Ghent University Academic Bibliography

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Contemporary global management of 21-hydroxylase deficiency congenital adrenal hyperplasia in early infancy : a multi-national registry study

David B N Lim, Jillian Bryce, Salma R Ali, Xanthippi Tseretopoulou, Niels H Birkebaek, Sabine E Hannema, Ariadna Campos-Martorell, Maria Clemente, Uta Neumann, Christa E Flück, et al.

(2026) EUROPEAN JOURNAL OF ENDOCRINOLOGY. 194(2). p.123-135
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Gynecomastia and its management in boys with partial androgen insensitivity syndrome

Supitcha Patjamontri, Angela K Lucas-Herald, Jillian Bryce, Erica van den Akker, Martine Cools (UGent) , Evgenia Globa, Gil Guerra-Junior, Olaf Hiort, Paul Hofman, Paul-Martin Holterhus, et al.

(2025) JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 110(6). p.e2018-e2025
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Prevalence and management of hypertension in Turner syndrome : data from the International Turner Syndrome (I-TS) registry

Shani A D Mathara Diddhenipothage, Katharina J Beck, Gayana Amiyangoda, Jillian Bryce, Luminita Cima, Katya De Groote (UGent) , Yana Deyanova, Evgenia Globa, Gloria Herrmann, Anders Juul, et al.

(2025) ENDOCRINE CONNECTIONS. 14(2).
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Blood pressure and its associations in 554 children and young people with congenital adrenal hyperplasia

Neil R Lawrence, Irina Bacila, Joseph Tonge, Jeremy Dawson, Gary S Collins, Zi-Qiang Lang, Jillian Bryce, Malika Alimussina, Minglu Chen, Salma Rashid Ali, et al.

(2025) EUROPEAN JOURNAL OF ENDOCRINOLOGY. 192(5). p.529-539
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Phenotypic variation and pubertal outcomes in males and females with 46,XY partial gonadal dysgenesis

Rieko Tadokoro-Cuccaro, Ieuan A Hughes, Martine Cools (UGent) , Koen Van de Vijver (UGent) , Berenice Bilharinho de Mendonça, Sorahia Domenice, Rafael Loch Batista, Renata Thomazini Dallago, Elaine F Costa, Nathalia Lisboa Gomes, et al.

(2025) JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 110(12). p.e4086-e4100
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Oligogenic analysis across broad phenotypes of 46,XY differences in sex development associated with NR5A1/SF-1 variants : findings from the international SF1next study

Chrysanthi Kouri, Idoia Martinez de Lapiscina, Rawda Naamneh-Elzenaty, Grit Sommer, Kay-Sara Sauter, Christa E. Flück, Saygin Abali, Zehra Yavas Abali, S. Faisal Ahmed, Leyla Akin, et al.

(2025) EBIOMEDICINE. 113.
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Temporal trends in acute adrenal insufficiency events in children with congenital adrenal hyperplasia during 2019-2022

Xanthippi Tseretopoulou, Salma R Ali, Jillian Bryce, Nadia Amin, Navoda Atapattu, Tania A S S Bachega, Federico Baronio, Rita Ortolano, Niels H Birkebaek, Walter Bonfig, et al.

(2024) JOURNAL OF THE ENDOCRINE SOCIETY. 8(10).
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Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development

Chrysanthi Kouri, Grit Sommer, Idoia Martinez de Lapiscina, Rawda Naamneh Elzenaty, Lloyd Tack (UGent) , Martine Cools (UGent) , S. Faisal Ahmed, Christa E. Flück, Saygin Abali, Zehra Yavas Abali, et al.

(2024) EBIOMEDICINE. 99.
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Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia

Beatrice Righi, Salma R. Ali, Jillian Bryce, Jeremy W. Tomlinson, Walter Bonfig, Federico Baronio, Eduardo C. Costa, Guilherme Guaragna-Filho, Guy T'Sjoen (UGent) , Martine Cools (UGent) , et al.

(2023) ENDOCRINE. 80(3). p.630-638
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Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia : a retrospective multicenter cohort study

Mariska A M Schröder, Mihaela Neacşu, Bas P H Adriaansen, Fred C G J Sweep, S Faisal Ahmed, Salma R Ali, Tânia A S S Bachega, Federico Baronio, Niels Holtum Birkebæk, Christiaan de Bruin, et al.

(2023) EUROPEAN JOURNAL OF ENDOCRINOLOGY. 189(4). p.460-468

Academic Bibliography

Contemporary global management of 21-hydroxylase deficiency congenital adrenal hyperplasia in early infancy : a multi-national registry study

Gynecomastia and its management in boys with partial androgen insensitivity syndrome

Prevalence and management of hypertension in Turner syndrome : data from the International Turner Syndrome (I-TS) registry

Blood pressure and its associations in 554 children and young people with congenital adrenal hyperplasia

Phenotypic variation and pubertal outcomes in males and females with 46,XY partial gonadal dysgenesis

Oligogenic analysis across broad phenotypes of 46,XY differences in sex development associated with NR5A1/SF-1 variants : findings from the international SF1next study

Temporal trends in acute adrenal insufficiency events in children with congenital adrenal hyperplasia during 2019-2022

Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development

Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia

Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia : a retrospective multicenter cohort study

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