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- Bookeditor, Srdan Verstovsek.Contents:
Novel insights into myelofibrosis pathophysiology and treatment / Srdan Verstovsek
Primary myelofibrosis : diagnosis and risk stratification / Ben Y. Zhang & Naseema Gangat
Prognostication in myelofibrosis / Francesco Passamonti, Domenica Caramazza, Barbara Mora & Margherita Maffioli
Prognostic relevance of mutations in myelofibrosis / Paola Guglielmelli, Giada Rotunno, Annalisa Pacilli & Carmela Mannarelli
Disease burden for the patient with myelofibrosis : goals and response with therapy / Holly L. Geyer & Ruben A. Mesa
Myeloproliferative neoplasms and splanchnic vein thrombosis / Giovanni Barosi & Vittorio Rosti
Interferon therapy for myelofibrosis / Hans Carl Hasselbalch
JAK inhibitors as therapy for myelofibrosis / Srdan Verstovsek & Kate J. Newberry
What we can do about anemia in myelofibrosis / Francisco Cervantes & Arturo Pereira
Rationale for combination therapies in myelofibrosis / Alessandro M. Vannucchi, Niccolò Bartalucci, Lisa Pieri & Paola Guglielmelli
When and how to transplant patients with myelofibrosis / H. Joachim Deeg, Olga Sala-Torra & Bart L. Scot. - ArticleWaller T, Morein B, Fabiansson E.Lab Anim. 1978 Jul;12(3):145-8.Parenteral administration of Encephalitozoon cuniculi induced an antibody response within 7--11 days. Peroral administration was less effective since only 2 of 6 animals showed seroconversion; they became seropositive within 14--21 days. Sera from animals which became seropositive had high antibody titres during the whole test period. Immune sera from 3 animals were fractionated by gel filtration. With the india-ink immunoreaction test, antibodies to E. cuniculi were found only in the 7S fractions, while the indirect fluorescent-antibody test detected them in fractions 19S and 7S. The 7S fractions were identified as IgG and the 19S fractions as IgM. A program for eradication of encephalitozoonosis, based on these results, is discussed.