Publications by authors named "Hartmut Wollmann"

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Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany.
Helmuth G Dörr, Hartmut A Wollmann, Berthold P Hauffa, Joachim Woelfle,

BMC Endocr Disord· June 2018

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Patients with Silver-Russell-Syndrome from Birth to Adulthood: Diagnosis, Development and Medical Care.
Hartmut A Wollmann, Michael B Ranke

Pediatr Endocrinol Rev· November 2017

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Growth Hormone Treatment in Children With Prader-Willi Syndrome: Three Years of Longitudinal Data in Prepubertal Children and Adult Height Data From the KIGS Database.
Nienke E Bakker, Anders Lindberg, Joseph Heissler, Hartmut A Wollmann, Cecilia Camacho-Hübner

J Clin Endocrinol Metab· May 2017

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A 2-year multicentre, open-label, randomized, controlled study of growth hormone (Genotropin®) treatment in very young children born small for gestational age: Early Growth and Neurodevelopment (EGN) Study.
Jean De Schepper, Johan Vanderfaeillie, Primus-E Mullis, Raoul Rooman, Anna Robertson, Hartmut A Wollmann

Clin Endocrinol (Oxf)· March 2016

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Schoolchildren born VLBW or VLGA show height-related changes in body composition and muscle function but no evidence of metabolic syndrome risk factors. Results from the NEOLONG study.
Michael B Ranke, Roland Schweizer, Susanne M Rodemann, Andrea Bevot, David D Martin, Hartmut A Wollmann

J Pediatr Endocrinol Metab· February 2016

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Cross-cultural equivalence of the patient- and parent-reported quality of life in short stature youth (QoLISSY) questionnaire.
Monika Bullinger, Julia Quitmann, Neuza Silva, Anja Rohenkohl, John E Chaplin, Hartmut Wollmann

Horm Res Paediatr· March 2015

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Three-year growth response to growth hormone treatment in very young children born small for gestational age-data from KIGS.
Margaret C S Boguszewski, Anders Lindberg, Hartmut A Wollmann

J Clin Endocrinol Metab· August 2014

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Results from an international multicenter trial evaluating the ease-of-use of and preference for a newly developed disposable injection pen for the treatment of growth hormone deficiency in treatment-naïve children and adults.
Andreas M Pleil, Feyza Darendeliler, Helmuth G Dörr, Katherine Hutchinson, Hartmut A Wollmann

Med Devices (Auckl)· April 2014

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Parental perception of health-related quality of life in children and adolescents with short stature: literature review and introduction of the parent-reported QoLISSY instrument.
Julia Quitmann, Anja Rohenkohl, Monika Bullinger, John E Chaplin, Michael Herdman, Hartmut Wollmann

Pediatr Endocrinol Rev· December 2013

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IGF1R mutation analysis in short children with Silver-Russell syndrome features.
Lukas Soellner, Sabrina Spengler, Matthias Begemann, Hartmut A Wollmann, Gerhard Binder

J Pediatr Genet· September 2013

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Implications of a data-driven approach to treatment with growth hormone in children with growth hormone deficiency and Turner syndrome.
Stefan Kaspers, Michael B Ranke, Donald Han, Jane Loftus, Hartmut Wollmann

Appl Health Econ Health Policy· June 2013

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Assessing the quality of life of health-referred children and adolescents with short stature: development and psychometric testing of the QoLISSY instrument.
Monika Bullinger, Julia Quitmann, Mick Power, Michael Herdman, Emmanuelle Mimoun, Hartmut Wollmann

Health Qual Life Outcomes· May 2013

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Accurate long-term prediction of height during the first four years of growth hormone treatment in prepubertal children with growth hormone deficiency or Turner Syndrome.
Michael B Ranke, Anders Lindberg, Mathias Brosz, Stefan Kaspers, Jane Loftus, Hartmut Wollmann

Horm Res Paediatr· January 2013

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Growth hormone treatment in short children born prematurely--data from KIGS.
Margaret C S Boguszewski, Hanna Karlsson, Hartmut A Wollmann, Patrick Wilton, Jovanna Dahlgren

J Clin Endocrinol Metab· June 2011

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Discontinuation of growth hormone (GH) treatment during the transition phase is an important factor determining the phenotype of young adults with nonidiopathic childhood-onset GH deficiency.
Maria Kołtowska-Häggström, Mitchell E Geffner, Peter Jönsson, John P Monson, Roger Abs, Hartmut A Wollmann

J Clin Endocrinol Metab· June 2010

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Assessment of health-related quality of life and patient satisfaction in children and adolescents with growth hormone deficiency or idiopathic short stature - part 1: a critical evaluation of available tools.
Anna Levke Brütt, David E Sandberg, John Chaplin, Hartmut Wollmann, Meinolf Noeker

Horm Res· November 2009

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Health-related quality of life of children and adolescents with growth hormone deficiency or idiopathic short stature - part 2: available results and future directions.
Monika Bullinger, Maria Kołtowska-Häggström, David Sandberg, John Chaplin, Hartmut Wollmann

Horm Res· November 2009

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LOT1 (ZAC1/PLAGL1) as member of an imprinted gene network does not harbor Silver-Russell specific variants.
Susanne Jäger, Nadine Schönherr, Sabrina Spengler, Michael B Ranke, Hartmut A Wollmann

J Pediatr Endocrinol Metab· June 2009

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Network of European studies of genes in growth (NESTEGG).
Linda B Johnston, Wiestske Ester, Janina Caliebe, Catherine Molinas, Hartmut Wollmann

Horm Res· April 2009

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No evidence for isolated imprinting mutations in the PEG1/MEST locus in Silver-Russell patients.
Nadine Schöherr, Susanne Jäger, Michael B Ranke, Hartmut A Wollmann, Gerhard Binder

Eur J Med Genet· October 2008

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Are H19 variants associated with Silver-Russell syndrome?
Nadine Schönherr, Gerhard Binder, Eckard Korsch, Elke Kämmerer, Hartmut A Wollmann

J Pediatr Endocrinol Metab· October 2008

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The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alteration.
Gerhard Binder, Ann-Kathrin Seidel, David D Martin, Roland Schweizer, C Philipp Schwarze, Hartmut A Wollmann

J Clin Endocrinol Metab· April 2008

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Search for subtelomeric imbalances by multiplex ligation-dependent probe amplification in Silver-Russell syndrome.
Katja Eggermann, Nadine Schönherr, Michael B Ranke, Hartmut A Wollmann, Gerhard Binder

Genet Test· March 2008

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No evidence for additional imprinting defects in Silver-Russell syndrome patients with maternal uniparental disomy 7 or 11p15 epimutation.
Nadine Schönherr, Esther Meyer, Gerhard Binder, Hartmut A Wollmann, Thomas Eggermann

J Pediatr Endocrinol Metab· December 2007

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Growth and development are similar in VLBW children born appropriate and small for gestational age: an interim report on 97 preschool children.
Michael B Ranke, Brigitte Vollmer, Richard Traunecker, Hartmut A Wollmann, Rangmar R Goelz

J Pediatr Endocrinol Metab· September 2007

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