Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Audrey Davidow"'
Autor:
Dale C. Hesdorffer, PhD, Barbara L. Kroner, PhD, Jing Shen, PhD, Kathleen Farrell, MB, BCh, BAO, Steve Roberds, PhD, Brandy Fureman, PhD, Brianne McDonald, Lynn Egan, Monika Jones, Monica Weldon, Michael Harris, Kim Rice, Vinez Campbell, Juliann Brandish, Cindy Kercheval, Nichole Villas, Mary Ann Meskis, Vanessa Vogel-Farley, Ilene Miller, JD, Mike Bartenhagen, Heidi Grabenstatter, PhD, Karen Utley, Paige Nues, Angela Cherry, Gina Vozenilek, Scotty Sims, Tracy Dixon Salazar, PhD, Christina SanInocencio, MS, Stephanie Forman, Nora Wong, Kim Bischoff, Julie Walters, Megan O’Boyle, Geraldine Bliss, Audrey Davidow, Lisa Schoyer, Yssa DeWoody, PhD, Kira Wagner, Michael Arcieri, Amber Freed, Kim Nye, Jo Anne Nakagawa, JayEtta Hecker
Publikováno v:
The Journal of Pediatrics: X, Vol 2, Iss , Pp 100021- (2020)
Objective: To evaluate the impact of pediatric sleep disturbances and night-time seizure monitoring of children with rare epilepsy syndromes on the sleep quality and mental health of caregivers. Study design: A cross-sectional study was conducted usi
Externí odkaz:
https://doaj.org/article/4d344e0f844b48a68a42cce3eb0d52ce
Publikováno v:
Pharmaceutical Research. 37
Individuals with the rare genetic disorder Pitt Hopkins Syndrome (PTHS) do not have sufficient expression of the transcription factor 4 (TCF4) which is located on chromosome 18. TCF4 is a basic helix-loop-helix E protein that is critical for the norm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96552a51823c0e7e0ee50e7c6dd1cdf6
https://doi.org/10.1007/s11095-020-02853-5
https://doi.org/10.1007/s11095-020-02853-5
Publikováno v:
Pharm Res
PURPOSE: Individuals with the rare genetic disorder Pitt Hopkins Syndrome (PTHS) do not have sufficient expression of the transcription factor 4 (TCF4) which is located on chromosome 18. TCF4 is a basic helix-loop-helix E protein that is critical for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46316461f2c88d967abca769f47e52ab
https://pubmed.ncbi.nlm.nih.gov/32529312
https://pubmed.ncbi.nlm.nih.gov/32529312
Autor:
Ilene Miller, Amber Freed, Yssa DeWoody, Kim Nye, Karen Utley, Julie Walters, Heidi L. Grabenstatter, JayEtta Hecker, Jo Anne Nakagawa, Monica Weldon, Mary Ann Meskis, Cindy Kercheval, Dale C. Hesdorffer, Gina Vozenilek, Barbara Kroner, Monika Jones, Vinez Campbell, Nora Wong, Geraldine Bliss, Audrey Davidow, Michael R. Harris, Kira Wagner, Megan O’Boyle, Mike Bartenhagen, Scotty Sims, Kim Rice, Lisa Schoyer, Nichole Villas, Kim Bischoff, Jing Shen, Christina SanInocencio, Kathleen Farrell, Vanessa Vogel-Farley, Lynn Egan, Juliann Brandish, Angela Cherry, Brianne McDonald, Brandy E. Fureman, Steve Roberds, Tracy Dixon Salazar, Michael Arcieri, Paige Nues, Stephanie Forman
Publikováno v:
The Journal of Pediatrics: X, Vol 2, Iss, Pp 100021-(2020)
Objective To evaluate the impact of pediatric sleep disturbances and night-time seizure monitoring of children with rare epilepsy syndromes on the sleep quality and mental health of caregivers. Study design A cross-sectional study was conducted using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f723d49822266836e5033d3ce31e3d0c
https://doi.org/10.1016/j.ympdx.2020.100021
https://doi.org/10.1016/j.ympdx.2020.100021
Autor:
Nhan Thi Ho, Barbara Kroner, Zachary Grinspan, Brandy Fureman, Kathleen Farrell, Jingzhou Zhang, Janice Buelow, Dale C. Hesdorffer, Brianne McDonald, Monica Weldon, Juliann Bradish, Vanessa Vogel-Farley, Paige Nues, Tracy Dixon-Salazar, Geraldine Bliss, Yssa DeWoody, Jo Anne Nakagawa, Michael Harris, Glen Arm, Heather Jackson, Ilene Miller, Gina Vozenilek, Nora Wong, Audrey Davidow, Kira Wagner, JayEtta Hecker, Lynn Egan, Heidi Grabenstatter, Mary Anne Meskis, Mike Bartenhagen, Scotty Sims, Julie Walters, Lisa Schoyer, Kim Nye
Publikováno v:
The Journal of Pediatrics. 203:249-258.e5
To describe the prevalence and characteristics of comorbidities in persons with rare epilepsies.Persons with rare epilepsies and caregivers of those affected were recruited through the Epilepsy Foundation and more than 30 rare epilepsy advocacy organ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d8414b3fa41111f51f91266661bc69a
https://doi.org/10.1016/j.jpeds.2018.07.055
https://doi.org/10.1016/j.jpeds.2018.07.055