Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Elisabeth A, de Blieck"'
Autor:
Elizabeth McCusker, Michael P. McDermott, Wai Lun Alan Fung, Andrew McGarry, Merit Cudkowicz, Elisabeth A. de Blieck, Karl Kieburtz, Jing Peng, Coordinators
Publikováno v:
Neurology. 92(14)
ObjectiveMost suicidality literature in Huntington disease (HD) is based on natural history studies or retrospective reviews, but reports on risk factors from clinical trials are limited.MethodsWe analyzed 609 participants from 2CARE, a randomized, d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::847b77a8b7e211bbc4d086f9dbd48ab3
https://pubmed.ncbi.nlm.nih.gov/32253298
https://pubmed.ncbi.nlm.nih.gov/32253298
Autor:
Kelly L. Andrzejewski, Madhurima Majumder, Elisabeth A. de Blieck, Michael P. McDermott, Merit Cudkowicz, Haruhiko Banno, Peggy Auinger, Alyssa Murphy, Nazem Atassi
Publikováno v:
Journal of Huntington's disease. 6(2)
BACKGROUND Excellent retention in Huntington disease (HD) clinical trials is essential for testing new therapies. The stage of disease, cognitive status, and availability of a care partner may influence retention in HD clinical trials. OBJECTIVE We s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c91e1e8e235992d21dbfb9cb0a8d2b98
https://pubmed.ncbi.nlm.nih.gov/28922164
https://pubmed.ncbi.nlm.nih.gov/28922164
Autor:
Dai Watanabe, Elisabeth A. de Blieck, Mitsuaki Kitano, Kazunori Hosoe, M. Flint Beal, Padmaja Yerramilli-Rao, Iwao Funahashi, Karl Kieburtz, Merit Cudkowicz
Publikováno v:
International Journal of Toxicology. 31:58-69
To support phase III testing of coenzyme Q10 (CoQ10) in humans, we conducted pharmacokinetic and toxicology studies in beagle dogs. Following single gavage administration of CoQ10 at 600, 1200, 1800, or 2400 mg/kg per d no obvious dose response was o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb5244d640bfdc635d02e4a2596e038e
https://doi.org/10.1177/1091581811425256
https://doi.org/10.1177/1091581811425256
Autor:
Frederick J. Marshall, Elisabeth A. de Blieck, Paul G. Rothberg, Jennifer Cialone, Amy Vierhile, Erika F. Augustine, Nicole Newhouse, Jonathan W. Mink, Heather R. Adams, Jennifer M. Kwon
Publikováno v:
Journal of Inherited Metabolic Disease. 34:1075-1081
Juvenile neuronal ceroid lipofuscinosis (JNCL; CLN3 disease; Batten disease) is an autosomal recessive neurodegenerative disease of childhood that typically presents at school age with vision loss followed by progressive cognitive decline, motor dysf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67ef6423d5676541d57b5eb4a5a17d53
https://doi.org/10.1007/s10545-011-9346-0
https://doi.org/10.1007/s10545-011-9346-0
Autor:
Sam Frank, Michele Goldstein, Tammie Kelsey, Merit Cudkowicz, Kimberly L. Ferrante, Elisabeth A. de Blieck, Joseph Weber, Linda Metakis, Bernard Ravina, Ira Shoulson, Robert J. Ferrante, Karl Kieburtz, Danna Jennings, Francis O. Walker, Arthur Watts, Peter Como, Michael P. McDermott, Vicki Hunt, H. Christopher Hyson, Carol Zimmerman, Susan E. Browne, Susan Daigneault, M. Flint Beal, Kristyn Newhall
Publikováno v:
Movement Disorders. 25:1924-1928
Coenzyme Q10 (CoQ(10)), a potential neuroprotective compound, was previously investigated at a dosage of 600 mg/day in Huntington's disease (HD) patients and demonstrated a trend toward slowing disease progression. Higher CoQ(10) dosages may prove be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57941278e1c9c8de99960544f058b2a4
https://doi.org/10.1002/mds.22408
https://doi.org/10.1002/mds.22408
Autor:
Jennifer M. Kwon, Jonathan W. Mink, Rachel Jordan, Christopher A. Beck, Elisabeth A. de Blieck, Heather R. Adams, Frederick J. Marshall, David A. Pearce, Erika Levy, Erika F. Augustine, Amy Vierhile
Publikováno v:
Developmental Medicine & Child Neurology. 52:637-643
Aim The primary aim of this investigation was to examine genotype and clinical phenotype differences in individuals with juvenile neuronal ceroid lipofuscinosis (JNCL) who were homozygous for a common disease-causing deletion or compound heterozygous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84860ae11fcba8209ec3c6a7da41aa7c
https://doi.org/10.1111/j.1469-8749.2010.03628.x
https://doi.org/10.1111/j.1469-8749.2010.03628.x
Autor:
Cynthia R. Howard, Elisabeth A. de Blieck, Cynthia B. ten Hoopen, Fred M. Howard, Bruce P. Lanphear, Ruth A. Lawrence
Publikováno v:
Pediatrics. 104:1204-1207
Background. To prevent breastfeeding problems, cup-feeding has been recommended as a method of providing medically necessary supplemental feedings to breastfed infants. Objectives. To compare amounts ingested, administration time, and infant physiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b809b20408a80a5231611b8a02d300
https://doi.org/10.1542/peds.104.s6.1204
https://doi.org/10.1542/peds.104.s6.1204
Autor:
Jennifer Cialone, Nicole Newhouse, Leon S. Dure, Heather R. Adams, Katherine Rose, Elisabeth A. de Blieck, Erika Levy, Jonathan W. Mink, Amy Vierhile, Jennifer M. Kwon, Denia Ramirez-Montealegre, Erika F. Augustine, Frederick J. Marshall
Publikováno v:
Journal of inherited metabolic disease. 35(3)
Juvenile neuronal ceroid lipofuscinosis (JNCL; CLN3 disease; Batten disease) is an autosomal recessive neurodegenerative disease of childhood. Symptoms typically present at school age with vision loss followed by progressive cognitive decline, motor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79a61fcb40dd4cdf10357712143131a7
https://pubmed.ncbi.nlm.nih.gov/22167274
https://pubmed.ncbi.nlm.nih.gov/22167274
Autor:
H Christopher, Hyson, Karl, Kieburtz, Ira, Shoulson, Michael, McDermott, Bernard, Ravina, Elisabeth A, de Blieck, Merit E, Cudkowicz, Robert J, Ferrante, Peter, Como, Sam, Frank, Carol, Zimmerman, Kimberly, Ferrante, Kristyn, Newhall, Danna, Jennings, Tammie, Kelsey, Francis, Walker, Vicki, Hunt, Susan, Daigneault, Michele, Goldstein, Joseph, Weber, Arthur, Watts, M Flint, Beal, Susan E, Browne, Linda J, Metakis
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 25(12)
Coenzyme Q10 (CoQ(10)), a potential neuroprotective compound, was previously investigated at a dosage of 600 mg/day in Huntington's disease (HD) patients and demonstrated a trend toward slowing disease progression. Higher CoQ(10) dosages may prove be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::132468d80c70a2558f024c43eb71626b
https://pubmed.ncbi.nlm.nih.gov/20669312
https://pubmed.ncbi.nlm.nih.gov/20669312
Autor:
Heather R, Adams, Christopher A, Beck, Erika, Levy, Rachel, Jordan, Jennifer M, Kwon, Frederick J, Marshall, Amy, Vierhile, Erika F, Augustine, Elisabeth A, de Blieck, David A, Pearce, Jonathan W, Mink
Publikováno v:
Developmental medicine and child neurology. 52(7)
The primary aim of this investigation was to examine genotype and clinical phenotype differences in individuals with juvenile neuronal ceroid lipofuscinosis (JNCL) who were homozygous for a common disease-causing deletion or compound heterozygous. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a114d4eedc077011c98b8280ec401d9
https://pubmed.ncbi.nlm.nih.gov/20187884
https://pubmed.ncbi.nlm.nih.gov/20187884