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PHARMACEUTICAL INTERVENTION ON THE ADEQUACY OF THE INDICATION OF SEMAGLUTIDE IN DIABETES MELLITUS 2.
Autor:
Santana, C. M. Dominguez, Rivas, M. E. Blanco, Vela, V. Vazquez, Del Rey, E. J. Alegre, Rubio, J. M. Borrero
Publikováno v:
European Journal of Hospital Pharmacy; 2024 Supplement, Vol. 31, pA160-A161, 2p
Autor:
M Asensio-Asensio, D Tortosa-Conesa, V Bertol-Alegre, L Hernández-Rubio, M E Blanco-Cantó, M A Méndez-Miralles, J Montoya, A García-Escrivá, M L Galiano, Francisco Javier López-González, M D Castro-Vilanova, A Alfaro-Sáez, M Díaz-Román
Publikováno v:
REVISTA DE NEUROLOGIA
r-FIHGUV. Repositorio Institucional de Producción Científica de la Fundación de Investigación del Hospital General de Valencia
instname
r-FIHGUV. Repositorio Institucional de Producción Científica de la Fundación de Investigación del Hospital General de Valencia
instname
Introduccion. El acetato de eslicarbacepina es un nuevo bloqueante de los canales de sodio en el tratamiento de las crisis de inicio focal. Los estudios prospectivos sobre su efectividad en monoterapia en pacientes con epilepsia parcial de reciente d
Publikováno v:
Drug testing and analysis. 7(9)
In this study, a selective and sensitive high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method requiring low sample volume (≤100 μL) was developed and validated for the quantitative determination of the opioid drug fe
Publikováno v:
Pediatric Pathology & Molecular Medicine. 18:143-150
Publikováno v:
Fetal and Pediatric Pathology. 18:143-150
We report a stillborn female with most of the clinical, histologic, and radiographic characteristics of the short rib-polydactyly syndrome (SRPS) type IV (Beemer-Langer) but also presenting prominent metaphyseal and scapular irregularities and spikin
Publikováno v:
ChemInform. 25
Publikováno v:
Orthopedics. 28(3)
Madelung deformity of the wrist is a congenital defect caused by a growth disturbance in the volar-ulnar distal radial physis leading to a typical appearance of the upper extremities. The majority of Madelung deformity cases are caused by hereditary
Autor:
C. Medina, M.R. Rivera-Vega, Sergio A. Cuevas-Covarrubias, M. Valdes-Flores, Susana Kofman-Alfaro, W. B. Rizzo, M. E. Blanco-Aguirre
Publikováno v:
Pediatric dermatology. 18(5)
Multiple sulfatase deficiency (MSD) is an inborn error of metabolism that combines the clinical features of late infantile metachromatic leukodystrophy and mucopolysaccharidosis. The characteristic biochemical abnormality is a reduction in the activi
Publikováno v:
Scandinavian journal of immunology. 9(6)
Two HLA-B,D-identical siblings, who differed only for the HLA-A region because of a maternal recombinational event, were studied in primary (1 degrees) and secondary (2 degrees) mixed lymphocyte culture (MLC). The HLA-A:B recombinant child did not re