Michael Tranfaglia
Overview
Explore the profile of Michael Tranfaglia 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
5
Citations
496
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.
Cogram P, Alkon D, Crockford D, Deacon R, Hurley M, Altimiras F, et al.
Sci Rep
. 2020 Oct;
10(1):18058.
PMID: 33093534
Fragile X syndrome (FXS), an X-chromosome linked intellectual disability, is the leading monogenetic cause of autism spectrum disorder (ASD), a neurodevelopmental condition that currently has no specific drug treatment. Building...
2.
Gurney M, Cogram P, Deacon R, Rex C, Tranfaglia M
Sci Rep
. 2017 Nov;
7(1):14653.
PMID: 29116166
Fragile-X syndrome (FXS) patients display intellectual disability and autism spectrum disorder due to silencing of the X-linked, fragile-X mental retardation-1 (FMR1) gene. Dysregulation of cAMP metabolism is a consistent finding...
3.
Westmark C, Westmark P, ORiordan K, Ray B, Hervey C, Salamat M, et al.
PLoS One
. 2011 Nov;
6(10):e26549.
PMID: 22046307
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and the leading known genetic cause of autism. Fragile X mental retardation protein (FMRP), which is absent...
4.
Paribello C, Tao L, Folino A, Berry-Kravis E, Tranfaglia M, Ethell I, et al.
BMC Neurol
. 2010 Oct;
10:91.
PMID: 20937127
Background: Fragile X syndrome (FXS) is a disorder characterized by a variety of disabilities, including cognitive deficits, attention-deficit/hyperactivity disorder, autism, and other socio-emotional problems. It is hypothesized that the absence...
5.
Hagerman R, Berry-Kravis E, Kaufmann W, Ono M, Tartaglia N, Lachiewicz A, et al.
Pediatrics
. 2009 Jan;
123(1):378-90.
PMID: 19117905
The FMR1 mutations can cause a variety of disabilities, including cognitive deficits, attention-deficit/hyperactivity disorder, autism, and other socioemotional problems, in individuals with the full mutation form (fragile X syndrome) and...