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Di Fede, Elisabetta
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1

Characterization of a novel HDAC2 pathogenetic variant: a m..:

Di Fede, Elisabetta ; Lettieri, Antonella ; Taci, Esi...
Human Genetics.  143 (2024)  6 - p. 747-759 , 2024
Link: https://doi.org/10.1007/..
 
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2

Epigenetic disorders: Lessons from the animals–animal model..:

Di Fede, Elisabetta ; Grazioli, Paolo ; Lettieri, Antonella...
Frontiers in Cell and Developmental Biology.  10 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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3

Identical EP300 variant leading to Rubinstein–Taybi syndrom..:

Saettini, Francesco ; Fazio, Grazia ; Bonati, Maria Teresa...
American Journal of Medical Genetics Part A.  188 (2022)  7 - p. 2129-2134 , 2022
Link: https://doi.org/10.1002/..
 
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4

KMT2A: Umbrella Gene for Multiple Diseases:

Castiglioni, Silvia ; Di Fede, Elisabetta ; Bernardelli, Clara...
Genes.  13 (2022)  3 - p. 514 , 2022
Link: https://doi.org/10.3390/..
 
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5

SLC35F1 as a candidate gene for neurodevelopmental disorder..:

Di Fede, Elisabetta ; Peron, Angela ; Colombo, Elisa Adele..
American Journal of Medical Genetics Part A.  185 (2021)  7 - p. 2238-2240 , 2021
Link: https://doi.org/10.1002/..
 
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6

Insights into the Role of the Microbiota and of Short-Chain..:

Di Fede, Elisabetta ; Ottaviano, Emerenziana ; Grazioli, Paolo...
International Journal of Molecular Sciences.  22 (2021)  7 - p. 3621 , 2021
Link: https://doi.org/10.3390/..
 
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7

Chromatin Imbalance as the Vertex Between Fetal Valproate S..:

Parodi, Chiara ; Di Fede, Elisabetta ; Peron, Angela...
Frontiers in Cell and Developmental Biology.  9 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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8

Lithium as a possible therapeutic strategy for Cornelia de ..:

Grazioli, Paolo ; Parodi, Chiara ; Mariani, Milena...
Cell Death Discovery.  7 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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9

Expanding the phenotype associated to KMT2A variants: overl..:

Di Fede, Elisabetta ; Massa, Valentina ; Augello, Bartolomeo...
European Journal of Human Genetics.  29 (2020)  1 - p. 88-98 , 2020
Link: https://doi.org/10.1038/..
 
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10

Generation of the Becker muscular dystrophy patient derived..:

Rovina, Davide ; Castiglioni, Elisa ; Niro, Francesco...
Stem Cell Research.  45 (2020)  - p. 101819 , 2020
Link: https://doi.org/10.1016/..
 
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11

Exploring by whole exome sequencing patients with initial d..:

Negri, Gloria ; Magini, Pamela ; Milani, Donatella...
Human Genetics.  138 (2019)  3 - p. 257-269 , 2019
Link: https://doi.org/10.1007/..
 
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12

Chromatinopathies: A focus on Cornelia de Lange syndrome:

Avagliano, Laura ; Parenti, Ilaria ; Grazioli, Paolo...
Clinical Genetics.  97 (2019)  1 - p. 3-11 , 2019
Link: https://doi.org/10.1111/..
 
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13

Front Cover:

Avagliano, Laura ; Parenti, Ilaria ; Grazioli, Paolo...
Clinical Genetics.  97 (2019)  1 - p. , 2019
Link: https://doi.org/10.1111/..
 
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14

Insights into Mutation Effect in Three Poikiloderma with Ne..:

Colombo, Elisa A. ; Elcioglu, Nursel H. ; Graziano, Claudio...
Journal of Clinical Immunology.  38 (2018)  4 - p. 494-502 , 2018
Link: https://doi.org/10.1007/..
 
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15

MOLECULAR STUDY OF CHROMATINOPATHIES: THE CASE OF RUBINSTEI..:

DI FEDE, ELISABETTA
https://hdl.handle.net/2434/949952.  , 2023
Link: https://hdl.handle.net/2..
 
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