Suchergebnisse - "Young, Sarah"

PubPharm (15)

1

Characterization of liver GSD IX γ2 pathophysiology in a novel Phkg2-/- mouse model

enthalten in: Molecular genetics and metabolism | 2021

von Gibson, R. | Lim, J. | Choi, S. | +7

2

Fenofibrate rapidly decreases hepatic lipid and glycogen storage in neonatal mice with glycogen storage disease type Ia

enthalten in: Human molecular genetics | 2020

von Yavarow, Z. | Kang, H. | Waskowicz, L. | +4

3

Liver fibrosis during clinical ascertainment of glycogen storage disease type III : a need for improved and systematic monitoring

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2019

von Halaby, C. | Young, S. | Austin, S. | +9

4

Bezafibrate induces autophagy and improves hepatic lipid metabolism in glycogen storage disease type Ia

enthalten in: Human molecular genetics | 2019

von Waskowicz, L. | Zhou, J. | Landau, D. | +11

5

Natural Progression of Canine Glycogen Storage Disease Type IIIa

enthalten in: Comparative medicine | 2016

von Brooks, E. | Yi, H. | Austin, S. | +5

6

Adjunctive β2-agonist treatment reduces glycogen independently of receptor-mediated acid α-glucosidase uptake in the limb muscles of mice with Pompe disease

enthalten in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2014

von Farah, B. | Madden, L. | Li, S. | +6

7

Quantitative computed tomography for enzyme replacement therapy in Pompe disease

enthalten in: Brain & development | 2012

von Yonee, C. | Toyoshima, M. | Young, S. | +7

8

Assessing disease severity in Pompe disease : the roles of a urinary glucose tetrasaccharide biomarker and imaging techniques

enthalten in: American journal of medical genetics. Part C, Seminars in medical genetics | 2012

von Young, S. | Piraud, M. | Goldstein, J. | +7

9

Impaired clearance of accumulated lysosomal glycogen in advanced Pompe disease despite high-level vector-mediated transgene expression

enthalten in: The journal of gene medicine | 2009

von Sun, B. | Zhang, H. | Bird, A. | +3

10

Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2009

von Young, S. | Zhang, H. | Corzo, D. | +4