UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 47

Sortiert nach

Occurrence, outcomes and predictors of portal hypertension in cystic fibrosis: A longitudinal prospective birth cohort study

Journal of cystic fibrosis, 2020-05, Vol.19 (3), p.455-459

2020

Volltextzugriff (PDF)

Azithromycin Selectively Reduces Tumor Necrosis Factor Alpha Levels in Cystic Fibrosis Airway Epithelial Cells

Antimicrobial Agents and Chemotherapy, 2007-03, Vol.51 (3), p.975-981

2007

Volltextzugriff (PDF)

Defective CFTR expression and function are detectable in blood monocytes: development of a new blood test for cystic fibrosis

PloS one, 2011-07, Vol.6 (7), p.e22212-e22212

2011

Volltextzugriff (PDF)

Impact of MIF gene promoter polymorphism on F508del cystic fibrosis patients

PloS one, 2014-12, Vol.9 (12), p.e114274

2014

Volltextzugriff (PDF)

Anti-inflammatory effects of azithromycin in cystic fibrosis airway epithelial cells

Biochemical and biophysical research communications, 2006-12, Vol.350 (4), p.977-982

2006

Volltextzugriff (PDF)

Further characterization of Shwachman-Diamond syndrome: Psychological functioning and quality of life in adult and young patients

American journal of medical genetics. Part A, 2012-03, Vol.158A (3), p.567-573

2012

Volltextzugriff (PDF)

Inconclusive Cystic Fibrosis neonatal screening results: long-term psychosocial effects on parents

Acta Paediatrica, 2009-12, Vol.98 (12), p.1927-1934

2009

Volltextzugriff (PDF)

An interactive computer program can effectively educate potential users of cystic fibrosis carrier tests

American journal of medical genetics. Part A, 2011-04, Vol.155A (4), p.778-785

2011

Volltextzugriff (PDF)

Pancreatic phenotype in infants with cystic fibrosis identified by mutation screening

Archives of disease in childhood, 2007-10, Vol.92 (10), p.842-846

2007

Volltextzugriff (PDF)

Aztreonam inhalation solution for suppressive treatment of chronic Pseudomonas aeruginosa lung infection in cystic fibrosis

Expert review of anti-infective therapy, 2011-11, Vol.9 (11), p.967-973

Assael, Baroukh Maurice

2011

Volltextzugriff (PDF)

Association between carrier screening and incidence of cystic fibrosis

JAMA : the journal of the American Medical Association, 2009-12, Vol.302 (23), p.2573

2009

Volltextzugriff (PDF)

New insights into the Shwachman-Diamond Syndrome-related haematological disorder: hyper-activation of mTOR and STAT3 in leukocytes

Scientific reports, 2016-09, Vol.6 (1), p.33165-33165, Article 33165

2016

Volltextzugriff (PDF)

Mutations in the SPINK1 gene in idiopathic pancreatitis italian patients

European journal of human genetics : EJHG, 2003-07, Vol.11 (7), p.543-546

2003

Volltextzugriff (PDF)

Ataluren‐driven restoration of Shwachman‐Bodian‐Diamond syndrome protein function in Shwachman‐Diamond syndrome bone marrow cells

American journal of hematology, 2018-04, Vol.93 (4), p.527-536

2018

Volltextzugriff (PDF)

Absence of a gender gap in survival. An analysis of the Italian registry for cystic fibrosis in the paediatric age

Journal of cystic fibrosis, 2011-09, Vol.10 (5), p.313-317

2011

Volltextzugriff (PDF)

Nasal potential difference outcomes support diagnostic decisions in cystic fibrosis

Journal of cystic fibrosis, 2016-09, Vol.15 (5), p.579-582

2016

Volltextzugriff (PDF)

Electrophysiological evaluation of Cystic Fibrosis Conductance Transmembrane Regulator (CFTR) expression in human monocytes

Biochimica et biophysica acta, 2014-10, Vol.1840 (10), p.3088-3095

2014

Volltextzugriff (PDF)

Hyaluronic acid improves the tolerability of hypertonic saline in the chronic treatment of cystic fibrosis patients: a multicenter, randomized, controlled clinical trial

Journal of aerosol medicine and pulmonary drug delivery, 2014-04, Vol.27 (2), p.133

2014

Volltextzugriff (PDF)

Impact of the A (H1N1) pandemic influenza (season 2009–2010) on patients with cystic fibrosis

Journal of cystic fibrosis, 2011-09, Vol.10 (5), p.370-376

2011

Volltextzugriff (PDF)

Ratiometric sweat secretion optical test in cystic fibrosis, carriers and healthy subjects

Journal of cystic fibrosis, 2018-03, Vol.17 (2), p.186-189

2018

Volltextzugriff (PDF)

Detection of CFTR protein in human leukocytes by flow cytometry

Cytometry. Part A, 2014-07, Vol.85 (7), p.611-620

2014

Volltextzugriff (PDF)

Growth and long-term lung function in cystic fibrosis: A longitudinal study of patients diagnosed by neonatal screening

Pediatric pulmonology, 2009-03, Vol.44 (3), p.209-215

2009

Volltextzugriff (PDF)

Chest computed tomography scores in patients with cystic fibrosis colonized with methicillin‐resistant Staphylococcus aureus

The clinical respiratory journal, 2018-02, Vol.12 (2), p.779-785

2018

Volltextzugriff (PDF)

Challenging the diagnosis of cystic fibrosis in a patient carrying the 186-8T/C allelic variant in the CF transmembrane conductance regulator gene

BMC pulmonary medicine, 2014-03, Vol.14 (1), p.44-44, Article 44

2014

Volltextzugriff (PDF)

Cystic fibrosis transmembrane conductance regulator functional evaluations in a G542X+/- IVS8Tn:T7/9 patient with acute recurrent pancreatitis

World journal of clinical cases, 2019-11, Vol.7 (22), p.3757-3764

2019

Volltextzugriff (PDF)

1 – 25 von 47

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(43)
Mit Volltextzugriff
(42)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(36)
Life Sciences & Biomedicine
(33)
Humans
(28)
Cystic Fibrosis
(25)
Female
(19)
Male
(19)
Adult
(14)
Biological And Medical Sciences
(14)
Medical Sciences
(13)
Respiratory System
(13)
Adolescent
(11)
Child
(11)
Cystic Fibrosis - Diagnosis
(11)
Cystic Fibrosis Transmembrane Conductance Regulator - Genetics
(10)
Mutation
(9)
Cystic Fibrosis - Genetics
(8)
Child, Preschool
(7)
Errors Of Metabolism
(7)
Infant, Newborn
(7)
Metabolic Diseases
(7)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Occurrence, outcomes and predictors of portal hypertension in cystic fibrosis: A longitudinal prospective birth cohort study

Azithromycin Selectively Reduces Tumor Necrosis Factor Alpha Levels in Cystic Fibrosis Airway Epithelial Cells

Defective CFTR expression and function are detectable in blood monocytes: development of a new blood test for cystic fibrosis

Impact of MIF gene promoter polymorphism on F508del cystic fibrosis patients

Anti-inflammatory effects of azithromycin in cystic fibrosis airway epithelial cells

Further characterization of Shwachman-Diamond syndrome: Psychological functioning and quality of life in adult and young patients

Inconclusive Cystic Fibrosis neonatal screening results: long-term psychosocial effects on parents

An interactive computer program can effectively educate potential users of cystic fibrosis carrier tests

Pancreatic phenotype in infants with cystic fibrosis identified by mutation screening

Aztreonam inhalation solution for suppressive treatment of chronic Pseudomonas aeruginosa lung infection in cystic fibrosis

Association between carrier screening and incidence of cystic fibrosis

New insights into the Shwachman-Diamond Syndrome-related haematological disorder: hyper-activation of mTOR and STAT3 in leukocytes

Mutations in the SPINK1 gene in idiopathic pancreatitis italian patients

Ataluren‐driven restoration of Shwachman‐Bodian‐Diamond syndrome protein function in Shwachman‐Diamond syndrome bone marrow cells

Absence of a gender gap in survival. An analysis of the Italian registry for cystic fibrosis in the paediatric age

Nasal potential difference outcomes support diagnostic decisions in cystic fibrosis

Electrophysiological evaluation of Cystic Fibrosis Conductance Transmembrane Regulator (CFTR) expression in human monocytes

Hyaluronic acid improves the tolerability of hypertonic saline in the chronic treatment of cystic fibrosis patients: a multicenter, randomized, controlled clinical trial

Impact of the A (H1N1) pandemic influenza (season 2009–2010) on patients with cystic fibrosis

Ratiometric sweat secretion optical test in cystic fibrosis, carriers and healthy subjects

Detection of CFTR protein in human leukocytes by flow cytometry

Growth and long-term lung function in cystic fibrosis: A longitudinal study of patients diagnosed by neonatal screening

Chest computed tomography scores in patients with cystic fibrosis colonized with methicillin‐resistant Staphylococcus aureus

Challenging the diagnosis of cystic fibrosis in a patient carrying the 186-8T/C allelic variant in the CF transmembrane conductance regulator gene

Cystic fibrosis transmembrane conductance regulator functional evaluations in a G542X+/- IVS8Tn:T7/9 patient with acute recurrent pancreatitis

Suchergebnisse filtern