A model of neuronopathic Gaucher disease.

Campbell, P E; Harris, C M; Harris, C M; Sirimanna, T; Vellodi, A

Campbell, P E; Harris, C M; Harris, C M; Sirimanna, T; Vellodi, A.

Affiliation

Campbell PE; Department of Audiological Medicine, Great Ormond Street Hospital for Children, London. pauline.campbell@plymouth.ac.uk

J Inherit Metab Dis ; 26(7): 629-39, 2003.

Article in En | MEDLINE | ID: mdl-14707511

Subject(s)

Gaucher Disease/pathology; Airway Obstruction/etiology; Airway Obstruction/surgery; Audiometry; Auditory Pathways/physiopathology; Child; Disease Progression; Evoked Potentials, Auditory, Brain Stem/physiology; Fatal Outcome; Female; Gaucher Disease/drug therapy; Gaucher Disease/physiopathology; Glucosylceramidase/therapeutic use; Humans; Infant; Infant, Newborn; Laryngismus/etiology; Laryngismus/surgery; Leukocytes/enzymology; Models, Biological; Oculomotor Muscles/physiopathology; Otoacoustic Emissions, Spontaneous/physiology; Recombinant Proteins/therapeutic use; Remission Induction; beta-Galactosidase/blood

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Collection: 01-internacional Database: MEDLINE Main subject: Gaucher Disease Type of study: Etiology_studies / Prognostic_studies Limits: Child / Female / Humans / Infant / Newborn Language: En Journal: J Inherit Metab Dis Year: 2003 Document type: Article Country of publication: United States

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