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X Ferrer

Showing results (91-100 of 114) with videos related to

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Msystems|December 15, 2025
Dynamic reworking of marine diatom endometabolomes in response to temperature and a model bacteriumMalin Olofsson, Mario Uchimiya, Frank X Ferrer-González, et al.
ISME Communications|November 8, 2023
Growth-stage-related shifts in diatom endometabolome composition set the stage for bacterial heterotrophyMalin Olofsson, Frank X Ferrer-González, Mario Uchimiya, et al.
Journal of the Peripheral Nervous System : JPNS|December 13, 2002
Peripheral neuropathy associated with mitochondrial disorders: 8 cases and review of the literatureS Bouillot, M L Martin-Négrier, A Vital, et al.
Journal of Endocrinological Investigation|May 16, 2006
One-tube-PCR technique for CCL2, CCL3, CCL4 and CCL5 applied to fine needle aspiration biopsies shows different profiles in autoimmune and non-autoimmune thyroid disordersX Ferrer-Francesch, P Caro, L Alcalde, et al.
Journal of Medical Genetics|February 27, 2004
A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychiaC Goizet, R Ben Yaou, L Demay, et al.
Neurogenetics|June 20, 2008
Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosisL Blázquez, M Azpitarte, A Sáenz, et al.
Revista De Neurologia|March 26, 2003
[Chloroquine-induced myopathy and neuropathy: progressive tetraparesis with areflexia that simulates a polyradiculoneuropathy. Two case reports]J L Becerra-Cuñat, J Coll-Cantí, E Gelpí-Mantius, et al.
Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
Brain : a Journal of Neurology|May 4, 2001
Central nervous system disease in patients with macrophagic myofasciitisF J Authier, P Cherin, A Creange, et al.
Pageof 12

Showing results (91-100 of 114) with videos related to

Sort By:
Pageof 12
Msystems|December 15, 2025
Dynamic reworking of marine diatom endometabolomes in response to temperature and a model bacteriumMalin Olofsson, Mario Uchimiya, Frank X Ferrer-González, et al.
ISME Communications|November 8, 2023
Growth-stage-related shifts in diatom endometabolome composition set the stage for bacterial heterotrophyMalin Olofsson, Frank X Ferrer-González, Mario Uchimiya, et al.
Journal of the Peripheral Nervous System : JPNS|December 13, 2002
Peripheral neuropathy associated with mitochondrial disorders: 8 cases and review of the literatureS Bouillot, M L Martin-Négrier, A Vital, et al.
Journal of Endocrinological Investigation|May 16, 2006
One-tube-PCR technique for CCL2, CCL3, CCL4 and CCL5 applied to fine needle aspiration biopsies shows different profiles in autoimmune and non-autoimmune thyroid disordersX Ferrer-Francesch, P Caro, L Alcalde, et al.
Journal of Medical Genetics|February 27, 2004
A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychiaC Goizet, R Ben Yaou, L Demay, et al.
Neurogenetics|June 20, 2008
Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosisL Blázquez, M Azpitarte, A Sáenz, et al.
Revista De Neurologia|March 26, 2003
[Chloroquine-induced myopathy and neuropathy: progressive tetraparesis with areflexia that simulates a polyradiculoneuropathy. Two case reports]J L Becerra-Cuñat, J Coll-Cantí, E Gelpí-Mantius, et al.
Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
Brain : a Journal of Neurology|May 4, 2001
Central nervous system disease in patients with macrophagic myofasciitisF J Authier, P Cherin, A Creange, et al.
Pageof 12