[HTML][HTML] A global neuronopathic gaucher disease registry (GARDIAN): a patient-led initiative

T Collin-Histed, M Stoodley, K Beusterien… - Orphanet Journal of …, 2023 - Springer
Background Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …

A global neuronopathic gaucher disease registry (GARDIAN): a patient-led initiative.

T Collin-Histed, M Stoodley, K Beusterien… - Orphanet Journal of …, 2023 - europepmc.org
Background Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …

[HTML][HTML] A global neuronopathic gaucher disease registry (GARDIAN): a patient-led initiative

T Collin-Histed, M Stoodley, K Beusterien… - Orphanet Journal of …, 2023 - ncbi.nlm.nih.gov
Background Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …

A Global Neuronopathic Gaucher Disease Registry (GARDIAN): A Patient-Led Initiative

T Collin-Histed, M Stoodley, K Beusterien, D Elstein… - 2023 - researchsquare.com
Background Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …

[HTML][HTML] A global neuronopathic gaucher disease registry (GARDIAN): a patient-led initiative

T Collin-Histed, M Stoodley… - … Journal of Rare …, 2023 - ojrd.biomedcentral.com
Gaucher disease (GD) is a rare autosomal recessive lysosomal storage disorder. GD types 2
and 3 are known as neuronopathic Gaucher disease (nGD) because they have brain …

A global neuronopathic gaucher disease registry (GARDIAN): a patient-led initiative

T Collin-Histed, M Stoodley… - Orphanet journal of …, 2023 - pubmed.ncbi.nlm.nih.gov
Background Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …

A global neuronopathic gaucher disease registry (GARDIAN): a patient-led initiative

T Collin-Histed, M Stoodley… - Orphanet Journal of …, 2023 - search.proquest.com
Background Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …

A global neuronopathic gaucher disease registry (GARDIAN): a patient-led initiative.

T Collin-Histed, M Stoodley… - Orphanet Journal of …, 2023 - search.ebscohost.com
Background: Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …

[PDF][PDF] A global neuronopathic gaucher disease registry (GARDIAN): a patient‑led initiative

T Collin‑Histed, M Stoodley… - … Journal of Rare …, 2023 - ojrd.biomedcentral.com
Background Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …

A Global Neuronopathic Gaucher Disease Registry (GARDIAN): A Patient-Led Initiative

T Collin-Histed, M Stoodley, K Beusterien, D Elstein… - 2023 - europepmc.org
Background: Gaucher disease (GD) is a rare autosomal recessive lysosomal storage
disorder. GD types 2 and 3 are known as neuronopathic Gaucher disease (nGD) because …