المؤلفون: Miguel Sampayo-Cordero, Bernat Miguel-Huguet, Andrea Malfettone, Elena López-Miranda, María Gion, Elena Abad, Daniel Alcalá-López, Jhudit Pérez-Escuredo, José Manuel Pérez-García, Antonio Llombart-Cussac, Javier Cortés

المصدر: Frontiers in Oncology, Vol 13 (2023)

مصطلحات موضوعية: time-to-event, non-inferiority, single-arm, phase II, clinical trial, superiority, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fonc.2023.1048242/full; https://doaj.org/toc/2234-943X

URL الوصول: https://doaj.org/article/4129d5abe3b54a4aa1163a0967a18f28

المؤلفون: Miguel Sampayo-Cordero, Bernat Miguel-Huguet, Almudena Pardo-Mateos, Andrea Malfettone, José Pérez-García, Antonio Llombart-Cussac, Javier Cortés, Marc Moltó-Abad, Cecilia Muñoz-Delgado, Marta Pérez-Quintana, Jordi Pérez-López

المصدر: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)

مصطلحات موضوعية: Systematic review, Meta-analysis, Case reports, Clinical studies, Mucopolysaccharidosis type II, Enzyme replacement therapy, Medicine

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13023-019-1202-6; https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/9855a7d39b014bba9957133dc07f8cb6

المؤلفون: Miguel Sampayo-Cordero, Bernat Miguel-Huguet, Andrea Malfettone, José Manuel Pérez-García, Antonio Llombart-Cussac, Javier Cortés, Almudena Pardo, Jordi Pérez-López

المصدر: Frontiers in Molecular Biosciences, Vol 8 (2021)

مصطلحات موضوعية: systematic review, mucopolysaccharidosis, enzyme replacement therapy, rare disease, nonrandomized study, meta-analysis, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fmolb.2021.690615/full; https://doaj.org/toc/2296-889X

URL الوصول: https://doaj.org/article/9f4d7fc64b8344aa8a9954194506836c

المؤلفون: Miguel Sampayo-Cordero, Bernat Miguel-Huguet, José Pérez-García, David Páez, Ángel L. Guerrero-Zotano, Javier Garde-Noguera, Elena Aguirre, Esther Holgado, Elena López-Miranda, Xin Huang, Andrea Malfettone, Antonio Llombart-Cussac, Javier Cortés

المصدر: Contemporary Clinical Trials Communications, Vol 20, Iss , Pp 100678- (2020)

مصطلحات موضوعية: Non-inferiority, Switching to non-inferiority, Two-stage, Single-arm, Phase II, Group sequential designs, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2451865420301629; https://doaj.org/toc/2451-8654

URL الوصول: https://doaj.org/article/9bb5f763d2cb4e348ebf7d6ca9bbebc7

المؤلفون: Alejandro Solís-Peña, Gianluca Pellino, Miquel Kraft, Bernat Miguel Huguet, Eloy Espin-Basany

المساهمون: Pellino, Gianluca, Solís-Peña, Alejandro, Kraft, Miquel, Huguet, Bernat Miguel, Espín-Basany, Eloy

المصدر: Colorectal Disease. 23:2173-2181

مصطلحات موضوعية: medicine.medical_specialty, mechanical bowel preparation, Colon, medicine.drug_class, Antibiotics, Administration, Oral, complication, law.invention, 03 medical and health sciences, 0302 clinical medicine, Randomized controlled trial, law, Anti-Bacterial Agent, Preoperative Care, Surgical site, medicine, Antibiotic Prophylaxi, Humans, Surgical Wound Infection, colon resection, Randomized Controlled Trials as Topic, Protocol (science), Elective Surgical Procedure, Cathartics, business.industry, Incidence (epidemiology), Cathartic, Gastroenterology, surgical site infection, Antibiotic Prophylaxis, Colorectal surgery, Anti-Bacterial Agents, Surgery, Regimen, Elective Surgical Procedures, 030220 oncology & carcinogenesis, Bowel preparation, colorectal surgery, 030211 gastroenterology & hepatology, oral antibiotic, business, Human

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b63ec9167114d01e49025defe31d065
https://doi.org/10.1111/codi.15681

المؤلفون: Miguel Sampayo-Cordero, Bernat Miguel-Huguet, Andrea Malfettone, José Manuel Pérez-García, Antonio Llombart-Cussac, Javier Cortés, Almudena Pardo, Jordi Pérez-López

المصدر: MDPI, IJERPH. 17(18):1-16

الإتاحة: https://ideas.repec.org/a/gam/jijerp/v17y2020i18p6590-d411734.html

المؤلفون: Bernat Miguel-Huguet, Almudena Pardo, Javier Cortes, Jordi Pérez-López, Miguel Sampayo-Cordero, Antonio Llombart-Cussac, Andrea Malfettone, Jose Perez-Garcia

المساهمون: Institut Català de la Salut, [Sampayo-Cordero M, Malfettone A] Medica Scientia Innovation Research (MedSIR), Ridgewood, NJ, USA. Medica Scientia Innovation Research (MedSIR), Barcelona, Spain. [Miguel-Huguet B] Department of Surgery, Hospital de Bellvitge, L’Hospitalet de Llobregat, Barcelona, Spain. [Pérez-García JM] Medica Scientia Innovation Research (MedSIR), Ridgewood, NJ, USA. Medica Scientia Innovation Research (MedSIR), Barcelona, Spain. Institute of Breast Cancer, Quiron Group, Barcelona, Spain. [Llombart-Cussac A] Medica Scientia Innovation Research (MedSIR), Ridgewood, NJ, USA. Medica Scientia Innovation Research (MedSIR), Barcelona, Spain. Hospital Arnau de Vilanova, Universidad Católica de Valencia 'San Vicente Mártir', Valencia, Spain. [Cortés J] Medica Scientia Innovation Research (MedSIR), Ridgewood, NJ, USA. Medica Scientia Innovation Research (MedSIR), Barcelona, Spain. Institute of Breast Cancer, Quiron Group, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Pérez-López J] Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Dipòsit Digital de la UB
Universidad de Barcelona
Scientia
International Journal of Environmental Research and Public Health
Volume 17
Issue 18
International Journal of Environmental Research and Public Health, Vol 17, Iss 6590, p 6590 (2020)

مصطلحات موضوعية: Pediatrics, Health, Toxicology and Mutagenesis, Mucopolysaccharidosis, lcsh:Medicine, law.invention, 0302 clinical medicine, afecciones patológicas, signos y síntomas::procesos patológicos::atributos de la enfermedad::enfermedades raras [ENFERMEDADES], Clinical trials, systematic review, Randomized controlled trial, enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::enfermedades genéticas ligadas al cromosoma X::retraso mental ligado al cromosoma X::enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::mucopolisacaridosis II [ENFERMEDADES], law, nonrandomized study, Medicine, clinical studies, Mucopolysaccharidosis type II, terapéutica::farmacoterapia::terapia enzimática::tratamiento de sustitución enzimática [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Mucopolysaccharidosis II, 0303 health sciences, mucopolysaccharidosis, Enzyme replacement therapy, Rare diseases, Systematic review, Meta-analysis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Genetic Diseases, X-Linked::Mental Retardation, X-Linked::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Mucopolysaccharidosis II [DISEASES], Assaigs clinics, Malalties congènites, Malalties rares, Goals, enzyme replacement therapy, Cohort study, medicine.medical_specialty, rare disease, Article, 03 medical and health sciences, Rare Diseases, Humans, case report, 030304 developmental biology, business.industry, Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Rare Diseases [DISEASES], lcsh:R, Public Health, Environmental and Occupational Health, Enzims - Ús terapèutic, randomized clinical trial, medicine.disease, meta-analysis, business, 030217 neurology & neurosurgery, Therapeutics::Drug Therapy::Enzyme Therapy::Enzyme Replacement Therapy [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Assaigs clínics, Rare disease

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf0f92d3e9458936af60be8675134179
http://hdl.handle.net/2445/173426

المؤلفون: Jordi Pérez-López, Bernat Miguel-Huguet, Miguel Sampayo-Cordero, Almudena Pardo-Mateos, Marc Moltó-Abad, Cecilia Muñoz-Delgado

المصدر: Molecular Genetics and Metabolism. 123:69-75

مصطلحات موضوعية: Adult, medicine.medical_specialty, Mucopolysaccharidosis I, Endocrinology, Diabetes and Metabolism, Disease, Biochemistry, Iduronidase, 03 medical and health sciences, Mucopolysaccharidosis type I, Rare Diseases, 0302 clinical medicine, Endocrinology, Meta-Analysis as Topic, Positive predicative value, Internal medicine, Genetics, medicine, Humans, Enzyme Replacement Therapy, 030212 general & internal medicine, Molecular Biology, Evidence-Based Medicine, business.industry, Standard treatment, Evidence-based medicine, Enzyme replacement therapy, Regimen, Meta-analysis, business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa14cfe0220ff171584d4f8931ab95f5
https://doi.org/10.1016/j.ymgme.2018.01.002

المؤلفون: Sampayo-Cordero, Miguel, Bernat Miguel-Huguet, Pardo-Mateos, Almudena, Malfettone, Andrea, Pérez-García, José, Llombart-Cussac, Antonio, Cortés, Javier, Moltó-Abad, Marc, Muñoz-Delgado, Cecilia, Pérez-Quintana, Marta, Pérez-López, Jordi

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12ae2020b9a39126fd4e14568d40d82e

المؤلفون: Marc Moltó-Abad, Jose Perez-Garcia, Almudena Pardo-Mateos, Cecilia Muñoz-Delgado, Miguel Sampayo-Cordero, Javier Cortes, Bernat Miguel-Huguet, Jordi Pérez-López, Andrea Malfettone, Antonio Llombart-Cussac, Marta Pérez-Quintana

المساهمون: [Sampayo-Cordero M, Malfettone A] Medica Scientia Innovation Research (MedSIR), Barcelona, Spain. [Miguel-Huguet B] Colorectal Unit, Department of Surgery, Hospital de Bellvitge, Barcelona, Spain. [Pardo-Mateos A] Albiotech consultores y redacción científica S.L., Madrid, Spain. [Pérez-García J] Medica Scientia Innovation Research (MedSIR), Barcelona, Spain. IOB, Institute of Oncology, QuironSalud Group, Madrid & Barcelona, Spain. [Llombart-Cussac A] Medica Scientia Innovation Research (MedSIR), Barcelona, Spain. FISABIO - Hospital Arnau de Vilanova, Valencia, Spain. [Moltó-Abad M, Pérez López J] Unitat de Malalties Minoritàries, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: ORPHANET JOURNAL OF RARE DISEASES
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Scientia
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)

مصطلحات موضوعية: 0301 basic medicine, Meta-analysis, Information Science::Communications Media::Publications::Review Literature as Topic::Systematic Reviews as Topic [INFORMATION SCIENCE], Idursulfase, Systematic review, lcsh:Medicine, Other subheadings::Other subheadings::/drug therapy [Other subheadings], Clinical studies, 0302 clinical medicine, Clinical endpoint, Pharmacology (medical), Mucopolysaccharidosis type II, terapéutica::farmacoterapia::terapia enzimática::tratamiento de sustitución enzimática [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Genetics (clinical), Mucopolysaccharidosis II, Otros calificadores::Otros calificadores::/tratamiento farmacológico [Otros calificadores], education.field_of_study, Case reports, General Medicine, Evidence-based medicine, Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Genetic Diseases, X-Linked::Mental Retardation, X-Linked::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Mucopolysaccharidosis II [DISEASES], Enzyme replacement therapy, Malalties rares, medicine.drug, medicine.medical_specialty, Ciencias de la información::medios de comunicación::publicaciones::literatura de revisión como asunto::revisiones sistemáticas como asunto [CIENCIA DE LA INFORMACIÓN], Population, Iduronate Sulfatase, Ressenyes sistemàtiques (Investigació mèdica), enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::trastornos heredodegenerativos del sistema nervioso::retraso mental ligado al cromosoma X::enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::mucopolisacaridosis II [ENFERMEDADES], 03 medical and health sciences, Mucopolysaccharidosis type I, Rare Diseases, Internal medicine, medicine, Humans, education, business.industry, Research, lcsh:R, Publication bias, 030104 developmental biology, business, 030217 neurology & neurosurgery, Therapeutics::Drug Therapy::Enzyme Therapy::Enzyme Replacement Therapy [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT]

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0966dc2ff484133851db45b75023be66
https://fundanet.fisabio.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=5162