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Results of search for 'au:"Werlé, E"', page 16 of 16
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Authors
APPEL, W
Feifel, G
Fiedler, F
Fiehn, W
Fritz, H
Grau, A J
HOCHSTRASSER, K
Haendle, H
Hochstrasser, K
Hutzel, M
LEYSATH, G
Lorenz, W
SCHIEVELBEIN, H
Schmal, A
Schwarz, S
TRAUTSCHOLD, I
Trautschold, I
WERLE, E
Weicker, H
Werle, E
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301.
Reactivity profiles of autoantibodies to different phospholipids and the phospholipid-binding protein beta2-glycoprotein I in patients with clinical symptoms related to thromboembolic and/or vasculopathic events with or without connective tissue diseases.
[electronic resource]
by
Jaekel, H P
Schmid, D
Müller, E W
Ziutelis, V
Trabandt, A
Grobe, N
Kaskel-Paul, S
Höh, H
Bauer, B
Sudik, R
Baldauf, A
Werle, E
Producer:
20040309
In:
Clinical laboratory
vol. 49
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302.
Autoantibodies to prothrombin and phosphatidylserine/prothrombin-complexes: do they contribute to the serodiagnosis of primary and secondary anti-phospholipid syndrome?
[electronic resource]
by
Jaekel, H P
Trabandt, A
Schmid, D
Grobe, N
Müller, E W
Ziutelis, V
Kaskel-Paul, S
Höh, H
Bauer, B
Sudik, R
Baldauf, A
Werle, E
Producer:
20041202
In:
Clinical laboratory
vol. 50
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303.
L-2-hydroxyglutaric aciduria: identification of ten novel mutations in the L2HGDH gene.
[electronic resource]
by
Sass, J O
Jobard, F
Topçu, M
Mahfoud, A
Werlé, E
Cure, S
Al-Sannaa, N
Alshahwan, S A
Bataillard, M
Cimbalistiene, L
Grolik, C
Kemmerich, V
Omran, H
Sztriha, L
Tabache, M
Fischer, J
Producer:
20120111
In:
Journal of inherited metabolic disease
vol. 31 Suppl 2
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