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Garelli, Emanuela
60
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Online (60)
Mediatypes
Articles (Online) (23)
OpenAccess-fulltext (37)
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1
Implications of an Underlying Beckwith–Wiedemann Syndrome f..:
Quarello, Paola
;
Carli, Diana
;
Biasoni, Davide
...
Cancers. 15 (2023) 4 - p. 1292 , 2023
Link:
https://doi.org/10.3390/..
?
2
A 20‐year long term experience of the Italian Diamond‐Black..:
Quarello, Paola
;
Garelli, Emanuela
;
Carando, Adriana
...
British Journal of Haematology. 190 (2020) 1 - p. 93-104 , 2020
Link:
https://doi.org/10.1111/..
?
3
Reduction of CFU-GM and circulating hematopoietic progenito..:
Timeus, Fabio
;
Crescenzio, Nicoletta
;
Foglia, Luiselda
...
PLOS ONE. 14 (2019) 3 - p. e0213782 , 2019
Link:
https://doi.org/10.1371/..
?
4
Design of a multiplex ligation-dependent probe amplificatio..:
Giorgio, Elisa
;
Garelli, Emanuela
;
Carando, Adriana
...
Journal of Human Genetics. 64 (2019) 11 - p. 1083-1090 , 2019
Link:
https://doi.org/10.1038/..
?
5
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/..
?
6
Ribosomal RNA analysis in the diagnosis of Diamond‐Blackfan..:
Quarello, Paola
;
Garelli, Emanuela
;
Carando, Adriana
...
British Journal of Haematology. 172 (2016) 5 - p. 782-785 , 2016
Link:
https://doi.org/10.1111/..
?
7
Exploiting pre‐rRNA processing in Diamond Blackfan anemia g..:
Farrar, Jason E.
;
Quarello, Paola
;
Fisher, Ross
...
American Journal of Hematology. 89 (2014) 10 - p. 985-991 , 2014
Link:
https://doi.org/10.1002/..
?
8
Loss of GATA‐1 full length as a cause of Diamond–Blackfan a..:
Parrella, Sara
;
Aspesi, Anna
;
Quarello, Paola
...
Pediatric Blood & Cancer. 61 (2014) 7 - p. 1319-1321 , 2014
Link:
https://doi.org/10.1002/..
?
9
The Spectrum of Non-Classical Diamond-Blackfan Anemia: A Ca..:
Farruggia, Piero
;
Quarello, Paola
;
Garelli, Emanuela
...
Pediatric Reports. 4 (2012) 2 - p. e25 , 2012
Link:
https://doi.org/10.4081/..
?
10
Cleft palate and ADULT phenotype in a patient with a novel ..:
Prontera, Paolo
;
Garelli, Emanuela
;
Isidori, Ilenia
...
American Journal of Medical Genetics Part A. 155 (2011) 11 - p. 2746-2749 , 2011
Link:
https://doi.org/10.1002/..
?
11
The ribosomal basis of diamond-blackfan anemia: mutation an..:
Boria, Ilenia
;
Garelli, Emanuela
;
Gazda, Hanna T.
...
Human Mutation. 31 (2010) 12 - p. 1269-1279 , 2010
Link:
https://doi.org/10.1002/..
?
12
Remittent hyperammonemia in congenital portosystemic shunt:
Ferrero, Giovanni Battista
;
Porta, Francesco
;
Biamino, Elisa
...
European Journal of Pediatrics. 169 (2009) 3 - p. 369-372 , 2009
Link:
https://doi.org/10.1007/..
?
13
Fibroblasts from patients with Diamond-Blackfan anaemia sho..:
Avondo, Federica
;
Roncaglia, Paola
;
Crescenzio, Nicoletta
...
BMC Genomics. 10 (2009) 1 - p. , 2009
Link:
https://doi.org/10.1186/..
?
14
HDR syndrome: A novel "de novo" mutation in GATA3 gene:
Ferraris, Silvio
;
Del monaco, Angelo Giovanni
;
Garelli, Emanuela
...
American Journal of Medical Genetics Part A. 149A (2009) 4 - p. 770-775 , 2009
Link:
https://doi.org/10.1002/..
?
15
RPS19 mutations in patients with Diamond-Blackfan anemia:
Campagnoli, Maria Francesca
;
Ramenghi, Ugo
;
Armiraglio, Marta
...
Human Mutation. 29 (2008) 7 - p. 911-920 , 2008
Link:
https://doi.org/10.1002/..
1-15