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[PDF] Top 20 Micropuncture studies of the sweat formation in cystic fibrosis patients

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Micropuncture studies of the sweat formation in cystic fibrosis patients

Micropuncture studies of the sweat formation in cystic fibrosis patients

... by sweat glands during secretion was ...both patients and ...precursor sweat and plasma in the present ...of sweat secretion this finding supports the hypothesis that active solute transport ... See full document

9

STUDIES IN THE PHYSIOLOGY OF SWEATING IN CYSTIC FIBROSIS

STUDIES IN THE PHYSIOLOGY OF SWEATING IN CYSTIC FIBROSIS

... Two types of experimental sweat gland fatigue with repeated injections of methacholine, and the observed frequencies in patients with cystic. fibrosis and in controls[r] ... See full document

11

Is sweat testing for cystic fibrosis feasible in patients with down syndrome?

Is sweat testing for cystic fibrosis feasible in patients with down syndrome?

... of sweat that was available for ...further studies, it would be worthwhile to have just one analysis but the double amount of sweat to gener- ate more data ... See full document

8

Non ∆F 508 Cystic Fibrosis Diagnosed at Age 50 in an African American Male: A Primary Care Perspective

Non ∆F 508 Cystic Fibrosis Diagnosed at Age 50 in an African American Male: A Primary Care Perspective

... their sweat chloride levels varies from normal to elevated, confounding the use of sweat chloride levels as the pathognomonic feature of CF ...with cystic fibrosis associated bacteria should ... See full document

5

A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis

A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis

... German patients with CF uncovered four cases with the nonsense mutation E92X, a G-->T transversion that creates a termination codon and affects the first base of exon 4 of the CFTR ...CF patients ... See full document

9

A PATCH TEST FOR CHLORIDE IN SWEAT AS A SIMPLE SCREENING METHOD FOR DETECTING CYSTIC FIBROSIS OF THE PANCREAS

A PATCH TEST FOR CHLORIDE IN SWEAT AS A SIMPLE SCREENING METHOD FOR DETECTING CYSTIC FIBROSIS OF THE PANCREAS

... By con- trast, approximately 10 to 15% of patients with cystic fibrosis have normal values for duodenal tnypsin.16 Using the data of di Sant’Agnese2 on electrolytes in sweat, 50 meq/l co[r] ... See full document

9

STUDIES IN CYSTIC FIBROSIS

STUDIES IN CYSTIC FIBROSIS

... During this 20-year study period a num- ber of complications led to hospital admis- sion. Of 63 patients in Group A, 28 were admitted to the hospital for a total of 50 hos- pitalizations[r] ... See full document

11

RELATING MUCUS, CALCIUM, AND SWEAT IN A NEW CONCEPT OF CYSTIC FIBROSIS

RELATING MUCUS, CALCIUM, AND SWEAT IN A NEW CONCEPT OF CYSTIC FIBROSIS

... flow of water anti small ions, that CF is a disease in which mucus is hvperpermeabie and fails to per- form this function adequatelY, and that this failure is caused by an excess secreti[r] ... See full document

18

SWEAT CHLORIDE CONCENTRATION IN CHILDREN WITH ALLERGY AND WITH CYSTIC FIBROSIS OF THE PANCREAS

SWEAT CHLORIDE CONCENTRATION IN CHILDREN WITH ALLERGY AND WITH CYSTIC FIBROSIS OF THE PANCREAS

... Sixty-six subjects from the Pediatric and Allergy Services of Walter Reed General Hospital were divided into the following study groups: Group I: six children with cystic fibrosis; Group[r] ... See full document

7

Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis

Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis

... Cystic fibrosis (CF) is a common autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator ...of patients with CF with five escalating doses of up to 10(10) ... See full document

9

STUDIES IN CYSTIC FIBROSIS

STUDIES IN CYSTIC FIBROSIS

... STUDIES IN CYSTIC FIBROSIS: A Report on Sixty-Five Patients over 17 Years of. Services[r] ... See full document

13

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

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

... of patients expectorate sputum daily and 85% ...in patients who develop respiratory disease early in life due to heightened compliancy of the chest wall in ...all patients develop clubbing of the ... See full document

209

A European regulatory perspective on cystic fibrosis: current treatments, trends in drug development and translational challenges for CFTR modulators

A European regulatory perspective on cystic fibrosis: current treatments, trends in drug development and translational challenges for CFTR modulators

... of patients aged ⩾ 2 years with G551D, the main gating mutation, accounting for ∼ 4 – 5% of the CF patient population [23], and an additional eight other gating mutations (G1244E, G1349D, G178R, G551S, S1251N, ... See full document

11

Sweat Chloride Concentrations in Infants Homozygous or Heterozygous for F508 Cystic Fibrosis

Sweat Chloride Concentrations in Infants Homozygous or Heterozygous for F508 Cystic Fibrosis

... A total of 725 infants were evaluated in this study, including 481 with newborn screening test results positive for CF; the other infants had been referred to the University of Wisconsin[r] ... See full document

7

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

... of patients with CF has improved sub- stantially over the last three decades ...the patients still die in early adulthood [39], the life expectancy for patients has increased from 31 to 37 years over ... See full document

7

Effect of ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis patients with G551D-CFTR

Effect of ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis patients with G551D-CFTR

... Unlike sweat chloride measurements, or symptom scores, the change in WL and central lung MCC was significantly related to the observed change in FEV 1 , though it only explained ~25% of the lung function ... See full document

11

A NEW SCREENING TEST FOR CYSTIC FIBROSIS

A NEW SCREENING TEST FOR CYSTIC FIBROSIS

... Sabinga, Maarten S., and Barbero, Giuhio J.: Sweat sodium content and flow rate in cystic fibrosis of the pancreas. Sabinga, Nlaarten S., and Barbero, Giulio J.:[r] ... See full document

6

Pediatric Cystic Fibrosis Sputum Can Be Chemically Dynamic, Anoxic, and Extremely Reduced Due to Hydrogen Sulfide Formation

Pediatric Cystic Fibrosis Sputum Can Be Chemically Dynamic, Anoxic, and Extremely Reduced Due to Hydrogen Sulfide Formation

... insufficiency, cystic fibrosis-related diabetes, gastroesoph- ageal diseases, CF liver disease, or allergic bronchopulmonary Aspergillus infection, hemoglobin A1c [HbA1c] levels, IgE levels, blood glucose ... See full document

15

Calcium and Magnesium Concentration in Sweat of Normal Children and Patients With Cystic Fibrosis

Calcium and Magnesium Concentration in Sweat of Normal Children and Patients With Cystic Fibrosis

... related in various systems as the intestinal epithelium or the renal tubule, it became of in- terest to measure with great accuracy both cal- cium and magnesium in the sweat of normal ch[r] ... See full document

5

A TEST FOR CONCENTRATION OF ELECTROLYTES IN SWEAT IN CYSTIC FIBROSIS OF THE PANCREAS UTILIZING PILOCARPINE BY IONTOPHORESIS

A TEST FOR CONCENTRATION OF ELECTROLYTES IN SWEAT IN CYSTIC FIBROSIS OF THE PANCREAS UTILIZING PILOCARPINE BY IONTOPHORESIS

... A method of performing the test for chlo- ride or sodium in the sweat of patients with. cystic fibrosis of the pancreas is presented[r] ... See full document

7

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