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Silipigni, R.
57
results:
Search for persons
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Online (57)
Mediatypes
Articles (Online) (34)
OpenAccess-fulltext (23)
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english (53)
italian (1)
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1
Clinical features and magnesium levels: Novel insights in 1..:
Meossi, C.
;
Carrer, A.
;
Ciaccio, C.
...
Journal of Intellectual Disability Research. 67 (2023) 7 - p. 679-689 , 2023
Link:
https://doi.org/10.1111/..
?
2
Complex genomic alterations and intellectual disability: an..:
Silipigni, R.
;
Milani, D.
;
Tolva, G.
...
Journal of Intellectual Disability Research. 65 (2020) 2 - p. 113-124 , 2020
Link:
https://doi.org/10.1111/..
?
3
Structural brain anomalies in Cri-du-Chat syndrome: MRI fin..:
Villa, R.
;
Fergnani, V.G.C.
;
Silipigni, R.
...
European Journal of Paediatric Neurology. 28 (2020) - p. 110-119 , 2020
Link:
https://doi.org/10.1016/..
?
4
PO-450 Interplay between coding and non-coding genome in hu..:
Morotti, A.
;
Forno, I.
;
Verdelli, C.
...
ESMO Open. 3 (2018) - p. A408 , 2018
Link:
https://doi.org/10.1136/..
?
5
The intra-tumor heterogeneity of C19MC miRNA cluster expres..:
Colombo, F.
;
Augello, C.
;
Terrasi, A.
...
Digestive and Liver Disease. 48 (2016) - p. e14 , 2016
Link:
https://doi.org/10.1016/..
?
6
Clinical features and magnesium levels: Novel insights in 1..:
Meossi, C
;
Carrer, A
;
Ciaccio, C
...
info:eu-repo/semantics/altIdentifier/wos/WOS:000979023600001. , 2023
Link:
https://hdl.handle.net/2..
?
7
Isolation of single circulating trophoblasts from maternal ..:
Doffini A
;
Forcato C
;
Mangano C
...
info:eu-repo/semantics/altIdentifier/pmid/36443901. , 2023
Link:
https://hdl.handle.net/1..
?
8
Insights into the identification of a molecular signature f..:
Rizzuti M
;
Melzi V
;
Gagliardi D
...
info:eu-repo/semantics/altIdentifier/pmid/35286466. , 2022
Link:
http://hdl.handle.net/24..
?
9
Yes-associated protein 1 is a novel calcium sensing recepto..:
Tavanti G. S
;
Verdelli C
;
Morotti A
...
info:eu-repo/semantics/altIdentifier/pmid/33670622. , 2021
Link:
http://hdl.handle.net/24..
?
10
Incidental finding of APC deletion in a child: double troub..:
Rosina E
;
Rinaldi B
;
Silipigni R
...
info:eu-repo/semantics/altIdentifier/pmid/33588901. , 2021
Link:
http://hdl.handle.net/24..
?
11
Unexpected phenotype in a frameshift mutation of PTCH1:
BELTRAMI, BENEDETTA
;
Prada E
;
Tolva G
...
info:eu-repo/semantics/altIdentifier/pmid/31578813. , 2020
Link:
http://hdl.handle.net/24..
?
12
Incidence of chromosomal abnormalities in fetuses with firs..:
Persico N
;
Boito S
;
Volpe P
...
info:eu-repo/semantics/altIdentifier/pmid/33034897. , 2020
Link:
http://hdl.handle.net/24..
?
13
Structural brain anomalies in Cri-du-Chat syndrome: MRI fin..:
Villa R
;
Fergnani V. G. C
;
Silipigni R
...
info:eu-repo/semantics/altIdentifier/pmid/32800423. , 2020
Link:
http://hdl.handle.net/24..
?
14
Generation of an induced pluripotent stem cell line (EURACi..:
Zanon A
;
Riekschnitz D
;
von Troyer M
...
1873-5061. , 2019
Link:
https://doi.org/10.1016/..
?
15
The Genetic Landscape of Human Glioblastoma and Matched Pri..:
Pesenti C
;
Navone SE
;
Guarnaccia L
...
info:eu-repo/semantics/altIdentifier/pmid/30984267. , 2019
Link:
http://hdl.handle.net/24..
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