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<small> Simon, Laurence et al. “Bing-Neel Syndrome, a Rare Complication of Waldenström Macroglobulinemia: Analysis of 44 Cases and Review of the Literature. A Study on Behalf of the French Innovative Leukemia Organization (FILO).” Haematologica 100.12 (2015): 1587–1594. PMC. Web. 20 Feb. 2017. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666335 </small>
<small> Simon, Laurence et al. “Bing-Neel Syndrome, a Rare Complication of Waldenström Macroglobulinemia: Analysis of 44 Cases and Review of the Literature. A Study on Behalf of the French Innovative Leukemia Organization (FILO).” Haematologica 100.12 (2015): 1587–1594. PMC. Web. 20 Feb. 2017. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666335 </small>

<small>Halperin, Daniel et al. “Bing-Neel Syndrome Case Report: A Previously Undocumented IgG Variant with MRI, PET/CT, and PET/MRI Imaging.” Case Reports in Hematology 2016 (2016): 3931709. PMC. Web. 20 Feb. 2017. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837273/ </small>

Revision as of 17:04, 22 March 2017

Bing-Neel Syndrome

  • Introduction of the disease

History

  • discovery
  • Case work?


Symptoms

Diagnosis

Treatment

References

Monique C. Minnema, Eva Kimby, Shirley D’Sa, Luc-Matthieu Fornecker, Stéphanie Poulain, Tom J. Snijders, Efstathios Kastritis, Stéphane Kremer, Aikaterini Fitsiori, Laurence Simon, Frédéric Davi, Michael Lunn, Jorge J. Castillo, Christopher J. Patterson, Magali Le Garff-Tavernier, Myrto Costopoulos, Véronique Leblond, Marie-José Kersten, Meletios A. Dimopoulos, Steven P. Treon Haematologica Jan 2017, 102 (1) 43-51; DOI: 10.3324/haematol.2016.147728 http://www.haematologica.org/content/102/1/43

Simon, Laurence et al. “Bing-Neel Syndrome, a Rare Complication of Waldenström Macroglobulinemia: Analysis of 44 Cases and Review of the Literature. A Study on Behalf of the French Innovative Leukemia Organization (FILO).” Haematologica 100.12 (2015): 1587–1594. PMC. Web. 20 Feb. 2017. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666335