Lohse P - Search Results

1

Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases.

Kümpfel T, Hoffmann LA, Pellkofer H, Pöllmann W, Feneberg W, Hohlfeld R, Lohse P. Kümpfel T, et al. Among authors: lohse p. Neurology. 2008 Nov 25;71(22):1812-20. doi: 10.1212/01.wnl.0000335930.18776.47. Neurology. 2008. PMID: 19029521

2

Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis.

Blaschek A, Lohse P, Huss K, Borggraefe I, Mueller-Felber W, Heinen F, Hohlfeld R, Kümpfel T. Blaschek A, et al. Among authors: lohse p. Mult Scler. 2010 Dec;16(12):1517-20. doi: 10.1177/1352458510382933. Epub 2010 Sep 27. Mult Scler. 2010. PMID: 20876156

3

Familial Mediterranean fever-associated mutation pyrin E148Q as a potential risk factor for multiple sclerosis.

Kümpfel T, Gerdes LA, Wacker T, Blaschek A, Havla J, Krumbholz M, Pöllmann W, Feneberg W, Hohlfeld R, Lohse P. Kümpfel T, et al. Among authors: lohse p. Mult Scler. 2012 Sep;18(9):1229-38. doi: 10.1177/1352458512437813. Epub 2012 Feb 15. Mult Scler. 2012. PMID: 22337722

4

TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome.

Hoffmann LA, Lohse P, König FB, Feneberg W, Hohlfeld R, Kümpfel T. Hoffmann LA, et al. Among authors: lohse p. Neurology. 2008 Mar 25;70(13 Pt 2):1155-6. doi: 10.1212/01.wnl.0000296279.98236.8a. Epub 2008 Feb 20. Neurology. 2008. PMID: 18287568 No abstract available.

5

Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation.

Kümpfel T, Hoffmann LA, Rübsamen H, Pöllmann W, Feneberg W, Hohlfeld R, Lohse P. Kümpfel T, et al. Among authors: lohse p. Arthritis Rheum. 2007 Aug;56(8):2774-83. doi: 10.1002/art.22795. Arthritis Rheum. 2007. PMID: 17665448 Free article.

6

Havla J, Lohse P, Gerdes LA, Hohlfeld R, Kümpfel T. Havla J, et al. Among authors: lohse p. J Rheumatol. 2013 Mar;40(3):261-4. doi: 10.3899/jrheum.120729. Epub 2013 Jan 15. J Rheumatol. 2013. PMID: 23322460

7

TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis.

Blaschek A, V Kries R, Lohse P, Huss K, Vill K, Belohradsky BH, Heinen F, Müller-Felber W, Kümpfel T. Blaschek A, et al. Among authors: lohse p. Eur J Paediatr Neurol. 2018 Jan;22(1):72-81. doi: 10.1016/j.ejpn.2017.08.007. Epub 2017 Sep 1. Eur J Paediatr Neurol. 2018. PMID: 28927886

8

Multiple sclerosis-like lesions and type I interferon signature in a patient with RVCL.

Schuh E, Ertl-Wagner B, Lohse P, Wolf W, Mann JF, Lee-Kirsch MA, Hohlfeld R, Kümpfel T. Schuh E, et al. Among authors: lohse p. Neurol Neuroimmunol Neuroinflamm. 2014 Dec 23;2(1):e55. doi: 10.1212/NXI.0000000000000055. eCollection 2015 Feb. Neurol Neuroimmunol Neuroinflamm. 2014. PMID: 25566545 Free PMC article. No abstract available.

9

Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutations.

Schuh E, Lohse P, Ertl-Wagner B, Witt M, Krumbholz M, Frankenberger M, Gerdes LA, Hohlfeld R, Kümpfel T. Schuh E, et al. Among authors: lohse p. Neurol Neuroimmunol Neuroinflamm. 2015 May 14;2(4):e109. doi: 10.1212/NXI.0000000000000109. eCollection 2015 Aug. Neurol Neuroimmunol Neuroinflamm. 2015. PMID: 26020059 Free PMC article.

10

Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutation.

Hoffmann F, Lohse P, Stojanov S, Shin YS, Renner ED, Kéry A, Zellerer S, Belohradsky BH. Hoffmann F, et al. Among authors: lohse p. Eur J Hum Genet. 2005 Apr;13(4):510-2. doi: 10.1038/sj.ejhg.5201352. Eur J Hum Genet. 2005. PMID: 15657603

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