Scientific publications
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Alcaraz-Vidal, L, Velasco, I, Pascual, M, Gomez, RGI, Escuriet, R and Comas, C.
First alongside midwifery led unit in a high complexity public hospital in Spain: Maternal and neonatal outcomes
Women and Birth 37(3):
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Llurba, E, Crispi, F, Crovetto, F, Youssef, L, Delgado, JL, Puig, I, Mora, J, Krofta, L, Mackova, K, Martinez-Varea, A, Tubau, A, Ruiz, A, Paya, A, Prat, M, Chantraine, F, Comas, C, Kajdy, A, Lopez-Tinajero, MF, Figueras, F and Gratacos, E.
Multicentre randomised trial of screening with sFlt1/PlGF and planned delivery to prevent pre-eclampsia at term: protocol of the PE37 study
BMJ Open 14(3):
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Mazarico, E, Meler, E, Mendoza, M, Herraiz, I, Llurba, E, De Diego, R, Comas, M, Boada, D, González, A, Bonacina, E, Armengol-Alsina, M, Moline, E, Hurtado, I, Torre, N, Gomez-Roig, MD, Galindo, A and Figueras, F.
Mortality and severe neurological morbidity in extremely preterm growth-restricted fetuses
ULTRASOUND IN OBSTETRICS & GYNECOLOGY 62(6): 788-795
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Garcia, B, Catasus, N, Ros, A, Rosas, I, Negro, A, Guerrero-Murillo, M, Valero, AM, Duat-Rodriguez, A, Becerra, JL, Bonache, S, Garcia, CL, Comas, C, Bielsa, I, Serra, E, Hernandez-Chico, C, Martin, Y, Castellanos, E and Blanco, I.
Neurofibromatosis type 1 families with first-degree relatives harbouring distinct NF1 pathogenic variants. Genetic counselling and familial diagnosis: what should be offered?
Journal of Medical Genetics 59(10): 1017-1023
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Cobo, T, Aldecoa, V, Bartha, JL, Bugatto, F, Carrillo-Badillo, MP, Comas, C, Diago-Almeda, V, Ferrero, S, Goya, M, Herraiz, I, Marti-Malgosa, L, Olivella, A, Paules, C, Vives, A, Figueras, F, Palacio, M and Gratacos, E.
Assessment of an intervention to optimise antenatal management of women admitted with preterm labour and intact membranes using amniocentesis-based predictive risk models: study protocol for a randomised controlled trial (OPTIM-PTL Study)
BMJ Open 11(9):
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Ribera, I, Ruiz, A, Sanchez, O, Eixarch, E, Antolin, E, Gomez-Montes, E, Perez-Cruz, M, Cruz-Lemini, M, Sanz-Cortes, M, Arevalo, S, Ferrer, Q, Vazquez, E, Vega, L, Dolader, P, Montoliu, A, Boix, H, Simoes, RV, Masoller, N, Sanchez-de-Toledoll, J, Comas, M, Bartha, JM, Galindo, A, Martinez, JM, Gomez-Roig, L, Crispi, F, Gomez, O, Carreras, E, Caberol, L, Gratacos, E and Llurba, E.
Multicenter prospective clinical study to evaluate children short-term neurodevelopmental outcome in congenital heart disease (children NEURO-HEART): study protocol
BMC Pediatrics 19(1): 326-326
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Ros A, Hurtado I, Vázquez-Méndez É, Monlleó-Neila L, Pauta M, Rovira-Remisa MM, García B, Masotto B, Comas C, Blanco I and Zientalska A.
Prenatal FBXL4-Associated Mitochondrial DNA Depletion Syndrome-13: A New Case and Review of the Literature.
Prenatal Diagnosis :