Mall MA - Search Results

1

The future of cystic fibrosis care: a global perspective.

Bell SC, Mall MA, Gutierrez H, Macek M, Madge S, Davies JC, Burgel PR, Tullis E, Castaños C, Castellani C, Byrnes CA, Cathcart F, Chotirmall SH, Cosgriff R, Eichler I, Fajac I, Goss CH, Drevinek P, Farrell PM, Gravelle AM, Havermans T, Mayer-Hamblett N, Kashirskaya N, Kerem E, Mathew JL, McKone EF, Naehrlich L, Nasr SZ, Oates GR, O'Neill C, Pypops U, Raraigh KS, Rowe SM, Southern KW, Sivam S, Stephenson AL, Zampoli M, Ratjen F. Bell SC, et al. Among authors: mall ma. Lancet Respir Med. 2020 Jan;8(1):65-124. doi: 10.1016/S2213-2600(19)30337-6. Epub 2019 Sep 27. Lancet Respir Med. 2020. PMID: 31570318 Free PMC article. Review.

2

Regulation of epithelial ion channels by the cystic fibrosis transmembrane conductance regulator.

Greger R, Mall M, Bleich M, Ecke D, Warth R, Riedemann N, Kunzelmann K. Greger R, et al. J Mol Med (Berl). 1996 Sep;74(9):527-34. doi: 10.1007/BF00204979. J Mol Med (Berl). 1996. PMID: 8892058 Review.

3

Control of epithelial Na+ conductance by the cystic fibrosis transmembrane conductance regulator.

Kunzelmann K, Schreiber R, Nitschke R, Mall M. Kunzelmann K, et al. Pflugers Arch. 2000 Jun;440(2):193-201. doi: 10.1007/s004240000255. Pflugers Arch. 2000. PMID: 10898518 Review.

4

Cystic fibrosis and CFTR.

Greger R, Schreiber R, Mall M, Wissner A, Hopf A, Briel M, Bleich M, Warth R, Kunzelmann K. Greger R, et al. Pflugers Arch. 2001;443 Suppl 1:S3-7. doi: 10.1007/s004240100635. Epub 2001 Jul 7. Pflugers Arch. 2001. PMID: 11845294 Review.

5

Pharmacotherapy of the ion transport defect in cystic fibrosis: role of purinergic receptor agonists and other potential therapeutics.

Kunzelmann K, Mall M. Kunzelmann K, et al. Am J Respir Med. 2003;2(4):299-309. doi: 10.1007/BF03256658. Am J Respir Med. 2003. PMID: 14719996 Review.

6

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.

Mall M, Grubb BR, Harkema JR, O'Neal WK, Boucher RC. Mall M, et al. Nat Med. 2004 May;10(5):487-93. doi: 10.1038/nm1028. Epub 2004 Apr 11. Nat Med. 2004. PMID: 15077107

7

CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis.

Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M. Hirtz S, et al. Gastroenterology. 2004 Oct;127(4):1085-95. doi: 10.1053/j.gastro.2004.07.006. Gastroenterology. 2004. PMID: 15480987

8

Preventive but not late amiloride therapy reduces morbidity and mortality of lung disease in betaENaC-overexpressing mice.

Zhou Z, Treis D, Schubert SC, Harm M, Schatterny J, Hirtz S, Duerr J, Boucher RC, Mall MA. Zhou Z, et al. Among authors: mall ma. Am J Respir Crit Care Med. 2008 Dec 15;178(12):1245-56. doi: 10.1164/rccm.200803-442OC. Epub 2008 Oct 10. Am J Respir Crit Care Med. 2008. PMID: 18849497

9

Role of the amiloride-sensitive epithelial Na+ channel in the pathogenesis and as a therapeutic target for cystic fibrosis lung disease.

Mall MA. Mall MA. Exp Physiol. 2009 Feb;94(2):171-4. doi: 10.1113/expphysiol.2008.042994. Epub 2008 Dec 5. Exp Physiol. 2009. PMID: 19060118 Free article.

10

Initial evaluation of a biochemical cystic fibrosis newborn screening by sequential analysis of immunoreactive trypsinogen and pancreatitis-associated protein (IRT/PAP) as a strategy that does not involve DNA testing in a Northern European population.

Sommerburg O, Lindner M, Muckenthaler M, Kohlmueller D, Leible S, Feneberg R, Kulozik AE, Mall MA, Hoffmann GF. Sommerburg O, et al. Among authors: mall ma. J Inherit Metab Dis. 2010 Oct;33(Suppl 2):S263-71. doi: 10.1007/s10545-010-9174-7. Epub 2010 Aug 17. J Inherit Metab Dis. 2010. PMID: 20714932

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