[Enzyme replacement therapy in a patient with Pompe disease].

Fujikawa, Yoshinao; Kinoshita, Satoru; Miyamoto, Yusaku; Nakayama, Tojo; Endo, Yusaku; Sasaki, Masayuki

Fujikawa, Yoshinao; Kinoshita, Satoru; Miyamoto, Yusaku; Nakayama, Tojo; Endo, Yusaku; Sasaki, Masayuki.

Affiliation

Fujikawa Y; Department of Child Neurology, National Center Hospital for Mental, Nervous and Muscular Disorders, National Center of Neurology and Psychiatry, Kodaira, Tokyo. fuji@oha.toho-u.ac.jp

No To Hattatsu ; 39(5): 383-6, 2007 Sep.

Article in Ja | MEDLINE | ID: mdl-17879614

Subject(s)

Glycogen Storage Disease Type II/drug therapy; alpha-Glucosidases/therapeutic use; Child, Preschool; Drug Administration Schedule; Evoked Potentials, Auditory, Brain Stem; Glycogen Storage Disease Type II/physiopathology; Humans; Male

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Collection: 01-internacional Database: MEDLINE Main subject: Glycogen Storage Disease Type II / Alpha-Glucosidases Limits: Child, preschool / Humans / Male Language: Ja Journal: No To Hattatsu Year: 2007 Type: Article

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