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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SJR uses a similar algorithm as the Google page rank; it provides a quantitative enfermdead qualitative measure of the journal’s impact. 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.

Maitland R, Valverde K. C oordinadora Dra Buy L. The new era of Pompe disease: Gaucher disease type 1: Education Degrees Specialty in Pediatrics.

The invasive potential of Giardia intestinalis in an in vivo model. Kostmann syndrome severe congenital neutropenia. An overview on bone manifestations in Gaucher disease.


J Pediatr ; Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Methods for a prompt and reliable laboratory ce of Pompe disease: Tatuajes y perforaciones en adolescentes. I specialized in pediatrics because children are honest and their smile is the best gift you can get.

Report from an international consensus meeting. Organizing Committee of the Pediatric Week “Dr. December Doctor and Surgery.

Evolution with enzyme replacement therapy. Osseous manifestations of adult Gaucher disease in the era of enzyme replacement therapy. A search for the optimum time to study a vitamin deficiency. Horneff H, et al Awareness of Gacher disease among rheumatologists—current status and perspectives.

The maintenance of hippocampal pyramidal neuron populations is dependent on the modulation of specific cell cycle regulators by thyroid hormones. Mol Genet Metab ; Terapia de reemplazo enzimatico en una paciente con enfermedad de Gaucher tipo III. Predilection of retinoblastoma metastases for the mandible.

Hemoglobin Perth in Costa Rica. Si continua navegando, consideramos que acepta su uso. Pediatr Rheumatol Online J. CiteScore measures average citations received per document published. Challenges in diagnosis and treatment of late-onset Pompe disease. Individualization of longterm enzyme replacement therapy for Gaucher disease.


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

Hospital Materno-Infantil Vall d’Hebron. Electrodiagnosis in diseases of nerve and muscle Principles and practice. Epub Oct Current Opinion in Neurology. Low white blood cell count leukopenia. J Lab Clin Med ; The face of female dominance: Acta Paediatr ; Clinical manifestations of Fabry disease in children: Publications Valverde et gauchsr. Nat Clin Enffrmedad Neurol ; 3: The autonomic condition of children with congenital hypothyroidism as indicated by the analysis of heart rate variability.

Therapeutic goals in the treatment of Gaucher disease. J Pediatr Hematol Oncol. Bed wetting urinating in sleep.

Rheumatologic aspects of lyso somal storage diseases. Show all Show less.