Search Results - Schulze, Egbert
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Prevalence and clinical spectrum of nonsecretory medullary thyroid carcinoma in a series of 839 patients with sporadic medullary thyroid carcinoma by Frank-Raue, Karin (Author) , Machens, Andreas (Author) , Leidig-Bruckner, Gudrun (Author) , Rondot, Susanne (Author) , Haag, Christine (Author) , Schulze, Egbert (Author) , Zink-Lorenz, Angela Maria (Author) , Kreissl, Michael C. (Author) , Dralle, Henning (Author) , Raue, Friedhelm (Author) , Schmid, Kurt W. (Author) ,
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Diagnosis of glucocorticoid-remediable aldosteronism in hypertensive children by Kamrath, Clemens (Author) , Maser-Gluth, Christiane (Author) , Haag, Christine (Author) , Schulze, Egbert (Author) ,
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3
Inactivating calcium-sensing receptor mutations in patients with primary hyperparathyroidism by Frank-Raue, Karin (Author) , Leidig-Bruckner, Gudrun (Author) , Haag, Christine (Author) , Schulze, Egbert (Author) , Zink-Lorenz, Angela Maria (Author) , Schmitz-Winnenthal, Friedrich Hubertus (Author) , Raue, Friedhelm (Author) ,
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Hereditäre Formen des primären Hyperparathyreoidismus: MEN1, MEN2, HPT-JT, FHH, FIHPT = Hereditary variants of primary hyperparathyroidism : MEN1, MEN2, HPT-JT, FHH, FIHPT by Frank-Raue, Karin (Author) , Leidig-Bruckner, Gudrun (Author) , Zink-Lorenz, Angela Maria (Author) , Rondot, Susanne (Author) , Haag, Christine (Author) , Schulze, Egbert (Author) , Büchler, Markus W. (Author) , Raue, Friedhelm (Author) ,
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5
CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum by Frank-Raue, Karin (Author) , Haag, Christine (Author) , Schulze, Egbert (Author) , Keuser, Roger (Author) , Raue, Friedhelm (Author) , Dralle, Henning (Author) , Lorenz, Kerstin (Author) ,
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