Enfermedad de Gaucher: tratamiento enzimático sustitutivo iniciado en la edad pediátrica. Experiencia de 20 años. Article in Anales de Pediatría 84(6). Experiencia en el tratamiento de Enfermedad de Gaucher con Imiglucerasa en el departamento de Hemato-Oncología Pediátrica del Hospital de Clínicas. pediatra sobre la prevención de la enfermedad cardiovascular del enfermedad con el desarrollo, en la adolescencia y en la . Enf. de Gaucher. – Enf. de Tay-.

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Horneff H, et al Awareness of Fabry disease among rheumatologists—current status and perspectives. Diagnosis of glycogenosis type ii. Molecular Genetics and Metabolism. Annals pediaria Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate.

Genet Med ; Mendoza Torreblanca, Julieta Griselda. C oordinadora Dra Buy L.

Apraxia Oculomotora — AAPOS

Report from an international consensus meeting. The transition metals copper and iron in neurodegenerative diseases. J Lab Clin Med ; The hexokinase gene family in the zebrafish: Subscribe to our Newsletter. Zulema Man, Buenos Aires Argentina. Kostmann syndrome severe congenital neutropenia. Hospital Materno-Infantil Vall d’Hebron. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Testicular torsion and its effects on the spermatogenic cycle in the contralateral testis of the rat.


Low white blood cell count leukopenia.

Enfermedad de Gaucher by diana cedeño perez on Prezi

Buenos Aires, Argentina, Organizing Committee of the Pediatric Week “Dr. Education Degrees Specialty in Pediatrics. The effect of nordihydroguaiaretic acid on iodoacetate-induced toxicity in cultured neurons. Osseous manifestations of adult Gaucher disease in the era of enzyme replacement therapy. Are you a health professional able to prescribe or dispense drugs?

El Ramón y Cajal a la cabeza en investigación de la enfermedad de Gaucher

Tetralogia de Fallot, incidencia de las complicaciones post-operatorias: Methods for a prompt and reliable laboratory diagnosis of Pompe disease: The genotype-phenotype correlation in Pompe disease. The invasive potential of Giardia intestinalis in an in vivo model.

The nuclear receptor FXR, but not LXR, up-regulates bile acid transporter expression in non-alcoholic fatty liver disease. SNIP measures contextual citation impact by wighting citations based on the total number pediwtria citations in a subject field.

Clinical syndromes at higher risk for malignacy. I specialized in pediatrics because children are honest and their smile is the best gift you can get. Physicians and Surgeons College of Costa Rica cod.

Universidad de Costa Rica – Facultad de Medicina. Muscular strength as a predictor of bone gqucher density. Retinoblastoma with central retinal artery thrombosis that mimics extraocular disease.


The maintenance of hippocampal pyramidal neuron populations is dependent on the modulation of specific cell cycle regulators by thyroid hormones. Tatuajes y perforaciones en adolescentes. Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia C. De la Mora De la Mora Ignacio. Individualization of longterm enzyme replacement therapy for Gaucher disease. Maitland R, Valverde K. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.

The mossy fiber system of the hippocampal formation is decreased by chronic and postnatal but not by prenatal protein malnutrition in rats. Enfermedad por Hemoglobina H; primer caso de la variante de hemoglobina H. Consenso para le enfermedad de Gaucher. Tamoxifen treatment induces protection in murine cysticercosis.

Pompe disease diagnosis ppediatria management guideline. Gaucher disease type 1: Current Opinion in Neurology. Women with dominant faces have lower cortisol. Dec ; An overview on bone manifestations in Gaucher disease.