標(biāo)題: Titlebook: Congenital Anomalies of the Kidney and Urinary Tract; Clinical Implication Amin J. Barakat,H. Gil Rushton Book 2016 Springer International [打印本頁] 作者: Filament 時間: 2025-3-21 16:42
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書目名稱Congenital Anomalies of the Kidney and Urinary Tract讀者反饋學(xué)科排名
作者: browbeat 時間: 2025-3-21 22:23
http://image.papertrans.cn/c/image/235470.jpg作者: JEER 時間: 2025-3-22 01:38 作者: Flatter 時間: 2025-3-22 04:34
978-3-319-29217-5Springer International Publishing Switzerland 2016作者: 吸引人的花招 時間: 2025-3-22 09:58 作者: 四指套 時間: 2025-3-22 15:19 作者: 四指套 時間: 2025-3-22 19:44
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作者: 記憶 時間: 2025-3-22 21:31 作者: 逃避現(xiàn)實 時間: 2025-3-23 03:21 作者: 埋伏 時間: 2025-3-23 06:26 作者: languor 時間: 2025-3-23 11:07 作者: 有害 時間: 2025-3-23 14:27 作者: 直覺沒有 時間: 2025-3-23 21:58
Electron Diffraction and Crystallography,ral diverticula, urethral polyps, megalourethra, and urethral atresia. PUV represents the most common cause of congenital urethral obstruction by far. It should be suspected prenatally in all male fetuses with bilateral hydronephrosis and especially in those with a thick-walled bladder that is not s作者: 冥界三河 時間: 2025-3-24 00:32 作者: 創(chuàng)造性 時間: 2025-3-24 05:31
Patterson Functions and Diffuse Scattering,an be identified by prenatal sonography, but many are still discovered either at birth or later based on clinical concerns. Megacycstis–megaureter syndrome, megacystis–microcolon–intestinal hypoperistalsis syndrome (MMIHS), bladder hypoplasia, agenesis, diverticula, duplication, exstrophy, and urach作者: extemporaneous 時間: 2025-3-24 08:46
https://doi.org/10.1007/978-3-662-04901-3dominal testicles; and bladder enlargement with hydroureters. Developmental etiology is unknown with consideration given to both obstructive and mesodermal defects. Evaluation requires assessment of pulmonary and renal function along with other associated system disorders. Treatment should be focuse作者: laparoscopy 時間: 2025-3-24 13:33
Patterson Functions and Diffuse Scattering,identified until the adolescent years, in order to gain first-hand knowledge of management. It describes the controversies that still exist and the reasons why the author has chosen his path of care. It tries to explain the physiology involved so the reader can appreciate the therapeutic options cho作者: 信任 時間: 2025-3-24 18:30
Patterson Functions and Diffuse Scattering,ticated. However, imaging remains the cornerstone for diagnosis and management of urologic anomalies in children. Due to the noninvasive nature and lack of radiation, ultrasonography is often the initial diagnostic tool for evaluation of the urinary tract. It is also the primary imaging modality for作者: 粘 時間: 2025-3-24 21:59
https://doi.org/10.1007/978-3-662-04516-9its associated possible diagnoses. The evaluation of prenatal UTD should be practical and stride to minimize invasiveness while maintaining the ability to identify significant urologic disease. A summary of current grading systems for UTD, use of prophylactic antibiotics, and the utility of lower ur作者: 相一致 時間: 2025-3-25 00:50 作者: conscribe 時間: 2025-3-25 06:47
Electron Holography: AlAs/GaAs Superlattices life. Recently it has been discovered that over 12?% of CAKUT cases are due to mutations in ~30 different monogenic disease genes. The fraction of recognized causative genes will be likely increased with the help of next-generation sequencing techniques. Identification of causative mutations will p作者: 針葉 時間: 2025-3-25 11:29 作者: precede 時間: 2025-3-25 15:25
Congenital Hydronephrosis,Identifying the select group of patients who will benefit from early intervention to prevent renal damage as a consequence of hydronephrosis generally requires follow-up over time. Deterioration in hydronephrosis, parenchymal thickness, and renal function are the main indications for treatment.作者: Small-Intestine 時間: 2025-3-25 19:11 作者: intuition 時間: 2025-3-25 22:56
Congenital Anomalies of the Kidney and Urinary TractClinical Implication作者: sperse 時間: 2025-3-26 04:00
Congenital Anomalies of the Kidney and Urinary Tract978-3-319-29219-9作者: CLAM 時間: 2025-3-26 05:55
Patterson Functions and Diffuse Scattering,Identifying the select group of patients who will benefit from early intervention to prevent renal damage as a consequence of hydronephrosis generally requires follow-up over time. Deterioration in hydronephrosis, parenchymal thickness, and renal function are the main indications for treatment.作者: 典型 時間: 2025-3-26 11:23
Electron Holography: AlAs/GaAs Superlatticesant abnormalities of the ear lobes, and supernumerary nipples. Chromosomal studies should be considered in any fetus with ultrasonographic evidence of CAKUT associated with other congenital anomalies.作者: Watemelon 時間: 2025-3-26 13:08 作者: 緯線 時間: 2025-3-26 16:57 作者: 打折 時間: 2025-3-26 21:16
Book 2016 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.作者: Inertia 時間: 2025-3-27 01:41
ious 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.978-3-319-29217-5978-3-319-29219-9作者: Nonthreatening 時間: 2025-3-27 05:32
Electron Diffraction and Crystallography,damage and prevent or delay the onset ESRD. In this chapter, I will present an overview of issues related to the etiology, pathobiology, diagnosis, and clinical management of CAKUT, which will serve as a foundation for more detailed presentation in subsequent chapters.作者: FADE 時間: 2025-3-27 10:01 作者: 出生 時間: 2025-3-27 14:56 作者: 大方不好 時間: 2025-3-27 20:46 作者: anarchist 時間: 2025-3-28 02:00
diagnosis and workup of different conditions.Serves as a comThis 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 urolog作者: 知道 時間: 2025-3-28 04:34 作者: Magisterial 時間: 2025-3-28 09:01 作者: 觀察 時間: 2025-3-28 13:23 作者: inundate 時間: 2025-3-28 18:31
Diffraction Contrast in TEM Images,th or without continuous antibiotic prophylaxis and surgical correction via endoscopic, open, or laparoscopic/robotic approaches. Need for surgical correction is influenced by a given child’s risk for further infections, potential for renal cortical scarring, and likelihood of spontaneous resolution, along with parental preferences.作者: Venules 時間: 2025-3-28 19:56
Patterson Functions and Diffuse Scattering,asons why the author has chosen his path of care. It tries to explain the physiology involved so the reader can appreciate the therapeutic options chosen by the author. Once the chapter is thoroughly analyzed, the reader should have the ability to decide his/her own style of management for these children based on solid foundation of information.作者: cortisol 時間: 2025-3-28 23:03
https://doi.org/10.1007/978-3-662-04516-9y to identify significant urologic disease. A summary of current grading systems for UTD, use of prophylactic antibiotics, and the utility of lower urinary tract imaging postnatally is given. Finally, a risk stratification for the evaluation and management that incorporates increasing degrees of UTD is reviewed.作者: expeditious 時間: 2025-3-29 06:07
Electron Holography: AlAs/GaAs Superlatticescognized causative genes will be likely increased with the help of next-generation sequencing techniques. Identification of causative mutations will provide diagnostics for individuals and families, allow for adequate stratification of clinical outcome studies, help generate pathogenic insights, and may lead to preventative measures.作者: 忘恩負(fù)義的人 時間: 2025-3-29 09:45 作者: insular 時間: 2025-3-29 14:44 作者: Missile 時間: 2025-3-29 16:05 作者: 松果 時間: 2025-3-29 23:01 作者: 輕觸 時間: 2025-3-30 03:50 作者: MEN 時間: 2025-3-30 07:44 作者: Nucleate 時間: 2025-3-30 11:38
Genetics of Congenital Anomalies of the Kidneys and Urinary Tract,cognized causative genes will be likely increased with the help of next-generation sequencing techniques. Identification of causative mutations will provide diagnostics for individuals and families, allow for adequate stratification of clinical outcome studies, help generate pathogenic insights, and may lead to preventative measures.作者: 仇恨 時間: 2025-3-30 14:09
https://doi.org/10.1007/978-3-662-04901-3d on preservation of renal function through management of stagnant urine and prevention of UTIs. Operative intervention when required is discussed and includes the upper and lower urinary tract, the testicles, and the appearance of the abdominal wall.作者: Ordeal 時間: 2025-3-30 19:59 作者: 向外 時間: 2025-3-31 00:39 作者: 引起痛苦 時間: 2025-3-31 01:57
Electron Diffraction and Crystallography,ble prognostic indicators of PUV include nadir serum creatinine <0.8 mg% before age 1 year, absent vesicoureteral reflux (VUR), continence at the age of 5 years, and persistence of pop-off phenomenon. In this chapter, we will focus on PUV.作者: 野蠻 時間: 2025-3-31 08:58
https://doi.org/10.1007/978-3-540-73886-2nes consist of preventing morbidity from urinary tract infections, preserving adequate renal function and urinary continence, and eliminating complications associated with obstruction or vesicoureteral reflux.作者: 一美元 時間: 2025-3-31 11:33
Congenital Anomalies of the Urethra,ble prognostic indicators of PUV include nadir serum creatinine <0.8 mg% before age 1 year, absent vesicoureteral reflux (VUR), continence at the age of 5 years, and persistence of pop-off phenomenon. In this chapter, we will focus on PUV.作者: BLANC 時間: 2025-3-31 14:58 作者: EVICT 時間: 2025-3-31 19:57 作者: expunge 時間: 2025-4-1 00:04
Anatomy, Applied Embryology, and Pathogenesis of Congenital Anomalies of the Kidney and Urinary Trant challenges to practising physicians. In order to frame the clinical implications of CAKUT, it is critical to understand the normal development of the kidney and urinary tract. Although accounts on pathogenesis focus predominantly on genetic causes of CAKUT, it is also important to consider other 作者: 拱墻 時間: 2025-4-1 05:41 作者: 錯 時間: 2025-4-1 08:34 作者: 未完成 時間: 2025-4-1 10:39
Congenital Hydronephrosis,ot clinically significant, there are a number of patients who would suffer if hydronephrosis were left untreated. Since congenital hydronephrosis is largely asymptomatic, management is a clinical challenge with a wide gray zone. In the majority of cases, a postnatal ultrasound is the initial step in
