Publications by authors named "Peter Lohse"

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Genome-wide significant association with seven novel multiple sclerosis risk loci.
J Med Genet 2015 Dec 16;52(12):848-55. Epub 2015 Oct 16.
Platform for Genome Analytics, Institutes of Neurogenetics & Integrative and Experimental Genomics, University of Lübeck, Lübeck, Germany Department of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Berlin, Germany Department of Medicine, School of Public Health, Imperial College London, London, UK.


Early detection of sensorineural hearing loss in Muckle-Wells-syndrome.
Pediatr Rheumatol Online J 2015 Nov 4;13(1):43. Epub 2015 Nov 4.
Department of Pediatrics, Division of Pediatric Rheumatology, University Hospital Tuebingen, Hoppe-Seyler-Str. 1, D-72076, Tuebingen, Germany.

Lipocalin-2 Is a Disease Activity Marker in Inflammatory Bowel Disease Regulated by IL-17A, IL-22, and TNF-α and Modulated by IL23R Genotype Status.
Inflamm Bowel Dis 2015 Oct;21(10):2327-40
*Department of Medicine II, Grosshadern, Ludwig-Maximilians-Universität (LMU), Munich, Germany; †Clinic for Preventive Dentistry and Parodontology, LMU Munich, Munich, Germany; ‡Clinic for Pediatric Pneumology and Neonatology, Hannover Medical School, Hannover, Germany; §Department of Clinical Chemistry, Grosshadern, LMU Munich, Munich, Germany; and ‖Institute of Human Genetics, RWTH Aachen University, Aachen, Germany.

Categorizing diffuse parenchymal lung disease in children.
Orphanet J Rare Dis 2015 Sep 25;10:122. Epub 2015 Sep 25.
Department of Pediatric Pneumology, Dr. von Haunersches Kinderspital, University of Munich, German Center for Lung Research, Lindwurmstraße 4, 80337, Munich, Germany.

Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutations.
Neurol Neuroimmunol Neuroinflamm 2015 Aug 14;2(4):e109. Epub 2015 May 14.
Institute of Clinical Neuroimmunology (E.S., M.K., L.-A.G., R.H., T.K.), Institute of Clinical Radiology (B.E.-W.), and Department of Rheumatology (M.W.), Ludwig-Maximillians University, Munich, Germany; Department of Neuroimmunology (E.S.), Center of Brain Research, Vienna, Austria; Institute of Laboratory Medicine and Human Genetics (P.L.), Singen, Germany; Comprehensive Pneumology Center (M.F.) (Ludwig-Maximilians University Munich, Asklepios Kliniken Gauting, Helmholtz Zentrum München, Germany); and Munich Cluster for Systems Neurology (SyNergy) (R.H.), Munich, Germany.

Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients.
Eur Respir J 2015 Jul 5;46(1):197-206. Epub 2015 Feb 5.
Department of Pediatric Pneumology, Hauner Children's Hospital, Ludwig-Maximilians University, Comprehensive Pneumology Center Munich (CPC-M), German Center for Lung Research (DZL), Munich, Germany

Multiple sclerosis-like lesions and type I interferon signature in a patient with RVCL.
Neurol Neuroimmunol Neuroinflamm 2015 Feb 23;2(1):e55. Epub 2014 Dec 23.
Institute of Clinical Neuroimmunology (E.S., R.H., T.K.) and Institute of Clinical Radiology (B.E.-W.), Ludwig-Maximilians University, Munich, Germany; Department of Neuroimmunology (E.S.), Center of Brain Research, Vienna, Austria; Institute of Laboratory Medicine and Human Genetics (P.L.), Singen, Germany; Department of Ophthalmology (W.W.), Outpatient Clinic Neuhann, Munich, Germany; Department of Nephrology (J.F.M.), Clinical Centre Schwabing, Munich, Germany; Department of Pediatrics (M.A.L.-K.), Technische Universität Dresden, Germany; and Munich Cluster for Systems Neurology (SyNergy) (R.H.), Munich, Germany.

Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis.
Orphanet J Rare Dis 2014 Nov 26;9:171. Epub 2014 Nov 26.
Department of Pediatric Pneumology, Hauner Children's Hospital, Ludwig-Maximilians-University, Member of the German Center for Lung Research (DZL), Munich, Germany.


Homozygosity for a partial deletion of apoprotein A-V signal peptide results in intracellular missorting of the protein and chylomicronemia in a breast-fed infant.
Atherosclerosis 2014 Mar 8;233(1):97-103. Epub 2014 Jan 8.
Department of Medicine, Asklepios Clinic St. Georg, Lohmuehlenstr. 5, 20099 Hamburg, Germany. Electronic address:


Skeletal scintigraphy indicates disease severity of cardiac involvement in patients with senile systemic amyloidosis.
Int J Cardiol 2013 Apr 20;164(2):179-84. Epub 2011 Jul 20.
Department of Cardiology, Angiology, and Respiratory Medicine, Im Neuenheimer Feld 410, Heidelberg, Germany.



Symptoms related to tumor necrosis factor receptor 1-associated periodic syndrome, multiple sclerosis, and severe rheumatoid arthritis in patients carrying the TNF receptor superfamily 1A D12E/p.Asp41Glu mutation.
J Rheumatol 2013 Mar 15;40(3):261-4. Epub 2013 Jan 15.
Institute of Clinical Neuroimmunology and the Department of Clinical Chemistry, Ludwig-Maximilians University, Munich, Germany.

A defect of CD16-positive monocytes can occur without disease.
Immunobiology 2013 Feb 28;218(2):169-74. Epub 2012 Feb 28.
Comprehensive Pneumology Center (CPC), Ludwig-Maximilians University, Asklepios Klinik Gauting and Helmholtz Center Munich, München, Germany.














Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid.
Am J Surg Pathol 2009 Jan;33(1):58-65
Department of Pathology, Medical Clinic of Gastroenterology, Hepatology, and Endocrinology, Charité University Hospital, Berlin, Germany.

Ultrafast intramolecular electronic energy transfer in rigidly linked aminopyrenyl-aminobenzanthronyl dyads--a femtosecond study.
Phys Chem Chem Phys 2009 Jan 30;11(2):317-23. Epub 2008 Oct 30.
Department of Physical Electronics, Faculty of Nuclear Science and Engineering, Czech Technical University, V Holesovickách 2, 180 00, Prague 8, Czech Republic.

Successful treatment of progressive cutaneous mastocytosis with imatinib in a 2-year-old boy carrying a somatic KIT mutation.
Blood 2008 Sep 20;112(5):1655-7. Epub 2008 Jun 20.
Division of Pediatric Hematology/Oncology, Department of Pediatrics and Adolescent Medicine, Medical University Graz, Graz, Austria.






NLRP3 E311K mutation in a large family with Muckle-Wells syndrome--description of a heterogeneous phenotype and response to treatment.
Arthritis Res Ther 2011 6;13(6):R196. Epub 2011 Dec 6.
Division of Pediatric Rheumatology, Dept, of Pediatrics, University Hospital Tübingen, Hoppe-Seyler-Straße 1, 72076 Tuebingen, Germany.







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