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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 25

Zeitschriftenartikel

Tschaidse, Lea; Auer, Matthias K.; Dubinski, Ilja; Lottspeich, Christian; Nowotny, Hanna; Schmidt, Heinrich; Gut, Nadezda und Reisch, Nicole (2022): Ectopic Prostate Tissue in the Uterine Cervix of a Female with Non-Classic Congenital Adrenal Hyperplasia-A Case Report. In: Journal of Clinical Medicine, Bd. 11, Nr. 15 [PDF, 1MB]

Sydlik, Carmen; Dubinski, Ilja; Bechtold, Susanne und Schmidt, Heinrich (2022): Free triiodothyronine/free thyroxine ratio in children with congenital hypothyroidism. In: Endocrine Connections, Bd. 11, Nr. 7 [PDF, 915kB]

Odenwald, Birgit; Fischer, Aline; Röschinger, Wulf; Liebl, Bernhard; Schmidt, Heinrich und Nennstiel, Uta (2021): Long-Term Course of Hypothyroidism Detected through Neonatal TSH Screening in a Population-Based Cohort of Very Preterm Infants Born at Less Than 32 Weeks of Gestation. In: International Journal of Neonatal Screening, Bd. 7, Nr. 4, 65

Nowotny, Hanna Franziska; Auer, Matthias K.; Lottspeich, Christian; Schmidt, Heinrich; Dubinski, Ilja; Bidlingmaier, Martin; Adaway, Jo; Hawley, James; Keevil, Brian und Reisch, Nicole (2021): Salivary Profiles of 11-oxygenated Androgens Follow a Diurnal Rhythm in Patients With Congenital Adrenal Hyperplasia. In: Journal of Clinical Endocrinology & Metabolism, Bd. 106, Nr. 11, E4509-E4519

Dubinski, Ilja; Dalla-Pozza, Susanne Bechtold; Bidlingmaier, Martin; Reisch, Nicole und Schmidt, Heinrich (2021): Reverse circadian glucocorticoid treatment in prepubertal children with congenital adrenal hyperplasia. In: Journal of Pediatric Endocrinology & Metabolism, Bd. 34, Nr. 12: S. 1543-1548

Auer, Matthias K.; Paizoni, Luisa; Neuner, Meike; Lottspeich, Christian; Schmidt, Heinrich; Bidlingmaier, Martin; Hawley, James; Keevil, Brian und Reisch, Nicole (2021): 11-oxygenated androgens and their relation to hypothalamus-pituitary-gonadal-axis disturbances in adults with congenital adrenal hyperplasia. In: Journal of Steroid Biochemistry and Molecular Biology, Bd. 212, 105921

Sydlik, Carmen; Dürr, Hans Roland; Bechtold-Dalla Pozza, Susanne; Weißenbacher, Claudia; Roeb, Julia und Schmidt, Heinrich (2020): Hypercalcaemia after treatment with denosumab in children: bisphosphonates as an option for therapy and prevention? In: World journal of pediatrics : WJP, Bd. 16: S. 520-527 [PDF, 1MB]

Neuhofer, Christiane M.; Catarino, Claudia B.; Schmidt, Heinrich; Seelos, Klaus; Alhaddad, Bader; Haack, Tobias B. und Klopstock, Thomas (2020): LINS1-associated neurodevelopmental disorder: Family with novel mutation expands the phenotypic spectrum. In: Neurology-Genetics, Bd. 6, Nr. 5, e500

Doerr, Helmuth-Guenther; Bettendorf, Markus; Binder, Gerhard; Braemswig, Jürgen; Hauffa, Berthold P.; Holterhus, Paul-Martin; Mohnike, Klaus; Schmidt, Heinrich; Stalla, Guenter K.; Wabitsch, Martin und Woelfle, Joachim (2020): Medizinische Betreuung von jungen Frauen mit Ullrich-Turner-Syndrom in Deutschland. In: Deutsche Medizinische Wochenschrift, Bd. 145, Nr. 4, E18-E23

Auer, Matthias K.; Paizoni, Luisa; Hofbauer, Lorenz C.; Rauner, Martina; Chen, Yiqing; Schmidt, Heinrich; Huebner, Angela; Bidlingmaier, Martin und Reisch, Nicole (2020): Effects of androgen excess and glucocorticoid exposure on bone health in adult patients with 21-hydroxylase deficiency. In: Journal of Steroid Biochemistry and Molecular Biology, Bd. 204, 105734

Paizoni, Luisa; Auer, Matthias K.; Schmidt, Heinrich; Huebner, Angela; Bidlingmaier, Martin und Reisch, Nicole (2020): Effect of androgen excess and glucocorticoid exposure on metabolic risk profiles in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. In: Journal of Steroid Biochemistry and Molecular Biology, Bd. 197, 105540

Doerr, Helmuth-Guenther; Bettendorf, Markus; Binder, Gerhard; Braemswig, Jürgen; Hauffa, Berthold P.; Holterhus, Paul-Martin; Mohnike, Klaus; Schmidt, Heinrich; Stalla, Gunter K.; Wabitsch, Martin und Woelfle, Joachim (2019): Lebenssituation von jungen Frauen mit Ullrich-Turner-Syndrom nach dem Ende der Wachstumshormontherapie: Ergebnisse einer Umfrage in Deutschland. In: Deutsche Medizinische Wochenschrift, Bd. 144, Nr. 14, E87-E93

Benz, Marcus R.; Ehren, Rasmus; Kleinert, Daniela; Müller, Carsten; Gellermann, Jutta; Fehrenbach, Henry; Schmidt, Heinrich und Weber, Lutz T. (2019): Generation and Validation of a Limited Sampling Strategy to Monitor Mycophenolic Acid Exposure in Children With Nephrotic Syndrome. In: Therapeutic Drug Monitoring, Bd. 41, Nr. 6: S. 696-702

Bechtold, Susanne; Blaschek, Astrid; Müller-Felber, Wolfgang; Weissenbacher, Claudia; Roeb, Julia; Sydlik, Carmen und Schmidt, Heinrich (2017): Muscle Density Measurement in Duchenne Muscular Dystrophy. In: Hormone Research in Paediatrics, Bd. 88: S. 258-259

Bahrami, Ehsan; Witzel, Maximilian; Racek, Tomas; Puchaka, Jacek; Hollizeck, Sebastian; Greif-Kohistani, Naschla; Kotlarz, Daniel; Horny, Hans-Peter; Feederle, Regina; Schmidt, Heinrich; Sherkat, Roya; Steinemann, Doris; Göhring, Gudrun; Schlegelbeger, Brigitte; Albert, Michael H.; Al-Herz, Waleed und Klein, Christoph (2017): Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations. In: Journal of Allergy and Clinical Immunology, Bd. 140, Nr. 4: S. 1112-1119

Witzel, Maximilian; Petersheim, Daniel; Fan, Yanxin; Bahrami, Ehsan; Racek, Tomas; Rohlfs, Meino; Puchalka, Jacek; Mertes, Christian; Gagneur, Julien; Ziegenhain, Christoph; Enard, Wolfgang; Stray-Pedersen, AsbJörg; Arkwright, Peter D.; Abboud, Miguel R.; Pazhakh, Vahid; Lieschke, Graham J.; Krawitz, Peter M.; Dahlhoff, Maik; Schneider, Marlon R.; Wolf, Eckhard; Horny, Hans-Peter; Schmidt, Heinrich; Schäffer, Alejandro A. und Klein, Christoph (2017): Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes. In: Nature Genetics, Bd. 49, Nr. 5: S. 742-752

Sydlik, Carmen; Weissenbacher, Claudia; Bechtold-Dalla Pozza, Susanne und Schmidt, Heinrich (2016): Evaluation of Prepubertal Patients with Suspected Neurosecretory Dysfunction of Growth Hormone Secretion: Diagnostic Steps and Treatment Response. In: Hormone Research in Paediatrics, Bd. 86: S. 378-379

Schmidt, Heinrich; Weissenbacher, Claudia; Bechtold-Dalla Pozza, Susanne; Roeb, Julia und Sydlik, Carmen (2016): Off-Label Use of the Aromatase Inhibitor Letrozole in Pubertal Boys to Improve Final Height: Laboratory, Auxological and Bone Age Data. In: Hormone Research in Paediatrics, Bd. 86: S. 179-180

Korte, Alexander; Schmidt, Heinrich; Bosinski, Hartmut A. G.; Mersmann, Maik und Beier, Klaus M. (2016): Zur Debatte über das TSG: Abschaffung der Begutachtung zur Vornamensänderung auch bei Minderjährigen mit der Diagnose Geschlechtsidentitätsstörung? In: Zeitschrift für Sexualforschung, Bd. 29, Nr. 1: S. 48-56

Odenwald, Brigitte; Nennstiel-Ratzel, Uta; Dörr, Helmuth-Günther; Schmidt, Heinrich; Wildner, Manfred und Bonfig, Walter (2016): Children with classic congenital adrenal hyperplasia experience salt loss and hypoglycemia: evaluation of adrenal crises during the first 6 years of life. In: European Journal of Endocrinology, Bd. 174, Nr. 2: S. 177-186

Dörr, Helmuth G.; Bettendorf, Markus; Binder, Gerhard; Karges, Beate; Kneppo, Carolin; Schmidt, Heinrich; Voss, Egbert; Wabitsch, Martin und Dötsch, Jörg (2015): Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled Trial. In: Hormone Research in Paediatrics, Bd. 84, Nr. 4: S. 266-274 [PDF, 224kB]

Bechtold, Susanne; Beyerlein, Andreas; Bonfig, Walter; Dalla Pozza, Robert; Putzker, Stephanie; Otto, Ragna; Schmidt, Heinrich und Schwarz, Hans Peter (2014): Sexual difference in bone geometry of adult patients with classical congenital adrenal hyperplasia: Data using peripheral quantitative computed tomography. In: Hormone Research in Paediatrics, Bd. 82, Nr. 3: S. 171-178 [PDF, 621kB]

Rivera-Brugués, Nuria; Albrecht, Beate; Wieczorek, Dagmar; Schmidt, Heinrich; Keller, Thomas; Göhring, Ina; Ekici, Arif B.; Tzschach, Andreas; Garshasbi, Masoud; Franke, Kathlen; Klopp, Norman; Wichmann, Heinz-Erich; Meitinger, Thomas; Strom, Tim M. und Hempel, Maja (Februar 2011): Cohen syndrome diagnosis using whole genome arrays. In: Journal of medical genetics, Bd. 48, Nr. 2: S. 136-140 [PDF, 423kB]

Dalla Pozza, Robert; Beyerlein, Andreas; Thilmany, Claude; Weissenbacher, Claudia; Netz, Heinrich; Schmidt, Heinrich und Bechtold, Susanne (2011): The effect of cardiovascular risk factors on the longitudinal evolution of the carotid intima medial thickness in children with type 1 diabetes mellitus. In: Cardiovascular Diabetology 10:53 [PDF, 251kB]

Schmidt, Heinrich; Giese, Renate; Enders, Angelika; Kern, W. und Hallschmid, M. (2009): Intranasal insulin to improve developmental delay in children with 22q13 deletion syndrome: an exploratory clinical trial. In: Journal of Medical Genetics, Bd. 46: S. 217-222 [PDF, 584kB]

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