๐
|
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.
17 auth.
Katherine R. Smith,
John A. Damiano,
S. Franceschetti,
S. Carpenter,
L. Canafoglia,
M. Morbin,
G. Rossi,
D. Pareyson,
S. Mole,
J. Staropoli,
...
K. Sims,
Jada Lewis,
Wenโlang Lin,
D. Dickson,
H. Dahl,
M. Bahlo,
S. Berkovic
|
8 |
2012 |
8 ๐
|
๐
|
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.
16 auth.
O. Bugiani,
J. Murrell,
G. Giaccone,
M. Hasegawa,
Giuseppe Ghigo,
M. Tabaton,
M. Morbin,
A. Primavera,
F. Carella,
C. Solaro,
...
M. Grisoli,
M. Savoiardo,
M. Spillantini,
F. Tagliavini,
M. Goedert,
B. Ghetti
|
8 |
1999 |
8 ๐
|
๐
|
A Recessive Mutation in the APP Gene with Dominant-Negative Effect on Amyloidogenesis
23 auth.
G. Di Fede,
M. Catania,
M. Morbin,
G. Rossi,
Silvia Suardi,
Giulia Mazzoleni,
M. Merlin,
A. Giovagnoli,
S. Prioni,
A. Erbetta,
...
C. Falcone,
M. Gobbi,
L. Colombo,
A. Bastone,
M. Beeg,
C. Manzoni,
Bruna Francescucci,
A. Spagnoli,
L. Cantu',
E. Del Favero,
E. Levy,
M. Salmona,
F. Tagliavini
|
8 |
2009 |
8 ๐
|
๐
|
Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies
7 auth.
G. Lauria,
M. Morbin,
R. Lombardi,
M. Borgna,
Giulia Mazzoleni,
A. Sghirlanzoni,
...
D. Pareyson
|
7 |
2003 |
7 ๐
|
๐
|
Loss of Prohibitin Membrane Scaffolds Impairs Mitochondrial Architecture and Leads to Tau Hyperphosphorylation and Neurodegeneration
8 auth.
Carsten Merkwirth,
P. Martinelli,
A. Korwitz,
M. Morbin,
H. Brรถnneke,
S. Jordan,
...
E. Rugarli,
T. Langer
|
7 |
2012 |
7 ๐
|
๐
|
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6.
22 auth.
T. Arsov,
Katherine R. Smith,
John A. Damiano,
S. Franceschetti,
L. Canafoglia,
C. Bromhead,
E. Andermann,
D. Vears,
P. Cossette,
S. Rajagopalan,
...
A. McDougall,
V. Sofia,
M. Farrell,
U. Aguglia,
A. Zini,
S. Meletti,
M. Morbin,
S. Mullen,
F. Andermann,
S. Mole,
M. Bahlo,
S. Berkovic
|
7 |
2011 |
7 ๐
|
๐
|
Expression of capsaicin receptor immunoreactivity in human peripheral nervous system and in painful neuropathies
8 auth.
G. Lauria,
M. Morbin,
R. Lombardi,
R. Capobianco,
Francesca Camozzi,
D. Pareyson,
...
M. Manconi,
P. Geppetti
|
6 |
2006 |
6 ๐
|
๐
|
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.
23 auth.
Katherine R. Smith,
H. Dahl,
L. Canafoglia,
E. Andermann,
John A. Damiano,
M. Morbin,
A. Bruni,
G. Giaccone,
P. Cossette,
P. Saftig,
...
J. Groฬtzinger,
M. Schwake,
F. Andermann,
J. Staropoli,
K. Sims,
S. Mole,
S. Franceschetti,
Noreen A. Alexander,
J. Cooper,
H. Chapman,
S. Carpenter,
S. Berkovic,
M. Bahlo
|
6 |
2013 |
6 ๐
|
๐
|
Amyloid ฮฒ plaque-associated proteins C1q and SAP enhance the Aฮฒ1โ42 peptide-induced cytokine secretion by adult human microglia in vitro
7 auth.
R. Veerhuis,
M. V. van Breemen,
J. Hoozemans,
M. Morbin,
Jamal Ouladhadj,
F. Tagliavini,
...
P. Eikelenboom
|
6 |
2003 |
6 ๐
|
๐
|
IgM deposits on skin nerves in antiโmyelinโassociated glycoprotein neuropathy
11 auth.
R. Lombardi,
B. Erne,
G. Lauria,
D. Pareyson,
M. Borgna,
M. Morbin,
...
Andreas Arnold,
A. Czapliลski,
P. Fuhr,
N. Schaeren-Wiemers,
A. Steck
|
6 |
2005 |
6 ๐
|
๐
|
Mutant Prion Protein Expression Causes Motor and Memory Deficits and Abnormal Sleep Patterns in a Transgenic Mouse Model
20 auth.
Sara Dossena,
L. Imeri,
M. Mangieri,
Anna Garofoli,
L. Ferrari,
Assunta Senatore,
Elena Restelli,
C. Balducci,
F. Fiordaliso,
M. Salio,
...
S. Bianchi,
L. Fioriti,
M. Morbin,
A. Pincherle,
G. Marcon,
F. Villani,
M. Carli,
F. Tagliavini,
G. Forloni,
R. Chiesa
|
6 |
2008 |
6 ๐
|