Elke Wühl

ORCID: 0000-0002-1205-2620
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About
Contact & Profiles
Research Areas
  • Blood Pressure and Hypertension Studies
  • Birth, Development, and Health
  • Dialysis and Renal Disease Management
  • Renal function and acid-base balance
  • Cardiovascular Health and Disease Prevention
  • Renal and related cancers
  • Biomedical Research and Pathophysiology
  • Pediatric Urology and Nephrology Studies
  • Sodium Intake and Health
  • Neonatal Health and Biochemistry
  • Renal Diseases and Glomerulopathies
  • Chronic Kidney Disease and Diabetes
  • Genetic and Kidney Cyst Diseases
  • Parathyroid Disorders and Treatments
  • Heart Rate Variability and Autonomic Control
  • Hemodynamic Monitoring and Therapy
  • Renal and Vascular Pathologies
  • Electrolyte and hormonal disorders
  • Hormonal Regulation and Hypertension
  • Metabolism and Genetic Disorders
  • Obesity, Physical Activity, Diet
  • Renal Transplantation Outcomes and Treatments
  • Genetic Syndromes and Imprinting
  • Cardiovascular Function and Risk Factors
  • Ion Transport and Channel Regulation

Heidelberg University
2016-2025

University Hospital Heidelberg
2016-2025

German Center for Pediatric and Adolescent Rheumatology
2010-2024

Heidelberg University
2006-2024

RELX Group (United States)
2022

Ege University
2020

University Medical Center Groningen
2020

University of Groningen
2020

KU Leuven
2019

Society of Interventional Radiology
2018

Increasing prevalence of hypertension (HTN) in children and adolescents has become a significant public health issue driving considerable amount research. Aspects discussed this document include advances the definition HTN 16 year or older, clinical significance isolated systolic youth, importance out office central blood pressure measurement, new risk factors for HTN, methods to assess vascular phenotypes, clustering cardiovascular treatment strategies among others. The recommendations...

10.1097/hjh.0000000000001039 article EN Journal of Hypertension 2016-07-27

Background Twenty-four-hour ambulatory blood pressure monitoring (ABPM) is an essential tool in the diagnosis and therapeutic of arterial hypertension children. The statistical use pediatric ABPM reference values has been compromised by non-Gaussian distribution 24-h (BP) Objective To develop distribution-adjusted tables. Methods From cross-sectional data obtained 949 healthy children adolescents aged 5–20 years, a set tables was developed for 24-h, daytime night-time mean systolic,...

10.1097/00004872-200210000-00019 article EN Journal of Hypertension 2002-10-01

Hypertension in children and adolescents has gained ground cardiovascular medicine, thanks to the progress made several areas of pathophysiological clinical research. These guidelines represent a consensus among specialists involved detection control high blood pressure adolescents. The synthesize considerable amount scientific data experience best wisdom upon which physicians, nurses families should base their decisions. They call attention burden hypertension adolescents, its contribution...

10.1097/hjh.0b013e32832f4f6b article EN Journal of Hypertension 2009-08-19

Congenital nephrotic syndrome (CNS) is clinically and genetically heterogeneous, with mutations in WT1, NPHS1 NPHS2 accounting for part of cases. We recently delineated a new autosomal recessive entity comprising CNS diffuse mesangial sclerosis distinct ocular anomalies microcoria as the leading clinical feature (Pierson syndrome). On basis homozygosity mapping to markers on chromosome 3p14-p22, we identified homozygous or compound heterozygous LAMB2 patients from five unrelated families....

10.1093/hmg/ddh284 article EN Human Molecular Genetics 2004-09-14

Objective Sonographic evaluation of arterial wall morphology and elasticity is increasingly accepted as a non-invasive tool in cardiovascular assessment. Several studies suggest that intima–media thickness (IMT) indices may sensitively reflect different vasculopathic processes children. However, normative values the impact adolescent growth are largely unknown. Methods We assessed IMT common carotid (cIMT) femoral arteries (fIMT), interacting anthropometric factors 247 healthy subjects aged...

10.1097/01.hjh.0000178834.26353.d5 article EN Journal of Hypertension 2005-08-08

Renal hypodysplasia (RHD) is characterized by a reduced nephron number, small kidney size, and disorganized renal tissue. A hereditary basis has been established for subset of affected patients, suggesting major role developmental genes that are involved in early organogenesis. Gene mutations have dominant inheritance cause RHD, urinary tract anomalies, defined extrarenal symptoms identified TCF2 (renal cysts diabetes syndrome), PAX2 (renal-coloboma EYA1 SIX1 (branchio-oto-renal SALL1...

10.1681/asn.2006030277 article EN Journal of the American Society of Nephrology 2006-09-14

Carotid intima-media thickness (cIMT) and carotid artery distensibility are reliable screening methods for vascular alterations the assessment of cardiovascular risk in adult pediatric cohorts. We sought to establish an international reference data set childhood adolescence period explore impact developmental changes body dimensions blood pressure (BP) on wall elasticity. cIMT, coefficient, incremental modulus elasticity, stiffness index β were assessed 1155 children aged 6 18 years...

10.1161/hypertensionaha.113.01297 article EN Hypertension 2013-07-02

Congenital anomalies of the kidney and urinary tract (CAKUT) are leading cause ESRD in children, but proportion patients with individual CAKUT entities progressing to during adulthood their long-term clinical outcomes unknown. This study assessed age at onset renal replacement therapy (RRT) patient graft survival across entire range.Patients were compared age-matched who undergoing RRT for other disorders on basis data from European Renal Association-European Dialysis Transplant Association...

10.2215/cjn.03310412 article EN Clinical Journal of the American Society of Nephrology 2012-10-20

Cystinosis is caused by mutations in the CTNS gene (17p13.2), which encodes for a lysosomal cystine/proton symporter termed cystinosin. It most common cause of inherited renal Fanconi syndrome young children. Because its rarity, diagnosis and specific treatment cystinosis are frequently delayed, has significant impact on overall prognosis. In this document, we have summarized expert opinions several aspects disease to improve knowledge provide guidance treatment.

10.1093/ndt/gfu090 article EN Nephrology Dialysis Transplantation 2014-08-27

10.1007/978-3-030-18167-3 article EN Updates in hypertension and cardiovascular protection 2019-01-01

Growth hormone treatment stimulates growth in short children with chronic renal failure. However, the extent to which this therapy increases final adult height is not known.

10.1056/nejm200009283431304 article EN New England Journal of Medicine 2000-09-28

Left ventricular hypertrophy (LVH) is the most important independent marker of cardiovascular risk in adults with chronic kidney disease. Cardiovascular morbidity seems increased even children renal insufficiency (CRI), but age and stage CRI when cardiac alterations become manifest are unknown. For assessing prevalence factors associated abnormal LV geometry CRI, echocardiograms, ambulatory BP monitoring, biochemical profiles were obtained 156 aged 3 to 18 yr stages 2 through 4 disease (GFR...

10.1681/asn.2005030276 article EN Journal of the American Society of Nephrology 2005-11-10

Background and objectives Cardiovascular disease is the most important comorbidity affecting long-term survival in children with CKD. Design, setting, participants, & measurements The Comorbidity Children CKD Study a multicenter, prospective, observational study ages 6–17 years old initial GFR of 10–60 ml/min per 1.73 m 2 . cardiovascular status monitored annually, subclinical assessed by noninvasive surrogate markers, including left ventricular mass index, carotid intima-media...

10.2215/cjn.01090216 article EN Clinical Journal of the American Society of Nephrology 2016-11-08

Hypertension is the leading risk factor for cardiovascular disease. Although accumulating evidence suggests tracking of blood pressure from childhood into adult life, there little information regarding relative contributions genetic, prenatal, biological, behavioral, environmental, and social determinants to pressure.Blood an array potential anthropometric, familial factors high pressure, including parental smoking habits, were determined as part a screening project in 4236 preschool...

10.1161/circulationaha.110.958769 article EN Circulation 2011-01-11

Children and adolescents with chronic kidney disease (CKD) are at high risk for cardiovascular morbidity mortality. A systemic arteriopathy cardiomyopathy has been characterized in pediatric dialysis patients by the presence of morphologic functional abnormalities.The Cardiovascular Comorbidity CKD (4C) Study is a multicenter, prospective, observational study aiming to recruit more than 600 children, aged 6 17 years, initial GFR 10 45 ml/min per 1.73 m(2). The prevalence, degree, progression...

10.2215/cjn.08791209 article EN Clinical Journal of the American Society of Nephrology 2010-06-25

BACKGROUND Aortic pulse wave velocity (PWV), an indicator of arterial stiffness, independently predicts cardiovascular mortality risk in adults. Arterial stiffening advances with age and seems accelerated children certain disease conditions such as chronic kidney or diabetes. The Vicorder, oscillometric device to measure PWV, has been validated children, but reference values a large pediatric cohort, association carotid stiffness influence individual family factors have not determined....

10.1093/ajh/hpv048 article EN American Journal of Hypertension 2015-05-05

Primary distal renal tubular acidosis (dRTA) is a rare disorder, and we aimed to gather data on treatment long-term outcome. We contacted paediatric adult nephrologists through European professional organizations. Responding clinicians entered demographic, biochemical, genetic clinical in an online form. Adequate were collected 340 patients (29 countries, female 52%). Mutation testing had been performed 206 (61%); pathogenic mutations identified 170 (83%). The median (range) presentation age...

10.1093/ndt/gfy409 article EN Nephrology Dialysis Transplantation 2018-12-21
Kathrin Burgmaier Leonie Violetta Brinker Florian Erger Bodo B. Beck Marcus R. Benz and 95 more Carsten Bergmann Olivia Boyer Laure Collard Claudia Dafinger Marc Fila Claudia Kowalewska Bärbel Lange-Sperandio Laura Massella Antonio Mastrangelo Djalila Mekahli Monika Miklaszewska Nadina Ortiz-Bruechle Ludwig Patzer Larisa Prikhodina Bruno Ranchin Nadejda Ranguelov Raphael Schild Tomáš Seeman Lale Sever Przemysław Sikora Maria Szczepańska Ana Teixeira Julia Thumfart Barbara Uetz Lutz T. Weber Elke Wühl Klaus Zerres Jörg Dötsch Franz Schaefer Max C. Liebau Loai Eid Klaus Arbeiter Nathalie Godefroid Jacques Lombet Aurélie De Mul Markus Feldkoetter Jakub Zieg Franziska Grundmann Matthias Galiano Bjoern Buchholz Anja Buescher Karsten Häffner Oliver Groß Ludwig Patzer Jun Oh Dieter Haffner Wanja M. Bernhardt Susanne Schaefer Simone Wygoda Jan Halbritter Ute Derichs Günter Klaus Felix Lechner Sabine Ponsel Jens König Hagen Staude Donald Wurm Martin Bald Michaela Geßner Neveen A. Soliman Gema Ariceta Juan David González-Rodríguez Francisco de la Cerda Ojeda Jérôme Harambat Denis Morin Claire Dossier Guillaume Dorval Rukshana Shroff Stella Stabouli Nakysa Hooman Francesca Mencarelli William Morello Germana Longo Francesco Emma Augustina Jankauskienė Katarzyna Taranta‐Janusz Ilona Zagożdżon Katarzyna Zachwieja Małgorzata Stańczyk Beata Bieniaś Mieczysław Litwin Aurelia Morawiec‐Knysak Alberto Caldas Afonso Oliver Dunand Andreea Liana Rãchişan Gordana Miloševski‐Lomić Svetlana Papizh Rina Rus Houweyda Jilani Bahriye Atmış Ali Düzova Alper Soylu Cengiz Candan Salim Çalışkan Alev Yılmaz

10.1016/j.kint.2021.04.019 article EN Kidney International 2021-04-30
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