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Minerva Pediatrica
|
December 15, 1980
[A case of pneumothorax frequently recurring as a complication of severe asthma: treatment by creation of pleural adherence]
A Iester, A Marchesi, A Di Stefano, et al.
Minerva Pediatrica
|
August 18, 1971
[Panmyelophthisis of the Fanconi type. Presentation of 2 brothers; chromosome changes in the father]
G Vignola, G Cordone, P G Mori, et al.
Minerva Pediatrica
|
July 14, 1974
[Pachydermoperiostosis. Report of a case]
G Cordone, G Pinelli, A Comelli, et al.
Neurology
|
May 1, 1996
Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency
C Minetti, M Bado, G Morreale, et al.
Minerva Pediatrica
|
May 5, 1975
[Louis-Bar disease. A recent case]
G Gemme, G Cordone, A Comelli, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
August 1, 1996
Severe dystrophinopathy in a patient with congenital hypotonia
G Cordone, M Bado, G Morreale, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 1, 1984
[Critical evaluation of changes of serum CK after exertion in the identification of carriers of Duchenne's muscular dystrophy]
G Cordone, V Venzano, G Rossi, et al.
Muscle & Nerve
|
February 18, 1998
Disorganization of dystrophin costameric lattice in Becker muscular dystrophy
C Minetti, G Cordone, F Beltrame, et al.
Journal of Child Neurology
|
June 27, 2000
Novel mutation in the CPT II gene in a child with periodic febrile myalgia and myoglobinuria
C Bruno, M Bado, C Minetti, et al.
Minerva Pediatrica
|
November 15, 1982
[Clinical and histomorphological study of congenital myopathy with minimal lesions]
G Meola, E Scarpini, C Minetti, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 82) with videos related to
Sort By:
Page
of 9
Minerva Pediatrica
|
December 15, 1980
[A case of pneumothorax frequently recurring as a complication of severe asthma: treatment by creation of pleural adherence]
A Iester, A Marchesi, A Di Stefano, et al.
Minerva Pediatrica
|
August 18, 1971
[Panmyelophthisis of the Fanconi type. Presentation of 2 brothers; chromosome changes in the father]
G Vignola, G Cordone, P G Mori, et al.
Minerva Pediatrica
|
July 14, 1974
[Pachydermoperiostosis. Report of a case]
G Cordone, G Pinelli, A Comelli, et al.
Neurology
|
May 1, 1996
Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency
C Minetti, M Bado, G Morreale, et al.
Minerva Pediatrica
|
May 5, 1975
[Louis-Bar disease. A recent case]
G Gemme, G Cordone, A Comelli, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
August 1, 1996
Severe dystrophinopathy in a patient with congenital hypotonia
G Cordone, M Bado, G Morreale, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 1, 1984
[Critical evaluation of changes of serum CK after exertion in the identification of carriers of Duchenne's muscular dystrophy]
G Cordone, V Venzano, G Rossi, et al.
Muscle & Nerve
|
February 18, 1998
Disorganization of dystrophin costameric lattice in Becker muscular dystrophy
C Minetti, G Cordone, F Beltrame, et al.
Journal of Child Neurology
|
June 27, 2000
Novel mutation in the CPT II gene in a child with periodic febrile myalgia and myoglobinuria
C Bruno, M Bado, C Minetti, et al.
Minerva Pediatrica
|
November 15, 1982
[Clinical and histomorphological study of congenital myopathy with minimal lesions]
G Meola, E Scarpini, C Minetti, et al.
Page
of 9