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M Bado

Showing results (11-20 of 31) with videos related to

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Minerva Pediatrica|February 28, 1984
[The myopathy of congenital fiber type disproportion]C Minetti, G Meola, E Scarpini, et al.
Cell Death and Differentiation|February 1, 1997
Induction of differentiation and apoptosis by interferon-gamma in human neuroblastoma cells in vitro as a dual and alternative early biological responseP G Montaldo, V Chiesa, M Bado, et al.
Neurology|January 27, 1998
Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuriaC Bruno, C Minetti, S Shanske, et al.
Minerva Pediatrica|November 30, 1983
[Ophthalmoplegia plus and ragged red fibers. Description of a case manifested in childhood]E De Langlade, G Corazza, C Minetti, et al.
Minerva Pediatrica|March 1, 1991
[The defect in muscular glucose-6-phosphate dehydrogenase]M Bado, C Minetti, L Mallamaci, et al.
American Journal of Medical Genetics. Part A|April 11, 2003
Long-term survival in Stuve-Wiedemann syndrome: a neuro-myo-skeletal disorder with manifestations of dysautonomiaM Di Rocco, G Stella, C Bruno, et al.
Minerva Pediatrica|October 1, 1995
[Cardiofacial syndrome. A case report]M Bado, G Morreale, M Pelegrini, et al.
Clinical Dysmorphology|May 11, 2002
Auriculo-condylar syndrome or new syndrome?M T Divizia, A Cordone, M Bado, et al.
Minerva Pediatrica|October 1, 1994
[Muscle phosphorylase deficiency in childhood. A case report]C Bruno, A Iester, M Bado, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophyM Di Rocco, L Leveratto, A Cama, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Minerva Pediatrica|February 28, 1984
[The myopathy of congenital fiber type disproportion]C Minetti, G Meola, E Scarpini, et al.
Cell Death and Differentiation|February 1, 1997
Induction of differentiation and apoptosis by interferon-gamma in human neuroblastoma cells in vitro as a dual and alternative early biological responseP G Montaldo, V Chiesa, M Bado, et al.
Neurology|January 27, 1998
Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuriaC Bruno, C Minetti, S Shanske, et al.
Minerva Pediatrica|November 30, 1983
[Ophthalmoplegia plus and ragged red fibers. Description of a case manifested in childhood]E De Langlade, G Corazza, C Minetti, et al.
Minerva Pediatrica|March 1, 1991
[The defect in muscular glucose-6-phosphate dehydrogenase]M Bado, C Minetti, L Mallamaci, et al.
American Journal of Medical Genetics. Part A|April 11, 2003
Long-term survival in Stuve-Wiedemann syndrome: a neuro-myo-skeletal disorder with manifestations of dysautonomiaM Di Rocco, G Stella, C Bruno, et al.
Minerva Pediatrica|October 1, 1995
[Cardiofacial syndrome. A case report]M Bado, G Morreale, M Pelegrini, et al.
Clinical Dysmorphology|May 11, 2002
Auriculo-condylar syndrome or new syndrome?M T Divizia, A Cordone, M Bado, et al.
Minerva Pediatrica|October 1, 1994
[Muscle phosphorylase deficiency in childhood. A case report]C Bruno, A Iester, M Bado, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophyM Di Rocco, L Leveratto, A Cama, et al.
Pageof 4