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Schnitzler's syndrome - a novel hypothesis of a shared pathophysiologic mechanism with Waldenström's disease.
van Leersum, F S; Potjewijd, J; van Geel, M; Steijlen, P M; Vreeburg, M.
Affiliation
  • van Leersum FS; Department of Dermatology, Maastricht University Medical Centre, P. Debyelaan 25, 6229, HX, Maastricht, The Netherlands. frank.van.leersum@mumc.nl.
  • Potjewijd J; Department of Internal Medicine, Division of Clinical and Experimental Immunology, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • van Geel M; Department of Dermatology, Maastricht University Medical Centre, P. Debyelaan 25, 6229, HX, Maastricht, The Netherlands.
  • Steijlen PM; Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Vreeburg M; Grow Research School for Oncology And Developmental Biology, Maastricht University Medical Centre, Maastricht, The Netherlands.
Orphanet J Rare Dis ; 14(1): 151, 2019 06 22.
Article in En | MEDLINE | ID: mdl-31228950
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Schnitzler Syndrome / Hereditary Autoinflammatory Diseases Limits: Animals / Humans Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2019 Document type: Article Affiliation country: Países Bajos
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Schnitzler Syndrome / Hereditary Autoinflammatory Diseases Limits: Animals / Humans Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2019 Document type: Article Affiliation country: Países Bajos