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C Orellana

Showing results (11-20 of 102) with videos related to

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Medicina Clinica|October 1, 1994
[Trigeminal sensitive neuropathy associated with polymyositis]C Orellana, J Vivancos, J M Grau, et al.
Clinical Rheumatology|February 10, 1998
Spondyloarthropathy presenting as a polymyalgia rheumatica-like syndromeA Ponce, R Sanmarti, C Orellana, et al.
The Journal of Investigative Dermatology|September 1, 1999
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T > G (Leu55Arg)F Martínez, J M Millán, C Orellana, et al.
Clinical Genetics|May 11, 2007
Clinical findings and molecular characterization of six subtelomeric imbalancesC Orellana, S Monfort, M Roselló, et al.
Lupus|February 14, 2009
Noonan syndrome associated with systemic lupus erythematosusM P Lisbona, M Moreno, C Orellana, et al.
Brain Research Bulletin|August 1, 1990
Sleep variables are unaltered by zolantidine in rats: are histamine H2-receptors not involved in sleep regulation?J M Monti, C Orellana, M Boussard, et al.
Updates in Surgery|October 6, 2017
Prognostic risk factors for conversion in laparoscopic cholecystectomyKarla V Chávez, Horacio Márquez-González, Itzé Aguirre, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|December 15, 2010
[Nijmegen breakage syndrome phenotype: a disorder to consider in the diagnosis of microcephaly]M Tomás Vila, J Pérez Verdú, M Roselló Piera, et al.
Clinical and Experimental Rheumatology|September 19, 2008
Sexual dysfunction in fibromyalgia patientsC Orellana, E Casado, M Masip, et al.
Sleep|December 1, 1994
Life events in the year preceding the onset of narcolepsyC Orellana, E Villemin, M Tafti, et al.
Pageof 11

Showing results (11-20 of 102) with videos related to

Sort By:
Pageof 11
Medicina Clinica|October 1, 1994
[Trigeminal sensitive neuropathy associated with polymyositis]C Orellana, J Vivancos, J M Grau, et al.
Clinical Rheumatology|February 10, 1998
Spondyloarthropathy presenting as a polymyalgia rheumatica-like syndromeA Ponce, R Sanmarti, C Orellana, et al.
The Journal of Investigative Dermatology|September 1, 1999
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T > G (Leu55Arg)F Martínez, J M Millán, C Orellana, et al.
Clinical Genetics|May 11, 2007
Clinical findings and molecular characterization of six subtelomeric imbalancesC Orellana, S Monfort, M Roselló, et al.
Lupus|February 14, 2009
Noonan syndrome associated with systemic lupus erythematosusM P Lisbona, M Moreno, C Orellana, et al.
Brain Research Bulletin|August 1, 1990
Sleep variables are unaltered by zolantidine in rats: are histamine H2-receptors not involved in sleep regulation?J M Monti, C Orellana, M Boussard, et al.
Updates in Surgery|October 6, 2017
Prognostic risk factors for conversion in laparoscopic cholecystectomyKarla V Chávez, Horacio Márquez-González, Itzé Aguirre, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|December 15, 2010
[Nijmegen breakage syndrome phenotype: a disorder to consider in the diagnosis of microcephaly]M Tomás Vila, J Pérez Verdú, M Roselló Piera, et al.
Clinical and Experimental Rheumatology|September 19, 2008
Sexual dysfunction in fibromyalgia patientsC Orellana, E Casado, M Masip, et al.
Sleep|December 1, 1994
Life events in the year preceding the onset of narcolepsyC Orellana, E Villemin, M Tafti, et al.
Pageof 11