Zobrazeno 1 - 10
of 3 102
pro vyhledávání: '"J. Domı́nguez"'
Autor:
S. P. Bermúdez‐Rodríguez, A. Malagón‐Liceaga, G. Figueroa‐Ramos, Y. V. Estrada‐Caraveo, M. Gatica‐Torres, J. Domínguez‐Cherit
Publikováno v:
JEADV Clinical Practice, Vol 3, Iss 5, Pp 1529-1536 (2024)
Abstract Background Genital herpes (GH) is the main infectious cause of genital ulcers worldwide. Clinical diagnosis alone may be misleading, especially in immunocompromised patients in whom atypical presentations are common. Objectives To assess the
Externí odkaz:
https://doaj.org/article/33ac2668748e40779324b48fc2d2b24e
Autor:
S. Navarrete Espí, G. Cervera Ygual, S. Soto Fuster, M. Benavent Giménez, J. Domínguez Morán, F. Gascón Giménez
Publikováno v:
Neurology Perspectives, Vol 4, Iss , Pp 47- (2024)
Externí odkaz:
https://doaj.org/article/1e4a04df150b4f8f9acc7966f93237e4
Autor:
G. Cervera Ygual, M. Benavent Giménez, C. Quintanilla Bordás, M. Carcelén Gadea, L. Navarro Cantó, J. Domínguez Morán, C. Alcalá Vicente, J. López Arqueros, F. Pérez Miralles, E. Sánchez Villanueva, B. Casanova Estruch, F. Gascón Giménez
Publikováno v:
Neurology Perspectives, Vol 4, Iss , Pp 212- (2024)
Externí odkaz:
https://doaj.org/article/2b65cab54def46649c48eaea8437a323
Autor:
R. Alba Camilo, P. Izquierdo Ramírez, J. Domínguez Morán, A. Piera Balbastre, D. García López, J. Láinez Andrés
Publikováno v:
Neurology Perspectives, Vol 4, Iss , Pp 252- (2024)
Externí odkaz:
https://doaj.org/article/d1dfb5ba257746d79b1d89007af3fd9e
Autor:
A. Gómez-Ferrer, A. Collado, M. Ramírez, J. Domínguez, J. Casanova, C. Mir, A. Wong, J. L. Marenco, E. Nagore, V. Soriano, J. Rubio-Briones
Publikováno v:
Frontiers in Surgery, Vol 9 (2022)
BackgroundVideo-endoscopic inguinal lymphadenectomy (VEIL) is a minimally invasive approach that is increasingly indicated in oncological settings, with mounting evidence for its long-term oncological safety.ObjectivesTo present our single-center exp
Externí odkaz:
https://doaj.org/article/a6887c9c77204ff9b6dfe871072b9a7d
Autor:
G. Basile, M.M.F. Qadir, F. Mauvais-Jarvis, A. Vetere, V. Shoba, A.E. Modell, R.L. Pastori, H.A. Russ, B.K. Wagner, J. Dominguez-Bendala
Publikováno v:
Molecular Metabolism, Vol 60, Iss , Pp 101477- (2022)
Background: Stem cell therapies are finally coming of age as a viable alternative to pancreatic islet transplantation for the treatment of insulin-dependent diabetes. Several clinical trials using human embryonic stem cell (hESC)-derived β-like cell
Externí odkaz:
https://doaj.org/article/844528a494564264821b9d6ab2bdef0b
Autor:
F. Claps, M. Ramirez-Backhaus, M.C.Mir Maresma, A. Gomez-Ferrer, J.M. Mascaros, A. Collado-Serra, J. Marenco, J. Dominguez-Escrig, J. Casanova, A. Calatrava, C. Trombetta, J. Rubio-Briones
Publikováno v:
European Urology Open Science, Vol 20, Iss , Pp S50- (2020)
Externí odkaz:
https://doaj.org/article/0cba983635264197a8210fc07543255d
Autor:
B. Molina-Moya, A. Lacoma, N. García-Sierra, S. Blanco, L. Haba, S. Samper, J. Ruiz-Manzano, C. Prat, C. Arnold, J. Domínguez
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Abstract We developed a novel method, PyroTyping, for discrimination of Mycobacterium tuberculosis isolates combining pyrosequencing and IS6110 polymorphism. A total of 100 isolates were analysed with IS6110-restriction fragment length polymorphism (
Externí odkaz:
https://doaj.org/article/6466a499d7dc4df1a59d0b07e28432f0
Autor:
A.I. Maraña Pérez, M.L. Ruiz-Falcó Rojas, V. Puertas Martín, J. Domínguez Carral, I. Carreras Sáez, A. Duat Rodríguez, V. Sánchez González
Publikováno v:
Neurología (English Edition), Vol 32, Iss 6, Pp 363-370 (2017)
Introduction: Sturge–Weber syndrome is a congenital vascular disorder characterised by facial capillary malformation (port-wine stain) associated with venous and capillary malformations in the brain and eye. Neurological symptoms and alterations in
Externí odkaz:
https://doaj.org/article/8744259a79e84821abb4eda603fc0fa8
Autor:
A.I. Maraña Pérez, M.L. Ruiz-Falcó Rojas, V. Puertas Martín, J. Domínguez Carral, I. Carreras Sáez, A. Duat Rodríguez, V. Sánchez González
Publikováno v:
Neurología, Vol 32, Iss 6, Pp 363-370 (2017)
Resumen: Introducción: El síndrome de Sturge-Weber es un trastorno vascular congénito caracterizado por una malformación facial capilar (mancha en vino de Oporto) asociada a malformaciones venosas y capilares en el cerebro y en el ojo. También p
Externí odkaz:
https://doaj.org/article/1b1d6901113f4246846dd5415b616bb2