Timing of umbilical cord occlusion, delayed vs early, in preterm babies: A randomized controlled trial (CODE-P Trial)

Autor: Gregoraci, A., Carbonell, M., Linde, A., Goya, M., Maiz, N., Gabriel, P., Villena, Y., Bérgamo, S., Beneitez, D., Montserrat, I., Céspedes, M.C., Vargas, M., Castillo, F., Carreras, E.

Publikováno v: In European Journal of Obstetrics & Gynecology and Reproductive Biology October 2023 289:203-207

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Management of iron deficiency in various clinical conditions and the role of intravenous iron: Recommendations of the Spanish Erythropathology Group of he Spanish Society of Haematology and Haemotherapy

Autor: Erce, JAG, Altes, A, Rubio, ML, Remacha, AF, de la Abio, M, Beneitez, D, de la Iglesia, S, de la Maya, MD, Flores, E, Perez, G, Ricard, MP, Vagace, JM

Publikováno v: REVISTA CLINICA ESPANOLA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

Iron deficiency due to blood loss, absorption disorders and dietary deficiencies causes iron -deficiency anaemia, whose treatment seeks to eliminate the underlying cause and restore haemoglobin and iron deposits. Typically, the latter 2 of these obje

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::d528185e8f9e9ca15fc7be76d65dbb91
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=2164

Influence of hematopoietic microchimerism in organ tolerance after kidney or heart transplantation

Autor: Pujal, J.M, Grinyó, J.M, Manito, N, Gil-Vernet, S, Hueso, M, Caldés, A, Costa, S, Benéitez, D, Grañena, A, Gallardo, D

Publikováno v: In Transplantation Proceedings 2003 35(5):1775-1777

Usefulness of NGS for Diagnosis of Dominant Beta-Thalassemia and Unstable Hemoglobinopathies in Five Clinical Cases.

Autor: Rizzuto V; Translational Research in Child and Adolescent Cancer - Rare Anemia Disorders Research Laboratory, Vall d'Hebron Research Institute, ERN-EuroBloodNet Member, Barcelona, Spain.; Josep Carreras Leukaemia Research Institute, Badalona, Spain.; Department of Medicine, Universitat de Barcelona, Barcelona, Spain., Koopmann TT; Department of Clinical Genetics, Leiden University Medical Center, ERN-EuroBloodNet Member, Leiden, Netherlands., Blanco-Álvarez A; Hematologic Molecular Genetics Unit, Hematology Department, Hospital Universitari Vall d'Hebron, ERN-EuroBloodNet Member, Barcelona, Spain., Tazón-Vega B; Hematologic Molecular Genetics Unit, Hematology Department, Hospital Universitari Vall d'Hebron, ERN-EuroBloodNet Member, Barcelona, Spain., Idrizovic A; Translational Research in Child and Adolescent Cancer - Rare Anemia Disorders Research Laboratory, Vall d'Hebron Research Institute, ERN-EuroBloodNet Member, Barcelona, Spain., Díaz de Heredia C; Oncohematologic Pediatrics Department, Hospital Universitari Vall d'Hebron, ERN-EuroBloodNet Member, Barcelona, Spain., Del Orbe R; Hematology Department, Hospital Universitario Cruces, Barakaldo, Spain., Pampliega MV; Hematology Department, Hospital Universitario Cruces, Barakaldo, Spain., Velasco P; Oncohematologic Pediatrics Department, Hospital Universitari Vall d'Hebron, ERN-EuroBloodNet Member, Barcelona, Spain., Beneitez D; Red Blood Cell Disorders Unit, Hematology Department, Hospital Universitari Vall d'Hebron, ERN-EuroBloodNet Member, Barcelona, Spain., Santen GWE; Department of Clinical Genetics, Leiden University Medical Center, ERN-EuroBloodNet Member, Leiden, Netherlands., Waisfisz Q; Department of Clinical Genetics, VU Medical Center, Amsterdam, Netherlands., Elting M; Department of Clinical Genetics, VU Medical Center, Amsterdam, Netherlands., Smiers FJW; Department of Pediatric Hematology, Leiden University Medical Center, Leiden, Netherlands., de Pagter AJ; Department of Pediatric Hematology, Leiden University Medical Center, Leiden, Netherlands., Kerkhoffs JH; Department of Hematology, HAGA City Hospital, The Hague, Netherlands., Harteveld CL; Department of Clinical Genetics, Leiden University Medical Center, ERN-EuroBloodNet Member, Leiden, Netherlands., Mañú-Pereira MDM; Translational Research in Child and Adolescent Cancer - Rare Anemia Disorders Research Laboratory, Vall d'Hebron Research Institute, ERN-EuroBloodNet Member, Barcelona, Spain.

Publikováno v: Frontiers in physiology [Front Physiol] 2021 Feb 05; Vol. 12, pp. 628236. Date of Electronic Publication: 2021 Feb 05 (Print Publication: 2021).