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Cystic Fibrosis Mortality in Childhood. Data from European Cystic Fibrosis Society Patient Registry

International journal of environmental research and public health, 2018-09, Vol.15 (9), p.2020

2018

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High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients

BMC genomics, 2022-04, Vol.23 (1), p.252-252, Article 252

2022

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Comprehensive Assessment of CFTR Modulators' Therapeutic Efficiency for N1303K Variant

International journal of molecular sciences, 2024-02, Vol.25 (5), p.2770

2024

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Burkholderia cepacia in cystic fibrosis children and adolescents: overall survival and immune alterations

Frontiers in cellular and infection microbiology, 2024-07, Vol.14, p.1374318

2024

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Ethnic Differences in the Frequency of CFTR Gene Mutations in Populations of the European and North Caucasian Part of the Russian Federation

Frontiers in genetics, 2021-06, Vol.12, p.678374-678374

2021

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Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients

Genes, 2020-05, Vol.11 (5), p.554

2020

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Advances in the Study of Common and Rare CFTR Complex Alleles Using Intestinal Organoids

Journal of personalized medicine, 2024-02, Vol.14 (2), p.129

2024

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Safety and efficacy of Creon® Micro in children with exocrine pancreatic insufficiency due to cystic fibrosis

Journal of cystic fibrosis, 2015-03, Vol.14 (2), p.275-281

2015

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Clinical Presentation of the c.3844T>C (p.Trp1282Arg, W1282R) Variant in Russian Cystic Fibrosis Patients

Genes, 2020-09, Vol.11 (10), p.1137

2020

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Tu1299 International Prospective Study of Distal Intestinal Obstruction Syndrome (DIOS)

Gastroenterology (New York, N.Y. 1943), 2014-05, Vol.146 (5), p.S-806-S-807

2014

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Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening-Towards a Consistent Definition and Data Acquisition

International journal of neonatal screening, 2023-11, Vol.9 (4), p.65

2023

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Newborn Screening for Cystic Fibrosis in Russia: A Catalyst for Improved Care

International journal of neonatal screening, 2020-06, Vol.6 (2), p.34-34

2020

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Contribution of pancreatic enzyme replacement therapy to survival and quality of life in patients with pancreatic exocrine insufficiency

World journal of gastroenterology : WJG, 2019-05, Vol.25 (20), p.2430-2441

2019

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ECFS best practice guidelines: the 2018 revision

Journal of cystic fibrosis, 2018-03, Vol.17 (2), p.153-178

2018

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Characteristics of the L138ins (p.Leu138dup) mutation in Russian cystic fibrosis patients: L138ins (p.Leu138dup) mutation in Russian cystic fibrosis patients

Journal of medical science, 2020-03, Vol.89 (1), p.e383

2020

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European Cystic Fibrosis Society Standards of Care: Best Practice guidelines

Journal of cystic fibrosis, 2014-05, Vol.13, p.S23-S42

2014

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Comprehensive Assessment of ICFTR/I Modulators’ Therapeutic Efficiency for N1303K Variant

International journal of molecular sciences, 2024-02, Vol.25 (5)

2024

Volltextzugriff (PDF)

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

Journal of cystic fibrosis, 2021-09, Vol.20 (5), p.810-819

2021

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

Journal of cystic fibrosis, 2017-03, Vol.16 (2), p.207-213

2017

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The global impact of SARS-CoV-2 in 181 people with cystic fibrosis

Journal of cystic fibrosis, 2020-11, Vol.19 (6), p.868-871

2020

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International prospective study of distal intestinal obstruction syndrome in cystic fibrosis: Associated factors and outcome

Journal of cystic fibrosis, 2016-07, Vol.15 (4), p.531-539

2016

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Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis–data from the European cystic fibrosis society patient registry

Journal of cystic fibrosis, 2020-05, Vol.19 (3), p.376-383

2020

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Global access to affordable CFTR modulator drugs: Time for action

Journal of cystic fibrosis, 2022-05, Vol.21 (3), p.e215-e216

2022

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The future of cystic fibrosis care: a global perspective

Cystic Fibrosis Mortality in Childhood. Data from European Cystic Fibrosis Society Patient Registry

High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients

Comprehensive Assessment of CFTR Modulators' Therapeutic Efficiency for N1303K Variant

Burkholderia cepacia in cystic fibrosis children and adolescents: overall survival and immune alterations

Ethnic Differences in the Frequency of CFTR Gene Mutations in Populations of the European and North Caucasian Part of the Russian Federation

Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients

Advances in the Study of Common and Rare CFTR Complex Alleles Using Intestinal Organoids

Safety and efficacy of Creon® Micro in children with exocrine pancreatic insufficiency due to cystic fibrosis

Clinical Presentation of the c.3844T>C (p.Trp1282Arg, W1282R) Variant in Russian Cystic Fibrosis Patients

Tu1299 International Prospective Study of Distal Intestinal Obstruction Syndrome (DIOS)

Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening-Towards a Consistent Definition and Data Acquisition

Newborn Screening for Cystic Fibrosis in Russia: A Catalyst for Improved Care

Contribution of pancreatic enzyme replacement therapy to survival and quality of life in patients with pancreatic exocrine insufficiency

ECFS best practice guidelines: the 2018 revision

Characteristics of the L138ins (p.Leu138dup) mutation in Russian cystic fibrosis patients: L138ins (p.Leu138dup) mutation in Russian cystic fibrosis patients

European Cystic Fibrosis Society Standards of Care: Best Practice guidelines

Comprehensive Assessment of ICFTR/I Modulators’ Therapeutic Efficiency for N1303K Variant

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

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

The global impact of SARS-CoV-2 in 181 people with cystic fibrosis

International prospective study of distal intestinal obstruction syndrome in cystic fibrosis: Associated factors and outcome

Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis–data from the European cystic fibrosis society patient registry

Global access to affordable CFTR modulator drugs: Time for action

Clinical characteristics of SARS-CoV-2 infection in children with cystic fibrosis: An international observational study

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