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Origone, P.
27
results:
Search for persons
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Format
Online (27)
Mediatypes
Articles (Online) (5)
Bookchapter (Online) (1)
OpenAccess-fulltext (21)
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?
1
Molecular characterization of an Italian series of sporadic..:
Liguria GIST Unit
;
Origone, P.
;
Gargiulo, S.
...
Gastric Cancer. 16 (2013) 4 - p. 596-601 , 2013
Link:
https://doi.org/10.1007/..
?
2
GIST mutational status and survival:
De Cian, F.
;
Origone, P.
;
Mastracci, L.
...
European Journal of Surgical Oncology (EJSO). 39 (2013) 9 - p. S57 , 2013
Link:
https://doi.org/10.1016/..
?
3
SOD1 mutations in amyotrophic lateral sclerosis: Results fr..:
Battistini, S.
;
Giannini, F.
;
Greco, G.
...
Journal of Neurology. 252 (2005) 7 - p. 782-788 , 2005
Link:
https://doi.org/10.1007/..
?
4
Detection of a neurofibromatosis type I (NF1) homologous se..:
Gasparini, P.
;
Grifa, A.
;
Origone, P.
...
Molecular and Cellular Probes. 7 (1993) 5 - p. 415-418 , 1993
Link:
https://doi.org/10.1006/..
?
5
Genetic Workup for Charcot–Marie–Tooth Neuropathy: A Retros..:
Gemelli C
;
Geroldi A
;
Massucco S
...
info:eu-repo/semantics/altIdentifier/pmid/35330153. , 2022
Link:
http://hdl.handle.net/11..
?
6
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres‐Ciga, S
;
Noyce, AJ
;
Hemani, G
...
https://eprints.whiterose.ac.uk/166378/7/ana.25431.pdf. , 2019
Link:
https://eprints.whiteros..
?
7
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres-Ciga S
;
Noyce AJ
;
Hemani G
...
info:eu-repo/semantics/altIdentifier/pmid/30723964. , 2019
Link:
http://hdl.handle.net/11..
?
8
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres-Ciga S
;
Noyce A. J
;
Hemani G
...
info:eu-repo/semantics/altIdentifier/pmid/30723964. , 2019
Link:
http://hdl.handle.net/11..
?
9
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres-Ciga S
;
Noyce A. J
;
Hemani G
...
info:eu-repo/semantics/altIdentifier/pmid/30723964. , 2019
Link:
http://hdl.handle.net/11..
?
10
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres-Ciga S
;
Noyce A. J
;
Hemani G
...
info:eu-repo/semantics/altIdentifier/pmid/30723964. , 2019
Link:
http://hdl.handle.net/11..
?
11
Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA r..:
Origone P
;
Gotta F
;
Lamp M
...
info:eu-repo/semantics/altIdentifier/pmid/29564144. , 2018
Link:
http://hdl.handle.net/11..
?
12
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene:
Nicolas A
;
Kenna K. P
;
Renton A. E
...
info:eu-repo/semantics/altIdentifier/pmid/29566793. , 2018
Link:
http://hdl.handle.net/11..
?
13
Autosomal-dominant transthyretin (TTR)-related amyloidosis ..:
Grandis M
;
Geroldi A
;
Gulli R
...
info:eu-repo/semantics/altIdentifier/pmid/30286783. , 2018
Link:
http://hdl.handle.net/11..
?
14
ATNX2 is not a regulatory gene in Italian amyotrophic later..:
Chio A
;
Mora G
;
Sabatelli M
...
info:eu-repo/semantics/altIdentifier/wos/WOS:000370880700027. , 2016
Link:
http://hdl.handle.net/24..
?
15
HFE p.H63D polymorphism does not influence ALS phenotype an..:
Chiò, Adriano
;
Mora, Gabriele
;
Sabatelli, Mario
...
info:eu-repo/semantics/altIdentifier/pmid/26174855. , 2015
Link:
http://hdl.handle.net/24..
1-15