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E Alexandrakis

Showing results (1-10 of 7) with videos related to

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Virchows Archiv. B, Cell Pathology Including Molecular Pathology|January 1, 1981
[Hepatic reactions in erythropoietic protoporphyria (author's transl)]O Klinge, E Alexandrakis
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|February 1, 1990
[Erythema migrans arciforme et palpabile (T-cell pseudolymphoma)]I Lohrisch, E Alexandrakis, H Maywurm, et al.
Deutsche Medizinische Wochenschrift (1946)|September 1, 1989
[T-cell lymphoma associated with sprue]W Ormann, W D Hirschmann, E Alexandrakis, et al.
The European Respiratory Journal|June 19, 2001
Tracheobronchial stenosis in Keutel syndromeM Meier, L P Weng, E Alexandrakis, et al.
Klinische Padiatrie|March 1, 1985
[Severe hereditary protein C deficiency in a newborn infant with fulminant purpura--successful treatment with phenprocoumon]H Wehinger, E Geiger, V Freudenberg, et al.
European Journal of Pediatrics|December 1, 1983
Hereditary hypofibrinogenemia with fibrinogen storage in the liverH Wehinger, O Klinge, E Alexandrakis, et al.
Journal of Thrombosis and Haemostasis : JTH|March 26, 2011
Circulating matrix γ-carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndromeE C M Cranenburg, K Y VAN Spaendonck-Zwarts, L Bonafe, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Virchows Archiv. B, Cell Pathology Including Molecular Pathology|January 1, 1981
[Hepatic reactions in erythropoietic protoporphyria (author's transl)]O Klinge, E Alexandrakis
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|February 1, 1990
[Erythema migrans arciforme et palpabile (T-cell pseudolymphoma)]I Lohrisch, E Alexandrakis, H Maywurm, et al.
Deutsche Medizinische Wochenschrift (1946)|September 1, 1989
[T-cell lymphoma associated with sprue]W Ormann, W D Hirschmann, E Alexandrakis, et al.
The European Respiratory Journal|June 19, 2001
Tracheobronchial stenosis in Keutel syndromeM Meier, L P Weng, E Alexandrakis, et al.
Klinische Padiatrie|March 1, 1985
[Severe hereditary protein C deficiency in a newborn infant with fulminant purpura--successful treatment with phenprocoumon]H Wehinger, E Geiger, V Freudenberg, et al.
European Journal of Pediatrics|December 1, 1983
Hereditary hypofibrinogenemia with fibrinogen storage in the liverH Wehinger, O Klinge, E Alexandrakis, et al.
Journal of Thrombosis and Haemostasis : JTH|March 26, 2011
Circulating matrix γ-carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndromeE C M Cranenburg, K Y VAN Spaendonck-Zwarts, L Bonafe, et al.
Pageof 1