José Vicente Hervás García

Prof. José Vicente Hervás García

Hospital de Sant Joan Despí Moisès Broggi, Barcelona, Catalonia, Spain

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
15 April 2016 in CNS Neuroscience & Therapeutics
Verified
Journal Article
Closed access
PDF file
ATAina Teniente-Serra
Aina Teniente-Serra
JGJosé Vicente Hervás García
José Vicente Hervás García
BQBibiana Quirant‐Sánchez
Bibiana Quirant‐Sánchez
MMMaria Jose Mansilla
Maria Jose Mansilla
LGLaia Grau‐López
Laia Grau‐López
ECEva Mª Martínez Cáceres
Eva Mª Martínez Cáceres

17 April 2017 in Cytometry Part B: Clinical Cytometry
Verified
Journal Article
Closed access
PDF file
JOJoan Punet Ortiz
Joan Punet Ortiz
JGJosé Vicente Hervás García
José Vicente Hervás García
ATAina Teniente-Serra
Aina Teniente-Serra
ACAntonio Cano‐Orgaz
Antonio Cano‐Orgaz
MMMaria José Mansilla
Maria José Mansilla
ECEva Mª Martínez Cáceres
Eva Mª Martínez Cáceres

1 June 2016 in Journal of Stroke and Cerebrovascular Diseases
Verified
Journal Article
Closed access
LPLuis A. Prats-Sánchez
Luis A. Prats-Sánchez
JGJosé Vicente Hervás García
José Vicente Hervás García
JBJuan L. Becerra
Juan L. Becerra
MLManuel Lozano
Manuel Lozano
CCCarlos Castaño
Carlos Castaño
CGCarlos García-Esperón
Carlos García-Esperón

27 September 2012 in Journal of Neurology
Verified
Journal Article
Closed access
PDF file
DRDolores Vilas Rolán
Dolores Vilas Rolán
DVDolores Vilas
Dolores Vilas
MLMarta Milà Lopez
Marta Milà Lopez
GCGemma Cuberas-Borrós
Gemma Cuberas-Borrós
JCJuan Luis Becerra Cuñat
Juan Luis Becerra Cuñat
DEDomingo Escudero
Domingo Escudero

30 October 2015 in Neurodegenerative Disease Management
Verified
Journal Article
Closed access
JGJosé Vicente Hervás García
José Vicente Hervás García
SPSilvia Presas-Rodríguez
Silvia Presas-Rodríguez
ACAne Miren Crespo-Cuevas
Ane Miren Crespo-Cuevas
TCTamara Canento
Tamara Canento
MLManuel Lozano-Sánchez
Manuel Lozano-Sánchez
CRCristina M. Ramo-Tello
Cristina M. Ramo-Tello
A risk for developing progressive multifocal leukoencephalopathy is a major barrier to natalizumab use. Extended dosing intervals have been proposed as a way to maintain therapeutic efficacy and reduce progressive multifocal leukoencephalopathy incidence. This is the first reported case of progressive multifocal leukoencephalopathy in a patient using an extended dosing regimen (300 mg/6 weeks). A close clinical and imaging monitoring allowed early detection, which is a major prognostic factor. A favorable outcome was seen with a therapy comprising plasma exchange therapy, mirtazapine, mefloquine and cidofovir. Further studies will be needed to assess the potential role of extended dosing intervals to improve prognosis in patients receiving natalizumab and also to measure its impact clinically and/or radiologically.

1 March 2024 in CNS & Neurological Disorders - Drug Targets
Verified
Journal Article
Closed access
PDF file
AGAnna Gil-Sanchez
Anna Gil-Sanchez
MCMarc Canudes
Marc Canudes
PVPetya Valcheva
Petya Valcheva
LNLara Nogueras
Lara Nogueras
CGCristina González-Mingot
Cristina González-Mingot
LBLluís Brieva
Lluís Brieva
Introduction: Vortioxetine is a multimodal antidepressant drug that has been reported to have a positive impact on cognition, social function, and fatigue. Nevertheless, it has not been widely studied. Our objective was to explore the effects of vortioxetine on these and other parameters in patients with multiple sclerosis (MS) and depression. Patients and Methodology: This observational case series study included patients with MS and depression who received treatment with vortioxetine for at least 6 months. The patient history of depression and depressive symptoms was assessed. A neuropsychiatric evaluation was carried out using different scales, both before and after treatment. Results: Of the 25 patients who enrolled in the study, 17 completed the treatment. Significant improvements were observed in health status (EQ-5D; p = 0.002), mood (Beck’s Depression Inventory, BDI-II; p = 0.006), anxiety (State-Trait Anxiety Inventory, STAI-State; p = 0.021, and STAI-Trait; p = 0.011), and in the general health test (Short Form Health Survey, SF-36) for the vitality (p = 0.028) and mental health (p = 0.025) domains of the patients who completed the treatment. However, no statistically significant differences were observed in the cognitive tests related to attention, information processing speed, or fatigue. Conclusion: In this population, vortioxetine treatment was effective in reducing the symptoms of depression and improving anxiety, vitality, and mental health. In contrast, it did not produce any improvement in cognition or fatigue but an increase in sample size would be necessary to confirm these results.