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1

Individualized vitamin A supplementation for patients with cystic fibrosis

Brei, Christina, Simon, Annette, Krawinkel, Michael B., Naehrlich, Lutz

Journal:

Clinical Nutrition

Year:

2013

Language:

english

File:

PDF, 317 KB

english, 2013

2

Effects of Lumacaftor/Ivacaftor Therapy on CFTR Function in Phe508del Homozygous Patients with Cystic Fibrosis

Graeber, Simon Y, Dopfer, Christian, Naehrlich, Lutz, Gyulumyan, Lena, Scheuermann, Heike, Hirtz, Stephanie, Wege, Sabine, Mairbäurl, Heimo, Dorda, Marie, Hyde, Rebecca, Bagheri-Hanson, Azadeh, Ruecke

Journal:

American Journal of Respiratory and Critical Care Medicine

Year:

2018

Language:

english

File:

PDF, 1.45 MB

english, 2018

3

Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood

Hengst, Meike, Naehrlich, Lutz, Mahavadi, Poornima, Grosse-Onnebrink, Joerg, Terheggen-Lagro, Suzanne, Skanke, Lars Høsøien, Schuch, Luise A., Brasch, Frank, Guenther, Andreas, Reu, Simone, Ley-Zaporo

Journal:

Orphanet Journal of Rare Diseases

Year:

2018

Language:

english

File:

PDF, 2.56 MB

english, 2018

4

A phase 3, double-blind, parallel-group study to evaluate the efficacy and safety of tezacaftor in combination with ivacaftor in participants 6 through 11 years of age with cystic fibrosis homozygous for F508del or heterozygous for the F508del-CFTR mutation and a residual function mutation

Davies, Jane C., Sermet-Gaudelus, Isabelle, Naehrlich, Lutz, Harris, R. Scott, Campbell, Daniel, Ahluwalia, Neil, Short, Christopher, Haseltine, Eric, Panorchan, Paul, Saunders, Clare, Owen, Caroline

Journal:

Journal of Cystic Fibrosis

Year:

2020

File:

PDF, 672 KB

2020

5

Misdiagnosis of cystic fibrosis — Experience from Germany

Lutz Naehrlich, Azadeh Bagheri-Behrouzi

Journal:

Journal of Cystic Fibrosis

Year:

2013

Language:

english

File:

PDF, 7.32 MB

english, 2013

6

Iodine deficiency and subclinical hypothyroidism are common in cystic fibrosis patients

Naehrlich, Lutz, Dörr, Helmuth-Günther, Bagheri-Behrouzi, Azadeh, Rauh, Manfred

Journal:

Journal of Trace Elements in Medicine and Biology

Year:

2013

Language:

english

File:

PDF, 271 KB

english, 2013

7

Nasal potential difference measurements in diagnosis of cystic fibrosis: An international survey

Naehrlich, Lutz, Ballmann, Manfred, Davies, Jane, Derichs, Nico, Gonska, Tanja, Hjelte, Lena, van Konigsbruggen-Rietschel, Silke, Leal, Teresinha, Melotti, Paola, Middleton, Peter, Tümmler, Burkhard,

Journal:

Journal of Cystic Fibrosis

Year:

2014

Language:

english

File:

PDF, 249 KB

english, 2014

8

Is there evidence for correct diagnosis in cystic fibrosis registries?

Thomas, Muriel, Lemonnier, Lydie, Gulmans, Vincent, Naehrlich, Lutz, Vermeulen, François, Cuppens, Harry, Castellani, Carlo, Norek, Aleksandra, De Boeck, Kris

Journal:

Journal of Cystic Fibrosis

Year:

2014

Language:

english

File:

PDF, 193 KB

english, 2014

9

Nasal potential difference: Best or average result for CFTR function as diagnostic criteria for cystic fibrosis?

Keenan, Katherine, Avolio, Julie, Rueckes-Nilges, Claudia, Tullis, Elizabeth, Gonska, Tanja, Naehrlich, Lutz

Journal:

Journal of Cystic Fibrosis

Year:

2015

Language:

english

File:

PDF, 489 KB

english, 2015

10

Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: a case–control study

Bagheri-Hanson, Azadeh, Nedwed, Sebastian, Rueckes-Nilges, Claudia, Naehrlich, Lutz

Journal:

BMC Pulmonary Medicine

Year:

2014

Language:

english

File:

PDF, 687 KB

english, 2014

11

Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene

Dupuis, Annie, Keenan, Katherine, Ooi, Chee Y., Dorfman, Ruslan, Sontag, Marci K., Naehrlich, Lutz, Castellani, Carlo, Strug, Lisa J., Rommens, Johanna M., Gonska, Tanja

Journal:

Genetics in Medicine

Year:

2015

Language:

english

File:

PDF, 737 KB

english, 2015

12

[American Thoracic Society American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado - ()] A64. MUCINS AND CILIA - Serine Proteases Degrade Airway Mucins In Cystic Fibrosis

Henke, Markus O., John, Gerrit, Rheineck, Christina, Chillappagari, Shashi, Naehrlich, Lutz, Rubin, Bruce K.

Year:

2011

Language:

english

File:

PDF, 16 KB

english, 2011

13

Endoscopic Cystogastrostomy of a Pancreatic Retention Cyst in Cystic Fibrosis

Naehrlich, Lutz, Zapke, Maren, Rupprecht, Thomas, Becker, Dirk

Journal:

Journal of Pediatric Gastroenterology & Nutrition

Year:

2005

Language:

english

File:

PDF, 96 KB

english, 2005

14

Three-center feasibility of lung clearance index in infants and preschool children with cystic fibrosis and other lung diseases

Stahl, Mirjam, Graeber, Simon Y., Joachim, Cornelia, Barth, Sandra, Ricklefs, Isabell, Diekmann, Gesa, Kopp, Matthias V., Naehrlich, Lutz, Mall, Marcus A.

Journal:

Journal of Cystic Fibrosis

Year:

2017

Language:

english

File:

PDF, 343 KB

english, 2017

15

Repaglinide versus insulin for newly diagnosed diabetes in patients with cystic fibrosis: a multicentre, open-label, randomised trial

Ballmann, Manfred, Hubert, Dominique, Assael, Baroukh M, Staab, Doris, Hebestreit, Alexandra, Naehrlich, Lutz, Nickolay, Tanja, Prinz, Nicole, Holl, Reinhard W, Staden, Ute, Claßen, Martin, Schuster,

Journal:

The Lancet Diabetes & Endocrinology

Year:

2017

Language:

english

File:

PDF, 173 KB

english, 2017

16

High Variability in Oral Glucose Tolerance among 1,128 Patients with Cystic Fibrosis: A Multicenter Screening Study

Scheuing, Nicole, Holl, Reinhard W., Dockter, Gerd, Hermann, Julia M., Junge, Sibylle, Koerner-Rettberg, Cordula, Naehrlich, Lutz, Smaczny, Christina, Staab, Doris, Thalhammer, Gabriela, van Koningsbr

Journal:

Year:

2014

Language:

english

File:

PDF, 1.26 MB

english, 2014

17

Cystic Fibrosis

Naehrig, Susanne, Chao, Cho-Ming, Naehrlich, Lutz

Journal:

Deutsches "{A}rzteblatt international

Year:

2017

Language:

english

File:

PDF, 421 KB

english, 2017

18

Impact of COVID-19 on people with cystic fibrosis

Colombo, Carla, Burgel, Pierre-RÃ©gis, Gartner, Silvia, van Koningsbruggen-Rietschel, Silke, Naehrlich, Lutz, Sermet-Gaudelus, Isabelle, Southern, Kevin W

Journal:

The Lancet Respiratory Medicine

Year:

2020

File:

PDF, 48 KB

2020

19

Defective BACH1/HO-1 regulatory circuits in cystic fibrosis bronchial epithelial cells

Chillappagari, Shashipavan, Garapati, Virajith, Mahavadi, Poornima, Naehrlich, Lutz, Schmeck, Bernd T., Schmitz, M. Lienhard, Guenther, Andreas

Journal:

Journal of Cystic Fibrosis

Year:

2020

File:

PDF, 2.46 MB

2020

20

Have courage in using nasal potential difference for diagnostic decisions and clinical research

Naehrlich, Lutz

Journal:

Journal of Cystic Fibrosis

Year:

2020

File:

PDF, 217 KB

2020

21

The Changing Face of Cystic Fibrosis and Its Implications for Screening

Naehrlich, Lutz

Journal:

International Journal of Neonatal Screening

Year:

2020

File:

PDF, 187 KB

2020

22

Risk factors for respiratory Aspergillus fumigatus in German Cystic Fibrosis patients and impact on lung function

DÃ¼esberg, Uta, Wosniok, Julia, Naehrlich, Lutz, Eschenhagen, Patience, Schwarz, Carsten

Journal:

Scientific Reports

Year:

2020

File:

PDF, 1.25 MB

2020