FERRONE, Marina Maria Teresa
FERRONE, Marina Maria Teresa
SCIENZE MEDICHE
ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia
2019-01-01 Rubino E, Mancini C, Boschi S, Ferrero P, Ferrone M, Bianca S, Zucca M, Orsi L, Pinessi L4 Govone F, Vacca A, Gai A, Giordana MT, Brusco A, Rainero I.
Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene.
1998-01-01 ARDUINO C ;FERRONE M ;BRUSCO A ;GARNERONE S ;FONTANA D ;ROLLE L ;CARBONARA AO
Molecular genetic analysis of von Hippel-Lindau disease by denaturing high-performance liquid chromatography.
2001-01-01 MENEGATTI E ;FERRONE M ;GALLONE S ;MAMELI M ;GROSSO E ;MIGONE N
Mutations in the POLG1 gene are not a relevant cause of cerebellar ataxia in Italy
2008-01-01 CAGNOLI C; BRUSSINO A; DI GREGORIO E; CAROPPO P; STOLA S; DRAGONE E; FERRONE M; PADOVAN S; MIGONE N; ORSI L; BRUSCO A
Polyvariant mutant CFTR genes in patients with chronic pancreatitis.
1999-01-01 ARDUINO C ;GALLO M ;BRUSCO A ;GARNERONE S ;PIANA MR ;DI MAGGIO S ;GERBINO PROMIS G ;FERRONE M ;ANGELI A ;GAIA E
SCA Tethering-PCR: A Rapid Genetic Test for the Diagnosis of SCA1-3, 6, and 7 by PCR and Capillary Electrophoresis
2018-01-01 Cagnoli, Claudia; Brussino, Alessandro; Mancini, Cecilia; Ferrone, Marina; Orsi, Laura; Salmin, Paola; Pappi, Patrizia; Giorgio, Elisa; Pozzi, Elisa; Cavalieri, Simona; Di Gregorio, Eleonora; Ferrero, Marta; Filla, Alessandro; De Michele, Giuseppe; Gellera, Cinzia; Mariotti, Caterina; Nethisinghe, Suran; Giunti, Paola; Stevanin, Giovanni; Brusco, Alfredo
Spinocerebellar ataxia type 12 identified in two Italian families
2009-01-01 Brussino A; Graziano C; Giobbe D; Dragone E; Ferrone M; Lodi R; Tonon C; Gabellino AS; Rinaldi R; Miccoli S; Grosso E; Bellati MC; Orsi L; Migone N; Brusco A
Spinocerebellar ataxia type 12 identified in two italian families may mimic sporadic ataxia
2010-01-01 Brussino A; Graziano C; Giobbe D; Ferrone M.M.T.; Dragone E; Arduino C; Lodi R; Tonon C; Gabellino AS; Rinaldi R; Miccoli S; Grosso E; Bellati MC; Orsi L; Migone N; Brusco A
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia | 2019 | Rubino E, Mancini C, Boschi S, Ferrero P, Ferrone M, Bianca S, Zucca M, Orsi L, Pinessi L4 Govone F, Vacca A, Gai A, Giordana MT, Brusco A, Rainero I. | |
Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene. | 1998 | ARDUINO C ;FERRONE M ;BRUSCO A ;GARNERONE S ;FONTANA D ;ROLLE L ;CARBONARA AO | |
Molecular genetic analysis of von Hippel-Lindau disease by denaturing high-performance liquid chromatography. | 2001 | MENEGATTI E ;FERRONE M ;GALLONE S ;MAMELI M ;GROSSO E ;MIGONE N | |
Mutations in the POLG1 gene are not a relevant cause of cerebellar ataxia in Italy | 2008 | CAGNOLI C; BRUSSINO A; DI GREGORIO E; CAROPPO P; STOLA S; DRAGONE E; FERRONE M; PADOVAN S; MIGONE N; ORSI L; BRUSCO A | |
Polyvariant mutant CFTR genes in patients with chronic pancreatitis. | 1999 | ARDUINO C ;GALLO M ;BRUSCO A ;GARNERONE S ;PIANA MR ;DI MAGGIO S ;GERBINO PROMIS G ;FERRONE M ;ANGELI A ;GAIA E | |
SCA Tethering-PCR: A Rapid Genetic Test for the Diagnosis of SCA1-3, 6, and 7 by PCR and Capillary Electrophoresis | 2018 | Cagnoli, Claudia; Brussino, Alessandro; Mancini, Cecilia; Ferrone, Marina; Orsi, Laura; Salmin, Paola; Pappi, Patrizia; Giorgio, Elisa; Pozzi, Elisa; Cavalieri, Simona; Di Gregorio, Eleonora; Ferrero, Marta; Filla, Alessandro; De Michele, Giuseppe; Gellera, Cinzia; Mariotti, Caterina; Nethisinghe, Suran; Giunti, Paola; Stevanin, Giovanni; Brusco, Alfredo | |
Spinocerebellar ataxia type 12 identified in two Italian families | 2009 | Brussino A; Graziano C; Giobbe D; Dragone E; Ferrone M; Lodi R; Tonon C; Gabellino AS; Rinaldi R; Miccoli S; Grosso E; Bellati MC; Orsi L; Migone N; Brusco A | |
Spinocerebellar ataxia type 12 identified in two italian families may mimic sporadic ataxia | 2010 | Brussino A; Graziano C; Giobbe D; Ferrone M.M.T.; Dragone E; Arduino C; Lodi R; Tonon C; Gabellino AS; Rinaldi R; Miccoli S; Grosso E; Bellati MC; Orsi L; Migone N; Brusco A |