Suchergebnisse - "López, Merce"

PubPharm (21)

1

Effect of Bypassing the Closest Stroke Center in Patients with Intracerebral Hemorrhage : A Secondary Analysis of the RACECAT Randomized Clinical Trial

enthalten in: JAMA neurology | 2023

von Ramos-Pachón, A. | Rodríguez-Luna, D. | Martí-Fàbregas, J. | +46

2

Mental health consequences of isolation of patients with COVID-19.

enthalten in: Revista espanola de salud publica | 2022

von Navas, E. | López, M. | Muñoz, M. | +7

3

Academic integrity policies against assessment fraud in postgraduate studies : An analysis of the situation in Spanish universities

enthalten in: Heliyon | 2022

von Cerdà-Navarro, A. | Touza, C. | Morey-López, M. | +1

4

Impact of isolating COVID-19 patients in a supervised community facility on transmission reduction among household members

enthalten in: Journal of public health (Oxford, England) | 2021

von López, M. | Gallego, C. | Abós-Herrándiz, R. | +7

CommentIn: J Public Health (Oxf). 2021 Jun 7;43(2):e350-e351. - PMID 33693852

5

Reasons for Not Performing Mechanical Thrombectomy : A Population-Based Study of Stroke Codes

enthalten in: Stroke | 2021

von Guisado-Alonso, D. | Martínez-Domeño, A. | Prats-Sánchez, L. | +33

CommentIn: Stroke. 2021 Aug;52(9):2754-2756. - PMID 34289709

6

Bottlenecks in the Acute Stroke Care System during the COVID-19 Pandemic in Catalonia

enthalten in: Cerebrovascular diseases (Basel, Switzerland) | 2021

von Ramos-Pachón, A. | García-Tornel, �. | Millán, M. | +33

7

A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population

enthalten in: Genes | 2019

von Garcia-Solaesa, V. | Serrano-Lorenzo, P. | Ramos-Arroyo, M. | +6

8

Telestroke in Catalonia : Increasing Thrombolysis Rate and Avoiding Interhospital Transfers

enthalten in: Cerebrovascular diseases (Basel, Switzerland) | 2018

von López-Cancio, E. | Ribó, M. | Cardona, P. | +19

9

Delineation of a recognizable phenotype for the recurrent LCR22-C to D/E atypical 22q11.2 deletion

enthalten in: American journal of medical genetics. Part A | 2016

von Bengoa-Alonso, A. | Artigas-López, M. | Moreno-Igoa, M. | +3

10

Two novel SCN1A mutations identified in families with familial hemiplegic migraine

enthalten in: Cephalalgia : an international journal of headache | 2014

von Weller, C. | Pelzer, N. | de Vries, B. | +10