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http://scihub22266oqcxt.onion/ 19344005!ä!19344005 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\19344005.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Isr+Med+Assoc+J 2009 ; 11 (1): 6-10 Nephropedia Template TP {{tp|p=19344005|t=2009. Renal tubular dysgenesis in Israel: pathologist s experience and literature review |pdf=|usr=}}{{19344005}} gab.com Text Renal tubular dysgenesis in Israel: pathologist s experience and literature review JO: Isr Med Assoc J http://www.kidney.de/pget.php?&tw=1&pmid=19344005 #FOAvip BACKGROUND: Renal tubular dysgenesis is a rare lethal kidney abnormality clinically manifested by olighydramnios, anuria and respiratory distress. Most of the information on this entity is provided by case reports and short series. OBJECTIVES: To evaluate the incidence and comparative frequency of clinical manifestations in different etiologic-pathogenic variants of RTD in Israel and in summarized published data. METHODS: Stillborn and neonatal autopsy material from nine medical centers in northern and central Israel was studied. Information concerning pregnancy, labor and postnatal status and autopsy findings of cases with histologically, histochemically and immunohistochemically confirmed RTD were obtained from corresponding reports and from published material. RESULTS: From the 1538 autopsies of fetuses (2 20 weeks gestation) and neonates that were performed between 1976 and 2007 we identified 12 cases of RTD (0.78%). Abnormality occurred more often (1.4%) in the Upper and Western Galilee than in Israel as a whole. CONCLUSIONS: Our study and a review of the literature showed that the autosomal recessive variant of RTD was more frequent than twin-twin transfusion-induced. Most symptoms were similar in all variants of RTD, but their frequency was different in each of them. Twit Text FOAVip Renal tubular dysgenesis in Israel: pathologist s experience and literature review ????Isr Med Assoc J http://www.kidney.de/pget.php?&tw=1&pmid=19344005 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=19344005 #FOAvip English Wikipedia <ref>{{Cite pmid|19344005}}</ref> Renal tubular dysgenesis in Israel: pathologist s experience and literature review #MMPMID19344005 Moldavsky M Isr Med Assoc J 2009[Jan]; 11 (1): 6-10 PMID19344005show ga BACKGROUND: Renal tubular dysgenesis is a rare lethal kidney abnormality clinically manifested by olighydramnios, anuria and respiratory distress. Most of the information on this entity is provided by case reports and short series. OBJECTIVES: To evaluate the incidence and comparative frequency of clinical manifestations in different etiologic-pathogenic variants of RTD in Israel and in summarized published data. METHODS: Stillborn and neonatal autopsy material from nine medical centers in northern and central Israel was studied. Information concerning pregnancy, labor and postnatal status and autopsy findings of cases with histologically, histochemically and immunohistochemically confirmed RTD were obtained from corresponding reports and from published material. RESULTS: From the 1538 autopsies of fetuses (2 20 weeks gestation) and neonates that were performed between 1976 and 2007 we identified 12 cases of RTD (0.78%). Abnormality occurred more often (1.4%) in the Upper and Western Galilee than in Israel as a whole. CONCLUSIONS: Our study and a review of the literature showed that the autosomal recessive variant of RTD was more frequent than twin-twin transfusion-induced. Most symptoms were similar in all variants of RTD, but their frequency was different in each of them. |Anuria/*etiology/physiopathology[MESH] |Autopsy[MESH] |Congenital Abnormalities/*diagnosis/epidemiology/*physiopathology[MESH] |Female[MESH] |Humans[MESH] |Incidence[MESH] |Infant, Newborn[MESH] |Israel/epidemiology[MESH] |Kidney Tubules/*abnormalities[MESH] |Male[MESH] |Oligohydramnios/*etiology/physiopathology[MESH] |Pregnancy[MESH] |Respiratory Distress Syndrome, Newborn/*etiology/physiopathology[MESH]Renal tubular dysgenesis in Israel: pathologist s experience and liter(epmc).pdf DeepDyve Pubget Overpricing