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Breaking down the fences among registries on autoinflammatory diseases: the E-Merge project

Orphanet journal of rare diseases, 2023-07, Vol.18 (1), p.191-191, Article 191

2023

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Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease

Annals of the rheumatic diseases, 2009-02, Vol.68 (2), p.246-248

2009

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Unravelling the clinical heterogeneity of undefined recurrent fever over time in the European registries on Autoinflammation

Pediatric rheumatology online journal, 2024-05, Vol.22 (1), p.55-55, Article 55

2024

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IL-6 blockade in systemic juvenile idiopathic arthritis - achievement of inactive disease and remission (data from the German AID-registry)

Pediatric rheumatology online journal, 2018-04, Vol.16 (1), p.22-8, Article 22

2018

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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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Rekurrierende Fiebersyndrome – Subgruppe der autoinflammatorischen Erkrankungen

Monatsschrift Kinderheilkunde, 2021-05, Vol.169 (5), p.432-442

2021

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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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Genetic fever syndromes. Hereditary recurrent (periodic) fever syndromes

Zeitschrift für Rheumatologie, 2013-05, Vol.72 (4), p.332-338

2013

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Cholestasis After Pediatric Liver Transplantation–Recurrence of a Progressive Familial Intrahepatic Cholestasis Phenotype as a Rare Differential Diagnosis: A Case Report

Transplantation proceedings, 2017-09, Vol.49 (7), p.1628-1633

2017

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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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Atypical clinical presentation of a severe Tumor Necrosis Factor Receptor-associated Periodic Syndrome (TRAPS) without mutation in the TNFRSF1A gene and good response to anakinra. Case report of a ten year old girl with fever, skin edema and abdominal pain (AID-registry)

Pediatric rheumatology online journal, 2015-09, Vol.13 (S1), p.P43-P43, Article P43

2015

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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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THU0382 Familial mediterranean fever (FMF) - disease activity and quality of life in adult patients of turkish ancestry living in turkey or germany

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.284-285

2013

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Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristics

Klinische Padiatrie, 2010-11, Vol.222 (6), p.356

2010

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Genotype-phenotype and genotype-origin correlations in children with mediterranean fever in Germany - an AID-net study

Klinische Padiatrie, 2013-11, Vol.225 (6), p.325

2013

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Update Alpha-1-Antitrypsin-Mangel

Monatsschrift Kinderheilkunde, 2022-06

2022

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Colchicine therapy in children with FMF

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.O44-O44, Article O44

2015

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Persistierende Transaminasenerhöhung und Hepatopathie nach schwerer Grunderkrankung im frühen Kindesalter: Sekundär sklerosierende Cholangitis kritisch kranker Patienten

Monatsschrift Kinderheilkunde, 2022-02, Vol.170 (2), p.146-152

2022

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Recurrent fever syndromes--Subgroup of autoinflammatory diseases/Rekurrierende Fiebersyndrome -- Subgruppe der autoinflammatorischen Erkrankungen

Monatsschrift Kinderheilkunde, 2021-05, Vol.169 (5), p.432

2021

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PMU62 Improved Quality of Life in Children With Progressive Familial Intrahepatic Cholestasis Following 24 Weeks of Treatment With Odevixibat, an Ileal Bile Acid Transporter Inhibitor: Results From the Phase 3 PEDFIC 1 Study

Value in health, 2021-06, Vol.24, p.S155-S155

2021

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Self-medication to treat pain in attacks of familial Mediterranean fever: aiming to find a new approach to pain management

Schmerz (Berlin, Germany), 2013-12, Vol.27 (6), p.605-611

2013

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OC48 Odevixibat therapy in patients with FIC1-deficient progressive familial intrahepatic cholestasis and severe diarrhoea following liver transplantation: a retrospective case series

Frontline gastroenterology, 2023-07, Vol.14 (Suppl 1), p.A29-A30

2023

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Prevalence and complications of uveitis in juvenile idiopathic arthritis in a population-based nation-wide study in Germany: suggested modification of the current screening guidelines

Rheumatology (Oxford, England), 2007-06, Vol.46 (6), p.1015-1019

2007

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Genetische Fiebersyndrome: Hereditäre rekurrierende (periodische) Fiebersyndrome

Zeitschrift für Rheumatologie, 2013-05, Vol.72 (4), p.332-338

2013

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Breaking down the fences among registries on autoinflammatory diseases: the E-Merge project

Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease

Unravelling the clinical heterogeneity of undefined recurrent fever over time in the European registries on Autoinflammation

IL-6 blockade in systemic juvenile idiopathic arthritis - achievement of inactive disease and remission (data from the German AID-registry)

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

Rekurrierende Fiebersyndrome – Subgruppe der autoinflammatorischen Erkrankungen

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

Genetic fever syndromes. Hereditary recurrent (periodic) fever syndromes

Cholestasis After Pediatric Liver Transplantation–Recurrence of a Progressive Familial Intrahepatic Cholestasis Phenotype as a Rare Differential Diagnosis: A Case Report

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

Atypical clinical presentation of a severe Tumor Necrosis Factor Receptor-associated Periodic Syndrome (TRAPS) without mutation in the TNFRSF1A gene and good response to anakinra. Case report of a ten year old girl with fever, skin edema and abdominal pain (AID-registry)

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

THU0382 Familial mediterranean fever (FMF) - disease activity and quality of life in adult patients of turkish ancestry living in turkey or germany

Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristics

Genotype-phenotype and genotype-origin correlations in children with mediterranean fever in Germany - an AID-net study

Update Alpha-1-Antitrypsin-Mangel

Colchicine therapy in children with FMF

Persistierende Transaminasenerhöhung und Hepatopathie nach schwerer Grunderkrankung im frühen Kindesalter: Sekundär sklerosierende Cholangitis kritisch kranker Patienten

Recurrent fever syndromes--Subgroup of autoinflammatory diseases/Rekurrierende Fiebersyndrome -- Subgruppe der autoinflammatorischen Erkrankungen

PMU62 Improved Quality of Life in Children With Progressive Familial Intrahepatic Cholestasis Following 24 Weeks of Treatment With Odevixibat, an Ileal Bile Acid Transporter Inhibitor: Results From the Phase 3 PEDFIC 1 Study

Self-medication to treat pain in attacks of familial Mediterranean fever: aiming to find a new approach to pain management

Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial

OC48 Odevixibat therapy in patients with FIC1-deficient progressive familial intrahepatic cholestasis and severe diarrhoea following liver transplantation: a retrospective case series

Prevalence and complications of uveitis in juvenile idiopathic arthritis in a population-based nation-wide study in Germany: suggested modification of the current screening guidelines

Genetische Fiebersyndrome: Hereditäre rekurrierende (periodische) Fiebersyndrome

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