People / Staff

Antonio F Martinez Monseny

Search publications

Publications

  • Izquierdo-Renau M, Martinez-Monseny T, Pociello N, Gonzalez P, del Río-Florentino R, Iriondo-Sanz M and Iglesias-Platas I.

    Changes in Parenteral Nutrition During the First Week of Life Influence Early but Not Late Postnatal Growth in Very Low-Birth-Weight Infants

    NUTRITION IN CLINICAL PRACTICE . 31(5): 666-672. Number of citations: 8

    [doi:10.1177/0884533616649582]

  • Margarit Soler A, Martínez-Sánchez L, Martinez-Monseny T, Trenchs-Sainz de la Maza V, Picouto MD, Villar F and Luaces-Cubells C.

    Epidemiological characteristics in suicidal adolescents seen in the Emergency Department

    ANALES DE PEDIATRIA . 85(1): 13-17. Number of citations: 4

    [doi:10.1016/j.anpedi.2015.04.022]

  • Martinez-Monseny T, Bobillo-Perez S, Martínez Planas A and García-García JJ.

    The role of complementary examinations and home monitoring in patients at risk from apparent life threatening event, apneas and sudden infant death syndrome

    ANALES DE PEDIATRIA . 83(2): 104-108.

    [doi:10.1016/j.anpedi.2014.11.010]

  • Martinez-Monseny T.

    Repercusión ecocardiográfica del estado de hidratación en los pacientes en diálisis

    Nefrologia . : .

  • Brooks D, Burke E, Lee S, Eble TN, O'Leary M, Osei-Owusu I, Rehm HL, Dhar SU, Emrick L, Bick D, Nehrebecky M, Macnamara E, Casas-Alba D, Armstrong-Moron J, Prat-Torres CS, Martinez-Monseny T, Palau F, Liu P, Adams D, Lalani S, Rosenfeld JA and Burrage LC.

    Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies.

    HUMAN GENETICS . : .

    [doi:10.1007/s00439-024-02657-2]

  • Palma-Milla C, Prat-Planas A, Soengas-Gonda E, Centeno-Pla M, Sánchez-Pozo J, Lazaro-Rodriguez I, Quesada-Espinosa JF, Arteche-Lopez A, Olival J, Pacio-Miguez M, Palomares-Bralo M, Santos-Simarro F, Cancho-Candela R, Vázquez-López M, Seidel V, Martinez-Monseny T, Casas-Alba D, Grinberg-Vaisman DR, Balcells S, Serrano M, Rabionet-Janssen R, Martin MA and Urreizti R.

    Expanding the Phenotypic Spectrum of TRAF7-Related Cardiac, Facial, and Digital Anomalies With Developmental Delay: Report of 11 New Cases and Literature Review.

    PEDIATRIC NEUROLOGY . 155: 8-17.

    [doi:10.1016/j.pediatrneurol.2024.03.008]

  • Haghshenas S, Bout HJ, Schijns JM, Levy MA, Kerkhof J, Bhai P, McConkey H, Jenkins ZA, Williams EM, Halliday BJ, Huisman SA, Lauffer P, de Waard V, Witteveen L, Banka S, Brady AF, Galazzi E, van Gils J, Hurst ACE, Kaiser FJ, Lacombe D, Martinez-Monseny T, Fergelot P, Monteiro FP, Parenti I, Persani L, Simarro FS, Simpson BN, Alders M, Robertson SP, Sadikovic B and Menke LA.

    Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles.

    Human Genetics and Genomics Advances . : 100287-100287.

    [doi:10.1016/j.xhgg.2024.100287]