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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 29
2023
Boekstegers, Ann 
ORCID: https://orcid.org/0000-0002-1251-5410; Schmidt, Heinrich ORCID: https://orcid.org/0000-0003-1329-0118; Kurzay, Mathias ORCID: https://orcid.org/0000-0003-4201-3494; Vallée, Tanja; Jung, Eva; Dubinski, Ilja ORCID: https://orcid.org/0000-0003-3670-2453; Maxwell, Rebecca ORCID: https://orcid.org/0000-0001-8198-6358 und Schmid, Irene ORCID: https://orcid.org/0000-0002-5105-3597
(2023):
Cortisol response in children with cancer and fever during chemotherapy: A prospective, observational study using random serum cortisol levels.
In: Cancer Medicine, Bd. 12, Nr. 8: S. 9247-9259
[PDF, 538kB]
ORCID: https://orcid.org/0000-0002-1251-5410; Schmidt, Heinrich ORCID: https://orcid.org/0000-0003-1329-0118; Kurzay, Mathias ORCID: https://orcid.org/0000-0003-4201-3494; Vallée, Tanja; Jung, Eva; Dubinski, Ilja ORCID: https://orcid.org/0000-0003-3670-2453; Maxwell, Rebecca ORCID: https://orcid.org/0000-0001-8198-6358 und Schmid, Irene ORCID: https://orcid.org/0000-0002-5105-3597
(2023):
Cortisol response in children with cancer and fever during chemotherapy: A prospective, observational study using random serum cortisol levels.
In: Cancer Medicine, Bd. 12, Nr. 8: S. 9247-9259
[PDF, 538kB]
2022
Dubinski, Ilja; Bechtold-Dalla Pozza, Susanne und Schmidt, Heinrich
(2022):
Infection with SARS-CoV-2 may alter the half-life of desmopressin (DDAVP) in patients with central diabetes insipidus.
In: Journal of Pediatric Endocrinology & Metabolism, Bd. 35, Nr. 12: S. 1544-1546
Walther, Antonia; Haeberle, Beate; Kueppers, Julia; Lurz, Eberhard; Schmid, Irene; Schmidt, Heinrich und Dubinski, Ilja
(2022):
Severe consumptive hypothyroidism in hepatic hemangioendothelioma A rare complication of a common clinical condition.
In: Journal of Pediatric Endocrinology & Metabolism, Bd. 35, Nr. 12: S. 1560-1564
Almarzooqi, Layla; Schmidt, Esther; Schmidt, Heinrich und Dubinski, Ilja
(2022):
Abnormalities of the Eyelashes in Turner's Syndrome.
In: Journal of Pediatric Genetics
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]
2021
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
2020
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
[PDF, 348kB]
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]
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
2019
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
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
2017
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
2016
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
2015
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]
2014
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]
2011
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]
2009
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]