Ghent University Academic Bibliography

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Increased aortic stiffness in prepubertal girls with Turner syndrome

Katya De Groote (UGent) , Daniel Devos (UGent) , Koen Van Herck (UGent) , Daniël De Wolf (UGent) , Saskia van der Straaten (UGent) , Ernst Rietzschel (UGent) , Ann Raes (UGent) , Kristof Vandekerckhove (UGent) , Joseph Panzer (UGent) , Hans De Wilde (UGent) , et al.

(2017) JOURNAL OF CARDIOLOGY. 69(1-2). p.201-207
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Evidence for bone and mineral metabolism alterations in children with autosomal dominant polycystic kidney disease

Stephanie De Rechter, Justine Bacchetta, Nathalie Godefroid, Laurence Dubourg, Pierre Cochat, Julie Maquet, Ann Raes (UGent) , Jean De Schepper (UGent) , Pieter Vermeersch, Maria Van Dyck, et al.

(2017) PEDIATRIC NEPHROLOGY. 32(9). p.1673-1673
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Evidence for bone and mineral metabolism alterations in children with autosomal dominant polycystic kidney disease

Stéphanie De Rechter, Justine Bacchetta, Nathalie Godefroid, Laurence Dubourg, Pierre Cochat, Julie Maquet, Ann Raes (UGent) , Jean De Schepper (UGent) , Pieter Vermeersch, Maria Van Dyck, et al.

(2017) JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 102(11). p.4210-4217
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- Journal Article
- A1
- open access
Validation of prediction models for near adult height in children with idiopathic growth hormone deficiency treated with growth hormone : a Belgian Registry Study

Saartje Straetemans, Jean De Schepper (UGent) , Muriel Thomas, Franciska Verlinde and Raoul Rooman

(2016) HORMONE RESEARCH IN PAEDIATRICS. 86(3). p.161-168
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- Conference Paper
- C3
Sertoli-Leydig cell tumor as a rare cause of hirsutism in a young adolescent

Saskia van der Straaten (UGent) , Mireille Merckx (UGent) , Jo Van Dorpe (UGent) , Ingeborg Goethals (UGent) , Victoria Bordon, Philippe Timmers and Jean De Schepper (UGent)

(2016) HORMONE RESEARCH IN PAEDIATRICS. 86(suppl. 1). p.278-279
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PGM1 deficiency diagnosed during an endocrine work-up of low IGF-1 mediated growth failure

Renate Zeevaert, Emmanuel Scalais, Laura Muiño Mosquera (UGent) , Linda De Meirleir, Carine De Beaufort, Michael Witsch, Jaak Jaeken and Jean De Schepper (UGent)

(2016) ACTA CLINICA BELGICA. 71(6). p.435-437
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Proposal for an algorithm for screening for undernutrition in hospitalized children

Koen Huysentruyt, Jean De Schepper, Patrick Bontems, Philippe Alliet, Ellen Peeters, Mathieu Roelants, Stephanie Van Biervliet (UGent) , Bruno Hauser and Yvan Vandenplas

(2016) JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION. 63(5). p.E86-E91
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Delayed adrenarche may be an additional feature of immunoglobulin super family member 1 deficiency syndrome

Severine Van Hulle, Margarita Craen (UGent) , Bert Callewaert (UGent) , Sjoerd Joustra, Wilma Oostdijk, Monique Losekoot, Jan Maarten Wit, Marc Olivier Turgeon, Daniel J Bernard and Jean De Schepper (UGent)

(2016) JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY. 8(1). p.86-91
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Proximal aortic stiffening in Turner patients is more pronounced in the presence of a bicuspid valve : a segmental functional MRI study

Daniel Devos (UGent) , Katya De Groote (UGent) , Danilo Babin (UGent) , Laurent Demulier (UGent) , Yvo Taeymans (UGent) , Jos Westenberg, Lucas Van Bortel (UGent) , Patrick Segers (UGent) , Eric Achten (UGent) , Jean De Schepper (UGent) , et al.

(2016) EUROPEAN HEART JOURNAL-CARDIOVASCULAR IMAGING. 17(suppl. 1). p.i17-i18
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- Conference Paper
- C3
Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape

Hannah Verdin (UGent) , Ana Fernández-Miñán, Sara Benito-Sanz, Sandra Janssens (UGent) , Bert Callewaert (UGent) , Kathleen De Waele (UGent) , Jean De Schepper (UGent) , Inge François, Björn Menten (UGent) , Karen Heath, et al.

(2016) Research day Faculty of Medicine and Health Sciences, Abstracts.

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Academic Bibliography

Increased aortic stiffness in prepubertal girls with Turner syndrome

Evidence for bone and mineral metabolism alterations in children with autosomal dominant polycystic kidney disease

Evidence for bone and mineral metabolism alterations in children with autosomal dominant polycystic kidney disease

Validation of prediction models for near adult height in children with idiopathic growth hormone deficiency treated with growth hormone : a Belgian Registry Study

Sertoli-Leydig cell tumor as a rare cause of hirsutism in a young adolescent

PGM1 deficiency diagnosed during an endocrine work-up of low IGF-1 mediated growth failure

Proposal for an algorithm for screening for undernutrition in hospitalized children

Delayed adrenarche may be an additional feature of immunoglobulin super family member 1 deficiency syndrome

Proximal aortic stiffening in Turner patients is more pronounced in the presence of a bicuspid valve : a segmental functional MRI study

Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape

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