Results 141 to 150 of about 7,474,211 (311)
Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions
ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos +5 more
wiley +1 more source
Additional support needs and approaches to dispute resolution: the perspectives of Scottish parents [PDF]
This paper draws on data from an ESRC funded project (RES-062-23-0803) which explores the use of dispute resolution mechanisms in the field of special educational needs in England and additional support needs in Scotland. Here, we present findings from a
Weedon, Elisabet, Riddell, Sheila
core
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li +11 more
wiley +1 more source
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source
Uniform Interstate Family Support Act Ohio
Title from cover of PDF document (viewed Nov. 21, 2005); responsibility statement from p. 2 of cover.; "Created: 6/11/1999 ...; Modified: 8/24/1999 ..."--Document properties screen.; Harvested from the web on 11/21 ...
Center for the Support of Families.
core
EUROFOUND beauftragte sieben Länder, Berichte über die Unterstützungen zu verfassen, die Eltern bei der Kindererziehung in den jeweiligen Ländern erhalten. Das Ziel dabei ist, wichtige Aspekte der Unterstützungen als soziale Investition für die Vereinbarkeit von Familie und Beruf zu thematisieren.
Kapella, Olaf +2 more
openaire +3 more sources
ABSTRACT Objective Facioscapulohumeral muscular dystrophy (FSHD) is one of the most debilitating and common muscular dystrophies. Despite its severity, no approved therapy exists for FSHD patients. However, several therapeutic candidates are currently under development, and some have recently entered clinical trials, marking the need for reliable ...
Mustafa Bilal Bayazit +11 more
wiley +1 more source
Onasemnogene Abeparvovec in Patients With SMA: Interim Results of the RESTORE Registry in Japan
ABSTRACT Objective There are limited real‐world data regarding the safety and effectiveness of onasemnogene abeparvovec (OA; Zolgensma) infusion, a one‐time gene replacement therapy, for Japanese patients with spinal muscular atrophy (SMA). We aimed to improve understanding of the real‐world outcomes for OA in Japan.
Kayoko Saito +8 more
wiley +1 more source
ABSTRACT Objective Early risk stratification may support clinical decision‐making in spontaneous intracerebral hemorrhage (ICH). We aimed to develop and internally validate HAGIV, a score integrating frequency of imaging markers (FIM), a time‐adjusted non‐contrast computed tomography (CT) metric of hematoma expansion, with established predictors for 90‐
Lei Song +10 more
wiley +1 more source
Predictors and outcomes of parental burnout in a Swedish context
In Sweden, parental burnout has been examined among parents of children with serious diseases(e.g., cancer) and/or chronic diseases (e.g., diabetes). However, there is a lack of studies on nonclinical samples of parents and studies that compare parents ...
Osman, Fatuma, +2 more
core

