Daniel Glaze
Overview
Explore the profile of Daniel Glaze including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
13
Citations
384
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Duis J, Nespeca M, Summers J, Bird L, Bindels-de Heus K, Valstar M, et al.
Mol Genet Genomic Med
. 2022 Feb;
10(3):e1843.
PMID: 35150089
Background: Angelman syndrome (AS) is a rare neurogenetic disorder present in approximately 1/12,000 individuals and characterized by developmental delay, cognitive impairment, motor dysfunction, seizures, gastrointestinal concerns, and abnormal electroencephalographic background....
2.
Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, et al.
BMJ Paediatr Open
. 2020 Oct;
4(1):e000731.
PMID: 33024833
Background: Rett syndrome (RTT) is a severe, progressive neurodevelopmental disorder with multisystem comorbidities that evolve across a patient's lifespan requiring attentive coordination of subspecialty care by primary care providers. A...
3.
Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, et al.
BMJ Paediatr Open
. 2020 Sep;
4(1):e000717.
PMID: 32984552
Background: Rett syndrome (RTT) is a severe neurodevelopmental disorder with complex medical comorbidities extending beyond the nervous system requiring the attention of health professionals. There is no peer-reviewed, consensus-based therapeutic...
4.
Kaplan K, McCool C, Lupski J, Glaze D, Potocki L
Am J Med Genet A
. 2019 Jul;
179(10):1982-1986.
PMID: 31342617
Potocki-Lupski syndrome (PTLS; MIM 610883) is a neurodevelopmental disorder caused by a microduplication, a 3.7 Mb copy number variant, mapping within chromosome 17p11.2, encompassing the dosage-sensitive RAI1 gene. Whereas RAI1...
5.
Marafi D, Suter B, Schultz R, Glaze D, Pavlik V, Goldman A
Neurology
. 2018 Dec;
92(2):e108-e114.
PMID: 30552298
Objective: We characterized the epilepsy features and contribution to cognitive regression in 47 patients with duplication syndrome (MDS) and reviewed these characteristics in over 280 MDS published cases. Methods: The...
6.
Vendrame M, Loddenkemper T, Zarowski M, Gregas M, Shuhaiber H, Sarco D, et al.
Epilepsy Behav
. 2012 Feb;
23(3):261-5.
PMID: 22341959
We prospectively analyzed EEGs from participants in the ongoing NIH Rare Diseases Clinical Research Network Angelman Syndrome Natural History Study. Of the one-hundred-sixty enrolled patients (2006-2010), 115 had complete data...
7.
Huckeba W, Chapieski L, Hiscock M, Glaze D
J Clin Exp Neuropsychol
. 2008 Oct;
30(4):410-20.
PMID: 18938679
The study addressed the issue of arithmetic deficiencies in children with Tourette syndrome (TS) as well as explanations for such deficiencies. A total of 47 children with TS were assigned...
8.
Hopkins B, Glaze D
Pediatr Ann
. 2008 Aug;
37(7):481-7.
PMID: 18710138
Disorders of arousal from NREM sleep are common events in childhood. Although they are considered to be benign in most cases, recurrent events may be associated with other primary sleep...
9.
Owens J, Babcock D, Blumer J, Chervin R, Ferber R, Goetting M, et al.
J Clin Sleep Med
. 2007 Jun;
1(1):49-59.
PMID: 17561616
Objectives: To formulate a rational approach to the pharmacologic treatment of pediatric insomnia, and to develop clinical guidelines regarding indications, target populations, and parameters for the use of these medications,...
10.
Potocki L, Bi W, Treadwell-Deering D, Carvalho C, Eifert A, Friedman E, et al.
Am J Hum Genet
. 2007 Mar;
80(4):633-49.
PMID: 17357070
The duplication 17p11.2 syndrome, associated with dup(17)(p11.2p11.2), is a recently recognized syndrome of multiple congenital anomalies and mental retardation and is the first predicted reciprocal microduplication syndrome described--the homologous recombination...