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Secondary (AA) amyloidosis in cystic fibrosis. A report of three cases.
Travis WD, Castile R, Vawter G, Shwachman H, Warwick W, Burke BA, Skinner M. Travis WD, et al. Among authors: shwachman h. Am J Clin Pathol. 1986 Apr;85(4):419-24. doi: 10.1093/ajcp/85.4.419. Am J Clin Pathol. 1986. PMID: 3953498
Review of autopsy material in Boston from 23 additional cystic fibrosis patients with long-term survival did not reveal any evidence of amyloidosis. It appears that secondary amyloidosis is emerging as a significant, although rare, complication of cystic fibrosis as greate …
Review of autopsy material in Boston from 23 additional cystic fibrosis patients with long-term survival did not reveal any evidence …
Meconium ileus: ten patients over 28 years of age.
Shwachman H. Shwachman H. J Pediatr Surg. 1983 Oct;18(5):570-5. doi: 10.1016/s0022-3468(83)80361-3. J Pediatr Surg. 1983. PMID: 6644496
Genetic counseling for affected families is recommended when a baby is born with this condition. Usually such infants are born at full term and there is no sex predilection. Prognosis is uncertain and the outlook depends, as it does in cystic fibrosis, on the degree and ra …
Genetic counseling for affected families is recommended when a baby is born with this condition. Usually such infants are born at full te
Chloramphenicol for long-term therapy of cystic fibrosis.
LLOYD AV, GRIMES G, KHAW KT, SHWACHMAN H. LLOYD AV, et al. Among authors: shwachman h. JAMA. 1963 Jun 29;184:1001-6. doi: 10.1001/jama.1963.03700260033006. JAMA. 1963. PMID: 13931113 No abstract available.