prof. Martine Cools
- ORCID iD
- 0000-0002-9552-4899
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Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development
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Working towards convergence of the clinical management of differences of sex development/intersex conditions and the human rights framework : a case study
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Efficacy and safety of a 4-year combination therapy of growth hormone and gonadotropin-releasing hormone analogue in pubertal girls with short predicted adult height
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Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia
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Reduced serum concentrations of biomarkers reflecting Leydig and Sertoli cell function in male patients with congenital adrenal hyperplasia
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Early puberty suppression and gender-affirming hormones do not alter final height in transgender adolescents
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Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development : a cross-sectional study
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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
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Electronic reporting of rare endocrine conditions within a clinical network : results from the EuRRECa project
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Individuals with numerical and structural variations of sex chromosomes : interdisciplinary management with focus on fertility potential
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Outcome of COVID-19 infections in patients with adrenal insufficiency and excess
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Testosterone restores body composition, bone mass, and bone strength following early puberty suppression in a mouse model mimicking the clinical strategy in trans boys
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Ovotesticular difference of sex development : genetic background, histological features and clinical management
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The genetic diagnosis of rare endocrine disorders of sex development and maturation : a survey among Endo-ERN centres
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Long-term GnRHa use and bone health in transgender adolescents : can a mouse model inform clinical practice?
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Effects of long-term puberty suppression and gender-affirming hormones on body composition and metabolic profile in a preclinical mouse model and a cohort of transboys
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Growth, puberty and testicular function in boys born small for gestational age with a nonspecific disorder of sex development
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Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
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Treatment of congenital adrenal hyperplasia in children aged 0-3 years : a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure
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Endocrine outcome and seminal parameters in young adult men born with hypospadias : a cross-sectional cohort study
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Impact of gender affirming treatment on bone health in transgender and gender diverse youth
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Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia
(2021) HORMONE RESEARCH IN PAEDIATRICS. In Hormone Research in Paediatrics 94(Supplement 1). p.69-70 -
Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism
(2021) HORMONE RESEARCH IN PAEDIATRICS. In Hormone Research in Paediatrics 94(supplement 1). p.42-43 -
Hervorming van de geslachtsregistratie : suggesties UGent en UZ Gent
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Testosterone therapy and its monitoring in adolescent boys with hypogonadism : results of an international survey from the I-DSD Registry
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Gonadectomy in conditions affecting sex development : a registry-based cohort study
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Adolescent and young adult urogenital outcome following childhood hypospadias repair : perfection revisited
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International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia : data from the I-CAH registry
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Approach to the virilizing girl at puberty
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ENDO-ERN expert opinion on the differential diagnosis of pubertal delay
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Assessing the health-related management of people with differences of sex development
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Multidisciplinary approach to the child with sex chromosomal mosaicism including a Y-containing cell line
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Patients with rare endocrine conditions have corresponding views on unmet needs in clinical research
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Fertility and sexuality issues in congenital lifelong urology patients : male aspects
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Novel model to study the physiological effects of temporary or prolonged sex steroid deficiency in male mice
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The External Genitalia Score (EGS) : a European multicenter validation study
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Clinical findings and follow-up of 46,XY and 45,X/46,XY testicular dysgenesis
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- Journal Article
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The EuRRECa project as a model for data access and governance policies for rare disease registries that collect clinical outcomes
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Real-world estimates of adrenal insufficiency–related adverse events in children with congenital adrenal hyperplasia
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Androgen receptor expression in preputial dartos tissue correlates with physiological androgen exposure in congenital malformations of the penis and in controls
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Psychosexual outcome, sexual function, and long-term satisfaction of adolescent and young adult men after childhood hypospadias repair
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Under-reported aspects of diagnosis and treatment addressed in the Dutch-Flemish guideline for comprehensive diagnostics in disorders/differences of sex development
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Parental stress, anxiety and trait mindfulness : associations with parent–child mealtime interactions in children with type 1 diabetes
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Rare and special robotic surgery indications in the pediatric population : ectopic organs and differences of sexual development
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Families with pediatric type 1 diabetes : a comparison with the general population on child well-being, parental distress, and parenting behavior
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Sexual and fertility issues in congenital lifelong urology patients
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De 'differences of sex development' in een notendop
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45,X/46,XY gonadal dysgenesis, 46,XX/46,XY chimerism (and variants), and 46,XX testicular and ovotesticular DSD
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- Journal Article
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The current landscape of European registries for rare endocrine conditions
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Clinical but not histological outcomes in males with 45,X/46,XY mosaicism vary depending on reason for diagnosis