New Diagnostic Method for Lysosomal Acid Lipase Deficiency and the Need to Recognize Its Manifestation in Infants (Wolman Disease)

Author:

Gómez-Nájera Mariana,Barajas-Medina Hilario,Gallegos-Rivas Mayra C.,Mendez-Sashida Pedro,Goss Kendrick A.,Sims Katherine B.,Tripuraneni Radhika,Valles-Ayoub Yadira

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Pediatrics, Perinatology, and Child Health

Reference10 articles.

1. Prevalence of lysosomal storage disorders.;Meikle;JAMA,1999

2. Wolman disease (LIPA p.G87 V) genotype frequency in people of Iranian-Jewish ancestry.;Valles-Ayoub;Genet Test Mol Biomarkers,2011

3. A new method for measurement of lysosomal acid lipase in dried blood using the inhibitor Lalistat 2.;Hamilton;Clin Chim Acta,2012

4. Long-term metabolic, endocrine, and neuropsychological outcome of hematopoietic cell transplantation for Wolman disease.;Tolar;Bone Marrow Transplant,2009

5. Wolmans disease: a review of treatment with bone marrow transplantation and considerations for the future.;Krivit;Bone Marrow Transplant,1992

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