Mcardle's disease: Successful symptomatic therapy by high dose oral administration of ribose

Klinische Wochenschrift

Volumn 69, Issue 2, 1991, Pages 92-

  Wagner, D R ^a   Zollner N ^a  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIA; LACTIC ACID; RIBOSE;

ADULT; CASE REPORT; CONTROLLED STUDY; GLYCOGEN STORAGE DISEASE TYPE 5; HUMAN; ORAL DRUG ADMINISTRATION; PRIORITY JOURNAL; SHORT SURVEY;

ADMINISTRATION, ORAL; ADULT; AMMONIA; CASE REPORT; DOSE-RESPONSE RELATIONSHIP, DRUG; GLYCOGEN STORAGE DISEASE TYPE V; HUMAN; LACTATES; LACTIC ACID; MALE; RIBOSE;

EID: 0026063834     PISSN: 00232173     EISSN: 14321440     Source Type: Journal    
DOI: 10.1007/BF01666823     Document Type: Article

References (5)

1. Hypoxanthine and McArdle's disease: a clue to metabolic stress in the working forearm
2. Diagnostische Bedeutung von Muskelbiopsien bei metabolischen Myopathien
3. McArdle's disease with myoadenylate deaminase deficiency: observations in a combined enzyme deficiency
4. Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine
5. Myoadenylate deaminase deficiency: successful symptomatic therapy by high dose oral administration of ribose