Acquired generalized lipodystrophy under immune checkpoint inhibition

Rheumatoid Arthritis

Updated recommendations of the German Society for Rheumatology for the care of patients with inflammatory rheumatic diseases in times of SARS-CoV-2 - methodology, key messages and justifying information

Rheumatology (Oxford).

Schulze-Koops H, Krüger K, Hoyer BF, Leipe J, Iking-Konert C, Specker C, Commission for Pharmacotherapy and the Board of Directors of the German Society for Rheumatology

doi: 10.1093/rheumatology/keab072.

Juvenile Idiopathic Arthritis

Systemic juvenile idiopathic arthritis and recurrent macrophage activation syndrome due to a CASP1 variant causing inflammasome hyperactivation

Rheumatology (Oxford).

Jørgensen SE, Christiansen M, Høst C, Glerup M, Mahler B, Lausten MM, Gad HH, Hartmann R, Herlin T, Mogensen TH

doi: 10.1093/rheumatology/keaa242.

Systemic Sclerosis

Severe thrombotic microangiopathy after autologous stem cell transplantation in systemic sclerosis: a case report

Rheumatology (Oxford)

Sharif MO, Leavis HL, van Paassen P, van Rhenen A, Timmermans SAMEG, Ton E, van Laar JM, Spierings J

doi: 10.1093/rheumatology/keab239

Further Publications Rheumatology

Colitis expands the phenotype of PAAND patients: new case report and review of the literature

Rheumatology (Oxford)

Valdivieso Shephard JL, Plasencia Rodríguez C, Suárez Ferrer C, Peiteado López D, Balsa Criado A, López-Granados E, Bravo García-Morato M

doi: 10.1093/rheumatology/keab215

Further Publications DermatologyFurther Publications ImmunologyFurther Publications Rheumatology

New variant in the IL1RN-gene (DIRA) associated with late-onset, CRMO-like presentation

Rheumatology (Oxford).

Kuemmerle-Deschner JB, Welzel T, Hoertnagel K, Tsiflikas I, Hospach A, Liu X, Schlipf S, Hansmann S, Samba SD, Griesinger A, Benseler SM, Weber AN

doi: 10.1093/rheumatology/keaa119.

Further Publications DermatologyFurther Publications ImmunologyFurther Publications Rheumatology

Rituximab for Eosinophilic Granulomatosis with Polyangiitis: a Systematic Review of Observational Studies

Rheumatology (Oxford).

Menditto VG, Rossetti G, Olivari D, Angeletti A, Rocchi M, Gabrielli A, Pomponio G

doi: 10.1093/rheumatology/keab046. Visit the original publication at ncbi.nlm.nih.gov

Immunodeficiency

Immunological Features of Neuroblastoma Amplified Sequence Deficiency: Report of the First Case Identified Through Newborn Screening for Primary Immunodeficiency and Review of the Literature

Front Immunol.

Ricci S, Lodi L, Serranti D, Moroni M, Belli G, Mancano G, La Barbera A, Forzano G, Mangone G, Indolfi G, Azzari C

doi: 10.3389/fimmu.2019.01955.

Further Publications DermatologyFurther Publications ImmunologyFurther Publications Rheumatology

A curable case of lupus: a case report

No abstract available

Immunodeficiency

Classical and Non-classical Presentations of Complement Factor I Deficiency: Two Contrasting Cases Diagnosed via Genetic and Genomic Methods

Front Immunol.

Shields AM, Pagnamenta AT, Pollard AJ, OxClinWGS., Taylor JC, Allroggen H, Patel SY

doi: 10.3389/fimmu.

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Updated recommendations of the German Society for Rheumatology for the care of patients with inflammatory rheumatic diseases in times of SARS-CoV-2 - methodology, key messages and justifying information

Systemic juvenile idiopathic arthritis and recurrent macrophage activation syndrome due to a CASP1 variant causing inflammasome hyperactivation

Severe thrombotic microangiopathy after autologous stem cell transplantation in systemic sclerosis: a case report

Colitis expands the phenotype of PAAND patients: new case report and review of the literature

New variant in the IL1RN-gene (DIRA) associated with late-onset, CRMO-like presentation

Rituximab for Eosinophilic Granulomatosis with Polyangiitis: a Systematic Review of Observational Studies

Immunological Features of Neuroblastoma Amplified Sequence Deficiency: Report of the First Case Identified Through Newborn Screening for Primary Immunodeficiency and Review of the Literature

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Classical and Non-classical Presentations of Complement Factor I Deficiency: Two Contrasting Cases Diagnosed via Genetic and Genomic Methods