List of works - Dorota Sands

'Go for it, dream big, work hard and persist': A message to the next generation of CF leaders in recognition of International Women's Day 2020

scientific article published on 07 March 2020

A cross-sectional study of growth, nutritional status and body proportions in children and adolescents at a medical center specializing in the treatment of cystic fibrosis in Poland.

scientific article

A formulation of aerosolized tobramycin (Bramitob) in the treatment of patients with cystic fibrosis and Pseudomonas aeruginosa infection: a double-blind, placebo-controlled, multicenter study

scientific article published on 01 January 2007

A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patients.

scientific article

Aerosolized lancovutide in adolescents (≥12 years) and adults with cystic fibrosis - a randomized trial

scientific article published on 01 September 2020

Age of menarche in girls with cystic fibrosis

scientific article published in January 2010

Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis

scientific article published on 23 August 2019

An integrated LC-ESI-MS platform for quantitation of serum peptide ladders. Application for colon carcinoma study.

scientific article published on 30 July 2009

Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency

scientific article published on 01 September 2001

Analysis of hospital management of chronic respiratory diseases in light of the "Maps of Health Needs" project in Poland

scientific article published on 01 January 2020

Application of positive expiratory pressure PEP in cystic fibrosis patient inhalations

scientific article

Bilateral sweat tests with two different methods as a part of cystic fibrosis newborn screening (CF NBS) protocol and additional quality control

scientific article published on September 2010

Bone turnover markers, osteoprotegerin and RANKL cytokines in children with cystic fibrosis.

scientific article published in January 2013

Change in lung clearance index with microbiological status in children with cystic fibrosis

scientific article published on 05 March 2019

Clinical Phenotype and Genotype of Children with Borderline Sweat Test and Abnormal Nasal Epithelial Chloride Transport

scientific article published on 10 June 2010

Clinical characteristics of rare CFTR mutations causing cystic fibrosis in Polish population

scientific article published on 22 May 2020

Clinical outcomes for cystic fibrosis patients with Pseudomonas aeruginosa cross-infections

scientific article published on 26 September 2019

Clinical status and somatic development of patients with or without meconium ileus diagnosed through neonatal screening for cystic fibrosis.

scientific article published on January 2015

Comparison of health-related quality of life among children with cystic fibrosis and their parents in two Eastern European countries.

scientific article published on 5 May 2015

Comparison of two tobramycin nebuliser solutions: pharmacokinetic, efficacy and safety profiles of T100 and TNS.

scientific article published on 15 May 2014

Cystic fibrosis newborn screening enables diagnosis of elder siblings of recalled infants--additional benefit

scientific article published on 01 January 2010

Determinants of health-related quality of life in polish patients with CF - adolescents' and parents' perspectives.

scientific article published on January 2015

Diagnosing cystic fibrosis in newborn screening in Poland - 15 years of experience.

scientific article

Dietary pattern and its relationship between bone mineral density in girls and boys with cystic fibrosis - preliminary report

scientific article published on 01 January 2015

Early decline of pancreatic function in cystic fibrosis patients with class 1 or 2 CFTR mutations

scientific article published on 01 February 2005

Effect of selected factors associated with the clinical course of the disease on nutritional status in children with cystic fibrosis.

scientific article published on September 2014

End of Life: Have we got it right?

scientific article published on 04 December 2015

End of life care for patients with cystic fibrosis.

scientific article published on June 2011

European Cystic Fibrosis Society Standards of Care: Framework for the Cystic Fibrosis Centre ⬇️

scientific article published on May 2014

European best practice guidelines for cystic fibrosis neonatal screening

scholarly article by Carlo Castellani et al published May 2009 in Journal of Cystic Fibrosis

Evaluation of factors related to bone disease in Polish children and adolescents with cystic fibrosis

scientific article published on 3 June 2015

Fecal elastase-1 cut-off levels in the assessment of exocrine pancreatic function in cystic fibrosis

scientific article published on 01 December 2002

Gastroesophageal Reflux Disease in Children with Cystic Fibrosis

scientific article published on 01 January 2015

Impact of lipophilic antioxidants and level of antibodies against oxidized low-density lipoprotein in Polish children with phenylketonuria.

scientific article published on 6 September 2011

Influence of perfusate temperature on nasal potential difference.

scientific article published on 25 October 2012

Insights into the cystic fibrosis care in Eastern Europe: Results of survey

scientific article published on 19 April 2018

Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients.

scientific article

Lung Function Deterioration in School Children with Cystic Fibrosis

scientific article published on 06 August 2020

Metabolomic studies of Pseudomonas aeruginosa

scientific article published on 07 November 2019

Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis

scientific article

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results

scientific article

Newborn screening for cystic fibrosis: Polish 4 years' experience with CFTR sequencing strategy

scientific article

Physical development in children and adolescents with bronchial asthma

scientific article published on 21 February 2013

Possible metabolic switch between environmental and pathogenic Pseudomonas aeruginosa strains: 1H NMR based metabolomics study

scientific article published on 25 May 2020

Postural defects in children with cystic fibrosis - preliminary report.

scientific article published in January 2015

Pseudomonas aeruginosa eradicates Staphylococcus aureus by manipulating the host immunity.

scientific article published on 7 October 2014

Renal assessment in teenage patients with cystic fibrosis - preliminary report

scientific article published in January 2015

Serum lipase after secretin stimulation detects mild pancreatic involvement in cystic fibrosis.

scientific article

Silent lung zone - application of multi-breath nitrogen washout test (MBNW) in the diagnosis of small airways diseases in children - preliminary report based on literature and own experience

scientific article published in January 2017

Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki

scientific article published in September 2016

The activity of cathepsin D in saliva of cystic fibrosis patients

scientific article published on 01 January 2007

The clinical presentations of pulmonary aspergillosis in children with cystic fibrosis - preliminary report.

scientific article published on January 2015

The expansion and performance of national newborn screening programmes for cystic fibrosis in Europe.

scientific article published on 30 December 2016

Thiocyanate concentration in saliva of cystic fibrosis patients

scientific article

Transepithelial nasal potential difference (NPD) measurements in cystic fibrosis (CF)

scholarly article published 1 January 2013

Uncommon clinical presentation of cystic fibrosis in a patient homozygous for a rare CFTR mutation: a case report

scientific article published on 27 February 2020

Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID)

scientific article published on 27 November 2020

[A study evaluating the correlation between the phenotype and genotype among 65 cystic fibrosis patients]

scientific article published on 01 August 1995

[Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland]

scientific article published on 01 April 2000

[Assessment of selected bone metabolism marker concentrations in children with cystic fibrosis]

scientific article published on 01 April 2012

[Genetic risk markers of low bone mineral density in cystic fibrosis children]

scientific article published on 01 October 2010

[Long-term evaluation of effectiveness for selected chest physiotherapy methods used in the treatment of cystic fibrosis]

scientific article published on 01 July 2001

[Nutritional status and pulmonary function in children and adolescents with cystic fibrosis]

scholarly article by Wioleta Umławska et al published 1 January 2012 in Pediatric endocrinology, diabetes, and metabolism

[Prenatal diagnosis of cystic fibrosis in risk families in Poland--results of molecular analysis]

scientific article published on 01 October 2004

List of works by Dorota Sands

'Go for it, dream big, work hard and persist': A message to the next generation of CF leaders in recognition of International Women's Day 2020

A cross-sectional study of growth, nutritional status and body proportions in children and adolescents at a medical center specializing in the treatment of cystic fibrosis in Poland.

A formulation of aerosolized tobramycin (Bramitob) in the treatment of patients with cystic fibrosis and Pseudomonas aeruginosa infection: a double-blind, placebo-controlled, multicenter study

A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patients.

Aerosolized lancovutide in adolescents (≥12 years) and adults with cystic fibrosis - a randomized trial

Age of menarche in girls with cystic fibrosis

Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis

An integrated LC-ESI-MS platform for quantitation of serum peptide ladders. Application for colon carcinoma study.

Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency

Analysis of hospital management of chronic respiratory diseases in light of the "Maps of Health Needs" project in Poland

Application of positive expiratory pressure *PEP* in cystic fibrosis patient inhalations

Bilateral sweat tests with two different methods as a part of cystic fibrosis newborn screening (CF NBS) protocol and additional quality control

Bone turnover markers, osteoprotegerin and RANKL cytokines in children with cystic fibrosis.

Change in lung clearance index with microbiological status in children with cystic fibrosis

Clinical Phenotype and Genotype of Children with Borderline Sweat Test and Abnormal Nasal Epithelial Chloride Transport

Clinical characteristics of rare CFTR mutations causing cystic fibrosis in Polish population

Clinical outcomes for cystic fibrosis patients with Pseudomonas aeruginosa cross-infections

Clinical status and somatic development of patients with or without meconium ileus diagnosed through neonatal screening for cystic fibrosis.

Comparison of health-related quality of life among children with cystic fibrosis and their parents in two Eastern European countries.

Comparison of two tobramycin nebuliser solutions: pharmacokinetic, efficacy and safety profiles of T100 and TNS.

Cystic fibrosis newborn screening enables diagnosis of elder siblings of recalled infants--additional benefit

Determinants of health-related quality of life in polish patients with CF - adolescents' and parents' perspectives.

Diagnosing cystic fibrosis in newborn screening in Poland - 15 years of experience.

Dietary pattern and its relationship between bone mineral density in girls and boys with cystic fibrosis - preliminary report

Early decline of pancreatic function in cystic fibrosis patients with class 1 or 2 CFTR mutations

Effect of selected factors associated with the clinical course of the disease on nutritional status in children with cystic fibrosis.

End of Life: Have we got it right?

End of life care for patients with cystic fibrosis.

European Cystic Fibrosis Society Standards of Care: Framework for the Cystic Fibrosis Centre ⬇️

European best practice guidelines for cystic fibrosis neonatal screening

Evaluation of factors related to bone disease in Polish children and adolescents with cystic fibrosis

Fecal elastase-1 cut-off levels in the assessment of exocrine pancreatic function in cystic fibrosis

Gastroesophageal Reflux Disease in Children with Cystic Fibrosis

Impact of lipophilic antioxidants and level of antibodies against oxidized low-density lipoprotein in Polish children with phenylketonuria.

Influence of perfusate temperature on nasal potential difference.

Insights into the cystic fibrosis care in Eastern Europe: Results of survey

Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients.

Lung Function Deterioration in School Children with Cystic Fibrosis

Metabolomic studies of Pseudomonas aeruginosa

Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results

Newborn screening for cystic fibrosis: Polish 4 years' experience with CFTR sequencing strategy

Physical development in children and adolescents with bronchial asthma

Possible metabolic switch between environmental and pathogenic Pseudomonas aeruginosa strains: 1H NMR based metabolomics study

Postural defects in children with cystic fibrosis - preliminary report.

Pseudomonas aeruginosa eradicates Staphylococcus aureus by manipulating the host immunity.

Renal assessment in teenage patients with cystic fibrosis - preliminary report

Serum lipase after secretin stimulation detects mild pancreatic involvement in cystic fibrosis.

Silent lung zone - application of multi-breath nitrogen washout test (MBNW) in the diagnosis of small airways diseases in children - preliminary report based on literature and own experience

Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki

The activity of cathepsin D in saliva of cystic fibrosis patients

The clinical presentations of pulmonary aspergillosis in children with cystic fibrosis - preliminary report.

The expansion and performance of national newborn screening programmes for cystic fibrosis in Europe.

Thiocyanate concentration in saliva of cystic fibrosis patients

Transepithelial nasal potential difference (NPD) measurements in cystic fibrosis (CF)

Uncommon clinical presentation of cystic fibrosis in a patient homozygous for a rare CFTR mutation: a case report

Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID)

[A study evaluating the correlation between the phenotype and genotype among 65 cystic fibrosis patients]

[Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland]

[Assessment of selected bone metabolism marker concentrations in children with cystic fibrosis]

[Genetic risk markers of low bone mineral density in cystic fibrosis children]

[Long-term evaluation of effectiveness for selected chest physiotherapy methods used in the treatment of cystic fibrosis]

[Nutritional status and pulmonary function in children and adolescents with cystic fibrosis]

[Prenatal diagnosis of cystic fibrosis in risk families in Poland--results of molecular analysis]

Application of positive expiratory pressure PEP in cystic fibrosis patient inhalations