Found: 522
Select item for more details and to access through your institution.
Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification.
- Published in:
- 2017
- By:
- Publication type:
- journal article
The development of bronchiectasis on chest computed tomography in children with cystic fibrosis: can pre-stages be identified?
- Published in:
- 2016
- By:
- Publication type:
- journal article
Assessment of lung disease in children with cystic fibrosis using hyperpolarized 3-Helium MRI: comparison with Shwachman score, Chrispin-Norman score and spirometry.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Characterization of macrolide resistance genes in Haemophilus influenzae isolated from children with cystic fibrosis.
- Published in:
- Journal of Antimicrobial Chemotherapy (JAC), 2011, v. 66, n. 1, p. 100, doi. 10.1093/jac/dkq425
- By:
- Publication type:
- Article
Linezolid-resistant ST36 methicillin-resistant Staphylococcus aureus associated with prolonged linezolid treatment in two paediatric cystic fibrosis patients.
- Published in:
- Journal of Antimicrobial Chemotherapy (JAC), 2010, v. 65, n. 3, p. 442, doi. 10.1093/jac/dkp494
- By:
- Publication type:
- Article
Ion Channels: Fluid control.
- Published in:
- Nature Reviews Drug Discovery, 2003, v. 2, n. 2, p. 94, doi. 10.1038/nrd1021
- By:
- Publication type:
- Article
The concentration of calprotectin in the stools of children with diagnosed cystic fibrosis.
- Published in:
- Gastroenterology Review / Przegląd Gastroenterologiczny, 2017, v. 12, n. 1, p. 38, doi. 10.5114/pg.2016.58897
- By:
- Publication type:
- Article
Respiratory syncytial virus prophylaxis in cystic fibrosis: the Canadian registry of palivizumab data (2005-2016).
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2018, v. 37, n. 7, p. 1345, doi. 10.1007/s10096-018-3256-0
- By:
- Publication type:
- Article
Virulence factor expression patterns in <i>Pseudomonas aeruginosa</i> strains from infants with cystic fibrosis.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2013, v. 32, n. 12, p. 1583, doi. 10.1007/s10096-013-1916-7
- By:
- Publication type:
- Article
1587. Comparative In Vitro Antipseudomonal Activity of Ceftolozane/Tazobactam Against Pseudomonas aeruginosa Isolates from Children with Cystic Fibrosis.
- Published in:
- Open Forum Infectious Diseases, 2019, v. 6, p. S579, doi. 10.1093/ofid/ofz360.1451
- By:
- Publication type:
- Article
Influenza Virus Detection Following Administration of Live-Attenuated Intranasal Influenza Vaccine in Children With Cystic Fibrosis and Their Healthy Siblings.
- Published in:
- Open Forum Infectious Diseases, 2016, v. 3, n. 4, p. 1, doi. 10.1093/ofid/ofw187
- By:
- Publication type:
- Article
Evaluation of Patients Referred Following Cystic Fibrosis Newborn Screening: Four Year Experience of A Single-Center.
- Published in:
- Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2019, v. 13, n. 4, p. 270, doi. 10.12956/tchd.533602
- By:
- Publication type:
- Article
THE RELATIONSHIP BETWEEN FATIGUE AND PULMONARY FUNCTIONS IN CHILDREN AND ADOLESCENTS WITH CYSTIC FIBROSIS.
- Published in:
- Respirology, 2019, v. 24, p. 233, doi. 10.1111/resp.13700_433
- Publication type:
- Article
ASSOCIATIONS OF PERIPHERAL MUSCLE STRENGTH, PULMONARY FUNCTION AND FUNCTIONAL CAPACITY IN CHILDREN AND ADOLESCENTS WITH CYSTIC FIBROSIS.
- Published in:
- Respirology, 2019, v. 24, p. 233, doi. 10.1111/resp.13700_432
- Publication type:
- Article
Angiomatoid fibrous histiocytoma with cystic structures of sweat duct origin.
- Published in:
- Pathology International, 2007, v. 57, n. 8, p. 513, doi. 10.1111/j.1440-1827.2007.02133.x
- By:
- Publication type:
- Article
In vitro Activity of Ceftolozane/Tazobactam Alone or with an Aminoglycoside Against Multi-Drug-Resistant Pseudomonas aeruginosa from Pediatric Cystic Fibrosis Patients.
- Published in:
- 2017
- By:
- Publication type:
- Report
A comparison of food group variety between toddlers with and without cystic fibrosis.
- Published in:
- Journal of Human Nutrition & Dietetics, 2004, v. 17, n. 6, p. 523, doi. 10.1111/j.1365-277X.2004.00560.x
- By:
- Publication type:
- Article
Taste preference for oral calorie supplements in children with cystic fibrosis, healthy children and healthy adults.
- Published in:
- Journal of Human Nutrition & Dietetics, 1999, v. 12, n. 4, p. 301, doi. 10.1046/j.1365-277X.1999.00167.x
- By:
- Publication type:
- Article
Current Literature in Human Nutrition and Dietetics.
- Published in:
- 1999
- Publication type:
- Abstract
Dyadic Adjustment and Spiritual Activities in Parents of Children with Cystic Fibrosis.
- Published in:
- Religions, 2014, v. 5, n. 2, p. 385, doi. 10.3390/rel5020385
- By:
- Publication type:
- Article
Gray hair and acrodermatitis enteropathica-like dermatitis: an unexpected presentation of cystic fibrosis.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Investigation for cystic fibrosis in infants with jejunoileal atresia in the Netherlands: a 35-year experience with 114 cases.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Heroin withdrawal leads to metabolic alkalosis in an infant with cystic fibrosis.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Myelodysplastic features in an infant with cystic fibrosis presenting with anaemia, oedema and failure to thrive.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Rapidly developing Cushing syndrome in a 4-year-old patient during combined treatment with itraconazole and inhaled budesonide.
- Published in:
- European Journal of Pediatrics, 2003, v. 162, n. 7/8, p. 488, doi. 10.1007/s00431-003-1233-8
- By:
- Publication type:
- Article
Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Skinfold measurements in children with cystic fibrosis: monitoring fat-free mass and exercise effects.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Essential fatty acid deficiency in well nourished young cystic fibrosis patients.
- Published in:
- European Journal of Pediatrics, 1997, v. 156, n. 12, p. 952, doi. 10.1007/s004310050750
- By:
- Publication type:
- Article
Faecal elastase 1 in children with cystic fibrosis.
- Published in:
- European Journal of Pediatrics, 1997, v. 156, n. 10, p. 770, doi. 10.1007/s004310050709
- By:
- Publication type:
- Article
Cystic fibrosis mutations in Romania.
- Published in:
- European Journal of Pediatrics, 1997, v. 156, n. 3, p. 212, doi. 10.1007/s004310050586
- By:
- Publication type:
- Article
Maternal psychiatric disorders in pediatric inflammatory bowel disease and cystic fibrosis.
- Published in:
- Child Psychiatry & Human Development, 1994, v. 25, n. 1, p. 45, doi. 10.1007/BF02251099
- By:
- Publication type:
- Article
Cystic Fibrosis.
- Published in:
- JAMA: Journal of the American Medical Association, 2000, v. 284, n. 14, p. 1884
- Publication type:
- Article
ANTIMICROBIAL SUSCEPTIBILITY OF PSEUDOMONAS AERUGINOSA ISOLATED FROM SPUTUM OF PAEDIATRIC PATIENTS WITH CYSTIC FIBROSIS.
- Published in:
- Albanian Journal of Natural & Technical Sciences, 2009, v. 26, n. 2, p. 127
- By:
- Publication type:
- Article
Salt depletion syndrome as the initial presentation of cystic fibrosis in a toddler with the rare p.Ala309Gly (A309G) CFTR variant.
- Published in:
- Clinical Genetics, 2016, v. 90, n. 2, p. 186, doi. 10.1111/cge.12733
- By:
- Publication type:
- Article
Refining the continuum of CFTR-associated disorders in the era of newborn screening.
- Published in:
- Clinical Genetics, 2016, v. 89, n. 5, p. 539, doi. 10.1111/cge.12711
- By:
- Publication type:
- Article
Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 1, p. 42, doi. 10.1034/j.1399-0004.2001.590107.x
- By:
- Publication type:
- Article
Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 318, doi. 10.1034/j.1399-0004.1999.560410.x
- By:
- Publication type:
- Article
Homeostatic interactions: a longitudinal study of biological, psychosocial and family variables in children with cystic fibrosis.
- Published in:
- Journal of Family Therapy, 1996, v. 18, n. 2, p. 123, doi. 10.1111/j.1467-6427.1996.tb00040.x
- By:
- Publication type:
- Article
Ocena stanu odżywienia oraz czynności płuc dzieci i młodzieży z mukowiscydozą.
- Published in:
- Pediatric Endocrinology, Diabetes & Metabolism, 2012, v. 18, n. 4, p. 137
- By:
- Publication type:
- Article
Causes of `delayed' respiratory distress in infancy.
- Published in:
- 1978
- By:
- Publication type:
- journal article
Predictors of Malnutrition in Children with Cystic Fibrosis.
- Published in:
- Indian Pediatrics, 2019, v. 56, n. 10, p. 825, doi. 10.1007/s13312-019-1607-2
- By:
- Publication type:
- Article
Aquagenic Wrinkling of Skin: A Screening Test for Cystic Fibrosis.
- Published in:
- Indian Pediatrics, 2019, v. 56, n. 2, p. 109, doi. 10.1007/s13312-019-1481-y
- By:
- Publication type:
- Article
News in Brief.
- Published in:
- Indian Pediatrics, 2017, v. 54, n. 12, p. 1060, doi. 10.1007/s13312-017-1214-z
- By:
- Publication type:
- Article
Pulmonary exacerbations and clinical outcomes in a longitudinal cohort of infants and preschool children with cystic fibrosis.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Assessment of serology and spirometry and the combination of both to complement microbiological isolation for earlier detection of Pseudomonas aeruginosa infection in children with cystic fibrosis.
- Published in:
- BMC Pulmonary Medicine, 2016, v. 16, p. 1, doi. 10.1186/s12890-016-0327-9
- By:
- Publication type:
- Article
Effect of Habitual Activity, Lung Function, and Nutritional Measurements on 3-Minute Step Test Performance in Children with Cystic Fibrosis.
- Published in:
- Cardiopulmonary Physical Therapy Journal (American Physical Therapy Association, Cardiopulmonary Section), 2007, v. 18, n. 1, p. 15, doi. 10.1097/01823246-200718010-00003
- By:
- Publication type:
- Article
The Influence of Lean Body Mass and Leg Muscle Strength on 6-Minute Walk Test Performance in Children with Cystic Fibrosis.
- Published in:
- Cardiopulmonary Physical Therapy Journal (American Physical Therapy Association, Cardiopulmonary Section), 2005, v. 16, n. 3, p. 5, doi. 10.1097/01823246-200516030-00002
- By:
- Publication type:
- Article
When the Cystic Fibrosis Label Does Not Fit: A Modified Uncertainty Theory.
- Published in:
- Qualitative Health Research, 2010, v. 20, n. 2, p. 209, doi. 10.1177/1049732309356285
- By:
- Publication type:
- Article
Salivary Protease Activity in Children with Cystic Fibrosis.
- Published in:
- Meandros Medical & Dental Journal, 2023, v. 24, n. 1, p. 19, doi. 10.4274/meandros.galenos.2021.07078
- By:
- Publication type:
- Article
Intestinal Inflammation in Children with Cystic Fibrosis Is Associated with Crohn's-Like Microbiota Disturbances.
- Published in:
- Journal of Clinical Medicine, 2019, v. 8, n. 5, p. 645, doi. 10.3390/jcm8050645
- By:
- Publication type:
- Article