21-Hydroxylase and 11β-Hydroxylase Mutations in Romanian Patients with Classic Congenital Adrenal Hyperplasia von Grigorescu Sido, Anca, Weber, Matthias M., Grigorescu Sido, Paula, Clausmeyer, Susanne, Heinrich, Udo, Schulze, Egbert

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21-Hydroxylase and 11beta-hydroxylase mutations in Romanian patients with classic congenital adrenal hyperplasia von Grigorescu Sido, Anca, Weber, Matthias M, Grigorescu Sido, Paula, Clausmeyer, Susanne, Heinrich, Udo, Schulze, Egbert

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Growth Analysis in Patients with 21-Hydroxylase Deficiency Influence of Glucocorticoid Dosage, Age at Diagnosis, Phenotype and Genotype on Growth and Height Outcome von Grigorescu-Sido, Anca, Bettendorf, Markus, Schulze, Egbert, Duncea, Ileana, Heinrich, Udo

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Brief Report: 21-Hydroxylase and 11β-Hydroxylase Mutations in Romanian Patients with Classic Congenital Adrenal Hyperplasia von Sido, Anca Grigorescu, Weber, Matthias M, Sido, Paula Grigorescu, Clausmeyer, Susanne, Heinrich, Udo, Schulze, Egbert

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Cardiac Manifestations in a Group of Romanian Patients with Gaucher Disease Type 1 (a Monocentric Study) von Lazea, Cecilia, Bucerzan, Simona, Al-Khzouz, Camelia, Zimmermann, Anca, Vesa, Ștefan Cristian, Nașcu, Ioana, Creț, Victoria, Crișan, Mirela, Asăvoaie, Carmen, Miclea, Diana, Grigorescu-Sido, Paula

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Dynamic changes of lipid profile in Romanian patients with Gaucher disease type 1 under enzyme replacement therapy: a prospective study von Zimmermann, Anca, Grigorescu-Sido, Paula, Rossmann, Heidi, Lackner, Karl J., Drugan, Cristina, Al Khzouz, Camelia, Bucerzan, Simona, Naşcu, Ioana, Zimmermann, Tim, Leucuţa, Daniel, Weber, Matthias M.

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Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1 von Zimmermann, Anca, Popp, Radu A, Rossmann, Heidi, Bucerzan, Simona, Nascu, Ioana, Leucuta, Daniel, Weber, Matthias M, Grigorescu-Sido, Paula

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Bone mineral density and bone turnover in Romanian children and young adults with classical 21-hydroxylase deficiency are influenced by glucocorticoid replacement therapy von Zimmermann, Anca, Sido, Paula Grigorescu, Schulze, Egbert, Al Khzouz, Camelia, Lazea, Cecilia, Coldea, Cristina, Weber, Matthias M.

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A Novel Nonsense Mutation of the AGL Gene in a Romanian Patient with Glycogen Storage Disease Type IIIa von Grigorescu-Sido, Paula, Bucerzan, Simona, Rossmann, Heidi, Zimmermann, Anca

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Cholelithiasis in Patients with Gaucher Disease type 1: Risk Factors and the Role of ABCG5/ABCG8 Gene Variants von Zimmermann, Anca, Popp, Radu A, Al-Khzouz, Camelia, Bucerzan, Simona, Naşcu, Ioana, Leucuta, Daniel, Galle, Peter R., Grigorescu-Sido, Paula

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Alterations in Lipid and Carbohydrate Metabolism in Patients with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency von Zimmermann, Anca, Grigorescu-Sido, Paula, AlKhzouz, Camelia, Patberg, Karen, Bucerzan, Simona, Schulze, Egbert, Zimmermann, Tim, Rossmann, Heidi, Geiss, Hans-Christian, Lackner, Karl J., Weber, Matthias M.

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Baseline characteristics and outcome in Romanian patients with Gaucher disease type 1 von Grigorescu-Sido, Paula, Drugan, Cristina, AlKhzouz, Camelia, Zimmermann, Anca, Coldea, Cristina, Denes, Carmen, Grigorescu, Mircea Dan, Cret, Victoria, Bucerzan, Simona

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