196 results on '"Lainka, E."'
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2. Breaking down the fences among registries on autoinflammatory diseases: the E-Merge project
3. Update Alpha-1-Antitrypsin-Mangel
4. Persistierende Transaminasenerhöhung und Hepatopathie nach schwerer Grunderkrankung im frühen Kindesalter: Sekundär sklerosierende Cholangitis kritisch kranker Patienten
5. Unravelling the clinical heterogeneity of undefined recurrent fever over time in the European registries on Autoinflammation
6. Rekurrierende Fiebersyndrome – Subgruppe der autoinflammatorischen Erkrankungen
7. OC48 Odevixibat therapy in patients with FIC1-deficient progressive familial intrahepatic cholestasis and severe diarrhoea following liver transplantation: a retrospective case series
8. IL-6 blockade in systemic juvenile idiopathic arthritis – achievement of inactive disease and remission (data from the German AID-registry)
9. Persistent transaminase elevation and hepatopathy after severe underlying disease in early childhood Secondary sclerosing cholangitis of critically ill patients
10. P486 Immunization status of children and adolescents with inflammatory bowel disease or autoimmune hepatitis in Germany
11. Schmerztherapeutische Bedarfsmedikation bei Attacken von familiärem Mittelmeerfieber: Auf der Suche nach einem schmerztherapeutischen Ansatz
12. Fieber unklarer Genese
13. Genetische Fiebersyndrome: Hereditäre rekurrierende (periodische) Fiebersyndrome
14. Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population
15. 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
16. Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German children
17. Hereditäre rekurrierende Fiebersyndrome (HRF): Subgruppe der autoinflammatorischen Erkrankungen (AID)
18. Diagnostik und Therapie von Pseudorheumaknötchen (subkutanes Granuloma anulare)
19. Streptokokkeninfektion als Ursache für eine chronische perianale Dermatitis bei Kindern
20. Differences in the severity of the phenotype of children and adolescents with Familial Mediterranean Fever residing in Turkey and Germany
21. Spätmanifestierender kongenitaler Zwerchfelldefekt mit der klinischen Symptomatik rezidivierenden Erbrechens
22. Verlauf der Nierenfunktion und prognostische Faktoren einer Nierenfunktionsverschlechterung bei Kindern und Jugendlichen nach Lebertransplantation
23. Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease
24. Protokolle zur Klassifikation, Überwachung und Therapie in der Kinderrheumatologie (PRO-KIND): Autoinflammatorische Syndrome CAPS/TRAPS/HIDS
25. Analysis of quality of life, hepatic biochemical markers, and sleep in patients with progressive familial intrahepatic cholestasis who had a pruritus response with odevixibat treatment.
26. Persistierende Transaminasenerhöhung und Hepatopathie nach schwerer Grunderkrankung im frühen Kindesalter
27. Temporäre Colchizinbehandlung bei heterozygoten FMF-Patienten
28. Combination of clinical parameters and biomarkers for the prediction of colchicine dose increase in patients with Familial Mediterranean Fever
29. Entwicklung von konsensbasierten Protokollen für das Management der juvenilen Dermatomyositis in Deutschland
30. Cholestasis After Pediatric Liver Transplantation–Recurrence of a Progressive Familial Intrahepatic Cholestasis Phenotype as a Rare Differential Diagnosis: A Case Report
31. Harmonisierung der Diagnostik und Therapie der systemischen juvenilen idiopathischen Arthritis in Deutschland
32. Dysregulation of proinflammatory versus anti-inflammatory human TH17 cell functionalities in the autoinflammatory Schnitzler syndrome
33. Der Einfluss des Spendergeschlechts auf Gefäßkomplikationen nach Leberlebendtransplantationen für Kinder im Säuglingsalter
34. IL-6 Inhibition – Daten aus dem deutschen AID
35. Analyse autoinflammatorischer Erkrankungen (AID) unter Behandlung eines Interleukin-1-Inhibitors (Daten aus dem AID-Register)
36. TRAPS-Syndrom ohne Nachweis einer Mutation im TNFRSF1A-Gen mit gutem Ansprechen auf Anakinra
37. Interleukin (IL)- 6 inhibition - Follow-up data of the German AID-registry
38. 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)
39. 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)
40. Colchicine therapy in children with FMF
41. Interleukin (IL)- 6 inhibition - Follow-up data of the German AID-registry1
42. Kongenitale porto-systemische Shunts – multimodale Behandlung von 7 Patienten
43. FRI0515 Neutrophil-Specific S100A12 Phenotype Correlates to Genotype in Familial Mediterranean Fever
44. Klinische Charakteristika des PFAPA-Syndroms im AID-Register
45. PReS-FINAL-2215: Genotype-phenotype correlations in children with Familial Mediterranean Fever in Germany
46. PReS-FINAL-2216: Biomarkers MRP8/14 and S100A12 correspond with flare and remission clinical status in Sojia patients in the AID-NET register
47. P01-008 – FMF genotype-phenotype correlations in Germany
48. PW01-009 – Markers of inflammation in adult FMF patients
49. Genotype-Phenotype and Genotype-Origin Correlations in Children with Mediterranean Fever in Germany – an AID-Net Study
50. Ultrasound assessment of splenic size in patients with Familial Mediterranean Fever compared to healthy controls among Turkish migrants living in Germany.
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