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[PDF] Top 20 Early Diagnosis of Cystic Fibrosis

Has 10000 "Early Diagnosis of Cystic Fibrosis" found on our website. Below are the top 20 most common "Early Diagnosis of Cystic Fibrosis".

Early Diagnosis of Cystic Fibrosis

Early Diagnosis of Cystic Fibrosis

... of diagnosis is in the best interest of children with CF, ie, early recognition through screening or de- layed diagnosis by traditional methods? It should be pointed out that this question takes on ... See full document

9

Early Diagnosis of Cystic Fibrosis: To Screen or Not To Screen—An Important Question

Early Diagnosis of Cystic Fibrosis: To Screen or Not To Screen—An Important Question

... This would clearly be advantageous since population statistics suggest that many patients with CF die without their disease ever having been diagnosed.6 Since CF is poten- tially lethal [r] ... See full document

5

Early Diagnosis of Cystic Fibrosis in the Newborn Period and Risk of Pseudomonas aeruginosa Acquisition in the First 10 Years of Life: A Registry-Based Longitudinal Study

Early Diagnosis of Cystic Fibrosis in the Newborn Period and Risk of Pseudomonas aeruginosa Acquisition in the First 10 Years of Life: A Registry-Based Longitudinal Study

... National Cystic Fibrosis Patient ...asymptomatic diagnosis)—<6 weeks, by pre/neonatal screening, genotype, family history (n ⴝ 157); ESD (early symptomatic diagnosis) (n ⴝ 227); LAD ... See full document

8

Early Versus Late Diagnosis: Psychological Impact on Parents of Children With Cystic Fibrosis

Early Versus Late Diagnosis: Psychological Impact on Parents of Children With Cystic Fibrosis

... an early diagnosis in our study did not significantly have more confidence in the medical profession before diagnosis than fathers with a late ...diagnosed early had significantly fewer ... See full document

7

Cystic fibrosis overview and update on infant care

Cystic fibrosis overview and update on infant care

... CF diagnosis is now occurring at an earlier age than before ...for early onset of malnutrition [38], airway inflammation, and structural changes in infants with ...The early diagnosis group ... See full document

10

European Cystic Fibrosis Society standards of care: best practice guidelines

European Cystic Fibrosis Society standards of care: best practice guidelines

... at diagnosis and therefore have the potential to enjoy an excellent quality of life and an even greater life expectancy than was seen ...screening, diagnosis, pre-emptive treatment of lung disease, ... See full document

20

STUDIES ON THE LABORATORY DIAGNOSIS OF CYSTIC FIBROSIS OF THE PANCREAS

STUDIES ON THE LABORATORY DIAGNOSIS OF CYSTIC FIBROSIS OF THE PANCREAS

... A study of 78 patients with cystic fibrosis of the pancreas was carried out to determine whether gelatin-liquefying bacteria may be responsible for gelatin liquefaction of gelatin film b[r] ... See full document

10

Saliva as a potential tool for cystic fibrosis diagnosis

Saliva as a potential tool for cystic fibrosis diagnosis

... CF diagnosis, further stud- ies need to be carried out to evaluate this hypothesis, given that the methods for assessing salivary parameters differ, which hinders ... See full document

7

A prospective pilot study of home monitoring in adults with cystic fibrosis (HOME CF) : protocol for a randomised controlled trial

A prospective pilot study of home monitoring in adults with cystic fibrosis (HOME CF) : protocol for a randomised controlled trial

... tecting early pulmonary exacerbations has the potential not only to improve lung health, but also to improve quality of life and reduce expenditure from the patient and healthcare provider ... See full document

8

Utilization of Prenatal Diagnosis For Cystic Fibrosis Over the Past Seven Years

Utilization of Prenatal Diagnosis For Cystic Fibrosis Over the Past Seven Years

... Utilization of Prenatal Diagnosis For Cystic Fibrosis Over the Past Seven Years. http://pediatrics.aappublications.org/content/94/1/13[r] ... See full document

6

Contrast-enhanced ultrasonography of the pancreas shows impaired perfusion in pancreas insufficient cystic fibrosis patients

Contrast-enhanced ultrasonography of the pancreas shows impaired perfusion in pancreas insufficient cystic fibrosis patients

... During a 4-year period (December 2010–May 2014), CF patients aged > 15 years attending regular follow up in the CF clinic were offered a detailed evaluation of the pancreas in this prospective observational study. The ... See full document

8

Molecular screening of R117H mutation in non caucasian cystic fibrosis patients in the north of Iran

Molecular screening of R117H mutation in non caucasian cystic fibrosis patients in the north of Iran

... genotypes and phenotypes in CF patients, diagnosis and follow up of R117H may be necessary. However, many mutations occuring in CFTR gene may cause variable clinical phenotypes and may not be predictable due to ... See full document

6

Inconclusive Diagnosis of Cystic Fibrosis After Newborn Screening

Inconclusive Diagnosis of Cystic Fibrosis After Newborn Screening

... The weight and height of subjects with CF were significantly lower compared with subjects with CFSPID by the time of fi rst assessment, even though birth weight was not different. This finding suggests that a suboptimal ... See full document

11

Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene

Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene

... In the clinical case reported here, sweat tests and genetic analysis were inconclusive and CFTR functional testing, in accordance with a standard method (NPD), was car- ried out. In addition, we evaluated a possible exon ... See full document

7

Antibiotic Susceptibility of Pseudomonas Aeruginosa Isolated from Cystic Fibrosis Patients

Antibiotic Susceptibility of Pseudomonas Aeruginosa Isolated from Cystic Fibrosis Patients

... 9.Starner TD1, McCray PB Jr; American College of Physicians; American Physiological Society. Pathogenesis of Early Lung Disease in Cystic Fibrosis: A Window of Opportunity To Eradicate Bacteria. Ann ... See full document

7

EARLY DETECTION OF PULMONARY FUNCTION ABNORMALITIES IN CYSTIC FIBROSIS

EARLY DETECTION OF PULMONARY FUNCTION ABNORMALITIES IN CYSTIC FIBROSIS

... lung volumes, flow rates and airway conductance, diffusing capacity and mixing efficiency were nor- mal... A significant decrease in arterial oxygen ten- sion was found together with a s[r] ... See full document

10

SECRETIN TESTS WITH BILUMEN GASTRODUODENAL DRAINAGE IN INFANTS AND CHILDREN

SECRETIN TESTS WITH BILUMEN GASTRODUODENAL DRAINAGE IN INFANTS AND CHILDREN

... Diagnosis of cystic fibrosis of the pancreas depends largely on the trypsin determination.15 Without secretin, the coefficient of variation of the trypsin concentration was 42%.. With se[r] ... See full document

8

What Follows Newborn Screening? An Evaluation of a Residential Education Program for Parents of Infants With Newly Diagnosed Cystic Fibrosis

What Follows Newborn Screening? An Evaluation of a Residential Education Program for Parents of Infants With Newly Diagnosed Cystic Fibrosis

... the diagnosis of CF, 2) the perceived value of the 5-day assessment and education program, and 3) the perceived advantages and disadvantages of the resi- dential component (Care-By-Parent unit) of the ...child’s ... See full document

8

Cystic fibrosis and the relevance of the whole body vibration exercises in oscillating platforms: a short review

Cystic fibrosis and the relevance of the whole body vibration exercises in oscillating platforms: a short review

... The prognosis of patients with CF has improved sub- stantially over the last three decades [37]. Although the majority of the patients still die in early adulthood [39], the life expectancy for patients has ... See full document

7

Microbiological aspects of infection with Pseudomonas aeruginosa in patients with cystic fibrosis

Microbiological aspects of infection with Pseudomonas aeruginosa in patients with cystic fibrosis

... disease early in life due to heightened compliancy of the chest wall in ...fingers early in the course of the disease, irrespective of the severity of lung ... See full document

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