Stahl M - Search Results

1

Multiple-breath washout to detect lung disease in patients with inborn errors of immunity.

Busack LM, Thee S, Liu Y, Allomba C, Ziegahn N, Tosolini A, Pioch CO, Schnorr AN, Fuhlrott BR, Staudacher O, Völler M, Steinke E, Hanitsch LG, Röhmel J, Wahn V, Krüger R, Mall MA, von Bernuth H, Stahl M. Busack LM, et al. Among authors: stahl m. ERJ Open Res. 2024 Mar 11;10(2):01019-2023. doi: 10.1183/23120541.01019-2023. eCollection 2024 Mar. ERJ Open Res. 2024. PMID: 38469376 Free PMC article.

2

Multiple breath washout is feasible in the clinical setting and detects abnormal lung function in infants and young children with cystic fibrosis.

Stahl M, Joachim C, Blessing K, Hämmerling S, Sommerburg O, Latzin P, Mall MA. Stahl M, et al. Respiration. 2014;87(5):357-63. doi: 10.1159/000357075. Epub 2014 Jan 14. Respiration. 2014. PMID: 24434651 Free article.

3

Early cystic fibrosis lung disease: Role of airway surface dehydration and lessons from preventive rehydration therapies in mice.

Mall MA, Graeber SY, Stahl M, Zhou-Suckow Z. Mall MA, et al. Among authors: stahl m. Int J Biochem Cell Biol. 2014 Jul;52:174-9. doi: 10.1016/j.biocel.2014.02.006. Epub 2014 Feb 20. Int J Biochem Cell Biol. 2014. PMID: 24561284 Review.

4

Five years of experience with biochemical cystic fibrosis newborn screening based on IRT/PAP in Germany.

Sommerburg O, Hammermann J, Lindner M, Stahl M, Muckenthaler M, Kohlmueller D, Happich M, Kulozik AE, Stopsack M, Gahr M, Hoffmann GF, Mall MA. Sommerburg O, et al. Among authors: stahl m. Pediatr Pulmonol. 2015 Jul;50(7):655-64. doi: 10.1002/ppul.23190. Epub 2015 Apr 23. Pediatr Pulmonol. 2015. PMID: 25914230

5

Imaging of Cystic Fibrosis Lung Disease and Clinical Interpretation.

Wielpütz MO, Eichinger M, Biederer J, Wege S, Stahl M, Sommerburg O, Mall MA, Kauczor HU, Puderbach M. Wielpütz MO, et al. Among authors: stahl m. Rofo. 2016 Sep;188(9):834-45. doi: 10.1055/s-0042-104936. Epub 2016 Apr 13. Rofo. 2016. PMID: 27074425 Free article. Review. English.

6

Comparison of Lung Clearance Index and Magnetic Resonance Imaging for Assessment of Lung Disease in Children with Cystic Fibrosis.

Stahl M, Wielpütz MO, Graeber SY, Joachim C, Sommerburg O, Kauczor HU, Puderbach M, Eichinger M, Mall MA. Stahl M, et al. Am J Respir Crit Care Med. 2017 Feb 1;195(3):349-359. doi: 10.1164/rccm.201604-0893OC. Am J Respir Crit Care Med. 2017. PMID: 27575911 Clinical Trial.

7

Early detection and sensitive monitoring of CF lung disease: Prospects of improved and safer imaging.

Mall MA, Stahl M, Graeber SY, Sommerburg O, Kauczor HU, Wielpütz MO. Mall MA, et al. Among authors: stahl m. Pediatr Pulmonol. 2016 Oct;51(S44):S49-S60. doi: 10.1002/ppul.23537. Pediatr Pulmonol. 2016. PMID: 27662104 Review.

8

Reply to Verbanck and Vanderhelst: The Respective Roles of Lung Clearance Index and Magnetic Resonance Imaging in the Clinical Management of Patients with Cystic Fibrosis.

Stahl M, Wielpütz MO, Kauczor HU, Mall MA; all authors. Stahl M, et al. Am J Respir Crit Care Med. 2018 Feb 1;197(3):410-411. doi: 10.1164/rccm.201707-1367LE. Am J Respir Crit Care Med. 2018. PMID: 28800247 No abstract available.

9

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

Stahl M, Graeber SY, Joachim C, Barth S, Ricklefs I, Diekmann G, Kopp MV, Naehrlich L, Mall MA. Stahl M, et al. J Cyst Fibros. 2018 Mar;17(2):249-255. doi: 10.1016/j.jcf.2017.08.001. Epub 2017 Aug 12. J Cyst Fibros. 2018. PMID: 28811149 Free article.

10

Chronic but not intermittent infection with Pseudomonas aeruginosa is associated with global changes of the lung microbiome in cystic fibrosis.

Boutin S, Graeber SY, Stahl M, Dittrich AS, Mall MA, Dalpke AH. Boutin S, et al. Among authors: stahl m. Eur Respir J. 2017 Oct 5;50(4):1701086. doi: 10.1183/13993003.01086-2017. Print 2017 Oct. Eur Respir J. 2017. PMID: 28982777 Free article. No abstract available.

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