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MeSH:(Glycogen Storage Disease Type II/pathology*)

1.Analysis of lysosomal enzyme activity and genetic variants in a child with late-onset Pompe disease.

Tiantian HE ; Jieni JIANG ; Yueyue XIONG ; Dan YU ; Xuemei ZHANG

Chinese Journal of Medical Genetics 2023;40(6):711-717

2.A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation.

Dong Gyu KIM ; Kisuck JUNG ; Myung Koo LEE ; In Gyu HYUN ; Hwa Jung LIM ; Hong Go SONG ; Je Geun CHI

Journal of Korean Medical Science 1993;8(3):221-224

4.Analysis of clinical features of 6 patients with infantile type glycogen storage disease type II.

Juan DING ; Yu HUANG ; Haipo YANG ; Qingyou ZHANG ; Xinlin HOU ; Xueqin LIU ; Yanling YANG ; Hui XIONG

Chinese Journal of Pediatrics 2015;53(6):436-441

5.Clinical sequelae of 17 cases with glycogen storage disease type II/Pompe disease.

Han-bing ZHANG ; Wei-min ZHANG ; Jia-jing QIU ; Yan MENG ; Zheng-qing QIU

Chinese Journal of Pediatrics 2012;50(6):415-419

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