The relationship between anxiety and joint attention in boys and girls with Fragile X Syndrome
reservedLa Sindrome X Fragile è una malattia genetica ereditaria rara causata da una mutazione del gene FMR1, localizzato lungo il braccio lungo del cromosoma X (q27.3).
RIOLFI, BEATRICE
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Mitochondrial Remodeling and Impaired Bioenergetics Define Neuronal Vulnerability in Fragile X-Related Disorders. [PDF]
Niccolini B +14 more
europepmc +1 more source
Advancing Standardization in Fragile X Syndrome Molecular Diagnosis: A Dual-Structured and Scoping Review. [PDF]
Sallum BT +4 more
europepmc +1 more source
Phenotypic variability of Fragile-X syndrome in Asian population: A systematic review. [PDF]
Napitupulu CLM +4 more
europepmc +1 more source
EMG chacterizationn and processing in fragile X syndrome children during gait
openQuesta tesi si concentra sulla caratterizzazione e analisi del segnale elettromiografico (EMG) durante il cammino nei bambini affetti da sindrome di X fragile.
MARINO, VALENTINA ALICE
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Blarcamesine improves EEG biomarkers of cortical dysfunction in a mouse model of fragile X syndrome. [PDF]
Jonak CR +5 more
europepmc +1 more source
Essential tremor-like phenotype in Fragile X carrier women. [PDF]
Hall DA +4 more
europepmc +1 more source
SMCHD1 Is Dispensable for Repeat-Induced FMR1 Hypermethylation in Fragile X Pluripotent Stem Cells. [PDF]
Aviel U +5 more
europepmc +1 more source
Autonomic Function in Fragile X Syndrome: A Systematic Review. [PDF]
Weissgold S +4 more
europepmc +1 more source
Comparing feedback learning and arousal responses in Down, Fragile X, and Williams syndromes. [PDF]
Hallman AEZ +4 more
europepmc +1 more source

