健谈
发表于 2025-3-27 00:51:46
Drug Allergy in Cystic Fibrosis,riably effective empiric treatments aimed at various clinical manifestations and components of this complex and protean disease. The result is a remarkable polypharmaceutical regimen of antibiotics, pancreatic enzymes, nutritional supplements, bronchodilators, and assorted other medications. In this
neutral-posture
发表于 2025-3-27 01:08:45
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Isometric
发表于 2025-3-27 09:16:36
https://doi.org/10.1007/978-1-4612-0475-6allergy; bacteria; cell biology; infection; infections; infectious disease; inflammation; pathology; pseudom
outset
发表于 2025-3-27 12:50:47
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Wallow
发表于 2025-3-27 17:41:41
Introduction to Generative Recursionf spectacular progress in understanding the genetic and molecular basis of CF. The research breakthroughs of the decade began with the first fundamental insights, published in 1981–1983, into the basic cellular pathophysiology of CF with demonstrations of alteredion transport in specialized exocrine
波动
发表于 2025-3-27 21:41:16
https://doi.org/10.1007/978-3-031-04317-8ed as honorary members. In years past, few individuals with CF survived infancy. Up to 10% of affected children died shortly after birth as a result of complications from meconium ileus, and survivors, who were typically malnourished, usually succumbed to repeated and persistent lung infections. The
Certainty
发表于 2025-3-28 01:50:37
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Enthralling
发表于 2025-3-28 03:29:10
https://doi.org/10.1007/978-3-031-04317-8 . appears to play an important role in the pathogenesis of CF pulmonary tissue injury. In contrast . is found less frequently in CF respiratory secretions than ., and its role in pulmonary tissue injury is unclear. Presented below is a review of the microbiologie and immunologie data evaluating the
Congestion
发表于 2025-3-28 08:54:09
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男学院
发表于 2025-3-28 12:29:55
Janelle Applequist,Matthew P. McAllister other investigators have reported that ABPA occurs with an incidence of approx 10-11% in patients with CF(2-5). This is probably an underestimation because the underlying lung disease in patients with CF obscures many of the pulmonary findings considered cardinal signs of ABPA. However, distinguish