FANIN, MARINA

FANIN, MARINA  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
11-year clinical follow-up of a patient with dysferlinopathy-report on the first diagnosed slovenian case 2001 FANIN, MARINAANGELINI, CORRADO + - - Slovenia
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy. 2000 PEGORARO, ELENAFANIN, MARINATREVISAN, CARLO PIETROANGELINI, CORRADO + NEUROLOGY - -
A severe case of Duchenne-like muscular dystrophy due to a mutation in the alpha-sarcoglycan (adhalin) gene 1996 FANIN, MARINAPEGORARO, ELENASORARU', GIANNIMOSTACCIUOLO, MARIA LUISATREVISAN, CARLO PIETROANGELINI, CORRADO + BASIC AND APPLIED MYOLOGY - -
Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients. 1994 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO JOURNAL OF THE NEUROLOGICAL SCIENCES - -
Acute quadriplegic myopathy in a 17 month old boy 2000 SALVIATI, LEONARDOLAVERDA, ANNA MARIAZANCAN, LUCIAFANIN, MARINAANGELINI, CORRADO + JOURNAL OF CHILD NEUROLOGY - -
Adult acid maltase deficiency: an open trial with albuterol and branched- chain aminoacids 2004 ANGELINI, CORRADOPEGORARO, ELENAVERGANI, LODOVICANASCIMBENI, ANNA CHIARAFANIN, MARINA + BASIC AND APPLIED MYOLOGY - -
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations. 1996 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO + JOURNAL OF THE NEUROLOGICAL SCIENCES - -
Application of a cDNA microarray for the analysis of muscular dystrophies and childhood leukemias 2003 CAMPANARO, STEFANODE PITTA', CRISTIANOROMUALDI, CHIARABELLIN MCAGNIN, STEFANOTOMBOLAN, LUCIAFANIN, MARINAPEGORARO, ELENATE KRONNIE, GEERTRUDYVALLE, GIORGIOBASSO, GIUSEPPEANGELINI CLANFRANCHI, GEROLAMO + MINERVA BIOTECNOLOGICA - -
Autophagy dysregulation in Danon disease 2017 NASCIMBENI, ANNA CHIARAFANIN, MARINAANGELINI, CORRADOSANDRI, MARCO CELL DEATH & DISEASE - -
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript 2016 FANIN, MARINABELLO, LUCAPEGORARO, ELENA + NEUROMUSCULAR DISORDERS - -
Beta-sarcoglycan gene mutations cause plasma membrane dysruption in striated and smooth muscle, leading to severe dilated cardiomyopathy 2002 MELACINI, PAOLAFANIN, MARINABOITO, CHIARAPEGORARO, ELENAANGELINI, CORRADOILICETO, SABINO EUROPEAN HEART JOURNAL - -
Biochemical and ultrastructural evidence of endoplasmic reticulum stress in LGMD2I 2007 FANIN, MARINAANGELINI, CORRADOPEGORARO, ELENA + VIRCHOWS ARCHIV - -
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy 2001 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO + NEUROLOGY - -
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophy. 1996 MELACINI, PAOLAVIANELLO, ANDREAFANIN, MARINAMIORIN, MARTAANGELINI, CORRADODALLA VOLTA, SERGIO + NEUROMUSCULAR DISORDERS - -
Cardiac involvement in Becker muscular dystrophy 1993 MELACINI, PAOLAFANIN, MARINADANIELI, GIAN ANTONIOFASOLI, GIUSEPPEANGELINI, CORRADOVITIELLO, LIBEROBUJA, GIANFRANCOMOSTACCIUOLO, MARIA LUISAPEGORARO, ELENADALLA VOLTA, SERGIO + JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY - -
Cardiac transplantation in a Duchenne muscular dystrophy carrier 1998 MELACINI, PAOLAFANIN, MARINAANGELINI, ANNALISAPEGORARO, ELENADANIELI, GIAN ANTONIOTHIENE, GAETANODALLA VOLTA, SERGIOANGELINI, CORRADO + NEUROMUSCULAR DISORDERS - -
Cardioembolic stroke in Danon disease. 2008 SPINAZZI, MARCOFANIN, MARINAMELACINI, PAOLANASCIMBENI, ANNA CHIARAANGELINI, CORRADO CLINICAL GENETICS - -
Cardiomyopathy in b-sarcoglycanopathies: a new pathogenetic hypothesis 2002 ANGELINI, CORRADOFANIN, MARINAMELACINI, PAOLAPEGORARO, ELENA + BASIC AND APPLIED MYOLOGY - -
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency 2003 BOSCARO, MARCOFANIN, MARINATREVISAN, CARLO PIETROANGELINI, CORRADOPEGORARO, ELENA + HUMAN MUTATION - -
Clinical and molecular study in LGMD2I 2003 FANIN, MARINAANGELINI, CORRADOPEGORARO, ELENA + EUROPEAN JOURNAL OF NEUROLOGY - -