Peter W. Lohse

Adolf Reichwein Str. 2
Siegen, NW 57076, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 59 publications

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

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

Journal: Geburtshilfe und Frauenheilkunde

Published: April 27, 2022

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.

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.

Journal: PloS one

Published: February 20, 2020

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

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

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Published: October 10, 2018

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

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

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Published: August 30, 2018

Genetics of cryopyrin-associated periodic syndrome

Genetics of cryopyrin-associated periodic syndrome

Journal: Zeitschrift fur Rheumatologie

Published: February 16, 2017

Hyper-IgD and periodic fever syndrome (HIDS) due to compound heterozygosity for G336S and V377I in a 44-year-old patient with a 27-year history of fever.

Hyper-IgD and periodic fever syndrome (HIDS) due to compound heterozygosity for G336S and V377I in a 44-year-old patient with a 27-year history of fever.

Journal: BMJ case reports

Published: December 01, 2016

Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome: differential diagnosis of septic arthritis by regular detection of exceedingly high synovial cell counts.

Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome: differential diagnosis of septic arthritis by regular detection of exceedingly high synovial cell counts.

Journal: Infection

Published: November 11, 2016

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

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

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: September 26, 2016

TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis.

TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: June 02, 2016

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.

Journal: G3 (Bethesda, Md.)

Published: May 20, 2016

Lung disease caused by ABCA3 mutations.

Lung disease caused by ABCA3 mutations.

Journal: Thorax

Published: March 29, 2016

Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.

Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.

Journal: Molecular medicine (Cambridge, Mass.)

Published: November 29, 2015

Showing 1-12 of 59

Last Updated: 09/26/2026