, however, on the rates and characteristics of ASD i
Externí odkaz:
https://doaj.org/article/56302f464d3d41da9dff7034a544b7c9
Autor:
Elisabeth M Dykens, Elizabeth Roof, Hailee Hunt-Hawkins, Christopher Daniell, Sarah Jurgensmeyer
Publikováno v:
PLoS ONE, Vol 14, Iss 10, p e0223162 (2019)
IntroductionPeople with Prader-Willi syndrome (PWS) have a distinctive behavioral phenotype that includes intellectual disability, compulsivity, inattention, inflexibility and insistence on sameness. Inflexibility and inattention are at odds with the
Externí odkaz:
https://doaj.org/article/4b512e0a1d384517b2230f17029dfdb5
Publikováno v:
Brain and language. 236
Angelman syndrome (AS) is known to affect expressive and receptive communication abilities. This study examined individual differences in neural mechanisms underlying speech processing in children with AS (n = 24, M age = 10.01 years) and typical dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a57eefeb01b7256365f00829351c6912
https://pubmed.ncbi.nlm.nih.gov/36502770
https://pubmed.ncbi.nlm.nih.gov/36502770
Publikováno v:
Physiol Behav
Hyperphagia and the associated interest in food is a characteristic feature of Prader-Willi syndrome (PWS) that emerges during childhood and remains a life-long concern. This study examined neural responses reflecting food cue salience in children wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f09ccd5a016035607c1016dc65c71320
https://hdl.handle.net/20.500.12511/7689
https://hdl.handle.net/20.500.12511/7689
Autor:
Christopher Daniell, Hailee Hunt-Hawkins, Carolyn M. Shivers, Nathan Dankner, Soo Jeong Kim, Elizabeth Roof, Elisabeth M. Dykens, Evon Batey Lee
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 9, Iss 1, Pp 1-12 (2017)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
Background A small percentage of people with autism spectrum disorders (ASD) have alterations in chromosome 15q11.2-q3, the critical region for Prader-Willi syndrome (PWS). Data are limited, however, on the rates and characteristics of ASD in PWS. Pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1599d5f066153e71157672e7ef69a2c4
http://link.springer.com/article/10.1186/s11689-017-9200-2
http://link.springer.com/article/10.1186/s11689-017-9200-2
Autor:
Hailee Hunt-Hawkins, Christopher Daniell, Elizabeth Roof, Elisabeth M. Dykens, Sarah Jurgensmeyer
Publikováno v:
PLoS ONE, Vol 14, Iss 10, p e0223162 (2019)
PLoS ONE
PLoS ONE
IntroductionPeople with Prader-Willi syndrome (PWS) have a distinctive behavioral phenotype that includes intellectual disability, compulsivity, inattention, inflexibility and insistence on sameness. Inflexibility and inattention are at odds with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::938456b4a2e7e941814b41a0f0635fb6
https://doi.org/10.1371/journal.pone.0223162
https://doi.org/10.1371/journal.pone.0223162
Cognitive and adaptive advantages of growth hormone treatment in children with Prader-Willi syndrome
Publikováno v:
Journal of child psychology and psychiatry, and allied disciplines. 58(1)
Background People with Prader-Willi syndrome (PWS) typically have mild to moderate intellectual deficits, compulsivity, hyperphagia, obesity, and growth hormone deficiencies. Growth hormone treatment (GHT) in PWS has well-established salutatory effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3b73dae45377a4aa330d97625e545ca
https://pubmed.ncbi.nlm.nih.gov/27481444
https://pubmed.ncbi.nlm.nih.gov/27481444