F John Meaney
Overview
Explore the profile of F John Meaney including associated specialties, affiliations and a list of published articles.
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44
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1116
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Recent Articles
1.
Patterson M, Garver W, Giugliani R, Imrie J, Jahnova H, Meaney F, et al.
J Inherit Metab Dis
. 2020 Apr;
43(5):1060-1069.
PMID: 32324281
Miglustat has been indicated for the treatment of Niemann-Pick disease type C (NP-C) since 2009. The aim of this observational study was to assess the effect of miglustat on long-term...
2.
Andrews J, Pandya S, Trout C, Jaff T, Matthews D, Cunniff C, et al.
SAGE Open Med
. 2019 Apr;
7:2050312119840518.
PMID: 30944724
Introduction: Information on use of palliative care services among individuals with Duchenne and Becker muscular dystrophy is scant despite the clearly documented need. Methods: We examined associations between uptake of...
3.
Andrews J, Conway K, Westfield C, Trout C, Meaney F, Mathews K, et al.
Pediatrics
. 2018 Jun;
142(1).
PMID: 29925575
Background: Duchenne muscular dystrophy (DMD) is an X-linked disorder characterized by progressive muscle weakness and multisystem involvement. Recent advances in management of individuals with DMD have prolonged survival. Lack of...
4.
Andrews J, Galindo M, Meaney F, Benavides A, Mayate L, Fox D, et al.
Birth Defects Res
. 2018 Jan;
110(10):851-862.
PMID: 29368410
Background: The diagnosis of fetal alcohol syndrome (FAS) rests on identification of characteristic facial, growth, and central nervous system (CNS) features. Public health surveillance of FAS depends on documentation of...
5.
Castillo J, Jelinek D, Wei H, Gannon N, Vaughan R, Horwood L, et al.
Am J Physiol Endocrinol Metab
. 2017 May;
313(2):E183-E194.
PMID: 28487438
A genome-wide association study (GWAS) reported that common variation in the human Niemann-Pick C1 gene () is associated with morbid adult obesity. This study was confirmed using our BALB/cJ mouse...
6.
Meaney F, Butler M
Med Anthropol Q
. 2016 Oct;
3(3):294-305.
PMID: 27695159
A multidisciplinary study involving cytogenetic, clinical, and anthropometric assessments of Prader-Labhart-Willi Syndrome (PLWS) has focused on improving diagnosis and prognosis in this complex condition. Since one of the major features...
7.
Pedersen A, Pettygrove S, Lu Z, Andrews J, Meaney F, Kurzius-Spencer M, et al.
Child Psychiatry Hum Dev
. 2016 Aug;
48(4):537-545.
PMID: 27558812
Clinical characteristics of autism spectrum disorder (ASD) and intellectual disability (ID) overlap, creating potential for diagnostic confusion. Diagnostic and statistical manual of mental disorders (DSM) criteria that best differentiate children...
8.
Pandya S, Andrews J, Campbell K, Meaney F
J Pediatr Rehabil Med
. 2016 Mar;
9(1):45-53.
PMID: 26966800
Purpose: To document use of rehabilitative technology among individuals with Duchenne/Becker muscular dystrophy (DBMD) among sites of the Muscular Dystrophy Surveillance, Tracking, and Research network (MD STARnet). Methods: Data from...
9.
Pandya S, Campbell K, Andrews J, Meaney F, Ciafaloni E
Muscle Nerve
. 2015 Jun;
53(2):191-7.
PMID: 26044770
Introduction: Anecdotal reports from families and care providers suggest a wide variation in services received by individuals with Duchenne/Becker muscular dystrophy (DBMD). Methods: We documented the type and frequency of...
10.
OLeary L, Ortiz L, Montgomery A, Fox D, Cunniff C, Ruttenber M, et al.
Birth Defects Res A Clin Mol Teratol
. 2015 Mar;
103(3):196-202.
PMID: 25761572
Surveillance of fetal alcohol syndrome (FAS) is important for monitoring the effects of prenatal alcohol exposure and describing the public health burden of this preventable disorder. Building on the infrastructure...