Respiratory Complications in Patients With Myelodysplasia and Arnold-Chiari Malformation
- 1 March 1986
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Pediatrics & Adolescent Medicine
- Vol. 140 (3), 221-224
- https://doi.org/10.1001/archpedi.1986.02140170047026
Abstract
• Respiratory complications in four patients with myelodysplasia and the Arnold-Chiari malformation included abnormal control of breathing, upper-airway dysfunction, aspiration pneumonia, and cor pulmonale. Early and prolonged ventilatory support resulted in a favorable outcome in three of four patients. (AJDC 1986;140:221-224)This publication has 16 references indexed in Scilit:
- Posterior Fossa Decompression in Shunt-Treated Hydrocephalic ChildrenDevelopmental Medicine and Child Neurology, 2008
- Apnea as the sole manifestation of cord compression in achondroplasiaThe Journal of Pediatrics, 1984
- Management of the Newborn with MyelodysplasiaClinical Pediatrics, 1979
- Manifestations and Management of Arnold-Chiari Malformation in Patients with MyelomeningocelePediatric Neurosurgery, 1975
- Impaired Peripheral Chemosensitivity and Acute Respiratory Failure in Arnold-Chiari Malformation and SyringomyeliaNew England Journal of Medicine, 1973
- Airway Obstruction Due to Vocal Cord Paralysis in Infants with Hydrocephalus and MeningomyeloceleAnnals of Otology, Rhinology & Laryngology, 1972
- Spina Bifida Cystica: Results of Treatment of 270 Consecutive Cases with Criteria for Selection for the FutureArchives of Disease in Childhood, 1972
- Multiple cranial nerve deficits associated with the Arnold‐Chiari malformationNeurology, 1971
- Respiratory Function After Cervical CordotomyChest, 1971
- DEFECTIVE CLOSURE OF THE NEURAL TUBEArchives of Neurology & Psychiatry, 1940