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Journal of the Neurological Sciences
|
September 1, 1996
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
D J Duggan, M Fanin, E Pegoraro, et al.
Neuropathology and Applied Neurobiology
|
November 8, 2019
Review: Danon disease: Review of natural history and recent advances
G Cenacchi, V Papa, V Pegoraro, et al.
Neurology
|
May 1, 1990
Enormous dystrophin in a patient with Becker muscular dystrophy
C Angelini, A H Beggs, E P Hoffman, et al.
Muscle & Nerve
|
October 1, 1995
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course
M Fanin, G A Danieli, M Cadaldini, et al.
The New England Journal of Medicine
|
February 27, 1997
Mutations in the sarcoglycan genes in patients with myopathy
D J Duggan, J R Gorospe, M Fanin, et al.
Neuromuscular Disorders : NMD
|
July 1, 1994
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes
C Angelini, M Fanin, E Pegoraro, et al.
Journal of Child Neurology
|
January 21, 2000
Acute quadriplegic myopathy in a 17-month-old boy
L Salviati, A M Laverda, L Zancan, et al.
Cancer Chemotherapy and Pharmacology
|
January 4, 2001
Neuromuscular damage after hyperthermic isolated limb perfusion in patients with melanoma or sarcoma treated with chemotherapeutic agents
D M Bonifati, C Ori, C R Rossi, et al.
Muscle & Nerve
|
September 1, 1996
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?
M Fanin, M P Freda, L Vitiello, et al.
Virchows Archiv : an International Journal of Pathology
|
August 1, 2019
Update on polyglucosan storage diseases
Giovanna Cenacchi, V Papa, R Costa, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 68) with videos related to
Sort By:
Page
of 7
Journal of the Neurological Sciences
|
September 1, 1996
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
D J Duggan, M Fanin, E Pegoraro, et al.
Neuropathology and Applied Neurobiology
|
November 8, 2019
Review: Danon disease: Review of natural history and recent advances
G Cenacchi, V Papa, V Pegoraro, et al.
Neurology
|
May 1, 1990
Enormous dystrophin in a patient with Becker muscular dystrophy
C Angelini, A H Beggs, E P Hoffman, et al.
Muscle & Nerve
|
October 1, 1995
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course
M Fanin, G A Danieli, M Cadaldini, et al.
The New England Journal of Medicine
|
February 27, 1997
Mutations in the sarcoglycan genes in patients with myopathy
D J Duggan, J R Gorospe, M Fanin, et al.
Neuromuscular Disorders : NMD
|
July 1, 1994
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes
C Angelini, M Fanin, E Pegoraro, et al.
Journal of Child Neurology
|
January 21, 2000
Acute quadriplegic myopathy in a 17-month-old boy
L Salviati, A M Laverda, L Zancan, et al.
Cancer Chemotherapy and Pharmacology
|
January 4, 2001
Neuromuscular damage after hyperthermic isolated limb perfusion in patients with melanoma or sarcoma treated with chemotherapeutic agents
D M Bonifati, C Ori, C R Rossi, et al.
Muscle & Nerve
|
September 1, 1996
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?
M Fanin, M P Freda, L Vitiello, et al.
Virchows Archiv : an International Journal of Pathology
|
August 1, 2019
Update on polyglucosan storage diseases
Giovanna Cenacchi, V Papa, R Costa, et al.
Page
of 7