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Pediatric Hematology and Oncology Volume 7, 1990 - Issue 4
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Miscellaneous Article

Familial Essential Thrombocyteemia

E. Fernandez-Robles Department of Haematology, Cliniques Universitaires Saint-Luc, Catholic University of Louvain, avenue Hippocrate 10, 1200, Brussels, Belgium
,
C. Vermylen Department of Haematology, Cliniques Universitaires Saint-Luc, Catholic University of Louvain, avenue Hippocrate 10, 1200, Brussels, Belgium
,
P. Martiat Department of Haematology, Cliniques Universitaires Saint-Luc, Catholic University of Louvain, avenue Hippocrate 10, 1200, Brussels, Belgium
,
J. Ninane Department of Haematology, Cliniques Universitaires Saint-Luc, Catholic University of Louvain, avenue Hippocrate 10, 1200, Brussels, Belgium
&
G. Cornu Department of Haematology, Cliniques Universitaires Saint-Luc, Catholic University of Louvain, avenue Hippocrate 10, 1200, Brussels, Belgium
Pages 373-376 | Received 23 Apr 1990, Accepted 24 Apr 1990, Published online: 09 Jul 2009

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E. Fernandez-Robles, C. Vermylen, P. Martiat, J. Ninane & G. Cornu. (1992) Familiai Essential Thrombocythemia. Pediatric Hematology and Oncology 9:1, pages 89-89.
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Sinasi özsoylu. (1992) Thrombocytosis in Children. Pediatric Hematology and Oncology 9:1, pages 87-87.
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Articles from other publishers (19)

Luciana Teofili & Luigi M. Larocca. (2011) Advances in understanding the pathogenesis of familial thrombocythaemia. British Journal of Haematology 152:6, pages 701-712.
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Lisa Pleyer, Victoria Faber, Daniel Neureiter, Daniel Neureiter & Richard Greil. 2010. Chronic Myeloid Neoplasias and Clonal Overlap Syndromes. Chronic Myeloid Neoplasias and Clonal Overlap Syndromes 15 50 .
N. Tecuceanu, R. Dardik, E. Rabizadeh, P. Raanani & A. Inbal. (2006) A family with hereditary thrombocythaemia and normal genes for thrombopoietin and c‐Mpl. British Journal of Haematology 135:3, pages 348-351.
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V. Mialou, S. Kagialis-Girard, C. Galambrun, C. Pondarré, K. Kebaili, M. Ffrench, M-P. Pagès & Y. Bertrand. (2005) Thrombocytoses et thrombocytémies essentielles de l'enfant. Archives de Pédiatrie 12:8, pages 1249-1254.
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M Stuhrmann, L. Bashawri, M. A. Ahmed, B. H. Al‐Awamy, W. Kühnau, J. Schmidtke & E. A. El‐Harith. (2001) Familial thrombocytosis as a recessive, possibly X‐linked trait in an Arab family. British Journal of Haematology 112:3, pages 616-620.
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A. Wiestner, S. A. Padosch, N. Ghilardi, J. M. Cesar, J. Odriozola, A. Shapiro & R. C. Skoda. (2000) Hereditary thrombocythaemia is a genetically heterogeneous disorder: exclusion of TPO and MPL in two families with hereditary thrombocythaemia. British Journal of Haematology 110:1, pages 104-109.
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Mario CazzolaRadek C. Skoda. (2000) Translational pathophysiology: a novel molecular mechanism of human disease. Blood 95:11, pages 3280-3288.
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Yigal Dror & Victor S. Blanchette. (2001) Essential thrombocythaemia in children. British Journal of Haematology 107:4, pages 691-698.
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Nico Ghilardi, Adrian Wiestner, Masahiro Kikuchi, Akimichi Ohsaka & Radek C. Skoda. (1999) Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene. British Journal of Haematology 107:2, pages 310-316.
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Yigal Dror, Alvin Zipursky & Victor S. Blanchette. (1999) Essential Thrombocythemia in Children. Journal of Pediatric Hematology/Oncology 21:5, pages 356-363.
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T.C. Pearson. (1998) 1 Diagnosis and classification of erythrocytoses and thrombocytoses. Baillière's Clinical Haematology 11:4, pages 695-720.
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Adrian Wiestner, Ronald J. Schlemper, Anthonie P.C. van der Maas & Radek C. Skoda. (1998) An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia. Nature Genetics 18:1, pages 49-52.
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Natan Cohen, Dorit Almoznino-Sarafian, Joshua Weissgarten, Irena Alon, Ronit Zaidenstein, Victor Dishi, Naomi Rahimi-Levene, Kalman Fried, David Modai & Ahuva Golik. (2008) Benign familial microcytic thrombocytosis with autosomal dominant transmission. Clinical Genetics 52:1, pages 47-50.
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PJ van Dijken, KH Woldendorp & JP van Wouwe. (2008) Familial thrombocytosis in infancy presenting with a leukaemoid reaction. Acta Paediatrica 85:9, pages 1132-1134.
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J. G. van den Tweel & W. G. M. Spliet. 1996. Paediatric Pathology. Paediatric Pathology 661 680 .
M. Kikuchi, T. Tayama, H. Hayakawa, I. Takahashi, H. Hoshino & A. Ohsaka. (2008) Familial thrombocytosis. British Journal of Haematology 89:4, pages 900-902.
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M. Pérez‐Encinas, J. L. Bello, S. Pérez‐Crespo, R. De Miguel & S. Tome. (2006) Familial myeloproliferative syndrome. American Journal of Hematology 46:3, pages 225-229.
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R. J. Schlemper, A. P. C. van der Maas & J. C. J. Eikenboom. (1994) Familial essential thrombocythemia: Clinical characteristics of 11 cases in one family. Annals of Hematology 68:3, pages 153-158.
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I M Hann. (1992) Myelodysplastic syndromes.. Archives of Disease in Childhood 67:7, pages 962-966.
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