Lohse P - Search Results

1

Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndrome.

Bonfig W, Salem NJ, Heiliger K, Hempel M, Lederer G, Bornkamm M, Wieland K, Lohse P, Burdach S, Oexle K. Bonfig W, et al. Among authors: lohse p. J Pediatr Endocrinol Metab. 2012;25(9-10):991-5. doi: 10.1515/jpem-2012-0103. J Pediatr Endocrinol Metab. 2012. PMID: 23426831

2

GCK-MODY (MODY 2) Caused by a Novel p.Phe330Ser Mutation.

Bonfig W, Hermanns S, Warncke K, Eder G, Engelsberger I, Burdach S, Ziegler AG, Lohse P. Bonfig W, et al. Among authors: lohse p. ISRN Pediatr. 2011;2011:676549. doi: 10.5402/2011/676549. Epub 2011 Apr 26. ISRN Pediatr. 2011. PMID: 22389783 Free PMC article.

3

Recurrent multiple spinal paragangliomas as a manifestation of a metastatic composite paraganglioma-ganglioneuroblastoma.

Gempt J, Baldawa SS, Weirich G, Delbridge C, Hempel M, Lohse P, Meyer B, Ringel F. Gempt J, et al. Among authors: lohse p. Acta Neurochir (Wien). 2013 Jul;155(7):1241-2. doi: 10.1007/s00701-013-1678-0. Epub 2013 Mar 27. Acta Neurochir (Wien). 2013. PMID: 23532344 No abstract available.

4

Reduced Steroid Synthesis in the Follicular Fluid of MTHFR 677TT Mutation Carriers: Effects of Increased Folic Acid Administration.

Pavlik R, Hecht S, Noss U, Soldin OP, Mendu RD, Soldin SJ, Lohse P, Thaler CJ. Pavlik R, et al. Among authors: lohse p. Geburtshilfe Frauenheilkd. 2022 Sep 30;82(10):1074-1081. doi: 10.1055/a-1791-9358. eCollection 2022 Oct. Geburtshilfe Frauenheilkd. 2022. PMID: 36186148 Free PMC article.

5

Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgery.

Schnitzler F, Friedrich M, Angelberger M, Diegelmann J, Stallhofer J, Wolf C, Dütschler J, Truniger S, Olszak T, Beigel F, Tillack C, Lohse P, Brand S. Schnitzler F, et al. Among authors: lohse p. PLoS One. 2020 Jul 27;15(7):e0236421. doi: 10.1371/journal.pone.0236421. eCollection 2020. PLoS One. 2020. PMID: 32716958 Free PMC article.

6

[Optimization of long-term care of neurological patients through internet- and mobile-based interventions with and without persuasive elements including gamification].

Lohse P, Steinmetzer T, Reichmann H, Reckhardt M, Bönninger I, Reinhardt F. Lohse P, et al. Fortschr Neurol Psychiatr. 2020 Aug;88(8):500-513. doi: 10.1055/a-1028-7073. Epub 2020 Apr 17. Fortschr Neurol Psychiatr. 2020. PMID: 32303076 German.

7

Ein Fall von Muckle-Wells-Syndrom mit einer neuen NLRP3-Mutation.

Yuksel S, Metz M, Lohse P, Krause K. Yuksel S, et al. Among authors: lohse p. J Dtsch Dermatol Ges. 2018 Oct;16(10):1250-1252. doi: 10.1111/ddg.13640_g. J Dtsch Dermatol Ges. 2018. PMID: 30300484 No abstract available.

8

A Case of Muckle-Wells Syndrome due to novel NLRP3 mutation.

Yuksel S, Metz M, Lohse P, Krause K. Yuksel S, et al. Among authors: lohse p. J Dtsch Dermatol Ges. 2018 Oct;16(10):1250-1252. doi: 10.1111/ddg.13640. Epub 2018 Aug 29. J Dtsch Dermatol Ges. 2018. PMID: 30157308 No abstract available.

9

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

10

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

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