Skip navigation
Home
Browse
Communities
& Collections
Browse Items by:
Author
Title
Subject
Issue Date
Material Type
Language
Access Rights
Help
OAR@UM Help
FAQs
OAR@UM Policies
Submission Forms
Sign on to:
My OAR@UM
OAR@UM
Search
Search:
All of OAR@UM
Faculty of Medicine and Surgery
Department of Physiology and Biochemistry
Books - FacM&SPB
Dissertations - FacM&SPB
Scholarly Works - FacM&SPB
for
Current filters:
Title
Author
Subject
Date Issued
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Start a new search
Add filters:
Use filters to refine the search results.
Title
Author
Subject
Date Issued
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Results 1-10 of 12 (Search time: 0.019 seconds).
previous
1
2
next
Item hits:
Issue Date
Title
Author(s)
2007
Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvβ1.1
Imbrici, Paola
;
D'Adamo, Maria Cristina
;
Cusimano, Antonella
;
Pessia, Mauro
2015
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene
D'Adamo, Maria Cristina
;
Gallenmuller, Constanze
;
Servettini, Ilenio
;
Hartl, Elisabeth
;
Tucker, Stephen J.
;
Arning, Larissa
;
Biskup, Saskia
;
Grottesi, Alessandro
;
Guglielmi, Luca
;
Imbrici, Paola
;
Bernasconi, Pia
;
Di Giovanni, Giuseppe
;
Franciolini, Fabio
;
Catacuzzeno, Luigi
;
Pessia, Mauro
;
Klopstock, Thomas
1999
Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K+ channel function
D'Adamo, Maria Cristina
;
Imbrici, Paola
;
Sponcichetti, Fabio
;
Pessia, Mauro
2011
Episodic ataxia type 1 mutations affect fast inactivation of K + channels by a reduction in either subunit surface expression or affinity for inactivation domain
Imbrici, Paola
;
D'Adamo, Maria Cristina
;
Grottesi, Alessandro
;
Biscarini, Andrea
;
Pessia, Mauro
2006
Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvβ1.1 and Kv1.4-1.1/Kvβ1.2
Imbrici, Paola
;
D'Adamo, Maria Cristina
;
Kullmann, Dimitri M.
;
Pessia, Mauro
2008
A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1
Imbrici, Paola
;
Gualandi, Francesca
;
D'Adamo, Maria Cristina
;
Masieri, Marina Taddei
;
Cudia, Paola
;
De Grandis, Domenico
;
Mannucci, Roberta
;
Nicoletti, Ildo
;
Tucker, Stephen J.
;
Ferlini, Alessandra
;
Pessia, Mauro
2007
Functional characterisation of a novel mutation causing episodic ataxia type 1 occurring in the KCNA1 gene
Imbrici, Paola
;
Gualandi, Francesca
;
D'Adamo, Maria Cristina
;
Cudia, Paola
;
De Grandis, Domenico
;
Ferlini, Alessandra
;
Pessia, Mauro
2017
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions
Imbrici, Paola
;
Altamura, Concetta
;
Gualandi, Francesca
;
Felice Mangiatordi, Giuseppe
;
Neri, Marcella
;
De Maria, Giovanni
;
Ferlini, Alessandra
;
Padovani, Alessandro
;
D'Adamo, Maria Cristina
;
Nicolotti, Orazio
;
Pessia, Mauro
;
Conte, Diana
;
Filosto, Massimiliano
;
Desaphy, Jean-Francois
2012
Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature
Brunetti, Orazio
;
Imbrici, Paola
;
Botti, Fabio Massimo
;
Pettorossi, Vito Enrico
;
D'Adamo, Maria Cristina
;
Valentino, Mario
;
Zammit, Christian
;
Mora, Marina
;
Gibertini, Sara
;
Di Giovanni, Giuseppe
;
Muscat, Richard
;
Pessia, Mauro
2003
Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channels
Imbrici, Paola
;
Cusimano, Antonella
;
D'Adamo, Maria Cristina
;
Curtis, Amalia de
;
Pessia, Mauro
Discover
Author
10
D'Adamo, Maria Cristina
3
Botti, Fabio Massimo
3
Di Giovanni, Giuseppe
3
Ferlini, Alessandra
3
Gualandi, Francesca
2
Brunetti, Orazio
2
Cudia, Paola
2
Cusimano, Antonella
2
De Grandis, Domenico
.
next >
Subject
9
Potassium channels
3
Ion channels
3
Myokymia
2
Sciatic nerve
2
Xenopus laevis
1
Acetazolamide
1
Amino acid sequence
1
Articulation disorders
1
Ataxia telangiectasia -- Genetic ...
.
next >