The French Gaucher’s disease registry: clinical characteristics, complications and treatment of 562 patients

Mapping the genetic and clinical characteristics of Gaucher disease in the Iberian Peninsula

(2012) Pilar Giraldo et al.   Orphanet Journal of Rare Diseases

Phase 1/2 and extension study of velaglucerase alfa replacement therapy in adults with type 1 Gaucher disease: 48-month experience

(2010) A. Zimran et al.   BLOOD

Osteopenia in Gaucher disease develops early in life: Response to imiglucerase enzyme therapy in children, adolescents and adults

(2010) Pramod K. Mistry et al.   BLOOD CELLS MOLECULES AND DISEASES

The incidence of Parkinsonism in patients with type 1 Gaucher disease: Data from the ICGG Gaucher Registry

(2010) Barry Rosenbloom et al.   BLOOD CELLS MOLECULES AND DISEASES

The risk of Parkinson’s disease in type 1 Gaucher disease

(2010) Gilberto Bultron et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Neuronopathic Gaucher disease: demographic and clinical features of 131 patients enrolled in the International Collaborative Gaucher Group Neurological Outcomes Subregistry

(2010) Anna Tylki-Szymańska et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Bone events and evolution of biologic markers in Gaucher disease before and during treatment

(2010) Jerome Stirnemann et al.   ARTHRITIS RESEARCH & THERAPY

Gaucher disease and monoclonal gammopathy: A report of 17 cases and impact of therapy

(2009) Bernard Grosbois et al.   BLOOD CELLS MOLECULES AND DISEASES

Force Majeure: Therapeutic measures in response to restricted supply of imiglucerase (Cerezyme) for patients with Gaucher disease

(2009) Carla E.M. Hollak et al.   BLOOD CELLS MOLECULES AND DISEASES

Timing of initiation of enzyme replacement therapy after diagnosis of type 1 Gaucher disease: effect on incidence of avascular necrosis

(2009) Pramod K. Mistry et al.   BRITISH JOURNAL OF HAEMATOLOGY

Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort study

(2009) KB Sims et al.   CLINICAL GENETICS

Parkinsonism in Gaucher's disease type 1: Ten new cases and a review of the literature

(2009) Ichraf Kraoua et al.   MOVEMENT DISORDERS

Lysosomal Storage Disorders in the Newborn

(2009) O. Staretz-Chacham et al.   PEDIATRICS

A benchmark analysis of the achievement of therapeutic goals for type 1 Gaucher disease patients treated with imiglucerase

(2008) Neal Weinreb et al.   AMERICAN JOURNAL OF HEMATOLOGY

Life expectancy in Gaucher disease type 1

(2008) Neal J. Weinreb et al.   AMERICAN JOURNAL OF HEMATOLOGY

Immunoglobulin and free light chain abnormalities in Gaucher disease type I: data from an adult cohort of 63 patients and review of the literature

(2008) M. de Fost et al.   ANNALS OF HEMATOLOGY

Phenotypic heterogeneity of N370S homozygotes with type I Gaucher disease: An analysis of 798 patients from the ICGG Gaucher Registry

(2008) C. Fairley et al.   JOURNAL OF INHERITED METABOLIC DISEASE