Lohse P - Search Results

1

Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonate.

Parappil H, Al Baridi A, ur Rahman S, Kitchi MH, Ruef P, Griese M, Lohse P, Aslanidis C, Schmitz G, Koch L, Poeschl J. Parappil H, et al. Among authors: lohse p. BMJ Case Rep. 2011 Mar 3;2011:bcr1020103427. doi: 10.1136/bcr.10.2010.3427. BMJ Case Rep. 2011. PMID: 22707629 Free PMC article.

2

Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine.

Hepping N, Griese M, Lohse P, Garbe W, Lange L. Hepping N, et al. Among authors: lohse p. J Perinatol. 2013 Jun;33(6):492-4. doi: 10.1038/jp.2012.131. J Perinatol. 2013. PMID: 23719253

3

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. Griese M, et al. Among authors: lohse p. Clin Genet. 2010 Feb;77(2):119-30. doi: 10.1111/j.1399-0004.2009.01325.x. Epub 2009 Dec 10. Clin Genet. 2010. PMID: 20002450

4

Children with absent surfactant protein D in bronchoalveolar lavage have more frequently pneumonia.

Griese M, Steinecker M, Schumacher S, Braun A, Lohse P, Heinrich S. Griese M, et al. Among authors: lohse p. Pediatr Allergy Immunol. 2008 Nov;19(7):639-47. doi: 10.1111/j.1399-3038.2007.00695.x. Epub 2008 Feb 11. Pediatr Allergy Immunol. 2008. PMID: 18266831

5

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. Griese M, et al. Among authors: lohse p. BMC Pediatr. 2011 Aug 17;11:72. doi: 10.1186/1471-2431-11-72. BMC Pediatr. 2011. PMID: 21849033 Free PMC article.

6

Molecular analysis of the MVK and TNFRSF1A genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: a low-penetrance TNFRSF1A variant in a heterozygous MVK carrier possibly influences the phenotype of hyperimmunoglobulinemia D with periodic fever syndrome or vice versa.

Stojanov S, Lohse P, Lohse P, Hoffmann F, Renner ED, Zellerer S, Kéry A, Shin YS, Haas D, Hoffmann GF, Belohradsky BH. Stojanov S, et al. Among authors: lohse p. Arthritis Rheum. 2004 Jun;50(6):1951-8. doi: 10.1002/art.20264. Arthritis Rheum. 2004. PMID: 15188372 Free article.

7

Microsatellite instability, loss of heterozygosity, and loss of hMLH1 and hMSH2 protein expression in endometrial carcinoma.

Peiró G, Diebold J, Lohse P, Ruebsamen H, Lohse P, Baretton GB, Löhrs U. Peiró G, et al. Among authors: lohse p. Hum Pathol. 2002 Mar;33(3):347-54. doi: 10.1053/hupa.2002.32220. Hum Pathol. 2002. PMID: 11979377

8

Pseudodominant inheritance of the hyperimmunoglobulinemia D with periodic fever syndrome in a mother and her two monozygotic twins.

Hospach T, Lohse P, Heilbronner H, Dannecker GE, Lohse P. Hospach T, et al. Among authors: lohse p. Arthritis Rheum. 2005 Nov;52(11):3606-10. doi: 10.1002/art.21381. Arthritis Rheum. 2005. PMID: 16255052 Free article.

9

Genetic analyses permit the differentiation between reactive malfunctions ('promyelocyte arrest') and arising promyelocyte leukemia in a pregnant patient with a history of a medulloblastoma.

Poleck-Dehlin B, Duell T, Bartl R, Lohse P, Rhein A, Diebold J, Kohl P, Mittermueller J, Schmetzer H. Poleck-Dehlin B, et al. Among authors: lohse p. Leuk Lymphoma. 2004 Sep;45(9):1905-11. doi: 10.1080/10428190410001697377. Leuk Lymphoma. 2004. PMID: 15223653

10

R116C mutation of cationic trypsinogen in a Turkish family with recurrent pancreatitis illustrates genetic microheterogeneity of hereditary pancreatitis.

Tautermann G, Ruebsamen H, Beck M, Dertinger S, Drexel H, Lohse P. Tautermann G, et al. Among authors: lohse p. Digestion. 2001;64(4):226-32. doi: 10.1159/000048866. Digestion. 2001. PMID: 11842279

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