mucopolysaccharidoses/lafyèv

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A dose-optimization trial of laronidase (Aldurazyme) in patients with mucopolysaccharidosis I.

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Recombinant human alpha-l-iduronidase (Aldurazyme), laronidase) is approved as an enzyme replacement therapy to treat the lysosomal storage disorder, mucopolysaccharidosis type I (MPS I) at a dose of 0.58 mg/kg by once-weekly intravenous infusion. To assess whether alternate dosing regimens might

Collagenopathic cardiopathies.

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Collagenopathic cardiopathies are a subject of extreme etiologic, pathogenetic and clinical interest. These disorders are associated with congenital or acquired anomalies of the connective tissue and because of the diffusion and nearly total distribution of this tissue, have a higher frequency than

Clinical Practice Guideline: Tonsillectomy in Children (Update)-Executive Summary.

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This update of a 2011 guideline developed by the American Academy of Otolaryngology-Head and Neck Surgery Foundation provides evidence-based recommendations on the pre-, intra-, and postoperative care and management of children 1 to 18 years of age under consideration for

Blau Syndrome and Early-Onset Sarcoidosis: A Six Case Series and Review of the Literature

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Objectives: This study aims to discuss the clinical, laboratory and genetic findings, and treatment options for six patients who were diagnosed with Blau syndrome (BS)/early-onset sarcoidosis (EOS).

Clinical Practice Guideline: Tonsillectomy in Children (Update).
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