Results 191 to 200 of about 225,713 (333)

Sensory processing in autism spectrum disorders and Fragile X syndrome-From the clinic to animal models.

Neuroscience and Biobehavioral Reviews, 2017
D. Sinclair, B. Oranje, K. Razak, S. Siegel, S. Schmid   +4 more
semanticscholar   +1 more source

Oral Manifestations of Non Vascular Ehlers‐Danlos Syndrome Cross‐Sectional Study

Oral Diseases, EarlyView.
ABSTRACT Background Ehlers–Danlos syndromes are rare hereditary connective tissue disorders; however, their oral manifestations remain poorly characterized in molecularly confirmed individuals. The aim of this study was to describe the oral phenotype of patients with non‐vascular Ehlers‐Danlos syndromes compared to healthy controls.
Aude Grand, Benjamin P. J. Fournier, Grégoire Chevalier, Karelle Benistan, François Côme Ferré   +4 more
wiley   +1 more source

Gene Therapy for Fragile X Syndrome, Challenges, and Promises. [PDF]

J Gene Med
Velinov M.
europepmc   +1 more source

Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment

Pediatrics, 2017
Walter E. Kaufmann, Sharon A. Kidd, Howard F. Andrews, D. Budimirovic, A. Esler, Barbara Haas‐Givler, T. Stackhouse, C. Riley, G. Peacock, Stephanie L. Sherman, W. Ted Brown, E. Berry-Kravis   +11 more
semanticscholar   +1 more source

Genetic risk variants implicate impaired maintenance and repair of periodontal tissues as causal for periodontitis—A synthesis of recent findings

Periodontology 2000, EarlyView.
AbstractPeriodontitis is a complex inflammatory disease in which the host genome, in conjunction with extrinsic factors, determines susceptibility and progression. Genetic predisposition is the strongest risk factor in the first decades of life. As people age, chronic exposure to the periodontal microbiome puts a strain on the proper maintenance of ...
Arne S. Schaefer, Luigi Nibali, Noha Zoheir, Niki M. Moutsopoulos, Bruno G. Loos   +4 more
wiley   +1 more source

Genetic diagnosis of three intellectually disabled individuals in a pedigree and insights into fragile X syndrome diagnosis. [PDF]

Front Neurosci
Huang J, Kang B, Xia X, Guo Z, Lv Y, Yang W, Wang C, Wang J, Liao S.   +8 more
europepmc   +1 more source

P3 abnormality in fragile X syndrome [PDF]

, 1987
Blackwood, D, Dickens, P, Oliver, C, St. Clair, D   +3 more
core   +1 more source

Impaired thalamic burst firing in fragile X syndrome. [PDF]

Cell Rep
O'Shea RT, Priebe NJ, Brager DH.
europepmc   +1 more source

Sleep in a mouse model of fragile X syndrome is resistant to metabolic manipulations. [PDF]

Hum Mol Genet
Lopez Valencia M, Velázquez Aponte RA, Baur JA, Jongens TA, Sehgal A.   +4 more
europepmc   +1 more source

A multi‐omics investigation of sarcopenia and frailty: Integrating genomic, epigenomic and telomere length data

Experimental Physiology, EarlyView.
Abstract Sarcopenia and frailty are complex geriatric syndromes influenced by a combination of genetic and environmental factors. Recent studies suggest that specific genetic variants, DNA methylation patterns and shortened telomeres are associated with age‐related diseases and might contribute to the development of both sarcopenia and frailty. In this
Valentina Ginevičienė, Erinija Pranckevičienė, Alina Urnikytė, Laura Jurkūnaitė, Kristijona Gutauskaitė, Rūta Dadelienė, Justina Kilaitė, Ieva Eglė Jamontaitė, Asta Mastavičiūtė, Ildus I. Ahmetov, Vidmantas Alekna   +10 more
wiley   +1 more source