MTMR2 phospholipid phosphatase and membrane trafficking in Schwann cells
2007-01-01 Bolis, A; Coviello, S; Galbiati, C; Quattrini, A; Bolino, A
Expression analysis in the peripheral nerve of the myotubularin-related 2 protein phosphatase, mutated in CMT4B1
2003-01-01 Previtali, Sc; Zerega, B; Sherman, Dl; Brophy, Pj; Dina, G; King, Rhm; Salih, Mm; Feltri, L; Quattrini, A; Wrabetz, A; Monaco, Ap; Bolino, A
ISOLATION OF A HUMAN CHROMOSOME-22-SPECIFIC ALPHA SATELLITE CLONE
1991-01-01 Rocchi, M; Archidiacono, N; Carbone, R; Bolino, A; Shridhar, V; Ward, Dc; Baldini, A
TRAFFICKING THROUGH THE ENDO-LYSOSOMAL AXIS REGULATES MYELINATION AND REPAIR IN THE PERIPHERAL NERVOUS SYSTEM
2014-01-01 Vaccari, I; Carbone, A; Alberizzi, V; Bianchi, F; Del Carro, U; Meisler, Mh; Previtali, Sc; Bolino, A
Disruption of MTMR2 in Schwann cells produces CMT4B1-like neuropathy with myelin outfoldings
2005-01-01 Bolis, A; Bussini, S; Coviello, S; Dina, G; Previtali, Sc; Pardini, C; Malaguti, Mc; Quattrini, A; Wrabetz, L; Bolino, A
Mutation of the small HSP27/HSPB1 causes CMT neuropathy with abnormal neurofilament assembly
2007-01-01 Cerri, F; Coviello, S; Previtali, Sc; Benedetti, S; Scarlato, M; Dacci, P; Fazio, R; Comi, G; Quattrini, A; Bolino, A
Role of the MTMR2 phospholipid phosphatase in membrane homeostasis during Schwann cell myelination
2007-01-01 Bolis, A; Galbiati, C; Coviello, S; Bolino, A
GENOMIC APPROACH FOR INHERITED MOTOR AND CMT2 NEUROPATHIES: A COLLABORATIVE STUDY
2015-01-01 Previtali, Sc; Fabrizi, Gm; Schenone, A; Pareyson, D; Manganelli, F; Bellone, E; Lunetta, C; Penco, S; Mandich, P; Taroni, F; Corbo, M; Magri, S; Ferrarini, M; Piscosquito, G; Scarlato, M; Riva, N; Vigano, F; Carrera, P; Pisciotta, C; Santoro, L; Ferrari, M; Bucci, G; Lazarevic, D; Cittaro, D; Comi, G; Casari, G; Bolino, A
Phospholipid metabolism, the regulation of membrane trafficking and Charcot-Marie-Tooth neuropathies
2015-01-01 Bolino, A
AUTOPHAGY INDUCTION AS A THERAPEUTIC STRATEGY FOR DEMYELINATING CMT1A NEUROPATHIES
2017-01-01 Grandi, F; Alberizzi, V; Moreno, G; Guerrero-Valero, M; Bolino, A
KIF13B MOTOR PROTEIN REGULATES MYELINATION IN THE PERIPHERAL AND CENTRAL NERVOUS SYSTEM
2013-01-01 Noseda, R; Scarlino, S; Triolo, D; Sherman, D; Feltri, L; Wrabetz, L; Nave, Ka; Huganir, Rl; Previtali, Sc; Bolino, A
HOMOZYGOSITY MAPPING OF A NEW FORM OF HMSN - AUTOSOMAL RECESSIVE HYPERMYELINATING NEUROPATHY
1995-01-01 Bolino, A; Brancolini, V; Quattrone, A; Gambardella, A; Romeo, G; Devoto, M
CHARCOT-MARIE-TOOTH DISEASE TYPE 4B: A MULTICENTRE RETROSPECTIVE STUDY
2017-01-01 Pareyson, D; Stojkovic, T; Leonard-Louis, S; Reilly, Mm; Laura, M; Parman, Y; Battaloglu, E; Tazir, M; Bellatache, M; Bonello-Palot, N; Sacconi, S; Guimaraes-Costa, R; Attarian, S; Latour, P; Megarbane, A; Schenone, A; Ursino, G; Sabatelli, M; Luigetti, M; Santoro, L; Manganelli, F; Quattrone, A; Valentino, P; Murakami, T; Scherer, Ss; Dankwa, L; Shy, Me; Herrmann, D; Pisciotta, C; Previtali, S; Bolino, A
A NEW X-LINKED HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA LEADING TO PROGRESSIVE RENAL-FAILURE
1993-01-01 Enia, G; Zoccali, C; Bolino, A; Romeo, G
Role of the extracellular matrix in regenerating and non-regenerating axonal neuropathies
2007-01-01 Previtali, Sc; Malaguti, Mc; Riva, N; Scarlato, M; Dacci, P; Triolo, D; Lorenzetti, I; Fazio, R; Comi, G; Bolino, A
VOCAL CORD PARALYSIS IN CHARCOT-MARIE-TOOTH TYPE 4B1 DISEASE ASSOCIATED WITH A NOVEL MUTATION IN THE MYOTUBULARIN-RELATED PROTEIN 2 GENE: A CASE REPORT AND REVIEW OF THE LITERATURE
2017-01-01 Zambon, Aa; Sora, Mgn; Cantarella, G; Cerri, F; Quattrini, A; Comi, G; Previtali, Sc; Bolino, A
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22
1999-01-01 Bolino, A; Levy, Er; Muglia, M; Conforti, Fl; Gambardella, A; Le Guern, E; Christodoulou, K; Quattrone, A; Devoto, M; Monaco, Ap
LOSS OF FIG4 IN BOTH SCHWANN CELLS AND MOTOR NEURONS CONTRIBUTES TO CMT4J NEUROPATHY
2015-01-01 Vaccari, I; Carbone, A; Alberizzi, V; Lenk, Gm; Wrabetz, L; Previtali, Sc; Meisler, Mh; Bolino, A
Crystal structure of a hypoallergenic isoform of the major birch pollen allergen Bet v 1 and its biological function
2002-01-01 Markovic-Housley, Z; Degano, M; Lamba, D; Susani, M; Ferreira, F; Scheiner, O; Breiteneder, H
Nucleotide insertions and deletions in chronic lymphocytic leukemia. A CLL specific deletion among IGHV3-21 expressing cases with stereotyped receptors
2005-01-01 Belessi, C; Davi, F; Stamatopoulos, K; Degano, M; Andreou, T; Moreno, C; Merle-Beral, H; Crespo, M; Laoutaris, N; Montserrat, E; Caligaris-Cappio, F; Anagnostopoulos, A; Ghia, P
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| MTMR2 phospholipid phosphatase and membrane trafficking in Schwann cells | 1-gen-2007 | Bolis, A; Coviello, S; Galbiati, C; Quattrini, A; Bolino, A | |
| Expression analysis in the peripheral nerve of the myotubularin-related 2 protein phosphatase, mutated in CMT4B1 | 1-gen-2003 | Previtali, Sc; Zerega, B; Sherman, Dl; Brophy, Pj; Dina, G; King, Rhm; Salih, Mm; Feltri, L; Quattrini, A; Wrabetz, A; Monaco, Ap; Bolino, A | |
| ISOLATION OF A HUMAN CHROMOSOME-22-SPECIFIC ALPHA SATELLITE CLONE | 1-gen-1991 | Rocchi, M; Archidiacono, N; Carbone, R; Bolino, A; Shridhar, V; Ward, Dc; Baldini, A | |
| TRAFFICKING THROUGH THE ENDO-LYSOSOMAL AXIS REGULATES MYELINATION AND REPAIR IN THE PERIPHERAL NERVOUS SYSTEM | 1-gen-2014 | Vaccari, I; Carbone, A; Alberizzi, V; Bianchi, F; Del Carro, U; Meisler, Mh; Previtali, Sc; Bolino, A | |
| Disruption of MTMR2 in Schwann cells produces CMT4B1-like neuropathy with myelin outfoldings | 1-gen-2005 | Bolis, A; Bussini, S; Coviello, S; Dina, G; Previtali, Sc; Pardini, C; Malaguti, Mc; Quattrini, A; Wrabetz, L; Bolino, A | |
| Mutation of the small HSP27/HSPB1 causes CMT neuropathy with abnormal neurofilament assembly | 1-gen-2007 | Cerri, F; Coviello, S; Previtali, Sc; Benedetti, S; Scarlato, M; Dacci, P; Fazio, R; Comi, G; Quattrini, A; Bolino, A | |
| Role of the MTMR2 phospholipid phosphatase in membrane homeostasis during Schwann cell myelination | 1-gen-2007 | Bolis, A; Galbiati, C; Coviello, S; Bolino, A | |
| GENOMIC APPROACH FOR INHERITED MOTOR AND CMT2 NEUROPATHIES: A COLLABORATIVE STUDY | 1-gen-2015 | Previtali, Sc; Fabrizi, Gm; Schenone, A; Pareyson, D; Manganelli, F; Bellone, E; Lunetta, C; Penco, S; Mandich, P; Taroni, F; Corbo, M; Magri, S; Ferrarini, M; Piscosquito, G; Scarlato, M; Riva, N; Vigano, F; Carrera, P; Pisciotta, C; Santoro, L; Ferrari, M; Bucci, G; Lazarevic, D; Cittaro, D; Comi, G; Casari, G; Bolino, A | |
| Phospholipid metabolism, the regulation of membrane trafficking and Charcot-Marie-Tooth neuropathies | 1-gen-2015 | Bolino, A | |
| AUTOPHAGY INDUCTION AS A THERAPEUTIC STRATEGY FOR DEMYELINATING CMT1A NEUROPATHIES | 1-gen-2017 | Grandi, F; Alberizzi, V; Moreno, G; Guerrero-Valero, M; Bolino, A | |
| KIF13B MOTOR PROTEIN REGULATES MYELINATION IN THE PERIPHERAL AND CENTRAL NERVOUS SYSTEM | 1-gen-2013 | Noseda, R; Scarlino, S; Triolo, D; Sherman, D; Feltri, L; Wrabetz, L; Nave, Ka; Huganir, Rl; Previtali, Sc; Bolino, A | |
| HOMOZYGOSITY MAPPING OF A NEW FORM OF HMSN - AUTOSOMAL RECESSIVE HYPERMYELINATING NEUROPATHY | 1-gen-1995 | Bolino, A; Brancolini, V; Quattrone, A; Gambardella, A; Romeo, G; Devoto, M | |
| CHARCOT-MARIE-TOOTH DISEASE TYPE 4B: A MULTICENTRE RETROSPECTIVE STUDY | 1-gen-2017 | Pareyson, D; Stojkovic, T; Leonard-Louis, S; Reilly, Mm; Laura, M; Parman, Y; Battaloglu, E; Tazir, M; Bellatache, M; Bonello-Palot, N; Sacconi, S; Guimaraes-Costa, R; Attarian, S; Latour, P; Megarbane, A; Schenone, A; Ursino, G; Sabatelli, M; Luigetti, M; Santoro, L; Manganelli, F; Quattrone, A; Valentino, P; Murakami, T; Scherer, Ss; Dankwa, L; Shy, Me; Herrmann, D; Pisciotta, C; Previtali, S; Bolino, A | |
| A NEW X-LINKED HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA LEADING TO PROGRESSIVE RENAL-FAILURE | 1-gen-1993 | Enia, G; Zoccali, C; Bolino, A; Romeo, G | |
| Role of the extracellular matrix in regenerating and non-regenerating axonal neuropathies | 1-gen-2007 | Previtali, Sc; Malaguti, Mc; Riva, N; Scarlato, M; Dacci, P; Triolo, D; Lorenzetti, I; Fazio, R; Comi, G; Bolino, A | |
| VOCAL CORD PARALYSIS IN CHARCOT-MARIE-TOOTH TYPE 4B1 DISEASE ASSOCIATED WITH A NOVEL MUTATION IN THE MYOTUBULARIN-RELATED PROTEIN 2 GENE: A CASE REPORT AND REVIEW OF THE LITERATURE | 1-gen-2017 | Zambon, Aa; Sora, Mgn; Cantarella, G; Cerri, F; Quattrini, A; Comi, G; Previtali, Sc; Bolino, A | |
| Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22 | 1-gen-1999 | Bolino, A; Levy, Er; Muglia, M; Conforti, Fl; Gambardella, A; Le Guern, E; Christodoulou, K; Quattrone, A; Devoto, M; Monaco, Ap | |
| LOSS OF FIG4 IN BOTH SCHWANN CELLS AND MOTOR NEURONS CONTRIBUTES TO CMT4J NEUROPATHY | 1-gen-2015 | Vaccari, I; Carbone, A; Alberizzi, V; Lenk, Gm; Wrabetz, L; Previtali, Sc; Meisler, Mh; Bolino, A | |
| Crystal structure of a hypoallergenic isoform of the major birch pollen allergen Bet v 1 and its biological function | 1-gen-2002 | Markovic-Housley, Z; Degano, M; Lamba, D; Susani, M; Ferreira, F; Scheiner, O; Breiteneder, H | |
| Nucleotide insertions and deletions in chronic lymphocytic leukemia. A CLL specific deletion among IGHV3-21 expressing cases with stereotyped receptors | 1-gen-2005 | Belessi, C; Davi, F; Stamatopoulos, K; Degano, M; Andreou, T; Moreno, C; Merle-Beral, H; Crespo, M; Laoutaris, N; Montserrat, E; Caligaris-Cappio, F; Anagnostopoulos, A; Ghia, P |
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- 4 Contributo in Atti di Convegno ...2965
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