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Pediatric Nephrology (Berlin, Germany)|October 1, 1995
von Willebrand factor and factor XIII in children with Henoch-Schonlein purpuraD De Mattia, R Penza, P Giordano, et al.
British Journal of Haematology|December 1, 1992
Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS)M N Fukuda, G F Gaetani, P Izzo, et al.
Journal of Endocrinological Investigation|July 29, 2009
Thyroid function and thyroid autoimmunity in childhood acute lymphoblastic leukemia off-therapy patients treated only with chemotherapyM Delvecchio, V Cecinati, L P Brescia, et al.
European Journal of Haematology|August 26, 1998
Resistance to activated protein C in thalassaemic patients: an underlying cause of thrombosisP Giordano, G C Del Vecchio, M Altomare, et al.
British Journal of Haematology|October 1, 1994
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin NapoliR Wilmotte, E Miraglia del Giudice, J Marechal, et al.
Biochemical and Biophysical Research Communications|September 15, 1993
Multiple control elements regulate transcription from the most distal promoter of human aldolase A geneP Costanzo, A Lupo, E Rippa, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 24, 2004
The adiponectin gene SNP+45 is associated with coronary artery disease in Type 2 (non-insulin-dependent) diabetes mellitusC Lacquemant, P Froguel, S Lobbens, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|January 1, 1991
Functional properties of Hb-J Calabria, beta 64 (E8) Gly-AspE Rabino Massa, G Bonetti, P Izzo, et al.
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