Massenspektrometrie: Eine Einführung (German Edition)

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Amaral MD. Novel personalized therapies for cystic fibrosis: treating the basic defect in all patients. J Intern Med ;— Genotype-phenotype correlation for pulmonary function in cystic fibrosis.

Thorax ;— Recommendations for the classification of diseases as CFTR-related disorders. J Cyst Fibros ;S86— Curr Opin Pediatr ;—7. Intestinal current measurements detect activation of mutant CFTR in patients with cystic fibrosis with the GD mutation treated with Ivacaftor.

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Brennan ML, Schrijver I. Cystic fibrosis: a review of associated phenotypes, use of molecular diagnostic approaches, genetic characteristics, progress, and dilemmas. J Mol Diagn ;— Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis. Nat Commun ;—8. Characterizing responses to CFTR-modulating drugs using rectal organoids derived from subjects with cystic fibrosis. Sci Trans Med ;ra Nasal potential difference measurements to assess CFTR ion channel activity. Methods Mol Biol ;— European cystic fibrosis society standards of care: best practice guidelines.

J Cyst Fibros ;S23— A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med ;— Kelly T, Buxbaum J. Gastrointestinal manifestations of cystic fibrosis. Dig Dis Sci ;— Colombo C. Liver disease in cystic fibrosis. Curr Opin Pulm Med ;— Risk factors for bronchiectasis in children with cystic fibrosis. Boyle MP. Nonclassic cystic fibrosis and CFTR-related diseases. Mainz JG, Koitschev A. Pathogenesis and management of nasal polyposis in cystic fibrosis.

Curr Allergy Asthma Rep ;— Origins of cystic fibrosis lung disease. Lancet ;— Sinonasal alterations in computed tomography scans in cystic fibrosis: a literature review of observational studies. Int Forum Allergy Rhinol ;— Cystic fibrosis chronic rhinosinusitis: a comprehensive review. Am J Rhinol Allergy ;— Concordant genotype of upper and lower airways P aeruginosa and S aureus isolates in cystic fibrosis.

Prenatal detection of cystic fibrosis by ultrasonography: a retrospective study of more than pregnancies. J Med Genet ;—8. Intestinal obstruction syndromes in cystic fibrosis: meconium Ileus, distal intestinal obstruction syndrome, and constipation.

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Curr Gastroenterol Rep ;— Pancreatic pathophysiology in cystic fibrosis. J Pathol ;— Davis PB. Cystic fibrosis since Water and electrolytes in cervical mucus from patients with cystic fibrosis. Fertil Steril ;—6. Early intervention and prevention of lung disease in cystic fibrosis: a European consensus. J Cyst Fibros ;— Prevention of Pseudomonas aeruginosa infection in cystic fibrosis patients.

Int J Med Microbiol ;—7. Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: a European consensus. Airway inflammation in cystic fibrosis: molecular mechanisms and clinical implications. Failure to recover to baseline pulmonary function after cystic fibrosis pulmonary exacerbation.

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Treatment of lung infection in patients with cystic fibrosis: current and future strategies. Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis. Chichester, UK: Cochrane Library, Cystic fibrosis pulmonary guidelines: airway clearance therapies. Respir Care ;— Rhinosinusitis in cystic fibrosis, HNO ;— Nutrition in patients with cystic fibrosis: a European Consensus. Best practice guidance for the diagnosis and management of cystic fibrosis-associated liver disease.

J Cyst Fibros ;S29— Therapeutics based on stop codon readthrough. Annu Rev Genomics Hum Genet ;— De Boeck K. Cystic fibrosis: terminology and diagnostic algorithms. Newborn screening: a prime example for effective secondary prevention. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz ;— Bundesausschuss G. Nationaler screeningreport Deutschland , Sens B, Stern M. Bad Honnef: Hippocampus Verlag, Factors accounting for a missed diagnosis of cystic fibrosis after newborn screening.

A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis. Grundlegende Netzwerk-Dienstprogramme. Internetbrowser Add-on, das unfreies, nicht triviales JavaScript blockiert. Umsetzung des Kerberos 5-Netzwerk-Sicherheitssystems.

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Eine Scheme-Umsetzung mit integriertem Editor und Debugger. Unterschiede an Originalen anwenden, mit optionalen Sicherungen. Configure interface for Python-based packages. Eine einfache, effiziente und sichere objektorientierte Programmiersprache. The core concepts, strategies, and techniques of validation are explained by an international team of pre-eminent authorities …. This volume offers a unique and accessible overview of the most active fields in Stochastic Geometry, up to the frontiers of recent research.

This book discusses low power techniques for millimeter wave transmitter IC. Considerations for the front-end design are followed by several implementation examples in the 60GHz band in CMOS down to 28nm technology. Additionally, the design and ….