Victor Rodriguez-Sureda
Overview
Explore the profile of Victor Rodriguez-Sureda including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
24
Citations
336
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Nakaki A, Gomez Y, Darecka K, Borras R, Vellve K, Paules C, et al.
Fetal Diagn Ther
. 2024 Jul;
52(1):46-58.
PMID: 39079502
Introduction: We investigated whether structured maternal lifestyle interventions based on Mediterranean diet or stress reduction influence fetal-infant neurodevelopment detected by detailed fetal neurosonography and Ages and Stages Questionnaires 3rd edition...
2.
Soveral I, Guirado L, Escobar-Diaz M, Alcaide M, Martinez J, Rodriguez-Sureda V, et al.
J Clin Med
. 2022 Dec;
11(23).
PMID: 36498692
Fetal echocardiography has limited prognostic ability in the evaluation of left-sided congenital heart defects (left heart defects). Cord blood cardiovascular biomarkers could improve the prognostic evaluation of left heart defects....
3.
Carnicer-Caceres C, Villena-Ortiz Y, Castillo-Ribelles L, Barquin-Del-Pino R, Camprodon-Gomez M, Felipe-Rucian A, et al.
Blood Cells Mol Dis
. 2022 Oct;
98:102704.
PMID: 36265282
Lysosomal storage disorders (LSD) are a group of inherited metabolic diseases mainly caused by a deficiency of lysosomal hydrolases, resulting in a gradual accumulation of non-degraded substrates in different tissues...
4.
Garrido-Gimenez C, Mendoza M, Cruz-Lemini M, Galian-Gay L, Sanchez-Garcia O, Granato C, et al.
Hypertension
. 2020 Oct;
76(6):1808-1816.
PMID: 33012203
Preeclampsia is caused by placental impairment with increased expression of sFlt-1 (soluble fms-like tyrosine kinase 1) and decreased PlGF (placental growth factor); it has been associated with cardiovascular morbidity and...
5.
Franco-Jarava C, Wang H, Martin-Nalda A, Alvarez D, Garcia-Prat M, Bodet D, et al.
Clin Immunol
. 2018 Mar;
191:44-51.
PMID: 29572183
There is scarce literature about autoinflammation in syndromic patients. We describe a patient who, in addition to psychomotor and growth delay, presented with fevers, neutrophilic dermatosis, and recurrent orogenital ulcers....
6.
De Castro-Oros I, Irun P, Cebolla J, Rodriguez-Sureda V, Mallen M, Pueyo M, et al.
J Transl Med
. 2017 Feb;
15(1):43.
PMID: 28222799
Background: Niemann-Pick disease type C (NP-C) is a rare, autosomal recessive neurodegenerative disease caused by mutations in either the NPC1 or NPC2 genes. The diagnosis of NP-C remains challenging due...
7.
Triunfo S, Crovetto F, Crispi F, Rodriguez-Sureda V, Dominguez C, Nadal A, et al.
Placenta
. 2016 May;
42:44-50.
PMID: 27238713
Objective: To explore in women with late-onset preeclampsia (PE) the association between maternal levels of angiogenic/antiangiogenic factors in the first trimester of pregnancy and histological findings attributable to placental underperfusion...
8.
Rodriguez-Sureda V, Crovetto F, Triunfo S, Sanchez O, Crispi F, Llurba E, et al.
Biol Chem
. 2016 Jan;
397(3):269-79.
PMID: 26756094
The pathogenic basis of abnormal placentation and dysfunction in preeclampsia (PE) is highly complex and incompletely understood. Secretory sphyngomyelinase activity (S-ASM) was analyzed in plasma samples from 158 pregnant women...
9.
Triunfo S, Parra-Saavedra M, Rodriguez-Sureda V, Crovetto F, Dominguez C, Gratacos E, et al.
Fetal Diagn Ther
. 2015 Oct;
40(1):13-20.
PMID: 26421431
Objective: To evaluate in normally growing fetuses at routine 32-36 weeks scan the performance of maternal angiogenic factors, Doppler and ultrasound indices in predicting smallness for gestational age (SGA) at...
10.
Gomez-Grau M, Garrido E, Cozar M, Rodriguez-Sureda V, Dominguez C, Arenas C, et al.
PLoS One
. 2015 Aug;
10(8):e0135873.
PMID: 26287674
Nonsense mutations are quite prevalent in inherited diseases. Readthrough drugs could provide a therapeutic option for any disease caused by this type of mutation. Geneticin (G418) and gentamicin were among...