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Items: 1 to 50 of 303

1.

Metabolic labelling of choline phospholipids probes ABCA3 transport in lamellar bodies.

Li Y, Kinting S, Höppner S, Forstner ME, Uhl O, Koletzko B, Griese M.

Biochim Biophys Acta Mol Cell Biol Lipids. 2019 Aug 29;1864(12):158516. doi: 10.1016/j.bbalip.2019.158516. [Epub ahead of print]

PMID:
31473345
2.

Abandoning developmental silos: what can paediatricians and adult interstitial lung disease physicians learn from each other?

Spagnolo P, Griese M, Cocconcelli E, Bernardinello N, Bush A.

Curr Opin Pulm Med. 2019 Sep;25(5):418-425. doi: 10.1097/MCP.0000000000000594.

PMID:
31365375
3.

Bi-allelic missense ABCA3 mutations in a patient with childhood ILD who reached adulthood.

Manali ED, Legendre M, Nathan N, Kannengiesser C, Coulomb-L'Hermine A, Tsiligiannis T, Tomos P, Griese M, Borie R, Clement A, Amselem S, Crestani B, Papiris SA.

ERJ Open Res. 2019 Jul 22;5(3). pii: 00066-2019. doi: 10.1183/23120541.00066-2019. eCollection 2019 Jul.

4.

Clinical characteristics of patients with familial idiopathic pulmonary fibrosis (f-IPF).

Krauss E, Gehrken G, Drakopanagiotakis F, Tello S, Dartsch RC, Maurer O, Windhorst A, von der Beck D, Griese M, Seeger W, Guenther A.

BMC Pulm Med. 2019 Jul 18;19(1):130. doi: 10.1186/s12890-019-0895-6.

5.

Potentiation of ABCA3 lipid transport function by ivacaftor and genistein.

Kinting S, Li Y, Forstner M, Delhommel F, Sattler M, Griese M.

J Cell Mol Med. 2019 Aug;23(8):5225-5234. doi: 10.1111/jcmm.14397. Epub 2019 Jun 18.

6.

Phenotype characterisation of TBX4 mutation and deletion carriers with neonatal and paediatric pulmonary hypertension.

Galambos C, Mullen MP, Shieh JT, Schwerk N, Kielt MJ, Ullmann N, Boldrini R, Stucin-Gantar I, Haass C, Bansal M, Agrawal PB, Johnson J, Peca D, Surace C, Cutrera R, Pauciulo MW, Nichols WC, Griese M, Ivy D, Abman SH, Austin ED, Danhaive O.

Eur Respir J. 2019 Aug 22;54(2). pii: 1801965. doi: 10.1183/13993003.01965-2018. Print 2019 Aug.

PMID:
31151956
7.

Abandoning developmental silos: what can paediatricians and adult interstitial lung disease physicians learn from each other?

Spagnolo P, Griese M, Cocconcelli E, Bernardinello N, Bush A.

Curr Opin Pulm Med. 2019 May 28. doi: 10.1097/MCP.0000000000000594. [Epub ahead of print]

PMID:
31145142
8.

Lavage lipidomics signatures in children with cystic fibrosis and protracted bacterial bronchitis.

Seidl E, Kiermeier H, Liebisch G, Ballmann M, Hesse S, Paul-Buck K, Ratjen F, Rietschel E, Griese M.

J Cyst Fibros. 2019 Apr 24. pii: S1569-1993(18)30860-9. doi: 10.1016/j.jcf.2019.04.012. [Epub ahead of print]

PMID:
31029606
9.

Quantitative Lipidomics in Pulmonary Alveolar Proteinosis.

Griese M, Bonella F, Costabel U, de Blic J, Tran NB, Liebisch G.

Am J Respir Crit Care Med. 2019 Oct 1;200(7):881-887. doi: 10.1164/rccm.201901-0086OC.

PMID:
31002528
10.

De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism.

Diets IJ, van der Donk R, Baltrunaite K, Waanders E, Reijnders MRF, Dingemans AJM, Pfundt R, Vulto-van Silfhout AT, Wiel L, Gilissen C, Thevenon J, Perrin L, Afenjar A, Nava C, Keren B, Bartz S, Peri B, Beunders G, Verbeek N, van Gassen K, Thiffault I, Cadieux-Dion M, Huerta-Saenz L, Wagner M, Konstantopoulou V, Vodopiutz J, Griese M, Boel A, Callewaert B, Brunner HG, Kleefstra T, Hoogerbrugge N, de Vries BBA, Hwa V, Dauber A, Hehir-Kwa JY, Kuiper RP, Jongmans MCJ.

Am J Hum Genet. 2019 Apr 4;104(4):758-766. doi: 10.1016/j.ajhg.2019.02.023. Epub 2019 Mar 28.

11.

Pulmonary alveolar proteinosis.

Trapnell BC, Nakata K, Bonella F, Campo I, Griese M, Hamilton J, Wang T, Morgan C, Cottin V, McCarthy C.

Nat Rev Dis Primers. 2019 Mar 7;5(1):16. doi: 10.1038/s41572-019-0066-3. Review.

PMID:
30846703
12.

Lung disease in STAT3 hyper-IgE syndrome requires intense therapy.

Kröner C, Neumann J, Ley-Zaporozhan J, Hagl B, Meixner I, Spielberger BD, Dückers G, Belohradsky BH, Niehues T, Borte M, Rosenecker J, Kappler M, Nährig S, Reu S, Griese M, Renner ED.

Allergy. 2019 Sep;74(9):1691-1702. doi: 10.1111/all.13753. Epub 2019 Apr 4.

PMID:
30793327
13.

Patient education for children with interstitial lung diseases and their caregivers: A pilot study.

Niemitz M, Schrader M, Carlens J, Hengst M, Eismann C, Goldbeck L, Griese M, Schwerk N.

Patient Educ Couns. 2019 Jun;102(6):1131-1139. doi: 10.1016/j.pec.2019.01.016. Epub 2019 Jan 23.

PMID:
30709570
14.

Early onset children's interstitial lung diseases: Discrete entities or manifestations of pulmonary dysmaturity?

Bush A, Griese M, Seidl E, Kerem E, Reu S, Nicholson AG.

Paediatr Respir Rev. 2019 Apr;30:65-71. doi: 10.1016/j.prrv.2018.09.004. Epub 2018 Oct 9. Review.

PMID:
30552058
15.

Congenital Vertical Tracheal Septum Misdiagnosed as Laryngomalacia.

Reiter K, Kramer J, Griese M, Kammer B.

Am J Respir Crit Care Med. 2019 Apr 1;199(7):917-918. doi: 10.1164/rccm.201805-0891IM. No abstract available.

PMID:
30407842
16.

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.

17.

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
18.

Pathogenesis, imaging and clinical characteristics of CF and non-CF bronchiectasis.

Schäfer J, Griese M, Chandrasekaran R, Chotirmall SH, Hartl D.

BMC Pulm Med. 2018 May 22;18(1):79. doi: 10.1186/s12890-018-0630-8. Review.

19.

Development and validation of a health-related quality of life questionnaire for pediatric patients with interstitial lung disease.

Niemitz M, Schwerk N, Goldbeck L, Griese M.

Pediatr Pulmonol. 2018 Jul;53(7):954-963. doi: 10.1002/ppul.24018. Epub 2018 Apr 23.

PMID:
29687642
20.

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.

21.

ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypes.

Schindlbeck U, Wittmann T, Höppner S, Kinting S, Liebisch G, Hegermann J, Griese M.

Hum Mutat. 2018 Jun;39(6):841-850. doi: 10.1002/humu.23416. Epub 2018 Mar 25.

PMID:
29505158
22.

Chronic interstitial lung disease in children.

Griese M.

Eur Respir Rev. 2018 Feb 7;27(147). pii: 170100. doi: 10.1183/16000617.0100-2017. Print 2018 Mar 31. Review.

23.

Functional rescue of misfolding ABCA3 mutations by small molecular correctors.

Kinting S, Höppner S, Schindlbeck U, Forstner ME, Harfst J, Wittmann T, Griese M.

Hum Mol Genet. 2018 Mar 15;27(6):943-953. doi: 10.1093/hmg/ddy011.

PMID:
29325094
24.

An informative intragenic microsatellite marker suggests the IL-1 receptor as a genetic modifier in cystic fibrosis.

Stanke F, Hector A, Hedtfeld S, Hartl D, Griese M, Tümmler B, Mall MA.

Eur Respir J. 2017 Dec 28;50(6). pii: 1700426. doi: 10.1183/13993003.00426-2017. Print 2017 Dec. No abstract available.

25.

Assessment of the multiplex PCR-based assay Unyvero pneumonia application for detection of bacterial pathogens and antibiotic resistance genes in children and neonates.

Papan C, Meyer-Buehn M, Laniado G, Nicolai T, Griese M, Huebner J.

Infection. 2018 Apr;46(2):189-196. doi: 10.1007/s15010-017-1088-y. Epub 2017 Oct 31.

PMID:
29086343
26.

International management platform for children's interstitial lung disease (chILD-EU).

Griese M, Seidl E, Hengst M, Reu S, Rock H, Anthony G, Kiper N, Emiralioğlu N, Snijders D, Goldbeck L, Leidl R, Ley-Zaporozhan J, Krüger-Stollfuss I, Kammer B, Wesselak T, Eismann C, Schams A, Neuner D, MacLean M, Nicholson AG, Lauren M, Clement A, Epaud R, de Blic J, Ashworth M, Aurora P, Calder A, Wetzke M, Kappler M, Cunningham S, Schwerk N, Bush A; the other chILD-EU collaborators.

Thorax. 2018 Mar;73(3):231-239. doi: 10.1136/thoraxjnl-2017-210519. Epub 2017 Oct 22.

27.

Tezacaftor/Ivacaftor in Subjects with Cystic Fibrosis and F508del/F508del-CFTR or F508del/G551D-CFTR.

Donaldson SH, Pilewski JM, Griese M, Cooke J, Viswanathan L, Tullis E, Davies JC, Lekstrom-Himes JA, Wang LT; VX11-661-101 Study Group.

Am J Respir Crit Care Med. 2018 Jan 15;197(2):214-224. doi: 10.1164/rccm.201704-0717OC.

28.

Quantification of volume and lipid filling of intracellular vesicles carrying the ABCA3 transporter.

Höppner S, Kinting S, Torrano AA, Schindlbeck U, Bräuchle C, Zarbock R, Wittmann T, Griese M.

Biochim Biophys Acta Mol Cell Res. 2017 Dec;1864(12):2330-2335. doi: 10.1016/j.bbamcr.2017.08.013. Epub 2017 Sep 6.

29.

Pulmonary Alveolar Proteinosis: A Comprehensive Clinical Perspective.

Griese M.

Pediatrics. 2017 Aug;140(2). pii: e20170610. doi: 10.1542/peds.2017-0610. Review.

30.

Serum YKL-40 is a reliable biomarker for pulmonary alveolar proteinosis.

Bonella F, Long X, He X, Ohshimo S, Griese M, Guzman J, Costabel U.

Respirology. 2017 Oct;22(7):1371-1378. doi: 10.1111/resp.13082. Epub 2017 May 31.

31.

Increasing Total Serum IgE, Allergic Bronchopulmonary Aspergillosis, and Lung Function in Cystic Fibrosis.

Gothe F, Kappler M, Griese M.

J Allergy Clin Immunol Pract. 2017 Nov - Dec;5(6):1591-1598.e6. doi: 10.1016/j.jaip.2017.03.033. Epub 2017 May 16.

PMID:
28526275
32.

Increasing sputum levels of gamma-glutamyltransferase may identify cystic fibrosis patients who do not benefit from inhaled glutathione.

Corti A, Griese M, Hector A, Pompella A.

J Cyst Fibros. 2017 May;16(3):342-345. doi: 10.1016/j.jcf.2016.12.002. Epub 2016 Dec 14.

33.

Management of children with interstitial lung diseases: the difficult issue of acute exacerbations.

Clement A, de Blic J, Epaud R, Galeron L, Nathan N, Hadchouel A, Barbato A, Snijders D, Kiper N, Cunningham S, Griese M, Bush A, Schwerk N; chILD-EU collaboration.

Eur Respir J. 2016 Dec;48(6):1559-1563. doi: 10.1183/13993003.01900-2016. No abstract available.

34.

Pott's disease: a major issue for an unaccompanied refugee minor.

Papan C, von Both U, Kappler M, Kammer B, Griese M, Huebner J.

Thorax. 2017 Mar;72(3):282-283. doi: 10.1136/thoraxjnl-2016-209468. Epub 2016 Nov 21.

PMID:
27872320
35.

Serum YKL-40 as predictor of outcome in hypersensitivity pneumonitis.

Long X, He X, Ohshimo S, Griese M, Sarria R, Guzman J, Costabel U, Bonella F.

Eur Respir J. 2017 Feb 23;49(2). pii: 1501924. doi: 10.1183/13993003.01924-2015. Print 2017 Feb.

36.

Whole lung lavage therapy for pulmonary alveolar proteinosis: a global survey of current practices and procedures.

Campo I, Luisetti M, Griese M, Trapnell BC, Bonella F, Grutters J, Nakata K, Van Moorsel CH, Costabel U, Cottin V, Ichiwata T, Inoue Y, Braschi A, Bonizzoni G, Iotti GA, Tinelli C, Rodi G; WLL International Study Group.

Orphanet J Rare Dis. 2016 Aug 31;11(1):115. doi: 10.1186/s13023-016-0497-9.

37.

Delivery of Alpha-1 Antitrypsin to Airways.

Griese M, Scheuch G.

Ann Am Thorac Soc. 2016 Aug;13 Suppl 4:S346-51. doi: 10.1513/AnnalsATS.201507-469KV. Review.

PMID:
27564672
38.

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
39.

TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization.

Wallmeier J, Shiratori H, Dougherty GW, Edelbusch C, Hjeij R, Loges NT, Menchen T, Olbrich H, Pennekamp P, Raidt J, Werner C, Minegishi K, Shinohara K, Asai Y, Takaoka K, Lee C, Griese M, Memari Y, Durbin R, Kolb-Kokocinski A, Sauer S, Wallingford JB, Hamada H, Omran H.

Am J Hum Genet. 2016 Aug 4;99(2):460-9. doi: 10.1016/j.ajhg.2016.06.014.

40.

A Global Survey on Whole Lung Lavage in Pulmonary Alveolar Proteinosis.

Campo I, Luisetti M, Griese M, Trapnell BC, Bonella F, Grutters JC, Nakata K, Van Moorsel CH, Costabel U, Cottin V, Ichiwata T, Inoue Y, Braschi A, Bonizzoni G, Iotti GA, Tinelli C, Rodi G; WLL International Study Group.

Chest. 2016 Jul;150(1):251-3. doi: 10.1016/j.chest.2016.04.030. No abstract available.

41.

Eradication of methicillin resistant Staphylococcus aureus detected for the first time in cystic fibrosis: A single center observational study.

Kappler M, Nagel F, Feilcke M, Kröner C, Pawlita I, Naehrig S, Ripper J, Hengst M, von Both U, Forstner M, Hector A, Griese M.

Pediatr Pulmonol. 2016 Oct;51(10):1010-1019. doi: 10.1002/ppul.23519. Epub 2016 Jul 5.

PMID:
27378061
42.

European idiopathic pulmonary fibrosis Patient Charter: a missed opportunity.

Bush A, Barbato A, Clement A, Cunningham S, Blic Jd, Gilbert C, Goldbeck L, Kiper N, Schwerk N, Griese M.

Eur Respir J. 2016 Jul;48(1):282-3. doi: 10.1183/13993003.00505-2016. No abstract available.

43.

Homooligomerization of ABCA3 and its functional significance.

Frixel S, Lotz-Havla AS, Kern S, Kaltenborn E, Wittmann T, Gersting SW, Muntau AC, Zarbock R, Griese M.

Int J Mol Med. 2016 Aug;38(2):558-66. doi: 10.3892/ijmm.2016.2650. Epub 2016 Jun 21.

PMID:
27352740
44.

Serum Levels of Surfactant Proteins in Patients with Combined Pulmonary Fibrosis and Emphysema (CPFE).

Papaioannou AI, Kostikas K, Manali ED, Papadaki G, Roussou A, Spathis A, Mazioti A, Tomos I, Papanikolaou I, Loukides S, Chainis K, Karakitsos P, Griese M, Papiris S.

PLoS One. 2016 Jun 23;11(6):e0157789. doi: 10.1371/journal.pone.0157789. eCollection 2016.

45.

Lung clearance index for monitoring early lung disease in alpha-1-antitrypsin deficiency.

Fuchs SI, Schwerk N, Pittschieler K, Ahrens F, Baden W, Bals R, Fähndrich S, Gleiber W, Griese M, Hülskamp G, Köhnlein T, Reckling L, Rietschel E, Staab D, Gappa M.

Respir Med. 2016 Jul;116:93-9. doi: 10.1016/j.rmed.2016.04.015. Epub 2016 Apr 27.

46.

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
47.

MUC1 gene polymorphisms are associated with serum KL-6 levels and pulmonary dysfunction in pulmonary alveolar proteinosis.

Bonella F, Long X, Ohshimo S, Horimasu Y, Griese M, Guzman J, Kohno N, Costabel U.

Orphanet J Rare Dis. 2016 Apr 23;11:48. doi: 10.1186/s13023-016-0430-2.

48.

Chitinase activation in patients with fungus-associated cystic fibrosis lung disease.

Hector A, Chotirmall SH, Lavelle GM, Mirković B, Horan D, Eichler L, Mezger M, Singh A, Ralhan A, Berenbrinker S, Mack I, Ensenauer R, Riethmüller J, Graepler-Mainka U, Murray MA, Griese M, McElvaney NG, Hartl D.

J Allergy Clin Immunol. 2016 Oct;138(4):1183-1189.e4. doi: 10.1016/j.jaci.2016.01.031. Epub 2016 Apr 4.

PMID:
27056270
49.

Analysis of the Proteolytic Processing of ABCA3: Identification of Cleavage Site and Involved Proteases.

Hofmann N, Galetskiy D, Rauch D, Wittmann T, Marquardt A, Griese M, Zarbock R.

PLoS One. 2016 Mar 31;11(3):e0152594. doi: 10.1371/journal.pone.0152594. eCollection 2016.

50.

Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.

Wittmann T, Frixel S, Höppner S, Schindlbeck U, Schams A, Kappler M, Hegermann J, Wrede C, Liebisch G, Vierzig A, Zacharasiewicz A, Kopp MV, Poets CF, Baden W, Hartl D, van Kaam AH, Lohse P, Aslanidis C, Zarbock R, Griese M.

Mol Med. 2016 Sep;22:183-191. doi: 10.2119/molmed.2015.00244. Epub 2016 Feb 26.

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