Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Mora

Showing results (541-550 of 680) with videos related to

Pageof 68
Sort By:
Annals of Neurology|August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleM Mora, L Cartegni, C Di Blasi, et al.
Molecular Medicine (Cambridge, Mass.)|February 20, 2025
Matrix metalloproteinases and their tissue inhibitors as upcoming biomarker signatures of connective tissue diseases-related interstitial lung disease: towards an earlier and accurate diagnosisVerónica Pulito-Cueto, Belén Atienza-Mateo, Joao C Batista-Liz, et al.
Infection and Drug Resistance|May 2, 2019
Differential recognition of <i>Candida tropicalis</i>, <i>Candida guilliermondii</i>, <i>Candida krusei</i>, and <i>Candida auris</i> by human innate immune cellsMaría J Navarro-Arias, Marco J Hernández-Chávez, Laura C García-Carnero, et al.
Neuromuscular Disorders : NMD|March 21, 2001
Evaluation of cardiac and respiratory involvement in sarcoglycanopathiesL Politano, V Nigro, L Passamano, et al.
Environmental Science & Technology|March 8, 2014
Blood and hair manganese concentrations in pregnant women from the infants' environmental health study (ISA) in Costa RicaAna M Mora, Berna van Wendel de Joode, Donna Mergler, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.
European Journal of Neurology|November 27, 2019
Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophyV Galimberti, R Tironi, A Lerario, et al.
Revista Espanola De Sanidad Penitenciaria|November 7, 2012
[Job satisfaction of nursing staff in Spanish prisons]E J Vera-Remartínez, L M Mora Parra, J A González Gómez, et al.
Cell Surface (Amsterdam, Netherlands)|January 1, 2026
<i>Pap1</i> is an adhesin involved in the interaction of <i>Sporothrix schenckii</i> and <i>Sporothrix brasiliensis</i> with the hostLeonardo Padró-Villegas, Julieta I Aguilera-Domínguez, Luz A López-Ramírez, et al.
Revista De Calidad Asistencial : Organo De La Sociedad Espanola De Calidad Asistencial|June 13, 2015
[Consequences of errors in the translation of questionnaires: Spanish version of Downton index]M Aranda-Gallardo, J M Morales-Asencio, J C Canca-Sánchez, et al.
Pageof 68

Showing results (541-550 of 680) with videos related to

Sort By:
Pageof 68
Annals of Neurology|August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleM Mora, L Cartegni, C Di Blasi, et al.
Molecular Medicine (Cambridge, Mass.)|February 20, 2025
Matrix metalloproteinases and their tissue inhibitors as upcoming biomarker signatures of connective tissue diseases-related interstitial lung disease: towards an earlier and accurate diagnosisVerónica Pulito-Cueto, Belén Atienza-Mateo, Joao C Batista-Liz, et al.
Infection and Drug Resistance|May 2, 2019
Differential recognition of <i>Candida tropicalis</i>, <i>Candida guilliermondii</i>, <i>Candida krusei</i>, and <i>Candida auris</i> by human innate immune cellsMaría J Navarro-Arias, Marco J Hernández-Chávez, Laura C García-Carnero, et al.
Neuromuscular Disorders : NMD|March 21, 2001
Evaluation of cardiac and respiratory involvement in sarcoglycanopathiesL Politano, V Nigro, L Passamano, et al.
Environmental Science & Technology|March 8, 2014
Blood and hair manganese concentrations in pregnant women from the infants' environmental health study (ISA) in Costa RicaAna M Mora, Berna van Wendel de Joode, Donna Mergler, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.
European Journal of Neurology|November 27, 2019
Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophyV Galimberti, R Tironi, A Lerario, et al.
Revista Espanola De Sanidad Penitenciaria|November 7, 2012
[Job satisfaction of nursing staff in Spanish prisons]E J Vera-Remartínez, L M Mora Parra, J A González Gómez, et al.
Cell Surface (Amsterdam, Netherlands)|January 1, 2026
<i>Pap1</i> is an adhesin involved in the interaction of <i>Sporothrix schenckii</i> and <i>Sporothrix brasiliensis</i> with the hostLeonardo Padró-Villegas, Julieta I Aguilera-Domínguez, Luz A López-Ramírez, et al.
Revista De Calidad Asistencial : Organo De La Sociedad Espanola De Calidad Asistencial|June 13, 2015
[Consequences of errors in the translation of questionnaires: Spanish version of Downton index]M Aranda-Gallardo, J M Morales-Asencio, J C Canca-Sánchez, et al.
Pageof 68