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Origone, P.
27  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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