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10.4274/jcrpe.1740 http://scihub22266oqcxt.onion/10.4274/jcrpe.1740 C4563190!4563190 !26316441     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26316441 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 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\26316441 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       J+Clin+Res+Pediatr+Endocrinol 2015 ; 7 (2 ): 155-8 Nephropedia Template TP {{tp|p=26316441 |t=2015. Dermal and Ophthalmic Findings in Pseudohypoaldosteronism |pdf=|usr=}}{{26316441 }} gab.com Text Dermal and Ophthalmic Findings in Pseudohypoaldosteronism JO: J Clin Res Pediatr Endocrinol http://www.kidney.de/pget.php?&tw=1&pmid=26316441 #FOAvip Pseudohypoaldosteronism (PHA) is defined as a state of resistance to aldosterone, a hormone crucial for electrolyte equilibrium. The genetically transmitted type of PHA is primary hypoaldosteronism. Secondary hypoaldosteronism develops as a result of hydronephrosis or hydroureter. PHA patients suffer from severe hyponatremia and a severe clinical condition due to severe loss of salt can be encountered in the neonatal period. Dermal findings in the form of miliaria rubra can also develop in these patients. With the loss of salt, abnormal accumulation of sebum in the eye due to a defect in the sodium channels can also occur. In this paper, a case of PHA in a newborn showing typical dermatological and ophthalmological findings is presented. Twit Text FOAVip Dermal and Ophthalmic Findings in Pseudohypoaldosteronism ????J Clin Res Pediatr Endocrinol http://www.kidney.de/pget.php?&tw=1&pmid=26316441 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26316441 #FOAvip English Wikipedia <ref>{{Cite pmid|26316441 }}</ref> Dermal and Ophthalmic Findings in Pseudohypoaldosteronism #MMPMID26316441 Korkut S ; Gökalp E ; Özdemir A ; Kurto?lu S ; Demirta? ? ; Gül Ü ; Ba?tu? O J Clin Res Pediatr Endocrinol 2015[Jun]; 7 (2 ): 155-8 PMID26316441 show ga Pseudohypoaldosteronism (PHA) is defined as a state of resistance to aldosterone, a hormone crucial for electrolyte equilibrium. The genetically transmitted type of PHA is primary hypoaldosteronism. Secondary hypoaldosteronism develops as a result of hydronephrosis or hydroureter. PHA patients suffer from severe hyponatremia and a severe clinical condition due to severe loss of salt can be encountered in the neonatal period. Dermal findings in the form of miliaria rubra can also develop in these patients. With the loss of salt, abnormal accumulation of sebum in the eye due to a defect in the sodium channels can also occur. In this paper, a case of PHA in a newborn showing typical dermatological and ophthalmological findings is presented. |Eye/*pathology [MESH] |Female [MESH] |Fluid Therapy [MESH] |Humans [MESH] |Hydronephrosis/etiology [MESH] |Infant, Newborn [MESH] |Polyuria/etiology [MESH] |Pseudohypoaldosteronism/complications/*pathology [MESH] |Sebum/chemistry [MESH] |Skin/*pathology [MESH]Dermal and Ophthalmic Findings in Pseudohypoaldosteronism (epmc).pdf DeepDyve Pubget Overpricing