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Authors whose works are in public domain in at least one jurisdiction

List of works by Mikko Seppänen

1-50 of 69 results

Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease

scientific article

The evolution of cellular deficiency in GATA2 mutation

scientific article published on 17 December 2013

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.

scientific article

TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk

scientific article

Dermatologic Features of ADA2 Deficiency in Cutaneous Polyarteritis Nodosa

scientific article published in July 2015

Mannose-binding lectin 2 gene polymorphism in recurrent herpes simplex virus 2 infection

scientific article published on 4 February 2009

Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes

scientific article published on 20 January 2017

Complement C4 deficiency and HLA homozygosity in patients with frequent intraoral herpes simplex virus type 1 infections

scientific article published on 26 September 2001

Serum complement C3/C4 ratio, a novel marker for recurrent cardiovascular events

scientific article

Immunoglobulins and complement factor C4 in adult rhinosinusitis

scientific article published on 01 August 2006

Rhinovirus/enterovirus RNA in tonsillar tissue of children with tonsillar disease

scientific article published on 8 November 2005

Subtly impaired humoral immunity predisposes to frequently recurring genital herpes simplex virus type 2 infection and herpetic neuralgia

scientific article published on 24 July 2006

Proinflammatory HLA-DRB1*01-haplotype predisposes to ST-elevation myocardial infarction

scientific article published on 20 January 2012

Human MHC region harbors both susceptibility and protective haplotypes for coronary artery disease

scientific article published on 01 January 2007

HLA-DRB1 allele frequencies and C4 copy number variation in Finnish sarcoidosis patients and associations with disease prognosis

scientific article published on 23 October 2011

Major histocompatibility complex class II and BTNL2 associations in sarcoidosis

scientific article published in August 2013

Changes in brain function and morphology in patients with recurring herpes simplex virus infections and chronic pain

scientific article published on 15 May 2009

Copy number analysis of complement C4A, C4B and C4A silencing mutation by real-time quantitative polymerase chain reaction

scientific article

ADA2 deficiency: clonal lymphoproliferation in a subset of patients

scientific article published on 29 January 2018

Terminal deletion of 11q with significant late-onset combined immune deficiency

scientific article

Recurrent lymphocytic meningitis positive for herpes simplex virus type 2.

scientific article published on July 2009

Occurrence of human bocaviruses and parvovirus 4 in solid tissues

scientific article published in August 2012

Is there a need to redefine the diagnostic criteria for common variable immunodeficiency?

scientific article published on 10 December 2013

C4A deficiency in children and adolescents with recurrent respiratory infections

scientific article published on 26 February 2012

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland

scientific article published on 28 September 2017

Inhibition of rubella virus replication by the broad-spectrum drug nitazoxanide in cell culture and in a patient with a primary immune deficiency

scientific article published on 30 September 2017

Complement and C4 Null Alleles in Severe Chronic Adult Periodontitis

scientific article published on 01 February 2007

Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland

scientific article published on 04 May 2016

Widespread unilateral pain associated with herpes simplex virus infections

scientific article published on 15 April 2008

HLA-DRB1*01 allele and low plasma immunoglobulin G1 concentration may predispose to herpes-associated recurrent lymphocytic meningitis

scientific article

Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

scientific article published on 19 March 2019

Analysis of clinical and immunologic phenotype in a large cohort of children and adults with cartilage-hair hypoplasia

scientific article published on 8 March 2017

SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations

scientific article published on 19 April 2017

Complement C4 deficiency--a plausible risk factor for non-tuberculous mycobacteria (NTM) infection in apparently immunocompetent patients

scientific article

X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world

scientific article published on 22 March 2019

Myiasis during adventure sports race

scientific article published in January 2004

Diversity of extended HLA-DRB1 haplotypes in the Finnish population

scientific article

Binding of complement regulators factor H and C4b binding protein to group A streptococcal strains isolated from tonsillar tissue and blood

scientific article published on 16 April 2008

Genetic variation in schlafen genes in a patient with a recapitulation of the murine Elektra phenotype

article

Lymphotoxin alpha LTA+496C allele is a risk factor for periodontitis in patients with coronary artery disease

scientific article

A High Prevalence of Gastrointestinal Manifestations in Common Variable Immunodeficiency

scientific article published on 01 April 2019

Peripheral hypertrophic subepithelial corneal degeneration: characterization, treatment and association with human leucocyte antigen genes

scientific article published on 7 February 2013

Emerging Infections and Pertinent Infections Related to Travel for Patients with Primary Immunodeficiencies.

scientific article published on 7 August 2017

Echovirus type 4 as a probable cause of meningitis associated with bilateral optic neuritis: a case report

scientific article published in March 2004

Haploinsufficiency of A20 impairs protein-protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation

scientific article published on 17 October 2018

Primary immunodeficiency associated with chromosomal aberration - an ESID survey

scientific article published on 02 August 2016

Association of Chlamydia pneumoniae infection with HLA-B*35 in patients with coronary artery disease

scientific article

Novel DSP Spectrin 6 Region Variant Causes Neonatal Erythroderma, Failure to Thrive, Severe Herpes Simplex Infections and Brain Lesions

scientific article published on 01 July 2019

Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease

scientific article published on 27 June 2019

Immunoglobulin G treatment of secondary immunodeficiencies in the era of novel therapies

scientific article published on December 1, 2014