Publications by authors named "Markus Bettendorf"

50Publications

Evolving pituitary hormone deficits in primarily isolated GHD: a review and experts' consensus.

Authors:
Gerhard Binder Dirk Schnabel Thomas Reinehr Roland Pfäffle Helmuth-Günther Dörr Markus Bettendorf Berthold Hauffa Joachim Woelfle

Mol Cell Pediatr 2020 Nov 3;7(1):16. Epub 2020 Nov 3.

University Children's Hospital, Pediatric Endocrinology, Loschgestr. 15, 91054, Erlangen, Germany.

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November 2020

Relation of health-related quality of life to near final height and body composition in adolescents with chronic endocrinopathies during transition period.

Authors:
Janna Mittnacht Daniela Choukair Thomas Breil Daniela Klose Ioana Inta Markus Bettendorf

Clin Endocrinol (Oxf) 2020 Dec 27;93(6):696-704. Epub 2020 Aug 27.

Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics, University Hospital Heidelberg, Heidelberg, Germany.

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December 2020

Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:
Helmuth-Günther Dörr Nadja Schulze Markus Bettendorf Gerhard Binder Walter Bonfig Christian Denzer Desiree Dunstheimer Kirsten Salzgeber Heinrich Schmidt Karl Otfried Schwab Egbert Voss Martin Wabitsch Joachim Wölfle

Mol Cell Pediatr 2020 Jul 9;7(1). Epub 2020 Jul 9.

Paediatric Endocrinology, University Children's Hospital, Erlangen, Germany.

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July 2020

Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism.

Authors:
Daniela Choukair Birgit Eberle Philipp Vick Pia Hermanns Birgit Weiss Nagarajan Paramasivam Matthias Schlesner Katharina Lornsen Ralph Roeth Carina Klutmann Jennifer Kreis Georg F Hoffmann Joachim Pohlenz Gudrun A Rappold Markus Bettendorf

Horm Res Paediatr 2020 19;93(1):16-29. Epub 2020 May 19.

Division of Paediatric Endocrinology, Children's Hospital, University of Heidelberg, Heidelberg, Germany.

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May 2020

GHD Diagnostics in Europe and the US: An Audit of National Guidelines and Practice.

Authors:
Gerhard Binder Thomas Reinehr Lourdes Ibáñez Susanne Thiele Agnès Linglart Joachim Woelfle Paul Saenger Markus Bettendorf Agnieszka Zachurzok Bettina Gohlke Tabitha Randell Berthold P Hauffa Hedi L Claahsen van der Grinten Paul-Martin Holterhus Anders Juul Roland Pfäffle Stefano Cianfarani

Horm Res Paediatr 2019 8;92(3):150-156. Epub 2019 Nov 8.

Dipartimento Pediatrico Universitario Ospedaliero, "Bambino Gesù" Children's Hospital - Tor Vergata University, Rome, Italy.

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May 2020

[Medical care of young women with Turner syndrome in Germany].

Authors:
Helmuth-Günther Dörr Markus Bettendorf Gerhard Binder Jürgen Brämswig Berthold P Hauffa Paul-Martin Holterhus Klaus Mohnike Heinrich Schmidt Günter K Stalla Martin Wabitsch Joachim Wölfle

Dtsch Med Wochenschr 2020 02 24;145(4):e18-e23. Epub 2019 Jul 24.

Universitätskinderklinik, Pädiatrische Endokrinologie und Diabetologie, Bonn.

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February 2020

Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment.

Authors:
Julia Quitmann Janika Bloemeke Neuza Silva Monika Bullinger Stefanie Witt Ilker Akkurt Desiree Dunstheimer Christian Vogel Volker Böttcher Ursula Kuhnle Krahl Markus Bettendorf Eckhard Schönau Susanne Fricke-Otto Alexandra Keller Klaus Mohnike Helmuth-Günther Dörr

Front Pediatr 2019 29;7:164. Epub 2019 Apr 29.

Clinic for Children and Adolescents, Erlangen-Nürnberg Universtiy, Erlangen, Germany.

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April 2019

[Life Situation of Young women with Turner Syndrome: Results of a Questionnaire-based Study in Germany].

Authors:
Helmuth-Günther Dörr Markus Bettendorf Gerhard Binder Jürgen Brämswig Berthold P Hauffa Paul-Martin Holterhus Klaus Mohnike Heinrich Schmidt Günter K Stalla Martin Wabitsch Joachim Wölfle

Dtsch Med Wochenschr 2019 07 14;144(14):e87-e93. Epub 2019 Mar 14.

Universitäts-Kinderklinik, Pädiatrische Endokrinologie und Diabetologie, Bonn.

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July 2019

Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature.

Authors:
Thomas Breil Vira Yakovenko Ioana Inta Daniela Choukair Daniela Klose Janna Mittnacht Egbert Schulze Abdul Alrajab Jürgen Grulich-Henn Markus Bettendorf

J Pediatr Endocrinol Metab 2019 Mar;32(3):259-267

Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics, University Hospital Heidelberg, Heidelberg, Germany.

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March 2019

Risk Factors for Childhood Overweight and Obesity in Ukraine and Germany

Authors:
Vira Yakovenko Laura Henn Markus Bettendorf Natalia Zelinska Galyna Soloviova Georg F. Hoffmann Juergen Grulich-Henn

J Clin Res Pediatr Endocrinol 2019 09 11;11(3):247-252. Epub 2019 Jan 11.

Ruprecht-Karls-University Heidelberg, University Children’s Hospital, Department of General Pediatrics, Heidelberg, Germany

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September 2019

Genotype/phenotype correlations in 538 congenital adrenal hyperplasia patients from Germany and Austria: discordances in milder genotypes and in screened versus prescreening patients.

Authors:
Stefan Riedl Friedrich-Wilhelm Röhl Walter Bonfig Jürgen Brämswig Annette Richter-Unruh Susanne Fricke-Otto Markus Bettendorf Felix Riepe Gernot Kriegshäuser Eckhard Schönau Gertrud Even Berthold Hauffa Helmuth-Günther Dörr Reinhard W Holl Klaus Mohnike

Endocr Connect 2019 Feb;8(2):86-94

Department of Pediatrics, Pediatric Endocrinology, Otto von Guericke Universität Magdeburg, Magdeburg, Germany.

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February 2019

Sequential measurements of IGF-I serum concentrations in adolescents with Laron syndrome treated with recombinant human IGF-I (rhIGF-I).

Authors:
Thomas Breil Carolin Kneppo Markus Bettendorf Hermann L Müller Klaus Kapelari Dirk Schnabel Joachim Woelfle

J Pediatr Endocrinol Metab 2018 Aug;31(8):895-902

Division of Paediatric Endocrinology, Children's Hospital, University of Bonn, Bonn, Germany.

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August 2018

Clinical Features and Response to Treatment of Prolactinomas in Children and Adolescents: A Retrospective Single-Centre Analysis and Review of the Literature.

Authors:
Thomas Breil Catherine Lorz Daniela Choukair Janna Mittnacht Ioana Inta Daniela Klose Jessica Jesser Egbert Schulze Markus Bettendorf

Horm Res Paediatr 2018 16;89(3):157-165. Epub 2018 Feb 16.

Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics, University Hospital Heidelberg, Heidelberg, Germany.

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September 2018

Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency.

Authors:
Franziska Simm Anne Griesbeck Daniela Choukair Birgit Weiß Nagarajan Paramasivam Jürgen Klammt Matthias Schlesner Stefan Wiemann Cristina Martinez Georg F Hoffmann Roland W Pfäffle Markus Bettendorf Gudrun A Rappold

Genet Med 2018 07 26;20(7):728-736. Epub 2017 Oct 26.

Department of Human Molecular Genetics, Institute of Human Genetics, Heidelberg University Hospital, Heidelberg, Germany.

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July 2018

Sodium Chloride Supplementation Is Not Routinely Performed in the Majority of German and Austrian Infants with Classic Salt-Wasting Congenital Adrenal Hyperplasia and Has No Effect on Linear Growth and Hydrocortisone or Fludrocortisone Dose.

Authors:
Walter Bonfig Friedhelm Roehl Stefan Riedl Jürgen Brämswig Annette Richter-Unruh Susanne Fricke-Otto Angela Hübner Markus Bettendorf Eckhard Schönau Helmut Dörr Reinhard W Holl Klaus Mohnike

Horm Res Paediatr 2018 26;89(1):7-12. Epub 2017 Oct 26.

Pediatric Endocrinology, Department of Pediatrics, Otto von Guericke Universität Magdeburg, Magdeburg, Germany.

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October 2018

Pediatric use of tetracyclines: focus on neurodevelopmental effects.

Authors:
Ioana Inta Georg F Hoffmann Markus Bettendorf

Pediatr Res 2017 11 2;82(5):725-726. Epub 2017 Aug 2.

Division of Pediatric Endocrinology, Center for Pediatric and Adolescent Medicine, Heidelberg University Hospital, Heidelberg, Germany.

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November 2017

Amyloidosis Cutis Dyschromica, a Rare Cause of Hyperpigmentation: A New Case and Literature Review.

Authors:
Oya Kuseyri Dorothea Haas Nina Lang Knut Schäkel Markus Bettendorf

Pediatrics 2017 May;139(5)

Department of General Pediatrics and Division of Pediatric Endocrinology and Diabetes, University Children's Hospital Heidelberg, Heidelberg, Germany; and.

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May 2017

Puberty marks major changes in the hippocampal and cortical c-Fos activation pattern induced by NMDA receptor antagonists.

Authors:
Ioana Inta Emese Domonkos Natascha Pfeiffer Rolf Sprengel Markus Bettendorf Undine E Lang Dragos Inta Peter Gass

Neuropharmacology 2017 01 16;112(Pt A):181-187. Epub 2016 Mar 16.

Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Germany.

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January 2017

Minocycline exacerbates apoptotic neurodegeneration induced by the NMDA receptor antagonist MK-801 in the early postnatal mouse brain.

Authors:
Ioana Inta Miriam A Vogt Anne S Vogel Markus Bettendorf Peter Gass Dragos Inta

Eur Arch Psychiatry Clin Neurosci 2016 Oct 19;266(7):673-7. Epub 2015 Oct 19.

Department of Psychiatry and Psychotherapy, Medical Faculty Mannheim, Central Institute for Mental Health Mannheim, University of Heidelberg, Heidelberg, Germany.

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October 2016

Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled Trial.

Authors:
Helmuth G Dörr Markus Bettendorf Gerhard Binder Beate Karges Carolin Kneppo Heinrich Schmidt Egbert Voss Martin Wabitsch Jörg Dötsch

Horm Res Paediatr 2015 7;84(4):266-74. Epub 2015 Aug 7.

Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics, University of Erlangen, Erlangen, Germany.

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September 2016