Hughes-Stovin syndrome (HSS) preliminary diagnostic criteria: a report by the HSS International Study Group (HSSISG)

Pulmonary embolism versus pulmonary vasculitis in Hughes-Stovin syndrome: Characteristic computed tomography pulmonary angiographic findings and diagnostic and therapeutic implications. HSS International Study Group

Giant cell arteritis associated with scalp, tongue or lip necrosis: A French multicenter case control study

Clinical picture, outcomes, and predictors of relapse in eosinophilia-associated coronary vasospasm: Data from a European multicentric study

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Allogeneic stem cell transplantation compared to conservative management in adults with inborn errors of immunity

Clinics dedicated to transition preparation for adolescents and young adults with chronic conditions: Factors influencing their use

In inflammatory myopathies, dropped head/bent spine syndrome is associated with scleromyositis: an international case-control study

Bilateral gastrocnemius myositis: an extra-intestinal manifestation of Crohn's disease

Complex Allele with Additive Gain-of-Function STING1 Variants in a Patient with Cavitating Lung Lesions and Aspergillosis

Granulomatous manifestations associated with COVID19 infection: Is there a link between these two diseases?

Pulmonary vasculitis in Hughes-Stovin syndrome (HSS): a reference atlas and computed tomography pulmonary angiography guide-a report by the HSS International Study Group

A critical analysis of 57 cases of Hughes-Stovin syndrome (HSS). A report by the HSS International Study Group (HSSISG)

Direct examination of Gram-negative spiral-shaped rods: what is hidden behind the Campylobacter spp.?

Follow-up of COVID-19 patients: LA is transient but other aPLs are persistent

Flare of IGA glomerulonephritis under G-CSF stimulation regimen for autologous stem cell transplantation in systemic sclerosis

Rapid Radiological Worsening and Cytokine Storm Syndrome in COVID-19 Pneumonia

Immune Defect in Adults With Down Syndrome: Insights Into a Complex Issue

Inadequate Immune Humoral Response against JC Virus in Progressive Multifocal Leukoencephalopathy Non-Survivors

Epidemiology, clinical picture and long-term outcomes of FIP1L1-PDGFRA-positive myeloid neoplasm with eosinophilia: Data from 151 patients

Progressive multifocal leukoencephalopathy and sarcoidosis under interleukin 7: The price of healing

Primary Immunodeficiencies With Defects in Innate Immunity: Focus on Orofacial Manifestations

Worldwide trends in all-cause mortality of auto-immune systemic diseases between 2001 and 2014

Infection risk among adults with down syndrome: a two group series of 101 patients in a tertiary center

Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies

Anti-Ku syndrome with elevated CK and anti-Ku syndrome with anti-dsDNA are two distinct entities with different outcomes

Persistent Acrocyanosis-A Rare Manifestation Revealing Anti-PL-12 Syndrome

Tongue and Scalp Necrosis: Simultaneous Initial Complications Revealing Giant Cell Arteritis

Adolescents and young adults (AYAs) affected by chronic immunological disease: A tool-box for success during the transition to adult care

CAR-T cells for treating systemic lupus erythematosus: A promising emerging therapy

Systemic lupus erythematosus and neutropaenia: a hallmark of haematological manifestations

Transitional B cells in quiescent SLE: An early checkpoint imprinted by IFN

10 most important contemporary challenges in the management of SLE

Impaired TLR9 responses in B cells from patients with systemic lupus erythematosus

Defective germinal center selection results in persistence of self-reactive B cells from the primary to the secondary repertoire in Primary Antiphospholipid Syndrome

An immunogenomic exome landscape of triple positive primary antiphospholipid patients

B cells in primary antiphospholipid syndrome: Review and remaining challenges

IKZF1 Loss-of-Function Variant Causes Autoimmunity and Severe Familial Antiphospholipid Syndrome

Tolerance and efficacy of targeted therapies prescribed for off-label indications in refractory systemic autoimmune diseases: data of the first 100 patients enrolled in the TATA registry (TArgeted Therapy in Autoimmune Diseases)

Prevalence of Antineutrophil Cytoplasmic Antibody-Associated Vasculitis and Spatial Association With Quarries in a Region of Northeastern France: A Capture-Recapture and Geospatial Analysis

Incidence and predictors of COVID-19 and flares in patients with rare autoimmune diseases: a systematic survey and serological study at a national reference center in France

Case Report: A New Gain-of-Function Mutation of STAT1 Identified in a Patient With Chronic Mucocutaneous Candidiasis and Rosacea-Like Demodicosis: An Emerging Association

Case Report: Acquired Disseminated BCG in the Context of a Delayed Immune Reconstitution After Hematological Malignancy

Recommendations for Transitioning Young People with Primary Immunodeficiency Disorders and Autoinflammatory Diseases to Adult Care

Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN Survey

Mixed connective tissue disease: state of the art on clinical practice guidelines

Beyond Anti-viral Effects of Chloroquine/Hydroxychloroquine

T1 mapping cardiac magnetic resonance imaging frequently detects subclinical diffuse myocardial fibrosis in systemic sclerosis patients

Primary immunodeficiencies and lymphoma: a systematic review of literature

Primary immunodeficiencies and lymphoma: a systematic review of literature

New-onset systemic sclerosis and scleroderma renal crisis under docetaxel

Hughes-Stovin syndrome (HSS) preliminary diagnostic criteria: a paradigm shift in managing pulmonary vasculitis in HSS and Behçet's disease (BD). On behalf of the HSS International Study Group (HSSISG) : Reply on Tahir Saygın Öğüt and Veli Yazısız "Comments on the proposed diagnostic criteria for Hughes-Stovin syndrome: the role of Behçet syndrome" (CLRH-D-26-01350)