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Hereditary erythermalgia and acquired erythromelalgia.
van Genderen PJ, Michiels JJ, Drenth JP. van Genderen PJ, et al. Am J Med Genet. 1993 Feb 15;45(4):530-2. doi: 10.1002/ajmg.1320450426. Am J Med Genet. 1993. PMID: 8465864 No abstract available.
Classification and diagnosis of erythromelalgia and erythermalgia.
Michiels JJ, Drenth JP, Van Genderen PJ. Michiels JJ, et al. Among authors: van genderen pj. Int J Dermatol. 1995 Feb;34(2):97-100. doi: 10.1111/j.1365-4362.1995.tb03587.x. Int J Dermatol. 1995. PMID: 7737785 Review. No abstract available.
Decreased half-life time of plasma von Willebrand factor collagen binding activity in essential thrombocythaemia: normalization after cytoreduction of the increased platelet count.
van Genderen PJ, Prins FJ, Lucas IS, van de Moesdijk D, van Vliet HH, van Strik R, Michiels JJ. van Genderen PJ, et al. Among authors: van vliet hh, van strik r, van de moesdijk d. Br J Haematol. 1997 Dec;99(4):832-6. doi: 10.1046/j.1365-2141.1997.4823285.x. Br J Haematol. 1997. PMID: 9432029
Acquired von Willebrand disease.
van Genderen PJ, Michiels JJ. van Genderen PJ, et al. Baillieres Clin Haematol. 1998 Jun;11(2):319-30. doi: 10.1016/s0950-3536(98)80051-6. Baillieres Clin Haematol. 1998. PMID: 10097810 Review.
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