Airway nitric oxide in Duchenne muscular dystrophy

Journal of Pediatrics

Volumn 141, Issue 1, 2002, Pages 132-134

  Straub, Volker ^a   Ratjen, Felix ^a   Amthor, Helge ^a   Voit, Thomas ^a   Grasemann, Hartmut ^a  

^a UNIVERSITY OF DUISBURG ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AIRWAY; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; ENZYME ACTIVITY; EXPIRATORY FLOW RATE; GENE MUTATION; HUMAN; INSPIRATORY CAPACITY; MALE; PRIORITY JOURNAL; PROTEIN EXPRESSION; VITAL CAPACITY;

EID: 0036067402     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1067/mpd.2002.125226     Document Type: Article

References (10)

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3. Inducible nitric oxide synthase expression is reduced in cystic fibrosis murine and human airway epithelial cells
4. Exhaled nitric oxide in patients with asthma: Association with NOS1 genotype
5. Airway nitric oxide levels in cystic fibrosis patients are related to a polymorphism in the neuronal nitric oxide synthase gene
6. ε-sarcoglycan replaces α-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex
7. Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy
8. Recommendations for standardized procedures for the on-line and off-line measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide in adults and children: 1999
9. A simple flowdriven method for online measurement of exhaled NO starting at the age of 4 to 5 years
10. Contribution of nitric oxide synthases 1, 2, and 3 to airway hyperresponsiveness and inflammation in a murine model of asthma