Suchergebnisse - "Colantoni, Luca"

PubPharm (8)

1

Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families

enthalten in: Clinical genetics | 2024

von Strafella, C. | Colantoni, L. | Megalizzi, D. | +12

2

D4Z4 Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients

enthalten in: Cells | 2022

von Caputo, V. | Megalizzi, D. | Fabrizio, C. | +11

3

Update on the Molecular Aspects and Methods Underlying the Complex Architecture of FSHD

enthalten in: Cells | 2022

von Caputo, V. | Megalizzi, D. | Fabrizio, C. | +6

4

Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease : Lessons from ADH1B, CYP1A2 and MTHFR

enthalten in: Genes | 2022

von Barati, S. | Fabrizio, C. | Strafella, C. | +9

5

The variability of SMCHD1 gene in FSHD patients : evidence of new mutations

enthalten in: Human molecular genetics | 2019

von Strafella, C. | Caputo, V. | Galota, R. | +11

6

Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis : from traditional technology to the NGS era

enthalten in: Neurogenetics | 2019

von Zampatti, S. | Colantoni, L. | Strafella, C. | +10

7

Alzheimer's disease (AD) and Mild Cognitive Impairment (MCI) patients are characterized by increased BDNF serum levels

enthalten in: Current Alzheimer research | 2010

von Angelucci, F. | Spalletta, G. | di Iulio, F. | +8

8

The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure

enthalten in: BMC medical genetics | 2007

von Rossi, M. | Ricci, E. | Colantoni, L. | +4

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