Lohse P - Search Results

1

Familial Mediterranean fever in Germany: clinical presentation and amyloidosis risk.

Ebrahimi-Fakhari D, Schönland SO, Hegenbart U, Lohse P, Beimler J, Wahlster L, Ho AD, Lorenz HM, Blank N. Ebrahimi-Fakhari D, et al. Among authors: lohse p. Scand J Rheumatol. 2013;42(1):52-8. doi: 10.3109/03009742.2012.714796. Epub 2012 Nov 8. Scand J Rheumatol. 2013. PMID: 23137073

2

Risk factors for AA amyloidosis in Germany.

Blank N, Hegenbart U, Lohse P, Beimler J, Röcken C, Ho AD, Lorenz HM, Schönland SO. Blank N, et al. Among authors: lohse p. Amyloid. 2015 Mar;22(1):1-7. doi: 10.3109/13506129.2014.980942. Epub 2014 Nov 7. Amyloid. 2015. PMID: 25376380

3

Skeletal scintigraphy indicates disease severity of cardiac involvement in patients with senile systemic amyloidosis.

Kristen AV, Haufe S, Schonland SO, Hegenbart U, Schnabel PA, Röcken C, Hardt S, Lohse P, Ho AD, Haberkorn U, Dengler TJ, Altland K, Katus HA. Kristen AV, et al. Among authors: lohse p. Int J Cardiol. 2013 Apr 5;164(2):179-84. doi: 10.1016/j.ijcard.2011.06.123. Epub 2011 Jul 20. Int J Cardiol. 2013. PMID: 21764155

4

Immunohistochemistry in the classification of systemic forms of amyloidosis: a systematic investigation of 117 patients.

Schönland SO, Hegenbart U, Bochtler T, Mangatter A, Hansberg M, Ho AD, Lohse P, Röcken C. Schönland SO, et al. Among authors: lohse p. Blood. 2012 Jan 12;119(2):488-93. doi: 10.1182/blood-2011-06-358507. Epub 2011 Nov 21. Blood. 2012. PMID: 22106346 Free article.

5

Three German fibrinogen Aalpha-chain amyloidosis patients with the p.Glu526Val mutation.

Eriksson M, Schönland S, Bergner R, Hegenbart U, Lohse P, Schmidt H, Röcken C. Eriksson M, et al. Among authors: lohse p. Virchows Arch. 2008 Jul;453(1):25-31. doi: 10.1007/s00428-008-0619-4. Epub 2008 May 24. Virchows Arch. 2008. PMID: 18500534

6

Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid.

Eriksson M, Büttner J, Todorov T, Yumlu S, Schönland S, Hegenbart U, Kristen AV, Dengler T, Lohse P, Helmke B, Schmidt H, Röcken C. Eriksson M, et al. Among authors: lohse p. Am J Surg Pathol. 2009 Jan;33(1):58-65. doi: 10.1097/PAS.0b013e3181788566. Am J Surg Pathol. 2009. PMID: 18830126

7

Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens: identification of three novel mutations in the APOA1 gene.

Eriksson M, Schönland S, Yumlu S, Hegenbart U, von Hutten H, Gioeva Z, Lohse P, Büttner J, Schmidt H, Röcken C. Eriksson M, et al. Among authors: lohse p. J Mol Diagn. 2009 May;11(3):257-62. doi: 10.2353/jmoldx.2009.080161. Epub 2009 Mar 26. J Mol Diagn. 2009. PMID: 19324996 Free PMC article.

8

Clinical and Molecular Phenotypes of Low-Penetrance Variants of NLRP3: Diagnostic and Therapeutic Challenges.

Kuemmerle-Deschner JB, Verma D, Endres T, Broderick L, de Jesus AA, Hofer F, Blank N, Krause K, Rietschel C, Horneff G, Aksentijevich I, Lohse P, Goldbach-Mansky R, Hoffman HM, Benseler SM. Kuemmerle-Deschner JB, et al. Among authors: lohse p. Arthritis Rheumatol. 2017 Nov;69(11):2233-2240. doi: 10.1002/art.40208. Epub 2017 Oct 17. Arthritis Rheumatol. 2017. PMID: 28692792

9

Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population.

Lainka E, Bielak M, Lohse P, Timmann C, Stojanov S, von Kries R, Niehues T, Neudorf U. Lainka E, et al. Among authors: lohse p. Eur J Pediatr. 2012 Dec;171(12):1775-85. doi: 10.1007/s00431-012-1803-8. Epub 2012 Aug 19. Eur J Pediatr. 2012. PMID: 22903357

10

Genotype-phenotype and genotype-origin correlations in children with mediterranean fever in Germany - an AID-net study.

Jeske M, Lohse P, Kallinich T, Berger T, Rietschel C, Holzinger D, Kamlah C, Lankisch P, Berendes R, Dueckers G, Horneff G, Lilienthal E, Haas JP, Giese A, Dressler F, Berrang J, Braunewell L, Neudorf U, Niehues T, Föll D, Lainka E. Jeske M, et al. Among authors: lohse p. Klin Padiatr. 2013 Nov;225(6):325-30. doi: 10.1055/s-0033-1355372. Epub 2013 Oct 24. Klin Padiatr. 2013. PMID: 24158885

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