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Eduard Gallardo

Showing results (11-20 of 120) with videos related to

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Medicina Clinica|February 10, 2015
[Dysferlinopathy masquerading as a refractory polymyositis]Jose Loureiro Amigo, Eduard Gallardo, Pia Gallano, et al.
Muscle & Nerve|May 30, 2008
Chronic sensorimotor polyradiculopathy with antibodies to P2: an electrophysiological and immunoproteomic analysisRicard Rojas-Garcia, Eduard Gallardo, Carolina De La Torre, et al.
The International Journal of Biochemistry & Cell Biology|June 25, 2013
Dysferlin interacts with calsequestrin-1, myomesin-2 and dynein in human skeletal muscleBàrbara Flix, Carolina de la Torre, Juan Castillo, et al.
Annals of Neurology|January 10, 2002
A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathyMengfatt Ho, Eduard Gallardo, Diane McKenna-Yasek, et al.
Blood|July 11, 2006
Steady remission of scleromyxedema 3 years after autologous stem cell transplantation: an in vivo and in vitro studyIsabel Illa, Carolina de la Torre, Ricardo Rojas-Garcia, et al.
Journal of Human Genetics|May 23, 2014
Severe exacerbation of Andersen-Tawil syndrome secondary to thyrotoxicosisJordi Díaz-Manera, Luis Querol, Aída Alejaldre, et al.
Scientific Reports|August 19, 2017
Hypoxia triggers IFN-I production in muscle: Implications in dermatomyositisNoemí De Luna, Xavier Suárez-Calvet, Cinta Lleixà, et al.
Neuromuscular Disorders : NMD|February 18, 2006
Muscle inflammation, autoimmune Addison's disease and sarcoidosis in a patient with dysferlin deficiencyAlbert Selva-O'Callaghan, Moises Labrador-Horrillo, Eduard Gallardo, et al.
Archives of Neurology|December 14, 2005
Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this associationJordi Sanahuja, Elena Franco, Ricardo Rojas-García, et al.
Muscle & Nerve|May 10, 2005
X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterizationCarmen Paradas, Celedonio Márquez, Eduard Gallardo, et al.
Pageof 12

Showing results (11-20 of 120) with videos related to

Sort By:
Pageof 12
Medicina Clinica|February 10, 2015
[Dysferlinopathy masquerading as a refractory polymyositis]Jose Loureiro Amigo, Eduard Gallardo, Pia Gallano, et al.
Muscle & Nerve|May 30, 2008
Chronic sensorimotor polyradiculopathy with antibodies to P2: an electrophysiological and immunoproteomic analysisRicard Rojas-Garcia, Eduard Gallardo, Carolina De La Torre, et al.
The International Journal of Biochemistry & Cell Biology|June 25, 2013
Dysferlin interacts with calsequestrin-1, myomesin-2 and dynein in human skeletal muscleBàrbara Flix, Carolina de la Torre, Juan Castillo, et al.
Annals of Neurology|January 10, 2002
A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathyMengfatt Ho, Eduard Gallardo, Diane McKenna-Yasek, et al.
Blood|July 11, 2006
Steady remission of scleromyxedema 3 years after autologous stem cell transplantation: an in vivo and in vitro studyIsabel Illa, Carolina de la Torre, Ricardo Rojas-Garcia, et al.
Journal of Human Genetics|May 23, 2014
Severe exacerbation of Andersen-Tawil syndrome secondary to thyrotoxicosisJordi Díaz-Manera, Luis Querol, Aída Alejaldre, et al.
Scientific Reports|August 19, 2017
Hypoxia triggers IFN-I production in muscle: Implications in dermatomyositisNoemí De Luna, Xavier Suárez-Calvet, Cinta Lleixà, et al.
Neuromuscular Disorders : NMD|February 18, 2006
Muscle inflammation, autoimmune Addison's disease and sarcoidosis in a patient with dysferlin deficiencyAlbert Selva-O'Callaghan, Moises Labrador-Horrillo, Eduard Gallardo, et al.
Archives of Neurology|December 14, 2005
Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this associationJordi Sanahuja, Elena Franco, Ricardo Rojas-García, et al.
Muscle & Nerve|May 10, 2005
X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterizationCarmen Paradas, Celedonio Márquez, Eduard Gallardo, et al.
Pageof 12