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MeSH:(Glycogen Storage Disease Type II)

6.Glycogen Storage Disease Type II: A Case Report.

Jeong Lim MOON ; Sae Yoon KANG ; Seung Han YANG ; Su Jeong CHOE ; Youn Soo LEE

Journal of the Korean Academy of Rehabilitation Medicine 1997;21(6):1224-1230

7.Evaluation of the Urinary Glucose Tetrasaccharide Assay Using Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry for Diagnosis of Pompe Disease.

Youngwon NAM ; Kyunghoon LEE ; Sun Hee JUN ; Kyung Un PARK ; Sang Hoon SONG ; Hyung Doo PARK ; Junghan SONG

Laboratory Medicine Online 2015;5(4):211-214

8.Clinical characteristics and gene mutation analysis of one pedigree with infantile glycogen storage disease type II.

Lei ZHANG ; Xiao-Heng XU ; Ji WANG ; Si-Jin ZHANG

Chinese Journal of Contemporary Pediatrics 2015;17(11):1228-1231

9.Research progress of nervous system damage in Pompe disease.

Wen-Chao ZHANG ; Ying-Ying MAO ; Qian CHEN

Chinese Journal of Contemporary Pediatrics 2023;25(4):420-424

10.Two Patients with Atypical Infantile Pompe Disease Presenting with Hypertrophic Cardiomyopathy.

Eun Hee KIM ; Jung Min KO ; Beom Hee LEE ; Gu Hwan KIM ; Jin Ho CHOI ; Han Wook YOO

Journal of Genetic Medicine 2009;6(2):161-165

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