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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Holger Cario

Department of Pediatrics

University Children's Hospital Ulm

Germany

[email]@*.uni-ulm.de

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Affiliation

Department of Pediatrics, University Children's Hospital Ulm, Germany. 1999 - 2005

References

Childhood polycythemias/erythrocytoses: classification, diagnosis, clinical presentation, and treatment. Cario, H. Ann. Hematol. (2005) [Pubmed]
Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis. Cario, H., Schwarz, K., Jorch, N., Kyank, U., Petrides, P.E., Schneider, D.T., Uhle, R., Debatin, K.M., Kohne, E. Haematologica (2005) [Pubmed]
Congenital erythrocytosis and polycythemia vera in childhood and adolescence. Cario, H., Schwarz, K., Debatin, K.M., Kohne, E. Klin. Padiatr (2004) [Pubmed]
Disproportionately elevated fasting proinsulin levels in normoglycemic patients with thalassemia major are correlated to the degree of iron overload. Cario, H., Holl, R.W., Debatin, K.M., Kohne, E. Horm. Res. (2003) [Pubmed]
Insulin sensitivity and beta-cell secretion in thalassaemia major with secondary haemochromatosis: assessment by oral glucose tolerance test. Cario, H., Holl, R.W., Debatin, K.M., Kohne, E. Eur. J. Pediatr. (2003) [Pubmed]
Familial polycythemia vera with Budd-Chiari syndrome in childhood. Cario, H., Pahl, H.L., Schwarz, K., Galm, C., Hoffmann, M., Burdelski, M., Kohne, E., Debatin, K.M. Br. J. Haematol. (2003) [Pubmed]
Treatment with hydroxyurea in thalassemia intermedia with paravertebral pseudotumors of extramedullary hematopoiesis. Cario, H., Wegener, M., Debatin, K.M., Kohne, E. Ann. Hematol. (2002) [Pubmed]
Epidemiological situation and treatment of patients with thalassemia major in Germany: results of the German multicenter beta-thalassemia study. Cario, H., Stahnke, K., Sander, S., Kohne, E. Ann. Hematol. (2000) [Pubmed]
A microdeletion syndrome due to a 3-Mb deletion on 19q13.2--Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation. Cario, H., Bode, H., Gustavsson, P., Dahl, N., Kohne, E. Clin. Genet. (1999) [Pubmed]