Polyarteritis Nodosa

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  Subject Areas on Research

  • A 78-year-old woman with leg pain and weakness. 
  • Alpha-1 Antitrypsin Deficiency in an Infant With Polyarteritis Nodosa. 
  • Antiphospholipid antibodies in patients with Wegener's granulomatosis and polyarteritis nodosa. 
  • Arteritis with impaired renal function. 
  • Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation. 
  • Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency. 
  • Cutaneous polyarteritis nodosa localized to a region of lymphedema secondary to Streptococcus viridans cellulitis and multiple surgeries. 
  • Cutaneous polyarteritis nodosa. Report of a case associated with Crohn's disease. 
  • Cyclophosphamide therapy of severe systemic necrotizing vasculitis. 
  • Deficiency of Adenosine Deaminase 2 (DADA2), an Inherited Cause of Polyarteritis Nodosa and a Mimic of Other Systemic Rheumatologic Disorders. 
  • Dermatologic Features of ADA2 Deficiency in Cutaneous Polyarteritis Nodosa. 
  • Diagnosis and treatment of the systemic and cutaneous necrotizing vasculitis syndromes. 
  • Early-onset stroke and vasculopathy associated with mutations in ADA2. 
  • Fatal infantile polyarteritis nodosa with predominant central nervous system involvement. 
  • Granulomatous angiitis of the central nervous system: protean manifestations and response to treatment. 
  • Human adenosine deaminase 2 deficiency: A multi-faceted inborn error of immunity. 
  • Hyperrenin-hyperaldosterone-dependent malignant hypertension in polyarteritis nodosa. 
  • Limitations of the 1990 American College of Rheumatology classification criteria in the diagnosis of vasculitis. 
  • Neuroradiologic findings in polyarteritis nodosa. 
  • Novel compound heterozygous variants in CECR1 gene associated with childhood onset polyarteritis nodosa and deficiency of ADA2. 
  • Polyarteritis Nodosum of the Breast in a Patient with History of Bilateral Augmentation Mammoplasty. 
  • Sequence-Based Screening of Patients With Idiopathic Polyarteritis Nodosa, Granulomatosis With Polyangiitis, and Microscopic Polyangiitis for Deleterious Genetic Variants in ADA2. 
  • The spectrum of vasculitis: clinical, pathologic, immunologic and therapeutic considerations. 
  • Treatment of vasculitis with cyclophosphamide. 
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  Keywords of People

  • Allen, Nancy Bates, Professor Emeritus of Medicine, Medicine, Rheumatology and Immunology