Achalasie
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology
Link
https://link.springer.com/content/pdf/10.1007/s11377-020-00473-4.pdf
Reference67 articles.
1. Tryhus MR, Davis M, Griffith JK, Ablin DS, Gogel HK (1989) Familial achalasia in two siblings: significance of possible hereditary role. J Pediatr Surg 24:292–295
2. Eckardt AJ, Eckardt VF (2011) Treatment and surveillance strategies in achalasia: an update. Nat Rev Gastroenterol Hepatol 8(6):311–319
3. Mearin F, Mourelle M, Guarner F, Salas A, Riveros-Moreno V, Moncada S et al (1993) Patients with achalasia lack nitric oxide synthase in the gastro-oesophageal junction. Eur J Clin Invest 23(11):724–728
4. Saur D, Paehge H, Schusdziarra V, Allescher HD (2000) Distinct expression of splice variants of neuronal nitric oxide synthase in the human gastrointestinal tract. Gastroenterology 118(5):849–858
5. Dodds WJ, Dent J, Hogan WJ, Patel GK, Toouli J, Arndorfer RC (1981) Paradoxial lower esophageal sphincter contraction induced by cholecystokinin-octapeptide in patients with achalasia. Gastroenterology 80:327–333
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