Gaucher disease types 1 and 3: Phenotypic characterization of large populations from the ICGG Gaucher Registry

Risk factors for fractures and avascular osteonecrosis in type 1 Gaucher disease: A study from the International Collaborative Gaucher Group (ICGG) Gaucher Registry

(2012) Aneal Khan et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Long-term clinical outcomes in type 1 Gaucher disease following 10 years of imiglucerase treatment

(2012) Neal J. Weinreb et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Gaucher Disease Glucocerebrosidase and α-Synuclein Form a Bidirectional Pathogenic Loop in Synucleinopathies

(2011) Joseph R. Mazzulli et al.   CELL

Type 1 Gaucher Disease

(2010) Manisha Balwani et al.   ARCHIVES OF INTERNAL MEDICINE

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

Gaucher disease type I: Assessment of basal metabolic rate in patients from southern Brazil

(2010) Divair Doneda et al.   BLOOD CELLS MOLECULES AND DISEASES

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

Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

(2009) E. Sidransky et al.   NEW ENGLAND JOURNAL OF MEDICINE

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

Eight-Year Clinical Outcomes of Long-Term Enzyme Replacement Therapy for 884 Children With Gaucher Disease Type 1

(2008) H. Andersson et al.   PEDIATRICS