43 results on '"Gartner S"'
Search Results
2. 731 CFTR-related metabolic syndrome (CRMS)/cystic fibrosis screen positive, inconclusive diagnosis (CFSPID): experience during 18 years.
3. Inconclusive diagnosis after a positive newborn bloodspot screening result for cystic fibrosis; clarification of the harmonised international definition
4. Age, apolipoprotein E4, and the risk of HIV dementia: the Hawaii Aging with HIV Cohort
5. P088 Ventilation inhomogeneity in patients with cystic fibrosis and pancreatic sufficiency and insufficiency
6. P019 Inconclusive Cystic Fibrosis Positive Neonatal Screening (CFSPID): clinical outcomes
7. WS06.1 Defining key outcomes to evaluate performance of newborn screening programmes for cystic fibrosis
8. WS20-1 An international survey to determine understanding of the designation of infants with an inconclusive diagnosis after newborn bloodspot screening for cystic fibrosis
9. WS07-6 Clinical characteristics of patients with normal spirometry - not as normal as it would seem!
10. 20 years experience with newborn screening for cystic fibrosis in Catalonia
11. 425 The European cystic fibrosis patient registry in Spain: the long and winding road that leads to a National Registry Normal
12. 412 Spanish multicentre registry-based study on the phenotype of patients with cystic fibrosis carrying the V232D (c.695T>A) mutation
13. 219 Elevated prostaglandins urine levels is associated with disease severity in cystic fibrosis patients
14. 197 Bacteriophages and antibiotic resistance in cystic fibrosis
15. 24 Deep intronic mutations in cystic fibrosis patients detected by next generation sequencing
16. EPS2.6 Prevalence and characteristics of attention deficit hyperactivity disorder in patients with cystic fibrosis
17. WS02.1 Nasal nitric oxide levels as a useful additional tool to categorize patients with cystic fibrosis screen positive inconclusive diagnosis (CFSPID)
18. 2 Next Generation Sequencing genotyping project in Spanish cystic fibrosis patients with uncharacterized CFTR mutations
19. ePS06.7 Factors associated with failure to eradicate first or newly acquired Pseudomonas aeruginosa in patients with CF
20. 14 Updated survey of newborn screening for cystic fibrosis
21. 20 Inconclusive diagnosis following newborn screening for cystic fibrosis (CF): clinical outcomes in 56 infants from three Spanish CF centres
22. The German national consensus on wound documentation and outcomes: Rationale, working programme and current status.
23. 188 Association of lung function with adherence to inhaled antibiotic treatment in patients with cystic fibrosis (CF)
24. 174 Quantification of major urinary metabolite of PGE2 in cystic fibrosis (CF) patients: Correlation with parameters of disease severity
25. 21 Genotype–phenotype correlation of CFTR p.Leu206Trp mutation in 22 paediatric and adult cystic fibrosis (CF) patients
26. Valor del óxido nítrico nasal en el diagnóstico de la discinesia ciliar primaria.
27. Inducción de esputo en niños: desarrollo técnico.
28. Protocolo de diagnóstico y seguimiento de los pacientes con fibrosis quística.
29. 10 CFTR p.Leu206Trp mutation: genotype-phenotype correlation in 12 Spanish cystic fibrosis (CF) patients
30. 219* Monitoring cystic fibrosis patient's adherence to nebulized antibiotics with the i-neb adaptive aerosol delivery (AAD) system
31. Validation of ISEsweat: a new device for the direct measurement of sweat chloride concentration (SCC) for the diagnosis of cystic fibrosis
32. Neonatal screening for cystic fibrosis in Cataluña, Spain: 10 years of experience
33. Cribado neonatal para la fibrosis quística.
34. 97 Early treatment of first Pseudomonas aeruginosa isolation in Cystic Fibrosis patients
35. 188 Association of lung function with adherence to inhaled antibiotic treatment in patients with cystic fibrosis (CF).
36. 174 Quantification of major urinary metabolite of PGE2 in cystic fibrosis (CF) patients: Correlation with parameters of disease severity.
37. Iridium anomaly at the Cretaceous-Tertiary boundary in Texas
38. Late Pleistocene calcareous nannofossils in the caribbean and their interoceanic correlation
39. Neogene sedimentation on the Blake Plateau and the emergence of the Central American isthmus
40. Provenance and accumulation rates of opaline silica, Al, Ti, Fe, Mn, Cu, Ni and Co in Pacific pelagic sediments
41. Structure of anisole derivatives by total neutron and X-ray scattering: Evidences of weak C–H⋯O and C–H⋯π interactions in the liquid state
42. Antimicrobial therapy for pulmonary pathogenic colonisation and infection by Pseudomonas aeruginosa in cystic fibrosis patients.
43. Lung transplantation in young infants with interstitial pneumonia
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