Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laurie A. Bailey"'
Autor:
Arnold R. Gammaitoni, Bradley S. Galer, Carla Schad, Tracy Dixon-Salazar, Lauren Schwartz, Laurie D. Bailey, Mary Anne Meskis
Publikováno v:
Epilepsy & Behavior. 112:107377
Objective Caring for children with developmental and epileptic encephalopathies (DEEs) places substantial demands on the entire family unit, including siblings. The Sibling Voices Survey assesses parental and sibling responses to questions designed t
Publikováno v:
Journal of Neurotherapy. 17:3-34
The theta-over-alpha frequency crossover seen in alpha-theta neurofeedback, considered an important factor in the treatment's success, has had little definitive research. This study examined 182 alpha-theta session graphs from 10 subject case files f
Autor:
Laurie A. Bailey, Donna Hoffman
Publikováno v:
Current Sexual Health Reports. 5:208-212
Although a plethora of data support the link between male erectile dysfunction and cardiovascular disease (CVD), no studies specifically address a link between female sexual dysfunction (FSD) and CVD, which is the number one cause of death in women.
Publikováno v:
Macromolecules. 27:7713-7717
A series of alkyl- and fluoroalkyl-substituted polyphosphazenes, [Me(Ph)PN] x (RMe 2 SiCH 2 )-(Ph)PN] y , were prepared by deprotonation of the methyl groups on [Me(Ph)PN] n with n-BuLi, followed by treatment of the intermediate anion with the corres
Autor:
Jerzy Chrusciel, Christopher L. Claypool, Maneesh Bahadur, Laurie A. Bailey, Patty Wisian-Neilson
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 93:265-268
The deprotonation-substitution reactions of poly(alkyl/arylphosphazenes) such as [Me(Ph)PN]n have proven to be a simple, one-step method for modification of this class of phosphazene polymers. Recent studies of the anion intermediate produced by depr
Publikováno v:
Blood cells, moleculesdiseases. 30(1)
The clinical impact of neutralizing antibodies directed against the therapeutic enzyme was investigated in patients with Gaucher disease. Two patients with Gaucher disease type 1 were followed for their clinical progression during antibody developmen
Publikováno v:
American journal of medical genetics. Part A. (1)
Gaucher disease, a common lysosomal storage disorder, is associated with mutations at the acid beta-glucosidase (GCase) locus. Two affected individuals are described to share a common mutant allele, but manifest different clinical categorical phenoty