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How instability in virtual economies of mobile digital games drives and ruins profit

EAI endorsed transactions on context-aware systems and applications., 2019-08, Vol.6 (18), p.162632

Lohse, P.

2019

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Higher Education in an Age of Disruption: Comparing European Internationalisation Policies

Lohse, Anna P

2024

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

Arthritis & rheumatology (Hoboken, N.J.), 2017-11, Vol.69 (11), p.2233-2240

2017

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Successful treatment of PASH syndrome with infliximab, cyclosporine and dapsone

Journal of the European Academy of Dermatology and Venereology, 2015-11, Vol.29 (11), p.2243-2247

2015

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

Infection, 2017-08, Vol.45 (4), p.395-402

2017

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Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-09, Vol.20 (5), p.e372-e375

2014

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Brief Report: Clinical and Molecular Phenotypes of Low‐Penetrance Variants of NLRP3: Diagnostic and Therapeutic Challenges

Arthritis & rheumatology (Hoboken, N.J.), 2017-11, Vol.69 (11), p.2233-2240

2017

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MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromes

Annals of the rheumatic diseases, 2011-12, Vol.70 (12), p.2075-2081

2011

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Data Augmentation for SAR Sea Ice and Water Classification Based on Per-Class Backscatter Variation With Incidence Angle

IEEE transactions on geoscience and remote sensing, 2023, Vol.61, p.1-15

2023

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Chronology of Glacial Advances and Deglaciation in the Encierro River Valley (29° Lat. S), Southern Atacama Desert, Based on Geomorphological Mapping and Cosmogenic 10Be Exposure Ages

Frontiers in earth science (Lausanne), 2022-07, Vol.10

2022

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Autoinflammatorische (Fieber-)Syndrome - Klinik, Genetik und Therapie

Aktuelle Rheumatologie, 2007-06, Vol.32 (3), p.154-161

Lohse, P

2007

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Genetics of cryopyrin-associated periodic syndrome

Zeitschrift für Rheumatologie, 2017-05, Vol.76 (4), p.313-321

2017

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Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine

Journal of perinatology, 2013-06, Vol.33 (6), p.492-494

2013

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Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics

Rheumatology (Oxford, England), 2009-08, Vol.48 (8), p.987-991

2009

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Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children

Rheumatology international, 2012-10, Vol.32 (10), p.3253-3260

2012

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease

Gut, 2005-10, Vol.54 (10), p.1421-1427

2005

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Conditions for cross-border policy transfer and cooperation: Analysing differences between higher education and vocational training

Research in comparative and international education, 2021-12, Vol.16 (4), p.361-383

2021

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Clinical and functional characterisation of a novel TNFRSF1A c.605T>A/V173D cleavage site mutation associated with tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS), cardiovascular complications and excellent response to etanercept treatment

Annals of the rheumatic diseases, 2008-09, Vol.67 (9), p.1292-1298

2008

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Cholesteryl ester storage disease: an easily missed diagnosis in oligosymptomatic children

Zeitschrift fur Gastroenterologie, 2013-10, Vol.51 (10), p.1184

2013

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Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population

European journal of pediatrics, 2012-12, Vol.171 (12), p.1775-1785

2012

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Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis

Clinical genetics, 2010-02, Vol.77 (2), p.119-130

2010

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Family with marked hyperferritinemia as a result of hemochromatosis type 4 (ferroportin disease)

Zeitschrift fur Gastroenterologie, 2014-09, Vol.52 (9), p.1075

2014

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Polymorphisms in the ACE and PAI‐1 genes are associated with recurrent spontaneous miscarriages

Human reproduction (Oxford), 2003-11, Vol.18 (11), p.2473-2477

2003

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

Multiple sclerosis, 2012-09, Vol.18 (9), p.1229-1238

2012

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FRI0515 Neutrophil-Specific S100A12 Phenotype Correlates to Genotype in Familial Mediterranean Fever

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.615-615

2015

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How instability in virtual economies of mobile digital games drives and ruins profit

Higher Education in an Age of Disruption: Comparing European Internationalisation Policies

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

Successful treatment of PASH syndrome with infliximab, cyclosporine and dapsone

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

Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor

Brief Report: Clinical and Molecular Phenotypes of Low‐Penetrance Variants of NLRP3: Diagnostic and Therapeutic Challenges

MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromes

Data Augmentation for SAR Sea Ice and Water Classification Based on Per-Class Backscatter Variation With Incidence Angle

Chronology of Glacial Advances and Deglaciation in the Encierro River Valley (29° Lat. S), Southern Atacama Desert, Based on Geomorphological Mapping and Cosmogenic 10Be Exposure Ages

Autoinflammatorische (Fieber-)Syndrome - Klinik, Genetik und Therapie

Genetics of cryopyrin-associated periodic syndrome

Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine

Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics

Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease

Conditions for cross-border policy transfer and cooperation: Analysing differences between higher education and vocational training

Clinical and functional characterisation of a novel TNFRSF1A c.605T>A/V173D cleavage site mutation associated with tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS), cardiovascular complications and excellent response to etanercept treatment

Cholesteryl ester storage disease: an easily missed diagnosis in oligosymptomatic children

Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population

Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosis

Family with marked hyperferritinemia as a result of hemochromatosis type 4 (ferroportin disease)

Polymorphisms in the ACE and PAI‐1 genes are associated with recurrent spontaneous miscarriages

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

FRI0515 Neutrophil-Specific S100A12 Phenotype Correlates to Genotype in Familial Mediterranean Fever

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