H. Hardt

发表

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Mediated Residual Chloride Secretion Does Not Protect against Early Chronic Pseudomonas aeruginosa Infection in F508del Homozygous Cystic Fibrosis Patients

B. Tümmler, N. Derichs, M. Ballmann, 2004, Pediatric Research.

Long‐term tobramycin aerosol therapy in cystic fibrosis

M. Gappa, B. Tümmler, A. Albus, 1989, Pediatric pulmonology.

Pressure s sensor p plethysmography: a a m method ffor a assessment o of respiratory m motion iin c children

J. Seidenberg, P. Bánovčin, H. Hardt, 1995 .

Lung volumes in healthy boys and girls, 6–15 years of age

H. Hardt, R. Nowak-Beneke, 1976, Lung.

Fibrosing Alveolitis in Childhood A Long‐Term Follow‐up

K. Müller, H. Hardt, G. Steinkamp, 1990, Acta paediatrica Scandinavica.

Bodyplethysmography in healthy children

H. Hardt, M. Leben, 1976, European Journal of Pediatrics.

Failure of pulse oximeter to detect sensor detachment

C. Poets, J. Seidenberg, H. Hardt, 1993, The Lancet.

Atypical spondyloarthritis in children: proposed diagnostic criteria

H. Abdul-Khaliq, A. Hussein, H. Hardt, 1989, European Journal of Pediatrics.

Bronchial sensitivity to inhaled histamine in healthy, nonatopic children

F. Riedel, H. Hardt, 1986, Pediatric pulmonology.

Assessment of Tidal Breathing Patterns for Monitoring of Bronchial Obstruction in Infants

J. Seidenberg, P. Bánovčin, H. Hardt, 1995, Pediatric Research.

Long term follow up of changes in FEV1 and treatment intensity during Pseudomonas aeruginosa colonisation in patients with cystic fibrosis

M. Ballmann, H. Hardt, P. Rabsch, 1998 .

Long term follow up of changes in FEV 1 and treatment intensity during Pseudomonas aeruginosa colonisation in patients with cystic fibrosis

M. Ballmann, H. Hardt, P. Rabsch, 1998 .

Pseudomonas aeruginosa infection in patients with cystic

H. Hardt, G. Steinkamp, A. Drommer, 1993 .

Geographic distribution and origin of CFTR mutations in Germany

X. Estivill, T. Meitinger, T. Dörk, 1996, Human Genetics.

Computer-assisted documentation of the clinical course of cystic fibrosis patients

B. Tümmler, H. Hardt, 1987, Infection.

Increased Concentrations of Milk Antibodies in Recurrent Pulmonary Aspiration in Infants and Young Children

W. Müller, H. Hardt, C. Rieger, 1985, Acta paediatrica Scandinavica.

Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis

B. Tümmler, T. Neumann, U. Wulbrand, 1993, The Lancet.

Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients

T. Dörk, B. Tümmler, T. Neumann, 1994, Human Genetics.

Transcript analysis of CFTR nonsense mutations in lymphocytes and nasal epithelial cells from cystic fibrosis patients

T. Dörk, K. Will, B. Tümmler, 1995, Human mutation.

Pulmonary Resection for Localized Bronchiectasis in Cystic Fibrosis

H. Hardt, G. Steinkamp, H. Zimmermann, 1988, Acta paediatrica Scandinavica.

DNA Typing of a Cystic Fibrosis Family with Borderline Sweat Tests

B. Tümmler, H. Hardt, T. Darnedde, 1988, Acta paediatrica Scandinavica.

Prospective, double‐blind, placebo‐controlled, multicentre study on the effect of high‐dose, intravenous immunoglobulin in children and adolescents with severe bronchial asthma

B. Niggemann, U. Wahn, M. Eibl, 1998, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

GenomeFingerprinting ofPseudomonas aeruginosa Indicates Colonization ofCystic Fibrosis Siblings withClosely Related Strains

D. Grothues, H. Hardt, U. Koopmann, 1988 .

Mechanics of respiration in healthy children 6 to 15 years of age

H. Hardt, A. Nowak, 1976, Lung.

Diagnostic implications and treatment of massive spontaneous atelectasis in childhood

H. Hardt, C. Rieger, W. Müller, 1986, Pediatric pulmonology.

Conductive airway surfactant: surface-tension function, biochemical composition, and possible alveolar origin.

C. Poets, W. Bernhard, A. Postle, 1997, American journal of respiratory cell and molecular biology.

A method for the isolation and preparation of surfactant from tracheobronchial aspirates in infants and children for quantitative and pulsating bubble analysis

C. Poets, W. Bernhard, H. Hardt, 1996, European journal of clinical investigation.

Lung transplantation for cystic fibrosis--a single center experience over 8 years.

A. Haverich, K. Wiebe, T. Wahlers, 1998, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Active surfactant in pharyngeal aspirates of term neonates: lipid biochemistry and surface tension function

C. Poets, W. Bernhard, H. Hardt, 1997, European journal of clinical investigation.

Commercial versus native surfactants. Surface activity, molecular components, and the effect of calcium.

C. Poets, G. Rau, W. Bernhard, 2000, American journal of respiratory and critical care medicine.

Reliability of a pulse oximeter in the detection of hyperoxemia.

C. Poets, D. Southall, J. Seidenberg, 1993, The Journal of pediatrics.

Lpphoq tes and Nasal Epithelial Cells From Cystic Fibrosis Patients

K. Will, M. Stuhrmann, H. Ellemunter, 2005 .

Epidemiology of chronic Pseudomonas aeruginosa infections in the airways of lung transplant recipients with cystic fibrosis.

B. Tümmler, U. Römling, P. Gudowius, 1997, Thorax.

Regional Lung Function in Asthmatic Children Receiving Bronchodilating Treatment

H. Hundeshagen, H. Hardt, H. Creutzig, 1981 .

DNA concentration and length in sputum of patients with cystic fibrosis during inhalation with recombinant human DNase.

B. Tümmler, S. Breitenstein, T. Brandt, 1995, Thorax.

Phosphatidylcholine molecular species in lung surfactant: composition in relation to respiratory rate and lung development.

C. Poets, G. Rau, W. Bernhard, 2001, American journal of respiratory cell and molecular biology.

Airway Resistance, Airway Conductance, Specific Airway Resistance, and Specific Airway Conductance in Children

H. Hardt, M. Leben, 1983, Pediatric Research.