D. Sands

发表

Metabolomic studies of Pseudomonas aeruginosa

Sławomir Jabłoński, M. Łukaszewicz, P. Młynarz, 2019, World Journal of Microbiology and Biotechnology.

Serum Lipase After Secretin Stimulation Detects Mild Pancreatic Involvement in Cystic Fibrosis

K. Herzig, J. Walkowiak, A. Galli-Tsinopoulou, 2004, Journal of pediatric gastroenterology and nutrition.

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

J. Ostrowski, E. Hennig, M. Dadlez, 2009, Proteomics. Clinical applications.

Long-term amikacin liposome inhalation suspension in cystic fibrosis patients with chronic P. aeruginosa infection.

J. Clancy, A. Quittner, M. Konstan, 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

J. Clancy, A. Quittner, M. Konstan, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

A Formulation of Aerosolized Tobramycin (Bramitob®) in the Treatment of Patients with Cystic Fibrosis and Pseudomonas aeruginosa Infection

A. Chuchalin, H. Mazurek, E. Csiszér, 2007, Paediatric drugs.

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

Sławomir Jabłoński, M. Łukaszewicz, P. Młynarz, 2020, Journal of pharmaceutical and biomedical analysis.

Physical development in children and adolescents with bronchial asthma

D. Sands, W. Umławska, G. Gąszczyk, 2013, Respiratory Physiology & Neurobiology.

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

G. Bellon, F. Ratjen, E. Eber, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

A. Sobczyńska-Tomaszewska, J. Walkowiak, T. Mazurczak, 2012, European Journal of Human Genetics.

Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forward.

M. Claustres, I. Sermet-Gaudelus, E. Girodon, 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

J. Walkowiak, A. Lipowicz, D. Sands, 2015, Advances in medical sciences.

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

J. Gajewska, T. Laskowska-Klita, D. Sands, 2013, Advances in medical sciences.

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

J. Moczko, S. Drzymała-Czyż, J. Walkowiak, 2012, European Journal of Human Genetics.

Lung Clearance Index in Children with Cystic Fibrosis during Pulmonary Exacerbation

J. Milczewska, D. Sands, M. Postek, 2021, Journal of clinical medicine.

Lung function deterioration in school children with cystic fibrosis

J. Milczewska, D. Sands, M. Postek, 2020, Pediatric pulmonology.

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

T. Wołkowicz, J. Milczewska, D. Sands, 2020, Pediatric pulmonology.

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

J. Milczewska, D. Sands, M. Postek, 2019, Pediatric pulmonology.

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

H. Mazurek, D. Sands, Ewa Sapiejka, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

The Effects of the Addition of a New Airway Clearance Device to Chest Physiotherapy in Children with Cystic Fibrosis Pulmonary Exacerbations

A. Cichocka, J. Milczewska, D. Sands, 2020, Journal of mother and child.

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

O. Sommerburg, S. McColley, C. Castellani, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Early Decline of Pancreatic Function in Cystic Fibrosis Patients with Class 1 or 2 CFTR Mutations

K. Herzig, J. Walkowiak, A. Nowakowska, 2005, Journal of pediatric gastroenterology and nutrition.

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

J. Walkowiak, D. Sands, S. Nousia-Arvanitakis, 2002, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

'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.

M. Kabra, E. Tullis, C. Wainwright, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cytokines in WBC‐reduced apheresis PCs during storage: a comparison of two WBC‐reduction methods

M. Wadhwa, P. Dilger, R. Thorpe, 2000, Transfusion.

Gastroesophageal Reflux Disease in Children with Cystic Fibrosis.

J. Walkowiak, D. Sands, A. Lisowska, 2015, Advances in experimental medicine and biology.

Age of menarche in girls with cystic fibrosis.

A. Zielińska, D. Sands, W. Umławska, 2010, Folia histochemica et cytobiologica.

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

J. Walkowiak, A. Lipowicz, D. Sands, 2015, Developmental period medicine.

Clinical complications in children with false-negative results in cystic fibrosis newborn screening

D. Sands, M. Ołtarzewski, K. Zybert, 2021, Jornal de pediatria.

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. Zielińska, D. Sands, W. Umławska, 2015, Archives of medical science : AMS.

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

M. Krzyzanowska, A. Zielińska, D. Sands, 2014, Advances in clinical and experimental medicine : official organ Wroclaw Medical University.

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

Ian M. Balfour-Lynn, Milan Macek, Trudy Havermans, 2014, Journal of Cystic Fibrosis.

Thiocyanate concentration in saliva of cystic fibrosis patients.

Ł. Minarowski, M. Gacko, D. Sands, 2008, Folia histochemica et cytobiologica.

Pseudomonas aeruginosa eradicates Staphylococcus aureus by manipulating the host immunity

D. Leduc, L. Touqui, P. Burgel, 2014, Nature Communications.

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

D. Sands, K. Walicka-Serzysko, 2015, Developmental period medicine.

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

D. Sands, U. Borawska-Kowalczyk, 2015, Developmental period medicine.

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

R. Marciniak, A. Sobczyńska-Tomaszewska, E. Mojs, 2011, European Journal of Human Genetics.

The activity of cathepsin D in saliva of cystic fibrosis patients.

E. Dąbrowska, D. Sands, A. Karwowska, 2007, Folia histochemica et cytobiologica.

European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance.

O. Sommerburg, C. Castellani, M. Proesmans, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

European best practice guidelines for cystic fibrosis neonatal screening.

O. Sommerburg, M. Macek, C. Férec, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

D. Sands, K. Czerska, M. Ołtarzewski, 2020, Pediatric pulmonology.

End of life care for patients with cystic fibrosis.

L. Dupont, P. Catastini, S. Madge, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

O. Sommerburg, C. Castellani, J. Dankert-Roelse, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

D. Sands, M. Ołtarzewski, E. Mierzejewska, 2015, Developmental period medicine.

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

A. Nowakowska, D. Sands, M. Ołtarzewski, 2010, Folia histochemica et cytobiologica.

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

A. Nowakowska, D. Sands, K. Zybert, 2010, Folia histochemica et cytobiologica.

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

X. Estivill, J. Zieleński, I. Aznarez, 2000, Medycyna wieku rozwojowego.

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

M. Corey, L. Tsui, J. Zieleński, 2009, Human Genetics.

Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.

Milan Macek, Gérard Lenoir, J. Sarles, 2010, American journal of respiratory and critical care medicine.

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

Á. Mészáros, D. Sands, R. Bodnár, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Postural defects in children with cystic fibrosis - preliminary report.

D. Sands, Paweł Michalski, M. Tramś, 2015, Developmental period medicine.

Pediatric Pulmonology

T. Wołkowicz, J. Milczewska, D. Sands, 2019 .

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

J. Jaworska, D. Sands, Aleksandra Marach-Mocarska, 2020, BMC Pediatrics.

Lung Ultrasound in the Evaluation of Lung Disease Severity in Children with Clinically Stable Cystic Fibrosis: A Prospective Cross-Sectional Study

N. Buda, D. Sands, Anna Komorowska-Piotrowska, 2023, Journal of clinical medicine.

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

D. Sands, E. Mierzejewska, K. Zybert, 2015, Developmental period medicine.

Prostaglandin-endoperoxide synthase genesCOX1 andCOX2 — novel modifiers of disease severity in cystic fibrosis patients

J. Zieleński, A. Sobczyńska-Tomaszewska, D. Bąk, 2011, Journal of Applied Genetics.

Metabolomics Comparison of Drug-Resistant and Drug-Susceptible Pseudomonas aeruginosa Strain (Intra- and Extracellular Analysis)

Sławomir Jabłoński, M. Łukaszewicz, P. Młynarz, 2021, International journal of molecular sciences.

Cystic fibrosis in the general practitioner’s office

D. Sands, K. Walicka-Serzysko, A. Wołkowicz, 2018 .

A Novel Lipidomic Strategy Reveals Plasma Phospholipid Signatures Associated with Respiratory Disease Severity in Cystic Fibrosis Patients

J. Jais, D. Piomelli, G. Astarita, 2009, PloS one.

NPD MEASUREMENTS IN CYSTIC FIBROSIS CF

D. Sands, 2013 .

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

D. Sands, T. Orlik, 2001, Medycyna wieku rozwojowego.

Cystic fibrosis – a challenge also for a laryngologist

J. Milczewska, D. Sands, 2013 .

Availability of CFTR modulators in countries of Eastern Europe: The reality in 2022.

P. Dřevínek, G. Petrova, D. Sands, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

P. Dřevínek, D. Sands, M. Pecková, 2018, Journal of Cystic Fibrosis.

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

B. Więckowska, H. Batura-Gabryel, K. Jahnz-Różyk, 2020, Advances in respiratory medicine.

Efficacy of the Simeox® Airway Clearance Technology in the Homecare Treatment of Children with Clinically Stable Cystic Fibrosis: A Randomized Controlled Trial

A. Cichocka, J. Milczewska, D. Sands, 2023, Children.

Pulmonary Function Tests in the Evaluation of Early Lung Disease in Cystic Fibrosis

J. Milczewska, D. Sands, M. Postek, 2023, Journal of clinical medicine.

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

D. Sands, 2013, Developmental Period Medicine.

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

M. Witt, J. Walkowiak, D. Sands, 2001, European journal of clinical investigation.

14 Updated survey of newborn screening for cystic fibrosis

O. Sommerburg, C. Castellani, J. Dankert-Roelse, 2014 .

Defining key outcomes to evaluate performance of newborn screening programmes for cystic fibrosis.

O. Sommerburg, C. Castellani, M. Proesmans, 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Parents’ Knowledge of the Impact of Cystic Fibrosis on the Quality of Life of Children and Adolescents Suffering from This Disease as an Element of Patient Safety

Damian Gorczyca, D. Sands, M. Głowacka, 2023, Journal of clinical medicine.