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Publications by Karen Valdez-Gonzalez
Early Diagnosis of Infantile-Onset Lysosomal Acid Lipase Deficiency in the Advent of Available Enzyme Replacement Therapy
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Related publications
The Disease Is the Accumulation of Cholesterol Esters Due to Deficit of Lysosomal Acid Lipase. Clinical Case of Lysosomal Acid Lipase Deficiency Is Described in This Article
Medical Council
Enzyme Replacement Therapy for Late-Onset Pompe Disease
Cochrane Database of Systematic Reviews
Lysosomal Acid Lipase Deficiency Unmasked in Two Children With Nonalcoholic Fatty Liver Disease
Pediatrics
Child Health
Pediatrics
Perinatology
Promising CNS-directed Enzyme Replacement Therapy for Lysosomal Storage Diseases
Experimental Neurology
Developmental Neuroscience
Neurology
Late-Onset Pompe Disease: Preliminary Results of Enzyme Replacement Therapy
Nervno-Myshechnye Bolezni
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Lysosomal Acid Lipase (Acid Cholesterol Ester Hydrolase)
The Journal of Japan Atherosclerosis Society
Long Term Substrate Reduction Therapy With Ezetimibe Alone or Associated With Statins in Three Adult Patients With Lysosomal Acid Lipase Deficiency
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Engineering of GlcNAc-1-Phosphotransferase for Production of Highly Phosphorylated Lysosomal Enzymes for Enzyme Replacement Therapy
Molecular Therapy - Methods and Clinical Development
Molecular Medicine
Genetics
Molecular Biology
773 BOVINE Α-Glucosidase DEFICIENCY: A MODEL FOR ENZYME REPLACEMENT THERAPY
Pediatric Research
Child Health
Pediatrics
Perinatology
