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標(biāo)題: Titlebook: Cystic Fibrosis Pulmonary Infections: Lessons from Around the World; Adolf Bauernfeind,Melvin I. Marks (Professor and V Book 1996 Springer [打印本頁]

作者: panache    時(shí)間: 2025-3-21 19:44
書目名稱Cystic Fibrosis Pulmonary Infections: Lessons from Around the World影響因子(影響力)




書目名稱Cystic Fibrosis Pulmonary Infections: Lessons from Around the World影響因子(影響力)學(xué)科排名




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作者: Chivalrous    時(shí)間: 2025-3-21 23:01
Microbial Resistanceion of multiply resistant organisms within the lungs of these patients. With seeming predictability, . becomes progressively resistant to several classes of antimicrobial agents including .-lactam antibiotics, aminoglycosides, and the fluoroquinolones [1].
作者: eustachian-tube    時(shí)間: 2025-3-22 01:05

作者: Commodious    時(shí)間: 2025-3-22 08:34
Cystic Fibrosis in Japanese population. Twenty-eight percent of the total cases presented symptoms of meconium ileus, which is a higher frequency than that seen in the Caucasian population. This might probably reflect a genetic difference between CF of Northern Europe and Japan.
作者: 贊成你    時(shí)間: 2025-3-22 09:43

作者: 迷住    時(shí)間: 2025-3-22 13:11
Anisotropic Behaviour of Damaged Materialster transplantation [1]. The first successful heart-lung transplants (HLT) for CF were performed in the United Kingdom in 1985 [2] and encouraging intermediate term (51/2 year experience) results have been reported [3] which compare favorably with results of HLT performed for diseases other than CF [4].
作者: 迷住    時(shí)間: 2025-3-22 20:19

作者: strdulate    時(shí)間: 2025-3-23 01:08
Anion Carriers of Mitochondrial Membranesf . increases with age. Of the CF-patients with ., 73% showed elevated specific serum IgG to this fungus. No correlation was found between culture, specified IgG to . and either specific Aspergillus IgE or total serum IgE. Maintaining good pulmonary condition and reduction of exposure to . may prevent colonization and infection with this mold.
作者: Narcissist    時(shí)間: 2025-3-23 04:42
Infinite Space, Half Space and Bi-materials,approximate annual cost of treatment in Venezuela is US$10 000 per patient, making it very difficult to provide adequate therapy to low income patients without financial assistance from public and private institutions.
作者: 梯田    時(shí)間: 2025-3-23 08:52

作者: 爭吵加    時(shí)間: 2025-3-23 10:10

作者: DEBT    時(shí)間: 2025-3-23 17:16
Pulmonary Infections in Venezuelan Patients with Cystic Fibrosisapproximate annual cost of treatment in Venezuela is US$10 000 per patient, making it very difficult to provide adequate therapy to low income patients without financial assistance from public and private institutions.
作者: 極肥胖    時(shí)間: 2025-3-23 19:01

作者: 躲債    時(shí)間: 2025-3-23 22:58

作者: 黃油沒有    時(shí)間: 2025-3-24 04:35

作者: BLANK    時(shí)間: 2025-3-24 08:48

作者: 神刊    時(shí)間: 2025-3-24 13:55
Book 1996e the specific mechanisms predisposing the respiratory mucosa of cystic fibrosis patients to infection, so far no clinically relevant procedures for completely effective prevention or control of infection have resulted. Hence, in dealing with infections in cystic fibrosis, we continue to rely mainly
作者: GREG    時(shí)間: 2025-3-24 15:08
Holes/Cracks/Inclusions in Laminates,y update of changes in its CF care program as well as data for the Canadian patient data registry at the CCFF. Every five years each clinic receives a site visit by members of the CCFF Clinic Subcommittee to review the clinical program, personnel, and physical resources.
作者: Defense    時(shí)間: 2025-3-24 22:25
L. E. Toth,J. Zbasnik,Y. Sato,W. Gardnern of viral infections, and of . cross-infection. Therapy strategies against lung infection (early colonization, chronic infection; criteria for inhospital or home therapy) adopted in the different Italian centres are also presented. Prognosis and quality of life of Italian CF patients are improving thanks to this global approach to the disease.
作者: 美麗的寫    時(shí)間: 2025-3-25 00:35

作者: hallow    時(shí)間: 2025-3-25 03:26
The General Approach to Cystic Fibrosis Pulmonary Infection in Canaday update of changes in its CF care program as well as data for the Canadian patient data registry at the CCFF. Every five years each clinic receives a site visit by members of the CCFF Clinic Subcommittee to review the clinical program, personnel, and physical resources.
作者: 高貴領(lǐng)導(dǎo)    時(shí)間: 2025-3-25 08:22
The General Approach to Cystic Fibrosis Pulmonary Infection in Italyn of viral infections, and of . cross-infection. Therapy strategies against lung infection (early colonization, chronic infection; criteria for inhospital or home therapy) adopted in the different Italian centres are also presented. Prognosis and quality of life of Italian CF patients are improving thanks to this global approach to the disease.
作者: Hirsutism    時(shí)間: 2025-3-25 15:03
Cystic Fibrosis in the Western Part of Germany: A General Review about Cystic Fibrosis Managementlack Forest since 1979. The aim of these meetings is to train young doctors in CF management, to standardize the medical care of CF patients in Germany and to discuss new therapeutic concepts. These Titisee meetings also initiated the start of a CF register of all patients treated in the participating CF centers.
作者: CULP    時(shí)間: 2025-3-25 16:20

作者: IRATE    時(shí)間: 2025-3-25 21:58
Chang-Geun Chae,Ho-Bin Seo,Jae-Suk Leestics in this disease. There is also no evidence of impaired absorption of antibiotics in CF. Since the pharmacodynamic effect of antibiotics has recently been related to their plasma concentrations to MIC-relationships, our findings should lead to a complete reevaluation of antibiotic therapy in cystic fibrosis on rational data analysis.
作者: CULP    時(shí)間: 2025-3-26 01:19
Anisotropic Behaviour of Damaged Materialsion of multiply resistant organisms within the lungs of these patients. With seeming predictability, . becomes progressively resistant to several classes of antimicrobial agents including .-lactam antibiotics, aminoglycosides, and the fluoroquinolones [1].
作者: 遭遇    時(shí)間: 2025-3-26 06:53
Anisotropic Elasticity with Matlabin CF in this part of the world. This was a very important development for Latin American countries, where methods to diagnose and treat CF were often lacking, and most medical resources were focused on summer diarrhea, malnutrition and common respiratory and parasitic infections.
作者: glacial    時(shí)間: 2025-3-26 11:19
Michael Z. Hu,Matthew R. Sturgeonese population. Twenty-eight percent of the total cases presented symptoms of meconium ileus, which is a higher frequency than that seen in the Caucasian population. This might probably reflect a genetic difference between CF of Northern Europe and Japan.
作者: palette    時(shí)間: 2025-3-26 14:10
Viral, Fungal and Atypical Bacterial Infections in Cystic Fibrosiswas the most frequent (53%), followed by parainfluenza (24%) and RSV (20%); 54% of the episodes lead to hospital admission. A significant change in microbial flora of respiratory secretions was seen in 88% of the episodes, mainly with ., and 65% of cases with initial colonization with . are associat
作者: debble    時(shí)間: 2025-3-26 18:00

作者: mosque    時(shí)間: 2025-3-27 00:16
Antimicrobial Pharmacotoxicity In the general population, antimicrobial agents are frequently associated with drug-related toxicity. As reviewed by Anderson [1], antimicrobial agents, particularly the beta-lactam antibiotics, may account for 20–50% of the adverse drug effects reported in hospitalized patients.
作者: 我沒有強(qiáng)迫    時(shí)間: 2025-3-27 01:27
Microbial Resistancens and microbiologists caring for CF patients have been all too familiar with the consequences of prolonged courses of antibiotics, that is the selection of multiply resistant organisms within the lungs of these patients. With seeming predictability, . becomes progressively resistant to several clas
作者: Instantaneous    時(shí)間: 2025-3-27 07:47
Microbial Virulence and Pathogenesis in Cystic Fibrosising ., ., ., ., . species and various non-tuberculous mycobacteria. Patients with CF may initially become infected with a number of bacterial species including . [1] and . [2], however . is the principal respiratory tract pathogen leading to chronic infection in these patients [3]. Once CF patients
作者: Audiometry    時(shí)間: 2025-3-27 11:49

作者: Angiogenesis    時(shí)間: 2025-3-27 16:42

作者: 憎惡    時(shí)間: 2025-3-27 18:14

作者: hermetic    時(shí)間: 2025-3-27 22:49
Cystic Fibrosis in Latin Americae managed by individual doctors. In the 1960s a National Foundation was created in Argentina to improve care and promote medical-biochemical research in CF in this part of the world. This was a very important development for Latin American countries, where methods to diagnose and treat CF were often
作者: braggadocio    時(shí)間: 2025-3-28 03:35
Pulmonary Infections in Venezuelan Patients with Cystic Fibrosisonic and recurrent pulmonary infections [1, 2]. In addition, it is responsible for a large variety of manifestations, i.e. pancreatic insufficiency, nasal polyposis, pulmonary disease, sinusitis, rectal prolapse, hyperglycemia, short stature, etc. Therefore, it is considered a complex disease which
作者: 撤退    時(shí)間: 2025-3-28 06:37

作者: 連接    時(shí)間: 2025-3-28 14:10

作者: tackle    時(shí)間: 2025-3-28 17:41
The General Approach to Cystic Fibrosis Pulmonary Infection in Russiaies started to attract attention of medical authorities in Russia only in recent years. According to the data of the National Russian Cystic Fibrosis (Mucoviscidosis) Association about 2000 CF patients were registered in the country (the population of Russia is 180 million people). The CF Centre in
作者: Isometric    時(shí)間: 2025-3-28 22:37

作者: Respond    時(shí)間: 2025-3-29 01:55

作者: abstemious    時(shí)間: 2025-3-29 05:56
The General Approach to Cystic Fibrosis Pulmonary Infection in Greece 50–60 affected neonates expected each year. The carrier frequency is estimated at 5% of the general population. There are 287 CF patients attending the CF Centre which was started in 1966 at the Aghia Sophia Children’s Hospital in Athens. 25% of the patients are older than 16 years and the oldest k
作者: 盟軍    時(shí)間: 2025-3-29 10:55

作者: 禮節(jié)    時(shí)間: 2025-3-29 14:04
The General Approach to Cystic Fibrosis Pulmonary Infection in Spain 2000 patients for the whole country. The real number of well-identified patients currently registered in the different CF Units is 996. This figure is based on the data obtained by us from fifteen reference hospitals where the cases of smaller institutions are collected. The Social Security organiz
作者: convulsion    時(shí)間: 2025-3-29 16:22
Cystic Fibrosis in the Western Part of Germany: A General Review about Cystic Fibrosis Management centers were set up in some university hospitals. Regular conventions of the CF Association led to a better education of German pediatricians and stimulated the founding of further CF centers throughout the former FRG, preferably in the university pediatric medical centers. In addition to these con
作者: 伙伴    時(shí)間: 2025-3-29 23:34

作者: 不理會    時(shí)間: 2025-3-30 00:42
Chang-Geun Chae,Ho-Bin Seo,Jae-Suk Lee. Our findings show that neither the kidney nor the liver are “hyperorgans” in CF nor does the distribution of antibiotics follow different characteristics in this disease. There is also no evidence of impaired absorption of antibiotics in CF. Since the pharmacodynamic effect of antibiotics has rece
作者: nonchalance    時(shí)間: 2025-3-30 07:21
Andrew Goodwin,Nam-Goo Kang,Jimmy W. Mays In the general population, antimicrobial agents are frequently associated with drug-related toxicity. As reviewed by Anderson [1], antimicrobial agents, particularly the beta-lactam antibiotics, may account for 20–50% of the adverse drug effects reported in hospitalized patients.
作者: rectocele    時(shí)間: 2025-3-30 10:15
Anisotropic Behaviour of Damaged Materialsns and microbiologists caring for CF patients have been all too familiar with the consequences of prolonged courses of antibiotics, that is the selection of multiply resistant organisms within the lungs of these patients. With seeming predictability, . becomes progressively resistant to several clas
作者: Anguish    時(shí)間: 2025-3-30 16:11

作者: 豐富    時(shí)間: 2025-3-30 19:23

作者: Exploit    時(shí)間: 2025-3-31 00:01
https://doi.org/10.1007/978-1-4419-5915-7on, bronchiectasis, and pulmonary failure [1]. Endobronchial infection including pneumonia, with or without an appropriate inflammatory response, is nearly universal in cystic fibrosis patients. Our success at controlling albeit not curing, the pulmonary infection in cystic fibrosis has undoubtedly
作者: 條約    時(shí)間: 2025-3-31 02:02

作者: Respond    時(shí)間: 2025-3-31 07:00
Anisotropic Elasticity with Matlabe managed by individual doctors. In the 1960s a National Foundation was created in Argentina to improve care and promote medical-biochemical research in CF in this part of the world. This was a very important development for Latin American countries, where methods to diagnose and treat CF were often
作者: 鍍金    時(shí)間: 2025-3-31 11:46
Infinite Space, Half Space and Bi-materials,onic and recurrent pulmonary infections [1, 2]. In addition, it is responsible for a large variety of manifestations, i.e. pancreatic insufficiency, nasal polyposis, pulmonary disease, sinusitis, rectal prolapse, hyperglycemia, short stature, etc. Therefore, it is considered a complex disease which
作者: Vsd168    時(shí)間: 2025-3-31 14:56

作者: 漂浮    時(shí)間: 2025-3-31 19:32
Michael Z. Hu,Matthew R. Sturgeon on the numbers of reported cases and live births in the period suggests that the estimated incidence of CF might be about one in 680 000 in the Japanese population. Twenty-eight percent of the total cases presented symptoms of meconium ileus, which is a higher frequency than that seen in the Caucas
作者: 愉快嗎    時(shí)間: 2025-3-31 22:22
Evren ?zarslan,Thomas Schultz,Andrea Fusteries started to attract attention of medical authorities in Russia only in recent years. According to the data of the National Russian Cystic Fibrosis (Mucoviscidosis) Association about 2000 CF patients were registered in the country (the population of Russia is 180 million people). The CF Centre in
作者: Subdue    時(shí)間: 2025-4-1 05:32
Bernard D. Coleman,Daniel C. Newmant electrolytes, and other less common clinical findings including meconium ileus, nasal polyposis, and hepatobiliary disease [1]. Patients are diagnosed at different ages with various modes of presentation, and there is considerable variability in the severity or rate of disease progression of invol
作者: chlorosis    時(shí)間: 2025-4-1 06:38
Maria K. Duszek-Perzyna,Piotr Perzynas prevalance in most developing countries..In Turkey the infant mortality rate is still very high (59/1000). Respiratory infections and diarrhea are important causes of infant mortality (13%, and 9%, respectively) (1). There are no reliable statistical data available for the incidence of CF in our c




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