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Titlebook: Congenital Anomalies of the Kidney and Urinary Tract; Clinical Implication Amin J. Barakat,H. Gil Rushton Book 2016 Springer International

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書(shū)目名稱Congenital Anomalies of the Kidney and Urinary Tract
副標(biāo)題Clinical Implication
編輯Amin J. Barakat,H. Gil Rushton
視頻videohttp://file.papertrans.cn/236/235470/235470.mp4
概述Covers a complete scope of congenital anomalies of the kidney and urinary tract.Tables and algorithms assist the reader in the differential diagnosis and workup of different conditions.Serves as a com
圖書(shū)封面Titlebook: Congenital Anomalies of the Kidney and Urinary Tract; Clinical Implication Amin J. Barakat,H. Gil Rushton Book 2016 Springer International
描述This comprehensive, easy to read reference addresses the clinical implications of congenital anomalies of the kidney and urinary tract (CAKUT) in children. Authored by a panel of internationally recognized pediatric nephrologists and urologists, chapters discuss clinical presentation, workup, interpretation of imaging studies, genetics, prenatal diagnosis, prevention and treatment of various anomalies to help the practitioner understand, diagnose and manage CAKUT. Tables, figures, algorithms and an extensive appendix listing conditions and syndromes associated with CAKUT are featured to assist physicians in the differential diagnosis and workup of different conditions.
出版日期Book 2016
關(guān)鍵詞Congenital Anomalies of the Kidney and Urinary Tract; Prune Belly Syndrome, Neuropathic Bladder; Ureth
版次1
doihttps://doi.org/10.1007/978-3-319-29219-9
isbn_softcover978-3-319-29217-5
isbn_ebook978-3-319-29219-9
copyrightSpringer International Publishing Switzerland 2016
The information of publication is updating

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978-3-319-29217-5Springer International Publishing Switzerland 2016
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Electron Diffraction and Crystallography,es of end-stage renal disease (ESRD) in children. Additionally, they are the most frequent malformations detected by prenatal ultrasound. CAKUT occur in association with nonrenal malformations in about 30 % of cases. In the majority of patients, CAKUT are sporadic; however, mutations in several rena
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