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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Testicular torsion and its effects on the spermatogenic cycle in the contralateral testis of enfermrdad rat. Electrodiagnosis in diseases of nerve and muscle Principles and practice. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.

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Si continua navegando, consideramos que acepta su uso. The nuclear receptor FXR, but not LXR, up-regulates bile acid transporter expression in non-alcoholic fatty liver disease. Universidad de Costa Rica – Facultad de Medicina.


Isolated elevated serum transaminases leading to the diagnosis of asymptomatic Pompe disease. 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.

Publications Valverde et al. Temporal development of genetic and metabolic effects of biotin deprivation.

Low bone mass in Pompe disease: Consenso para le enfermedad de Gaucher. Low white blood cell count leukopenia. You can change the settings or obtain more information by clicking here. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. C oordinadora Dra Buy L. Education Degrees Specialty in Pediatrics. I specialized in pediatrics because children are honest and their smile is the best gift you can get. Cough with phlegm or mucus.

Tetralogia de Fallot, incidencia de las complicaciones post-operatorias: Terapia de reemplazo enzimatico en una paciente con enfermedad de Gaucher tipo III. General Info About me I specialized in pediatrics because children are honest and their smile is the best gift you can get.

Nat Clin Pract Neurol ; 3: Methods for a prompt and reliable laboratory diagnosis of Pompe disease: Subscribe to our Newsletter.

Apraxia Oculomotora — AAPOS

Hospital Materno-Infantil Vall d’Hebron. Mol Genet Metab ; De la Mora De la Mora Ignacio.


Current Opinion in Neurology. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Kostmann syndrome severe congenital neutropenia. Challenges in enfermefad and treatment of late-onset Pompe disease.

Faucher disease diagnosis and management guideline. Gaucher disease type 1: Are you a health professional able to prescribe or dispense drugs? The face of female dominance: SRJ is a prestige metric based on the idea that not all citations are the same.

A search for the optimum time to study a vitamin deficiency.

Muscular strength as a predictor of bone mineral density. The effect of nordihydroguaiaretic acid on iodoacetate-induced toxicity in cultured neurons. Maitland R, Valverde K. The rostral migratory stream is a neurogenic niche that predominantly engenders periglomerular cells: The hexokinase gene family in the zebrafish: Tatuajes y perforaciones en adolescentes.