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Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
May 21, 2016
Evaluation of Use of Belimumab In Clinical Practice Settings (Observe Study) In Spain: Health Resource Utilization and Labour Absenteeism
J Cortés, J L Andreu, J Calvo, et al.
Clinical and Experimental Rheumatology
|
November 1, 1993
Catastrophic antiphospholipid syndrome (CAS): a rare manifestation of the antiphospholipid antibody syndrome
R Mazzucchelli, C Barbadillo, H Youssef, et al.
JMIR Medical Education
|
February 21, 2023
Correction: Personalized Precision Medicine for Health Care Professionals: Development of a Competency Framework
Fernando Martin-Sanchez, Martín Lázaro, Carlos López-Otín, et al.
JMIR Medical Education
|
February 7, 2023
Personalized Precision Medicine for Health Care Professionals: Development of a Competency Framework
Fernando Martin-Sanchez, Martín Lázaro, Carlos López-Otín, et al.
Neuromuscular Disorders : NMD
|
June 26, 1999
A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's disease
A L Andreu, C Bruno, L Tamburino, et al.
Muscle & Nerve
|
July 27, 1999
A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contact
J Gamez, R Fernandez, C Bruno, et al.
Archivos De Bronconeumologia
|
December 24, 2005
[Description of a new procedure for fiberoptic bronchoscopy during noninvasive ventilation through a nasal mask in patients with acute respiratory failure]
E Chiner, M Llombart, J Signes-Costa, et al.
FEBS Letters
|
December 13, 2005
Free radicals-mediated damage in transmitochondrial cells harboring the T14487C mutation in the ND6 gene of mtDNA
Ricardo Gonzalo, Elena Garcia-Arumi, David Llige, et al.
Revista Espanola De Anestesiologia Y Reanimacion
|
July 1, 1985
[Presentation of a case of a silent genetic cholinesterase variant]
M S Carrasco, F Gómez Armenta, C Gil, et al.
Annals of Medicine
|
October 30, 2001
Exercise intolerance resulting from a muscle-restricted mutation in the mitochondrial tRNA(Leu (CUN)) gene
C Vives-Bauza, J Gamez, M Roig, et al.
Page
of 32
Search research articles
Search
Showing results (131-140 of 313) with videos related to
Sort By:
Page
of 32
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
May 21, 2016
Evaluation of Use of Belimumab In Clinical Practice Settings (Observe Study) In Spain: Health Resource Utilization and Labour Absenteeism
J Cortés, J L Andreu, J Calvo, et al.
Clinical and Experimental Rheumatology
|
November 1, 1993
Catastrophic antiphospholipid syndrome (CAS): a rare manifestation of the antiphospholipid antibody syndrome
R Mazzucchelli, C Barbadillo, H Youssef, et al.
JMIR Medical Education
|
February 21, 2023
Correction: Personalized Precision Medicine for Health Care Professionals: Development of a Competency Framework
Fernando Martin-Sanchez, Martín Lázaro, Carlos López-Otín, et al.
JMIR Medical Education
|
February 7, 2023
Personalized Precision Medicine for Health Care Professionals: Development of a Competency Framework
Fernando Martin-Sanchez, Martín Lázaro, Carlos López-Otín, et al.
Neuromuscular Disorders : NMD
|
June 26, 1999
A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's disease
A L Andreu, C Bruno, L Tamburino, et al.
Muscle & Nerve
|
July 27, 1999
A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contact
J Gamez, R Fernandez, C Bruno, et al.
Archivos De Bronconeumologia
|
December 24, 2005
[Description of a new procedure for fiberoptic bronchoscopy during noninvasive ventilation through a nasal mask in patients with acute respiratory failure]
E Chiner, M Llombart, J Signes-Costa, et al.
FEBS Letters
|
December 13, 2005
Free radicals-mediated damage in transmitochondrial cells harboring the T14487C mutation in the ND6 gene of mtDNA
Ricardo Gonzalo, Elena Garcia-Arumi, David Llige, et al.
Revista Espanola De Anestesiologia Y Reanimacion
|
July 1, 1985
[Presentation of a case of a silent genetic cholinesterase variant]
M S Carrasco, F Gómez Armenta, C Gil, et al.
Annals of Medicine
|
October 30, 2001
Exercise intolerance resulting from a muscle-restricted mutation in the mitochondrial tRNA(Leu (CUN)) gene
C Vives-Bauza, J Gamez, M Roig, et al.
Page
of 32