arrow
M

Martine Cools

Ghent University Hospital
H指数:50
被引数:8,144

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Genetic testing and reporting: What the endocrinologists should know and can expect (Joint position paper of the ENDO-ERN)

遗传检测与报告:内分泌科医生应知应会(ENDO-ERN联合立场文件)

2026-09-160
PRE
A laser capture microdissection-based method for high-sensitivity transcriptomics from archived FFPE tissue slides with single-cell resolution using LCM-FFPEseq

基于激光捕获显微切割技术的单细胞分辨率高通量转录组学方法,用于 Archived FFPE 组织切片的 LCM-FFPEseq 高灵敏度分析

2026-09-010
OAAI
Growth Patterns and Bone Maturation in Children with Sex Chromosomal (45,X/46,XY) DSD

性染色体(45,X/46,XY)DSD儿童的生长模式与骨骼成熟

2026-05-190
PRE
Variant Curation of the Largest Compendium of FOXL2 Coding and Noncoding Sequence and Structural Variants in BPES

FOXL2编码和非编码序列及结构变异的最大汇编的变异筛选

2026-05-060
OAAI
Prevalence and Changes in Genetic and Clinical Characteristics in Growth Hormone-Treated Belgian Girls with Turner Syndrome: A Study from the BELGROW Registry

特纳综合征接受生长激素治疗的比利时女孩遗传和临床特征的患病率及变化:一项来自BELGROW注册研究

2026-01-010
PRE
EndoCompass Project: Research Roadmap for Reproductive and Developmental Endocrinology

EndoCompass 项目:生殖与发育内分泌学的研究路线图

2025-12-010
OA
The gender incongruence module in the European Registries for Rare Endocrine & Bone Conditions (EuRREB): first results, current insights, and future directions

欧洲罕见内分泌与骨骼疾病登记系统(EuRREB)中的性别不一致模块:初步结果、当前见解和未来方向

2025-10-010
PRE
Phenotypic Variation and Pubertal Outcomes in Males and Females With 46,XY Partial Gonadal Dysgenesis

46,XY部分性性腺发育不全患者中男女两性的表型变异和青春期结局

2025-04-100
OA
Blood pressure and its associations in 554 children and young people with congenital adrenal hyperplasia

554例先天性肾上腺皮质增生症儿童及青少年的血压及其关联因素研究

2025-04-040
PRE
The attitudes of transgender and gender-diverse adolescents and their parents regarding fertility, parenthood, and fertility preservation before the start of puberty suppression or gender-affirming hormone therapy

在开始青春期抑制或性别肯定性激素治疗之前,跨性别和性别多样化的青少年及其父母对生育,生育和生育能力的态度

2025-03-010
OA
Gonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency
2025-01-090
OA