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DI GREGORIO, ELEONORA
218  results:
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1

DNA methylation analysis in patients with neurodevelopmenta..:

Trajkova, Slavica ; Kerkhof, Jennifer ; Rossi Sebastiano, Matteo...
Human Genetics and Genomics Advances.  5 (2024)  3 - p. 100309 , 2024
Link: https://doi.org/10.1016/..
 
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2

Spinocerebellar ataxia 38: structure–function analysis show..:

Ferrero, Enza ; Di Gregorio, Eleonora ; Ferrero, Marta...
Human Genetics.  142 (2023)  8 - p. 1055-1076 , 2023
Link: https://doi.org/10.1007/..
 
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3

Identifying phenotypic expansions for congenital diaphragma..:

Hardcastle, Amy ; Berry, Aliska M. ; Campbell, Ian M....
American Journal of Medical Genetics Part A.  188 (2022)  10 - p. 2958-2968 , 2022
Link: https://doi.org/10.1002/..
 
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4

CAPRIN1 haploinsufficiency causes a neurodevelopmental diso..:

Pavinato, Lisa ; Delle Vedove, Andrea ; Carli, Diana...
Brain.  146 (2022)  2 - p. 534-548 , 2022
Link: https://doi.org/10.1093/..
 
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5

Evidence that FGFRL1 contributes to congenital diaphragmati..:

Gofin, Yoel ; Mackay, Laura Palmer ; Machol, Keren...
Molecular Genetics and Metabolism.  132 (2021)  - p. S84 , 2021
Link: https://doi.org/10.1016/..
 
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6

Evidence that FGFRL1 contributes to congenital diaphragmati..:

Gofin, Yoel ; Mackay, Laura Palmer ; Machol, Keren...
American Journal of Medical Genetics Part A.  185 (2021)  3 - p. 836-840 , 2021
Link: https://doi.org/10.1002/..
 
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7

New Insights into Potocki-Shaffer Syndrome: Report of Two N..:

Trajkova, Slavica ; Di Gregorio, Eleonora ; Ferrero, Giovanni Battista...
Brain Sciences.  10 (2020)  11 - p. 788 , 2020
Link: https://doi.org/10.3390/..
 
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8

In vitro dexamethasone treatment does not induce alternativ..:

Pozzi, Elisa ; Giorgio, Elisa ; Mancini, Cecilia...
Scientific Reports.  10 (2020)  1 - p. , 2020
Link: https://doi.org/10.1038/..
 
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9

Long-term efficacy of docosahexaenoic acid (DHA) for Spinoc..:

Manes, Marta ; Alberici, Antonella ; Di Gregorio, Eleonora...
Parkinsonism & Related Disorders.  63 (2019)  - p. 191-194 , 2019
Link: https://doi.org/10.1016/..
 
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10

Mice harbouring a SCA28 patient mutation in AFG3L2 develop ..:

Mancini, Cecilia ; Hoxha, Eriola ; Iommarini, Luisa...
Neurobiology of Disease.  124 (2019)  - p. 14-28 , 2019
Link: https://doi.org/10.1016/..
 
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11

Congenital Sensorineural Hearing Loss and Inborn Pigmentary..:

Gironi, Laura Cristina ; Colombo, Enrico ; Brusco, Alfredo...
Medicina.  55 (2019)  7 - p. 345 , 2019
Link: https://doi.org/10.3390/..
 
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12

Combining Memory and Non-linearity in Echo State Networks:

, In: Artificial Neural Networks and Machine Learning – ICANN 2018; Lecture Notes in Computer Science,
Di Gregorio, Eleonora ; Gallicchio, Claudio ; Micheli, Alessio - p. 556-566 , 2018
Link: https://doi.org/10.1007/..
 
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13

Spontaneous remission in a Diamond‐Blackfan anaemia patient..:

Garelli, Emanuela ; Quarello, Paola ; Giorgio, Elisa...
British Journal of Haematology.  185 (2018)  5 - p. 994-998 , 2018
Link: https://doi.org/10.1111/..
 
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14

Docosahexaenoic acid is a beneficial replacement treatment ..:

Manes, Marta ; Alberici, Antonella ; Di Gregorio, Eleonora...
Annals of Neurology.  82 (2017)  4 - p. 615-621 , 2017
Link: https://doi.org/10.1002/..
 
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15

Exome sequencing in children of women with skewed X-inactiv..:

Giorgio, Elisa ; Brussino, Alessandro ; Biamino, Elisa...
European Journal of Paediatric Neurology.  21 (2017)  3 - p. 475-484 , 2017
Link: https://doi.org/10.1016/..
 
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