13 studies were found.

1.		Recruiting	Replagal Enzyme Replacement Therapy for Children with Fabry Disease Condition: Fabry Disease
2.		Recruiting	Alternative Dosing and Regimen of Replagal to Treat Fabry Disease Condition: Fabry Disease
3.		Recruiting	Expanded access use of Myozyme (alglucosidase alfa) in patients with infantile-onset Pompe disease Conditions: Glycogen Storage Disease Type II; Glycogenosis 2
4.		Recruiting	An Open-Label Clinical Trial of Replagal Enzyme Therapy in Children Ages 7-17 Years with Fabry Disease Condition: Fabry Disease
5.		Recruiting	Registry of Fabry Disease - A Multicenter Observational Study Condition: Fabry Disease
6.		Recruiting	OGT 918-006: A Phase I/II Randomized, Controlled Study of OGT 918 in Patients with Neuronopathic Gaucher Disease Condition: Gaucher Disease
7.		Recruiting	Nervous System Degeneration in Glycosphingolipid Storage Disorders Conditions: Gangliosidoses; Gaucher Disease
8.		Recruiting	The Natural History and Pathogenesis of Mucolipidosis Type IV Condition: Mucolipidosis Type IV
9.		Recruiting	Phase II Randomized Study of Alendronate Sodium for Osteopenia in Patients with Gaucher's Disease Conditions: Gaucher's Disease; Osteopenia
10.		Recruiting	Phase II Study of Glucocerebrosidase in Patients With Gaucher Disease Condition: Gaucher's Disease
11.		Recruiting	Analysis of the Nervous System in Patients with Fabry's Disease Condition: Fabry's Disease
12.		Recruiting	Effects of Enzyme Replacement in Gaucher's Disease Condition: Gaucher's Disease
13.		Recruiting	Genetic Studies of Lysosomal Storage Disorders Conditions: Gaucher's Disease; Lysosomal Storage Disease