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Results of search for 'au:"Alexandrakis, E"'
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Authors
Alexandrakis, E
Bauerle, H
Bonafe, L
Cranenburg, E C M
Dikkers, F G
Frangoulis, E
Freudenberg, V
Geiger, E
Goeckenjan, G
Hirschmann, W D
Klinge, O
Kouroumalis, E
Laverman, G D
Lionis, C
Lohrisch, I
Maywurm, H
Meier, M
Mittaz Crettol, L
Schürmann, J
Wehinger, H
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Topics
Abnormalities, Multiple
Adult
Female
Fibrin
Follow-Up Studies
Humans
Liver
Lymphoma
Male
Middle Aged
Porphyrias
Protoporphyrins
Skin
T-Lymphocytes
analysis
diagnosis
drug therapy
metabolism
pathology
therapeutic use
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Languages
English
German
Your search returned 9 results.
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1.
[Hepatic reactions in erythropoietic protoporphyria (author's transl)].
[electronic resource]
by
Klinge, O
Alexandrakis, E
Producer:
19820128
In:
Virchows Archiv. B, Cell pathology including molecular pathology
vol. 37
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2.
[Liver lesions in hereditary and experimental erythropoietic protoporphyria].
[electronic resource]
by
Alexandrakis, E
Klinge, O
Producer:
19830811
In:
Verhandlungen der Deutschen Gesellschaft fur Pathologie
vol. 66
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3.
[Erythema migrans arciforme et palpabile (T-cell pseudolymphoma)].
[electronic resource]
by
Lohrisch, I
Alexandrakis, E
Maywurm, H
Petres, J
Producer:
19900507
In:
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete
vol. 41
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4.
[T-cell lymphoma associated with sprue].
[electronic resource]
by
Ormann, W
Hirschmann, W D
Alexandrakis, E
Bauerle, H
Producer:
19891006
In:
Deutsche medizinische Wochenschrift (1946)
vol. 114
Online resources:
Available from publisher's website
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5.
How Greek GPs manage hepatitis C infected patients: experiences gained from a primary health care district in rural Crete.
[electronic resource]
by
Lionis, C
Frangoulis, E
Skliros, S
Alexandrakis, E
Kouroumalis, E
Producer:
19990428
In:
Australian family physician
vol. 28
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6.
Tracheobronchial stenosis in Keutel syndrome.
[electronic resource]
by
Meier, M
Weng, L P
Alexandrakis, E
Rüschoff, J
Goeckenjan, G
Producer:
20020503
In:
The European respiratory journal
vol. 17
Online resources:
Available from publisher's website
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7.
[Severe hereditary protein C deficiency in a newborn infant with fulminant purpura--successful treatment with phenprocoumon].
[electronic resource]
by
Wehinger, H
Geiger, E
Freudenberg, V
Schürmann, J
Alexandrakis, E
Witt, I
Producer:
19850620
In:
Klinische Padiatrie
vol. 197
Online resources:
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8.
Hereditary hypofibrinogenemia with fibrinogen storage in the liver.
[electronic resource]
by
Wehinger, H
Klinge, O
Alexandrakis, E
Schürmann, J
Witt, J
Seydewitz, H H
Producer:
19840227
In:
European journal of pediatrics
vol. 141
Online resources:
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9.
Circulating matrix γ-carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndrome.
[electronic resource]
by
Cranenburg, E C M
VAN Spaendonck-Zwarts, K Y
Bonafe, L
Mittaz Crettol, L
Rödiger, L A
Dikkers, F G
VAN Essen, A J
Superti-Furga, A
Alexandrakis, E
Vermeer, C
Schurgers, L J
Laverman, G D
Producer:
20111031
In:
Journal of thrombosis and haemostasis : JTH
vol. 9
Online resources:
Available from publisher's website
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