Genetic, environmental, and epigenetic factors involved in CAKUT
Nicolaou, Nayia, Renkema, Kirsten Y., Bongers, Ernie M. H. F., Giles, Rachel H., Knoers, Nine V. A. M.·2015·Nature Reviews Nephrology
Cited by (346)
Items 201–300 of 346
- Nadir Creatinine in Congenital Anomalies of the Kidney and Urinary Tract (CAKUT): A Single-Center ExperienceMarius-Cosmin Colceriu, Paul Luchian Aldea, Bogdan Bulată, Dan Delean, Alexandra Sevastre-Berghian, Simona Valeria Clichici, Andreea Liana Răchişan, Teodora Mocan · 2024 · Children
- Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi‐Center Cohort StudyKeying Li, Huilin Wang, Matthew Hoi Kin Chau, Zirui Dong, Ye Cao, Yu Zheng, Tak Yeung Leung, Kwong Wai Choy, Yuanfang Zhu · 2024 · Prenatal Diagnosis
- Kidney Programming and Hypertension: Linking Prenatal Development to AdulthoodYou‐Lin Tain, Chien‐Ning Hsu · 2024 · International Journal of Molecular Sciences
- Pediatric Obstructive UropathyBärbel Lange-Sperandio · 2015 · Springer eBooks
- Overlap of vitamin A and vitamin D target genes with CAKUT-related processesOzan Özışık, Friederike Ehrhart, Chris T. Evelo, Alberto Mantovani, Anaı̈s Baudot · 2022 · F1000Research
- Pediatric Obstructive UropathyBärbel Lange-Sperandio, Norman D. Rosenblum · 2022 · Springer eBooks
- A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning KidneySander Groen in ’t Woud, Carlo Maj, Kirsten Y. Renkema, Rik Westland, Tessel E. Galesloot, Iris A.L.M. van Rooij, Sita H. H. M. Vermeulen, Wout Feitz, Nel Roeleveld, Michiel F. Schreuder et al. · 2022 · Biomedicines
- Follow-up of children and adolescents with congenital anomalies of the kidneys and urinary tract, associated with rare hereditary syndromesI. E. Kutyrlo, Ж. Г. Левиашвили, D. D. Batrakov, Н. Д. Савенкова · 2023 · Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)
- Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomaliesYibo Lu, Yiyang Zhou, Jing Guo, Ming Xin QI, Yuwan Lin, Xingyu Zhang, Ying Xiang, Qihua Fu, Bo Wang · 2023 · Communications Biology
- Fetal renal cystic disease and post-natal follow up—a single center experienceLorena Botero-Calderon, Anne K. Lawrence, Natalie O’Toole, Lisa M. Guay‐Woodford · 2023 · Frontiers in Pediatrics
- Genetic and environmental factors driving congenital solitary functioning kidneySander Groen in ’t Woud, Marleen M. H. J. van Gelder, Iris A.L.M. van Rooij, Wout Feitz, Nel Roeleveld, Michiel F. Schreuder, Loes F.M. van der Zanden, for the SOFIA study group, Joanna A.E. van Wijk, Rik Westland et al. · 2023 · Nephrology Dialysis Transplantation
- Single Nucleotide Variants in A Family of Monozygotic Twins Discordant for the Phenotype Congenital Megaureter: A Genomic AnalysisAugusto César Soares dos Santos, Luciana Bastos Rodrigues, Raony Guimarães Corrêa do Carmo Lisboa Cardenas, Patrícia Gonçalves Pereira Couto, Luiz Armando Cunha de Marco, Eduardo Araujo OLIVEIRA, Débora Marques de Miranda, Ana Cristina Simões e Silva · 2017 · The Open Urology & Nephrology Journal
- Modeling development of genitourinary birth defects to understand disruption due to changes in gene dosage.Victor A. Ruthig, Dolores J. Lamb · 2022 · PubMed Central
- Conditional Knockout Kdm2a Reveals Crucial Involvement in Development and Function of Kidney Collecting DuctsXianrong Xiong, Hailing Yu, Xupeng Li, Yuan Li, Ruilan Zeng, Yufan Wang, Chunhai Zhang, Yan Xiong, Wei Fu, Honghong He et al. · 2025 · International Journal of Molecular Sciences
- Spatial and Temporal Expression Patterns of EDA2R, PCDH9, and TRAF7 in Yotari (Dab1−/−) Mice: Implicationsfor Understanding CAKUT PathogenesisJelena Komic, Nela Kelam, Anita Racetin, Natalija Filipović, Mirna Saraga‐Babić, Dai Ihara, Yu Katsuyama, Katarina Vukojević · 2025 · International Journal of Molecular Sciences
- Copy Number Variations Analysis Identifies QPRT as a Candidate Gene Associated With Susceptibility for Solitary Functioning KidneyXiao Zhou, Hao Zheng, Li Han, Yan Wang, Li Zhang, Xiao Ming Shu, Mu L. Zhang, Guan N. Liu, Lian Ding · 2021 · Frontiers in Genetics
- Clinical outcomes and temporal trends of immunological and non-immunological rare diseases in adult kidney transplantEster Gallo, Silvia Mingozzi, Alberto Mella, Fabrizio Fop, Roberto Presta, Manuel Burdese, Elena Boaglio, Maria Cristina Torazza, Roberta Giraudi, Gianluca Leonardi et al. · 2021 · BMC Nephrology
- Overexpression of long noncoding RNA 4933425B07Rik leads to renal hypoplasia by inactivating Wnt/β-catenin signaling pathwayShanshan Xue, Xuanjin Du, Minghui Yu, Haixin Ju, Lihong Tan, Yaxin Li, Jialu Liu, Chunyan Wang, Xiaohui Wu, Hong Ming Xu et al. · 2023 · Frontiers in Cell and Developmental Biology
- Plasma MCP-1 and TGF-β1 Levels are Associated with Kidney Injury in Children with Congenital Anomalies of the Kidney and Urinary TractXiaoqi Xuan, Xiao Pu, Yang Yu’e, JinLong Yang, YongLe Li, Hang Wu, JianGuo Xu · 2024 · Applied Biochemistry and Biotechnology
- A preliminary study of the miRNA restitution effect on CNV-induced miRNA downregulation in CAKUTKristina Mitrovic, Ivan Životić, Ivana Kolić, Jelena J. Žakula, Maja Živković, Aleksandra Stanković, Ivan B. Jovanović · 2024 · BMC Genomics
- Advances in Diagnosis and Treatment of Inherited Kidney Diseases in ChildrenGuozhen Wang, Mengqiu Liao, Danny Junyi Tan, Xiangjun Chen, Ran Chao, Yifan Zhu, Li Pan, Yuelin Guan, Jianhua Mao, Lidan Hu · 2024 · Kidney Diseases
- Fetal Pancake KidneySharon Perlman, Yael Borovitz, Sonya Bar‐Adon, Benjamin Dekel, Reuven Achiron, Yinon Gilboa · 2020 · Journal of Ultrasound in Medicine
- Overexpression of Long Non-coding RNA 4933425B07Rik Causes Urinary Malformations in MiceLihong Tan, Minghui Yu, Yaxin Li, Shanshan Xue, Jing Chen, Yihui Zhai, Xiaoyan Fang, Jialu Liu, Jiaojiao Liu, Xiaohui Wu et al. · 2021 · Frontiers in Cell and Developmental Biology
- Pathophysiology of Fetal and Neonatal KidneysFarid Boubred, Umberto Siméoni · 2017 · Springer eBooks
- Generation of kidney ureteric bud and collecting duct organoids that recapitulate kidney branching morphogenesisZipeng Zeng, Biao Huang, Riana K. Parvez, Yidan Li, Jyunhao Chen, Ariel C. Vonk, Matthew Edward Thornton, Tadrushi Patel, Elisabeth A. Rutledge, Albert D. Kim et al. · 2020 · bioRxiv (Cold Spring Harbor Laboratory)
- Congenital Anomalies of the Kidney and the Urinary Tract in Newborns from Lviv Region (West Ukraine) For 2006-2017Nataliya Kitsera, N. V. Helner, Z Osadchuk, N.S. Lukyanenko · 2019
- Challenges in genetic counseling for congenital anomalies of the kidneys and urinary tract (CAKUT) spectrumPing Gong, Myriam Pelletier, Neil S. Silverman, Kathleen A. Kuhlman, Robert J. Wallerstein · 2022 · Case Reports in Perinatal Medicine
- Comparative Study between Obstructive and Non-Obstructive Renal Anomalies Among a Group of Iraqi ChildrenShatha H. Ali, Sally Kadhim, Qahtan Mohammed Al-Obaidy · 2021 · Iraqi journal of Medical Sciences
- Epigenetic regulation of chronic kidney disease development following prenatal maternal stressVineeta Sharma, Sukhveer Singh, Jayant Maini, Vikas Kumar Srivastava · 2023 · Elsevier eBooks
- Association between Maternal Birth Weight and Prevalence of Congenital Malformations in Offspring: The Japanese Environment and Children’s StudyHirotaka Hamada, Noriyuki Iwama, Hasumi Tomita, Kazuma Tagami, Natsumi Kumagai, Rie Kudo, Hongxin Wang, Seiya Izumi, Zen Watanabe, Mami Ishikuro et al. · 2024 · Nutrients
- Integrative analysis of multi-omics data reveals importance of collagen and the PI3K AKT signalling pathway in CAKUTJumamurat R. Bayjanov, Cenna Doornbos, Ozan Özışık, Woosub Shin, Núria Queralt-Rosiñach, Daphne Wijnbergen, Jean Sébastien Saulnier‐Blache, Joost Peter Schanstra, Bénédicte Buffin‐Meyer, Julie Klein et al. · 2024 · Scientific Reports
- The etiology of congenital obstructive uropathy: developmental and genetic perspectivesMayke A C Ten Hoor, Brian Becknell, Peter Hohenstein, Jaap Mulder · 2024 · Current topics in developmental biology/Current Topics in Developmental Biology
- Hypoxia-inducible factor-1 alpha and nuclear factor erythroid 2-related factor 2 as biomarkers of renal scarring in children with congenital anomalies of the kidney and urinary tract: a prospective case-control studyAylin Gençler, Hakim Çelık, Fatih Padalı, Abit Demir, Safiye Kafadar · 2025 · BMC Nephrology
- A New Pathogenic Variant of CAKUTHED Diagnosed Based on Intellectual DisabilityShinichiro Morıchı, Shinji Suzuki, Akiko Kasuga, Yu Ishida, Gaku Yamanaka, Yasuyo Kashiwagi, Hisashi Kawashima · 2019 · The Indian Journal of Pediatrics
- Protein expression in vesicoureteral reflux: What about children?Eda Tokat, Mustafa Özgür Tan, Serhat Gürocak · 2021 · Journal of Pediatric Surgery
- Kidneys - kindergarten to graduationAA Iyengar · 2016 · Indian Journal of Nephrology
- Development of the Kidneys and Urinary Tract in Relation to Renal AnomaliesPaul J. D. Winyard · 2020 · Elsevier eBooks
- Zinner Syndrome Versus Herlyn-Werner-Wunderlich Syndrome; Rare Congenital Genitourinary Malformations and Literature ReviewSaim Türkoğlu, Cemil Göya, Murat Demir · 2024 · Yeni Üroloji Dergisi
- ODAMNet: A Python package to identify molecular relationships between chemicals and rare diseases using overlap, active module and random walk approachesMorgane Térézol, Anaı̈s Baudot, Ozan Özışık · 2024 · SoftwareX
- Prevalence of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) in the Greater Buffalo Region: A Retrospective ReviewM. Lauria, Andrew Toenniessen, Hula Al-Rashidy, Richard John Quigg, Xiaoyan Wu · 2022 · Journal of Urology and Renal Diseases
- A case report of congenital ureteral stricture: Obstructed, hydronephrotic solitary kidney with cystic dysplastic changesSeblewongel Aseme, Abnet Mengesha Tsegaye, Seyfe Bekele Tilahun, Tihitena Negussie Mammo · 2024 · International Journal of Surgery Case Reports
- Genetic and Clinical Factors Influencing Congenital Anomalies of the Kidney and Urinary Tract in Children: Insights from Prenatal and Postnatal AssessmentsHülya Gözde Önal, Hülya Nalçacıoğlu, Demet Tekcan Karalı, Mesut Önal, Beytullah Yağız, Meltem Necibe Ceyhan Bilgici · 2024 · Biomedicines
- Lactoferrin in Pediatric Chronic Kidney Disease and Its Relationship with Cardiovascular RiskChun-Yi Ho, Pei‐Chen Lu, Weiling Chen, Wei-Ting Liao, Chien‐Ning Hsu, You‐Lin Tain · 2024 · Children
- Functional Characterization of a Novel PBX1 De Novo Missense Variant Identified in a Pediatric Patient with CAKUTCaterina Scolari, Angelo Corso Faini, Giulia Verra, Martina Migliorero, Giulia Margherita Brach Del Prever, Claudia Saglia, Fiorenza Mioli, Carmelo Maria Romeo, Tullia Carradori, Maria Luca et al. · 2025 · Genes
- Single‐Position Robot‐Assisted Laparoscopic Nephroureterectomy for Duplicated Kidneys and Ureters: Technique and OutcomesWei-Cheng Sun, Chen-Yue Liu, Xiao-Yan Wang, Gong-Lin Tang, Yan-Tao Lou, Feng Zhang, Jianing Sun, Xin Chen, Jun-Dong Zhao, Hong-Wei Zhao · 2026 · International Journal of Clinical Practice
- Genetics of CAKUTAlina Christine Hilger, Rik Westland, Julia Hoefele · 2026 · Medizinische Genetik
- The population frequency of predicted pathogenic genetic variants in commonly affected CAKUT genes in the general populationMary Huang, Judy Savige · 2026 · Pediatric Nephrology
- Environmental exposures and pediatric kidney healthAnisha Gerber, Zoe Cacanindin, Julia J. Scialla, Nivedita Kamath · 2026 · Pediatric Research
- Expanding the knowledge on development of CAKUT: molecular genetics and beyondGabriel C. Dworschak, Heiko Martin Reutter, Alina Christine Hilger · 2019 · Annals of Translational Medicine
- Nephrology in the United States of AmericaSamaya Javed Anumudu, Stephen Z. Fadem · 2021 · Springer eBooks
- Dissecting nephron morphogenesis using kidney organoids from human pluripotent stem cellsElena Garreta, Zarina Nauryzgaliyeva, Andrés Marco, Wajima Safi, Núria Montserrat · 2021 · Current Opinion in Genetics & Development
- Pathophysiology of Fetal and Neonatal KidneysFarid Boubred, Umberto Siméoni · 2018 · Springer eBooks
- Hemostasis and oxidative stress in chronic kidney disease in children and adolescentsAna Cristina dos Santos Lopes, Letícia Parreiras Nunes Sousa, Rívia Mara Morais e Silva, Ana Cristina Simões e Silva, Luci Maria Sant’Ana Dusse, Patrícia Nessralla Alpoim · 2022 · Canadian Journal of Physiology and Pharmacology
- A RANGE OF MUTATIONS IN PATIENTS WITH ISOLATED AND SYNDROMAL FORMS OF CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACTA. Ch. Mazur, Alena P. Mikhalenka, Sergey Baiko, V. M. Malyshava, I. V. Shauchuk, Alexander V. Kilchevsky, Alexander V. Sukalo · 2022 · Молекулярная и прикладная генетика
- Analysis of the operational status of the three-level referral system for urologic ultrasound screening and risk factors for renal pelvic dilatation in high-risk childrenBaowei Ji, Yinv Gong, Ying Zhang, Yun Li, Yihui Zhai, Yinghua Sun, Xiang Wang, Lishan Jia, Hong Ming Xu, Qian Shen · 2023 · Frontiers in Pediatrics
- MicroRNAs in Renal Development and RegenerationElise J. Tucker, Darling Macarena Rojas‐Canales, Saira R. Ali, Jonathan Gleadle · 2023 · Elsevier eBooks
- Congenital Anomalies of the Kidney and Urinary TractMatthew Satariano, Angelina Magreni Dixon, Cozumel S. Pruette · 2024 · Nephrology Self-Assessment Program
- The role of chromatin-related epigenetic modulations in CAKUTLuise König, Miriam Schmidts · 2025 · Current topics in developmental biology/Current Topics in Developmental Biology
- Assessing Urinary Tract Junction Obstruction Defects by Methylene Blue Dye InjectionKangsun Yun · 2017 · Journal of Visualized Experiments
- Interleukin‐10‐1082 A/G polymorphism is associated with renal parenchymal damage in congenital anomalies of the kidney and urinary tractLyuba Dineva Miteva, Е. Kostadinova, Spaska Angelova Stanilova · 2018 · Nephrology
- Signs and symptoms of developmental abnormalities of the genitourinary tractPaulo César Koch Nogueira, Isabel de Pádua Paz · 2016 · Jornal de Pediatria (Versão em Português)
- Evaluation of insertion/deletion (I/D) polymorphisms of ACE gene and circulating levels of angiotensin II in congenital anomalies of the kidney and urinary tractPedro Antunes Pousa, Tamires Sara Campos Mendonça, Larissa Marques Fonseca, Eduardo Araujo OLIVEIRA, André Rolim Belisário, Ana Cristina Simões e Silva · 2022 · Molecular Biology Reports
- Patterns and Clinical Outcomes of Congenital Anomalies of the Kidney and Urinary Tract in Preterm InfantsEman Alfaraj, Hussain A Al Ghadeer, Zahra Hussain AlSannaa, Mohammad H AlDar, Fatimah S Albattat · 2025 · Cureus
- Overexpression of long noncoding RNA 4933425B07Rik leads to renal hypoplasia by inactivating the Wnt/β-catenin signaling pathwayShanshan Xue, Xuanjin Du, Minghui Yu, Haixin Ju, Lihong Tan, Yaxin Li, Jialu Liu, Chunyan Wang, Xiaohui Wu, Hong Ming Xu et al. · 2022 · Research Square
- Management von obstruktiven HarntransportstörungenH.-G. Dietz, Baerbel Lange‐Sperandio · 2016 · Kinder- und Jugendmedizin
- Genetik der Nierenfehlbildungen beim DiGeorge-SyndromM. Pohl · 2017 · Der Nephrologe
- Anomalías congénitas de los riñones y de las vías urinarias, una revisión de la literatura*Manuel S. Ordóñez-Bastidas, Nadia Ximena Molina Urbina, Roberth Alirio Ortiz, Jaime Manuel Restrepo, María A. Acosta-Aragón · 2017 · Revista Colombiana Salud Libre
- Renal and Urinary Tract AnomaliesRobin Dawn Clark, Cynthia J. Curry · 2019
- Copy Number Variation: A New Genetic Form of Polycystic Kidney and Liver DiseaseTakuya Fujimaru, Eisei Sohara · 2020 · Kidney International Reports
- Akutes Nierenversagen bei Neugeborenen als Risikofaktor für die chronische NiereninsuffizienzMoritz Scheerer, Jun Seok Oh · 2021 · Kinder- und Jugendmedizin
- Molecular Screening of PAX2 Gene Polymorphism in Primary Vesicoureteral Reflux Patients in Taif Governorate, KSAEhab I. El‐Hallous, Abdulla A. Alharthi, Ahmed Gaber, Mohamed M. Hassan · 2021 · Pakistan Journal of Biological Sciences
- Роль метаболической терапии в лечении гипоксии паренхимы почек у детей с пиелонефритом, ассоциированным с недифференцированной дисплазией соединительной тканиN.S. Lukyanenko, K.A. Kens, O.O. Dobrik · 2021 · KIDNEYS
- Evaluation of Insertion/deletion (I/D) Polymorphisms of ACE Gene in Congenital Anomalies of The Kidney and Urinary Tract From a Brazilian Pediatric PopulationPedro Antunes Pousa, Tamires Sara Campos Mendonça, Larissa Marques Fonseca, Eduardo Araujo OLIVEIRA, André Rolim Belisário, Ana Cristina Simões e Silva · 2021 · Research Square
- Pediatric Obstructive UropathyBärbel Lange-Sperandio, Norman D. Rosenblum · 2021 · Springer eBooks
- Pathophysiology of Fetal and Neonatal KidneysFarid Boubred, Umberto Siméoni · 2018 · Springer eBooks
- Intensivierte Hämodialyseverfahren bei Kindern und JugendlichenJulia Thumfart, D Müller · 2016 · Nieren- und Hochdruckkrankheiten
- Faculty Opinions recommendation of FAT4 Fine-Tunes Kidney Development by Regulating RET Signaling.Andreas Schedl · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Faculty Opinions recommendation of Developmental pathology of congenital kidney and urinary tract anomalies.Andreas Schedl · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Faculty Opinions recommendation of Genetics of congenital anomalies of the kidney and urinary tract: the current state of play.Andreas Schedl · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Genetic Basis of Congenital Anomalies of Kidney and Urinary TractAbu Sadat Mohammad Nurunnabi, Mahmud Javed Hasan, Amir Mohammad Kaiser, Arif Mohammad, Shuchana Chakma · 2022 · Community Based Medical Journal
- Angeborene Fehlbildungen von Nieren und Harntrakt (CAKUT)Stefan Kohl · 2022 · Dialyse aktuell
- Congenital Anomalies of the Kidneys and Urinary TractMelanie Chan, Angela D. Gupta, Dan N. Wood, John O. Connolly · 2022 · Springer eBooks
- A clinical case of surgical treatment of a 10-year-old girl with megaureter of the single kidneyA. A. Оganisyan, A. S. Vrublevskiy, Y. A. Galkina, R. Yu. Valiev, I. S. Ahmetzhanov, Sergey G. Vrublevskiy, Е. N. Vrublevskaya · 2022 · Russian Journal of Pediatric Surgery
- Congenital Anomalies of the Kidney and Urinary TractDervla M. Connaughton, Friedhelm Hildebrandt · 2022 · Elsevier eBooks
- The Significance of Expression Pattern of Dab1 and Reelin in the Postnatal Bladder of Dab1 -/- (Yotari) MiceJelena Čurčić, Anita Racetin, Nela Kelam, Katarina Vukojević · 2022 · Annals of biomedical and clinical research
- Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experienceJulia Hoefele, Korbinian Maria Riedhammer, Jasmina Ćomić, Velibor B. Tasic, Jovana Putnik, Nora Abazi‐Emini, Nataša Stajić, Thomas Meitinger, Valbona Nushi-Stavileci, Riccardo Berutti et al. · 2022 · Research Square
- Anomalías congénitas del riñón y las vías urinariasPierre Cochat, B. Fretes, Delphine Demede, Aurélia Bertholet‐Thomas, Laurence Michel‐Calemard, Sara Cabet, Justine Bacchetta · 2022 · EMC - Pediatría
- Fetal and Perinatal Nephrology: Small but MightyStefan Kohl, Max C. Liebau · 2023 · Kidney360
- Integrative analysis of CAKUT multi-omics dataJumamurat R. Bayjanov, Cenna Doornbos, Ozan Özışık, Woosub Shin, Núria Queralt-Rosiñach, Daphne Wijnbergen, Jean Sébastien Saulnier‐Blache, Joost Peter Schanstra, José M. Fernández, Rajaram Kaliyaperumal et al. · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
- Nephrologie der PerinatalperiodeSandra Habbig, Angela Kribs · 2023 · Springer eBooks
- The dominant findings of a recessive man: from Mendel’s kid pea to kidneyKálmán Tory · 2023 · Pediatric Nephrology
- Altered Development of the Kidneys and the Urinary TractJulie E. Goodwin, Akhil Maheshwari · 2024 · Elsevier eBooks
- Konjenital Üriner Sistem Anomalileri ile Ebeveyn Yaşı Arasındaki İlişkinin DeğerlendirilmesiDilek Orbatu, Alper Soylu, Salìh Kavukçu · 2024 · Balıkesir Medical Journal
- Prospective observational study on clinical profile of congenital anomalies of kidney and urinary tract (CAKUT) in children in central India: A study protocolAnirudh Kommareddy, Jayant Vagha · 2024 · F1000Research
- The Many Faces of Congenital Anomalies of the Kidney and Urinary TractMiriam Schmidts, Md Abdul Qader · 2024 · Kidney International Reports
- Komplexe Syndrome mit Fehlbildungen von Nieren- und ableitenden HarnwegenStefanie Weber · 2024 · Therapie der Krankheiten im Kindes- und Jugendalter
- Breaking the Rules: Upper Pole Ureteropelvic Junction Obstruction Causing Massive Urinary Tract Dilation in a Neonate With Prenatal Diagnosis of Multicystic Dysplastic KidneyR. Grant Owens, Gina A Lockwood, Douglas W. Storm · 2024 · Urology
- An Emerging Role for Primary Cilia of the Renal Glomerulus: Implications and Considerations for Pathogenesis of Glomerular DiseasesLindsey Avery Fitzsimons · 2024 · Physiology
- CLINLCAL CASE OF MULTICYSTIC DYSPLASIA OF THE LEFT KIDNEY IN A NEWBORN CHILD – SCIENTIFIC AND APPLIED REALITIESM. M. Kiselovа, M. Kushnir, R. Dub · 2024 · Neonatology surgery and perinatal medicine
- Antenatal Diagnosis of Congenital Anomalies of the Kidneys and Urinary Tract (CAKUT)Angela Yulia, D. Patel, Trevor Gaunt, Paul J. D. Winyard · 2024 · Springer eBooks