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C Angelini

Showing results (151-160 of 531) with videos related to

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Neurology|August 1, 1986
Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairmentC Angelini, N Bresolin, G Pegolo, 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.
Human Genetics|March 1, 1996
Genetic epidemiology of congenital muscular dystrophy in a sample from north-east ItalyM L Mostacciuolo, M Miorin, F Martinello, et al.
Virchows Archiv : an International Journal of Pathology|August 1, 2019
Update on polyglucosan storage diseasesGiovanna Cenacchi, V Papa, R Costa, et al.
Drug and Alcohol Dependence|May 19, 2018
A systematic review of community-based interventions to improve oral chronic disease medication regimen adherence among individuals with substance use disorderKaren M Clements, Tasmina Hydery, Mark A Tesell, et al.
Acta Neuropathologica. Supplementum|January 1, 1981
Fatal lipid storage with abnormal mitochondria in an infantC Angelini, P A Battistella, A Laverda, et al.
Journal of Child Neurology|January 21, 2000
Acute quadriplegic myopathy in a 17-month-old boyL 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 agentsD M Bonifati, C Ori, C R Rossi, et al.
Journal of Medical Genetics|March 1, 1995
Neonatal spinal muscular atrophy with diaphragmatic paralysis is unlinked to 5q11.2-q13G Novelli, F Capon, L Tamisari, et al.
Neuroepidemiology|January 1, 1995
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1M L Mostacciuolo, F Schiavon, C Angelini, et al.
Pageof 54

Showing results (151-160 of 531) with videos related to

Sort By:
Pageof 54
Neurology|August 1, 1986
Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairmentC Angelini, N Bresolin, G Pegolo, 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.
Human Genetics|March 1, 1996
Genetic epidemiology of congenital muscular dystrophy in a sample from north-east ItalyM L Mostacciuolo, M Miorin, F Martinello, et al.
Virchows Archiv : an International Journal of Pathology|August 1, 2019
Update on polyglucosan storage diseasesGiovanna Cenacchi, V Papa, R Costa, et al.
Drug and Alcohol Dependence|May 19, 2018
A systematic review of community-based interventions to improve oral chronic disease medication regimen adherence among individuals with substance use disorderKaren M Clements, Tasmina Hydery, Mark A Tesell, et al.
Acta Neuropathologica. Supplementum|January 1, 1981
Fatal lipid storage with abnormal mitochondria in an infantC Angelini, P A Battistella, A Laverda, et al.
Journal of Child Neurology|January 21, 2000
Acute quadriplegic myopathy in a 17-month-old boyL 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 agentsD M Bonifati, C Ori, C R Rossi, et al.
Journal of Medical Genetics|March 1, 1995
Neonatal spinal muscular atrophy with diaphragmatic paralysis is unlinked to 5q11.2-q13G Novelli, F Capon, L Tamisari, et al.
Neuroepidemiology|January 1, 1995
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1M L Mostacciuolo, F Schiavon, C Angelini, et al.
Pageof 54