Djalila Mekahli

Universitair Ziekenhuis Leuven — Belgium

Biochemistry, Genetics and Molecular Biology · Life Sciences

39h-index5.4kcitations241works9.62yr avg
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Research Topics

Genetic and Kidney Cyst Diseases(107), Renal and related cancers(69), Pediatric Urology and Nephrology Studies(31), Biomedical Research and Pathophysiology(30), Genetic Syndromes and Imprinting(24)

Publications239 total

KDIGO 2025 ADPKD guideline through pediatric eyes
Universität Zürich, ZORA·2025Open Access
KDIGO 2025 ADPKD guideline through pediatric eyes
Pediatric Nephrology·2025Open Access
Clinical and genetic characteristics of patients diagnosed with atypical hemolytic uremic syndrome (aHUS): epidemiological data from the Belgian cohort of the Global aHUS Registry
Journal of Nephrology·2025Open Access
#2357 Kidney volume based on multi-dimensional orthogonal ultrasound measurements is more accurate than kidney length in evaluation of kidney growth in paediatric ADPKD
Nephrology Dialysis Transplantation·2025Open Access
#694 Mitochondrial translation reveals a therapeutic vulnerability in autosomal dominant polycystic kidney disease
Nephrology Dialysis Transplantation·2025Open Access
Progression of the estimated glomerular filtration rate in asphyxiated neonates undergoing therapeutic hypothermia during the first 10 days of life
Pediatric Nephrology·2025Open Access
The authors reply
Kidney International·2025
The molecular landscape of polycystic kidneys is marked by common alterations in purine metabolism
2025Open Access
Machine learning based clinical decision tool to predict acute kidney injury and survival in therapeutic hypothermia treated neonates
Scientific Reports·2025· 5 citedOpen Access
Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries
Kidney International·2025· 6 citedOpen Access
Polycystic Kidney Disease in Children: The Current Status and the Next Horizon
American Journal of Kidney Diseases·2025· 5 citedOpen Access
A risk score to predict kidney survival in patients with autosomal recessive polycystic kidney disease at the age of two months
Kidney International·2025· 3 citedOpen Access
Characteristics of patients with autosomal polycystic kidney disease reaching kidney failure by age 40
Pediatric Nephrology·2025· 2 citedOpen Access
KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summary
Kidney International·2025· 58 citedOpen Access
KDIGO 2025 Clinical Practice Guideline for the Evaluation, Management, and Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Kidney International·2025· 64 citedOpen Access
Tuberous sclerosis complex–associated kidney disease in children
Pediatric Nephrology·2025Open Access
Pseudo-Bartter syndrome: A CFTR-related disorder?
Journal of Cystic Fibrosis·2024· 1 cited
mRNA Translation Reprogramming in Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Journal of the American Society of Nephrology·2024
Bardet-Biedl syndrome improved diagnosis criteria and management: Inter European Reference Networks consensus statement and recommendations
European Journal of Human Genetics·2024· 50 citedOpen Access
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions
Kidney International Reports·2024· 13 citedOpen Access
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Frequent Co-authors

Franz Schaefer(13), Elena Levtchenko(12), Max C. Liebau(9), Carsten Bergmann(7), Augustina Jankauskienė(7), Karel Allegaert(7), Geert Bultynck(6), Humbert De Smedt(6), Ludwig Missiaen(6), Bruno Ranchin(6), Albert Ong(6), Tomáš Seeman(6), Stéphanie De Rechter(6), Bert Bammens(5), Jan B. Parys(5), Tess Harris(5), Jens König(5), Roser Torrá(5), Dieter Haffner(5), Gema Ariceta(5)