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Brugnoni, R.
45
results:
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Online (45)
Mediatypes
Articles (Online) (24)
OpenAccess-fulltext (21)
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1
VP.41 Congenital myasthenic syndrome: natural history of an..:
Gallone, A.
;
Pugliese, A.
;
Brugnoni, R.
...
Neuromuscular Disorders. 32 (2022) - p. S83 , 2022
Link:
https://doi.org/10.1016/..
?
2
ClC‐1 mutations in myotonia congenita patients: insights in..:
Imbrici, P.
;
Maggi, L.
;
Mangiatordi, G. F.
...
The Journal of Physiology. 593 (2015) 18 - p. 4181-4199 , 2015
Link:
https://doi.org/10.1113/..
?
3
G.P.137:
Imbrici, P.
;
Desaphy, J.F.
;
Brugnoni, R.
...
Neuromuscular Disorders. 24 (2014) 9-10 - p. 842 , 2014
Link:
https://doi.org/10.1016/..
?
4
G.P.136:
Maggi, L.
;
Brugnoni, R.
;
Colleoni, L.
...
Neuromuscular Disorders. 24 (2014) 9-10 - p. 841-842 , 2014
Link:
https://doi.org/10.1016/..
?
5
P.12.4 Great phenotypic variability in two siblings affecte..:
Maggi, L.
;
Brugnoni, R.
;
Confalonieri, P.
...
Neuromuscular Disorders. 23 (2013) 9-10 - p. 806 , 2013
Link:
https://doi.org/10.1016/..
?
6
Marked phenotypic variability in two siblings with congenit..:
Maggi, Lorenzo
;
Brugnoni, R.
;
Scaioli, V.
...
Journal of Neurology. 260 (2013) 11 - p. 2894-2896 , 2013
Link:
https://doi.org/10.1007/..
?
7
Efficacy of propafenone in paramyotonia congenita:
Alfonsi, E.
;
Merlo, I. M.
;
Tonini, M.
...
Neurology. 68 (2007) 13 - p. 1080-1081 , 2007
Link:
https://doi.org/10.1212/..
?
8
Is the CACNA1A gene involved in familial migraine with aura:
Brugnoni, R.
;
Leone, M.
;
Rigamonti, A.
...
Neurological Sciences. 23 (2002) 1 - p. 1-5 , 2002
Link:
https://doi.org/10.1007/..
?
9
DMD and BMD in the same family due to two distinct mutation:
Morandi, L.
;
Mora, M.
;
Tedeschi, S.
...
American Journal of Medical Genetics. 59 (1995) 4 - p. 501-505 , 1995
Link:
https://doi.org/10.1002/..
?
10
Clinical and Molecular Spectrum of Myotonia and Periodic Pa..:
Maggi L
;
Brugnoni R
;
Canioni E
...
info:eu-repo/semantics/altIdentifier/pmid/32849172. , 2020
Link:
http://hdl.handle.net/11..
?
11
ClC-1 mutations in myotonia congenita patients: insights in..:
Imbrici, P
;
Maggi, L
;
Mangiatordi, G F
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594292/. , 2015
Link:
http://www.ncbi.nlm.nih...
?
12
ClC-1 mutations in myotonia congenita patients: insights in..:
Imbrici, P
;
Maggi, L
;
Mangiatordi, G F
...
info:eu-repo/semantics/altIdentifier/pmid/26096614. , 2015
Link:
http://hdl.handle.net/11..
?
13
Disruption of heart sarcoglycan complex and severe cardiomy..:
Barresi, R
;
Di, B
;
Negri, T
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1734518. , 2000
Link:
http://www.ncbi.nlm.nih...
?
14
Expression of transforming growth factor-beta 1 in dystroph..:
Bernasconi, P
;
Torchiana, E
;
Confalonieri, P
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC185304. , 1995
Link:
http://www.ncbi.nlm.nih...
?
15
Identifying a stable and generalizable factor structure of ..:
Tseng, Vincent W.S.
;
Tharp, Jordan A.
;
Reiter, Jacob E.
...
Psychiatry Research. 333 (2024) - p. 115702 , 2024
Link:
https://doi.org/10.1016/..
1-15