Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 78

1.

Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function.

Xu Z, Lo WS, Beck DB, Schuch LA, Oláhová M, Kopajtich R, Chong YE, Alston CL, Seidl E, Zhai L, Lau CF, Timchak D, LeDuc CA, Borczuk AC, Teich AF, Juusola J, Sofeso C, Müller C, Pierre G, Hilliard T, Turnpenny PD, Wagner M, Kappler M, Brasch F, Bouffard JP, Nangle LA, Yang XL, Zhang M, Taylor RW, Prokisch H, Griese M, Chung WK, Schimmel P.

Am J Hum Genet. 2018 Jul 5;103(1):100-114. doi: 10.1016/j.ajhg.2018.06.006.

2.

Pulmonary interstitial glycogenosis - A systematic analysis of new cases.

Seidl E, Carlens J, Reu S, Wetzke M, Ley-Zaporozhan J, Brasch F, Wesselak T, Schams A, Rauch D, Schuch L, Kappler M, Schelstraete P, Wolf M, Stehling F, Haarmann E, Borensztajn D, van de Loo M, Rubak S, Lex C, Hinrichs B, Reiter K, Schwerk N, Griese M.

Respir Med. 2018 Jul;140:11-20. doi: 10.1016/j.rmed.2018.05.009. Epub 2018 May 17. Review.

PMID:
29957271
3.

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

Hengst M, Naehrlich L, Mahavadi P, Grosse-Onnebrink J, Terheggen-Lagro S, Skanke LH, Schuch LA, Brasch F, Guenther A, Reu S, Ley-Zaporozhan J, Griese M.

Orphanet J Rare Dis. 2018 Mar 27;13(1):42. doi: 10.1186/s13023-018-0780-z.

4.

Neuroendocrine Cell Hyperplasia of Infancy (NEHI) – hilft Bildgebung Lungenbiopsien zu vermeiden?

Beeskow AB, Hirsch FW, Brasch F, Prenzel F.

Rofo. 2017 Aug;189(8):765-766. doi: 10.1055/s-0043-108686. Epub 2017 May 16. German. No abstract available.

5.

Lung disease caused by ABCA3 mutations.

Kröner C, Wittmann T, Reu S, Teusch V, Klemme M, Rauch D, Hengst M, Kappler M, Cobanoglu N, Sismanlar T, Aslan AT, Campo I, Proesmans M, Schaible T, Terheggen-Lagro S, Regamey N, Eber E, Seidenberg J, Schwerk N, Aslanidis C, Lohse P, Brasch F, Zarbock R, Griese M.

Thorax. 2017 Mar;72(3):213-220. doi: 10.1136/thoraxjnl-2016-208649. Epub 2016 Aug 11.

PMID:
27516224
6.

Tools to explore ABCA3 mutations causing interstitial lung disease.

Wittmann T, Schindlbeck U, Höppner S, Kinting S, Frixel S, Kröner C, Liebisch G, Hegermann J, Aslanidis C, Brasch F, Reu S, Lasch P, Zarbock R, Griese M.

Pediatr Pulmonol. 2016 Dec;51(12):1284-1294. doi: 10.1002/ppul.23471. Epub 2016 May 13.

PMID:
27177387
7.

Persistent Tachypnea of Infancy. Usual and Aberrant.

Rauch D, Wetzke M, Reu S, Wesselak W, Schams A, Hengst M, Kammer B, Ley-Zaporozhan J, Kappler M, Proesmans M, Lange J, Escribano A, Kerem E, Ahrens F, Brasch F, Schwerk N, Griese M; PTI (Persistent Tachypnea of Infancy) Study Group of the Kids Lung Register.

Am J Respir Crit Care Med. 2016 Feb 15;193(4):438-47. doi: 10.1164/rccm.201508-1655OC.

8.

Categorizing diffuse parenchymal lung disease in children.

Griese M, Irnstetter A, Hengst M, Burmester H, Nagel F, Ripper J, Feilcke M, Pawlita I, Gothe F, Kappler M, Schams A, Wesselak T, Rauch D, Wittmann T, Lohse P, Brasch F, Kröner C.

Orphanet J Rare Dis. 2015 Sep 25;10:122. doi: 10.1186/s13023-015-0339-1.

9.

Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients.

Kröner C, Reu S, Teusch V, Schams A, Grimmelt AC, Barker M, Brand J, Gappa M, Kitz R, Kramer BW, Lange L, Lau S, Pfannenstiel C, Proesmans M, Seidenberg J, Sismanlar T, Aslan AT, Werner C, Zielen S, Zarbock R, Brasch F, Lohse P, Griese M.

Eur Respir J. 2015 Jul;46(1):197-206. doi: 10.1183/09031936.00129414. Epub 2015 Feb 5.

10.

Hypersensitivity pneumonitis: lessons for diagnosis and treatment of a rare entity in children.

Griese M, Haug M, Hartl D, Teusch V, Glöckner-Pagel J, Brasch F; National EAA Study Group.

Orphanet J Rare Dis. 2013 Aug 8;8:121. doi: 10.1186/1750-1172-8-121.

11.

Multimodality treatment for poorly differentiated neuroendocrine head and neck carcinomas--a single institution experience.

Görner M, Brasch F, Hirnle P, Gehl HB, Scholtz LU, Wegehenkel K, Sudhoff H.

Eur J Cancer Care (Engl). 2013 Sep;22(5):648-52. doi: 10.1111/ecc.12070. Epub 2013 May 23.

PMID:
23701280
12.

Pulmonary hypertension presenting with apnea, cyanosis, and failure to thrive in a young child.

Navarini S, Bucher B, Pavlovic M, Pfammatter JP, Casaulta C, Brasch F, Griese M, Regamey N.

Chest. 2011 Oct;140(4):1086-1089. doi: 10.1378/chest.10-2607. No abstract available.

PMID:
21972389
13.

Long-term follow-up and treatment of congenital alveolar proteinosis.

Griese M, Ripper J, Sibbersen A, Lohse P, Lohse P, Brasch F, Schams A, Pamir A, Schaub B, Muensterer OJ, Schön C, Glöckner-Pagel J, Nicolai T, Reiter K, Hector A.

BMC Pediatr. 2011 Aug 17;11:72. doi: 10.1186/1471-2431-11-72.

14.

[Poorly differentiated neuroendocrine small-cell carcinoma of the gallbladder].

Benkel M, Brasch F, Neumann JD, Altendorf-Hofmann A, Sendt W.

Zentralbl Chir. 2012 Feb;137(1):71-2. doi: 10.1055/s-0030-1262764. Epub 2011 Mar 1. German.

PMID:
21365540
15.

Incidence and classification of pediatric diffuse parenchymal lung diseases in Germany.

Griese M, Haug M, Brasch F, Freihorst A, Lohse P, von Kries R, Zimmermann T, Hartl D.

Orphanet J Rare Dis. 2009 Dec 12;4:26. doi: 10.1186/1750-1172-4-26.

16.

Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis.

Griese M, Brasch F, Aldana VR, Cabrera MM, Goelnitz U, Ikonen E, Karam BJ, Liebisch G, Linder MD, Lohse P, Meyer W, Schmitz G, Pamir A, Ripper J, Rolfs A, Schams A, Lezana FJ.

Clin Genet. 2010 Feb;77(2):119-30. doi: 10.1111/j.1399-0004.2009.01325.x. Epub 2009 Dec 10.

PMID:
20002450
17.

[Interstitial lung diseases].

Junker K, Brasch F.

Pathologe. 2008 Nov;29 Suppl 2:273-9. doi: 10.1007/s00292-008-1026-y. German.

PMID:
18766344
18.

Surfactant protein B deficiency caused by a novel mutation involving multiple exons of the SP-B gene.

Schuerman FA, Griese M, Gille JP, Brasch F, Noorduyn LA, van Kaam AH.

Eur J Med Res. 2008 Jun 24;13(6):281-6.

PMID:
18558554
19.

Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation.

Pasutto F, Sticht H, Hammersen G, Gillessen-Kaesbach G, Fitzpatrick DR, Nürnberg G, Brasch F, Schirmer-Zimmermann H, Tolmie JL, Chitayat D, Houge G, Fernández-Martínez L, Keating S, Mortier G, Hennekam RC, von der Wense A, Slavotinek A, Meinecke P, Bitoun P, Becker C, Nürnberg P, Reis A, Rauch A.

Am J Hum Genet. 2007 Mar;80(3):550-60. Epub 2007 Jan 29.

20.

CR10/80--Lymphoid interstitial pneumonia and Kabuki-Syndrome in a young man.

Zimmermann T, Brasch F, Rauch A, Stachel D, Holter W, Beck JD.

Paediatr Respir Rev. 2006;7 Suppl 1:S329. No abstract available.

PMID:
17036410
21.

CR3/108--Congenital alveolar capillary dysplasia with familiary microphthalmia.

Schirmer-Zimmerman H, Hammersen G, Scheuerlen W, Griese M, Brasch F, Rauch A.

Paediatr Respir Rev. 2006;7 Suppl 1:S326. No abstract available.

PMID:
17036407
22.

Microfibril-associated protein 4 binds to surfactant protein A (SP-A) and colocalizes with SP-A in the extracellular matrix of the lung.

Schlosser A, Thomsen T, Shipley JM, Hein PW, Brasch F, Tornøe I, Nielsen O, Skjødt K, Palaniyar N, Steinhilber W, McCormack FX, Holmskov U.

Scand J Immunol. 2006 Aug;64(2):104-16.

23.

Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency.

Brasch F, Schimanski S, Mühlfeld C, Barlage S, Langmann T, Aslanidis C, Boettcher A, Dada A, Schroten H, Mildenberger E, Prueter E, Ballmann M, Ochs M, Johnen G, Griese M, Schmitz G.

Am J Respir Crit Care Med. 2006 Sep 1;174(5):571-80. Epub 2006 May 25.

PMID:
16728712
24.

Prevalence of the mismatch-repair-deficient phenotype in colonic adenomas arising in HNPCC patients: results of a 5-year follow-up study.

German HNPCC Consortium, Müller A, Beckmann C, Westphal G, Bocker Edmonston T, Friedrichs N, Dietmaier W, Brasch FE, Kloor M, Poremba C, Keller G, Aust DE, Fass J, Büttner R, Becker H, Rüschoff J.

Int J Colorectal Dis. 2006 Oct;21(7):632-41. Epub 2006 Mar 2.

PMID:
16511680
25.

[Interstitial pulmonary diseases].

Brasch F.

Pathologe. 2006 Mar;27(2):116-32. Review. German.

PMID:
16456642
26.

Distribution of surfactant proteins in type II pneumocytes of newborn, 14-day old, and adult rats: an immunoelectron microscopic and stereological study.

Schmiedl A, Ochs M, Mühlfeld C, Johnen G, Brasch F.

Histochem Cell Biol. 2005 Dec;124(6):465-76. Epub 2005 Sep 27.

PMID:
16187065
27.

[Pulmonary megakaryocyte-embolism in contact with osteomyelofibrosis].

Steppling H, Müller KM, Brasch F.

Pneumologie. 2005 Jun;59(6):376-7. German. No abstract available.

PMID:
15991073
28.

Decrease of the surface fraction of surfactant proteins containing clara cells and type II pneumocytes in a rat asthma model.

Schmiedl A, Tschernig T, Brasch F, Pabst R, Bargsten G.

Exp Toxicol Pathol. 2005 Mar;56(4-5):265-72.

PMID:
15816355
29.

HNPCC-associated small bowel cancer: clinical and molecular characteristics.

Schulmann K, Brasch FE, Kunstmann E, Engel C, Pagenstecher C, Vogelsang H, Krüger S, Vogel T, Knaebel HP, Rüschoff J, Hahn SA, Knebel-Doeberitz MV, Moeslein G, Meltzer SJ, Schackert HK, Tympner C, Mangold E, Schmiegel W; German HNPCC Consortium.

Gastroenterology. 2005 Mar;128(3):590-9.

PMID:
15765394
30.

Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene.

Stevens PA, Pettenazzo A, Brasch F, Mulugeta S, Baritussio A, Ochs M, Morrison L, Russo SJ, Beers MF.

Pediatr Res. 2005 Jan;57(1):89-98. Epub 2004 Nov 19.

PMID:
15557112
31.

[Rare pulmonary occupational diseases--importance of microanalytical examination].

Brasch F, Müller KM.

Wien Klin Wochenschr. 2004;116 Suppl 1:18-24. German.

PMID:
15518087
32.

Surfactant proteins in pulmonary alveolar proteinosis in adults.

Brasch F, Birzele J, Ochs M, Guttentag SH, Schoch OD, Boehler A, Beers MF, Müller KM, Hawgood S, Johnen G.

Eur Respir J. 2004 Sep;24(3):426-35.

33.

Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene.

Brasch F, Griese M, Tredano M, Johnen G, Ochs M, Rieger C, Mulugeta S, Müller KM, Bahuau M, Beers MF.

Eur Respir J. 2004 Jul;24(1):30-9. Review.

34.

[Classification of pulmonary alveolar proteinosis in newborns, infants, and children].

Brasch F, Müller KM.

Pathologe. 2004 Jul;25(4):299-309. German.

PMID:
15241624
35.

HNPCC: six new pathogenic mutations.

Kunstmann E, Vieland J, Brasch FE, Hahn SA, Epplen JT, Schulmann K, Schmiegel W.

BMC Med Genet. 2004 Jun 24;5:16.

36.

Pivotal role of cathepsin K in lung fibrosis.

Bühling F, Röcken C, Brasch F, Hartig R, Yasuda Y, Saftig P, Brömme D, Welte T.

Am J Pathol. 2004 Jun;164(6):2203-16.

37.

[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)].

Rüschoff J, Roggendorf B, Brasch F, Mathiak M, Aust DE, Plaschke J, Mueller W, Poremba C, Kloor M, Keller G, Muders M, Blasenbreu-Vogt S, Rümmele P, Müller A, Büttner R; Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)].

Pathologe. 2004 May;25(3):178-92. Review. German.

PMID:
15138699
38.

Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease.

Tredano M, Griese M, Brasch F, Schumacher S, de Blic J, Marque S, Houdayer C, Elion J, Couderc R, Bahuau M.

Am J Med Genet A. 2004 Apr 1;126A(1):18-26.

PMID:
15039969
39.

Collagenous colitis: implications for the role of vascular endothelial growth factor in repair mechanisms.

Griga T, Tromm A, Schmiegel W, Pfisterer O, Müller KM, Brasch F.

Eur J Gastroenterol Hepatol. 2004 Apr;16(4):397-402.

PMID:
15028972
40.

Microsatellite instability and expression of MLH1 and MSH2 in carcinomas of the small intestine.

Schulmann K, Hahn SA, Brasch F, Schmiegel W.

Cancer. 2003 Oct 15;98(8):1774-5; author reply 1775-6. No abstract available.

41.

Involvement of napsin A in the C- and N-terminal processing of surfactant protein B in type-II pneumocytes of the human lung.

Brasch F, Ochs M, Kahne T, Guttentag S, Schauer-Vukasinovic V, Derrick M, Johnen G, Kapp N, Muller KM, Richter J, Giller T, Hawgood S, Buhling F.

J Biol Chem. 2003 Dec 5;278(49):49006-14. Epub 2003 Sep 16.

42.

Surfactant protein B in type II pneumocytes and intra-alveolar surfactant forms of human lungs.

Brasch F, Johnen G, Winn-Brasch A, Guttentag SH, Schmiedl A, Kapp N, Suzuki Y, Müller KM, Richter J, Hawgood S, Ochs M.

Am J Respir Cell Mol Biol. 2004 Apr;30(4):449-58. Epub 2003 Sep 11.

PMID:
12972403
43.

Adult polyglucosan body disease: a postmortem correlation study.

Sindern E, Ziemssen F, Ziemssen T, Podskarbi T, Shin Y, Brasch F, Müller KM, Schröder JM, Malin JP, Vorgerd M.

Neurology. 2003 Jul 22;61(2):263-5.

PMID:
12874416
44.

Cysteine protease activity is required for surfactant protein B processing and lamellar body genesis.

Guttentag S, Robinson L, Zhang P, Brasch F, Bühling F, Beers M.

Am J Respir Cell Mol Biol. 2003 Jan;28(1):69-79.

PMID:
12495934
45.

Effect of surfactant on ventilation-induced mediator release in isolated perfused mouse lungs.

Stamme C, Brasch F, von Bethmann A, Uhlig S.

Pulm Pharmacol Ther. 2002;15(5):455-61.

PMID:
12406668
46.

Involvement of cathepsin H in the processing of the hydrophobic surfactant-associated protein C in type II pneumocytes.

Brasch F, Ten Brinke A, Johnen G, Ochs M, Kapp N, Müller KM, Beers MF, Fehrenbach H, Richter J, Batenburg JJ, Bühling F.

Am J Respir Cell Mol Biol. 2002 Jun;26(6):659-70.

PMID:
12034564
47.

Immunohistochemical localization of vascular endothelial growth factor in colonic mucosa of patients with inflammatory bowel disease.

Griga T, May B, Pfisterer O, Müller KM, Brasch F.

Hepatogastroenterology. 2002 Jan-Feb;49(43):116-23.

PMID:
11941933
48.

Intracellular and intraalveolar localization of surfactant protein A (SP-A) in the parenchymal region of the human lung.

Ochs M, Johnen G, Müller KM, Wahlers T, Hawgood S, Richter J, Brasch F.

Am J Respir Cell Mol Biol. 2002 Jan;26(1):91-8.

PMID:
11751208
49.

Can airways close completely?

Uhlig S, Wohlsen A, Brasch F.

J Appl Physiol (1985). 2000 Dec;89(6):2521-2. No abstract available.

50.

Computed chest tomography in an animal model for decompression sickness: radiologic, physiologic, and pathologic findings.

Reuter M, Tetzlaff K, Brasch F, Gerriets T, Weiher M, Struck N, Hirt S, Hansen J, Müller KM, Heller M.

Eur Radiol. 2000;10(3):534-41.

PMID:
10757012

Supplemental Content

Loading ...
Support Center