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10 in total

Review 1. Are there useful biochemical markers of disease activity in lysosomal storage diseases?

Authors: B Winchester
Journal: J Inherit Metab Dis Date: 2001 Impact factor: 4.982

2. Antibody-mediated enzyme replacement therapy targeting both lysosomal and cytoplasmic glycogen in Pompe disease.

Authors: Haiqing Yi; Tao Sun; Dustin Armstrong; Scott Borneman; Chunyu Yang; Stephanie Austin; Priya S Kishnani; Baodong Sun
Journal: J Mol Med (Berl) Date: 2017-02-02 Impact factor: 4.599

Review 3. The natural course of non-classic Pompe's disease; a review of 225 published cases.

Authors: Léon P F Winkel; Marloes L C Hagemans; Pieter A van Doorn; M Christa B Loonen; Wim J C Hop; Arnold J J Reuser; Ans T van der Ploeg
Journal: J Neurol Date: 2005-08 Impact factor: 4.849

Review 4. Urinary oligosaccharides in lysosomal and other metabolic disorders.

Authors: A Federico; G Guazzi
Journal: Ital J Neurol Sci Date: 1982-03

5. Determination of a glucose-containing tetrasaccharide in urine of patients with acute pancreatitis.

Authors: J Kumlien; A Andrén-Sandberg; D Zopf; A Lundblad
Journal: Int J Pancreatol Date: 1989-03

6. Sensitive quantification of α-glucans in mouse tissues, cell cultures, and human cerebrospinal fluid.

Authors: Silvia Nitschke; Sara Petković; Saija Ahonen; Berge A Minassian; Felix Nitschke
Journal: J Biol Chem Date: 2020-08-13 Impact factor: 5.157

7. Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis.

Authors: A C Sewell
Journal: Eur J Pediatr Date: 1980-09 Impact factor: 3.183

Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).