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http://scihub22266oqcxt.onion/ C4261656!4261656!25610058     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Eurasian+J+Med 2009 ; 41 (1): 15-21 Nephropedia Template TP {{tp|p=25610058|t=2009. Congenital Cystic Pulmonary Malformations in Children: Our Experience with 19 Patients |pdf=|usr=}}{{25610058}} gab.com Text Congenital Cystic Pulmonary Malformations in Children: Our Experience with 19 Patients JO: Eurasian J Med http://www.kidney.de/pget.php?&tw=1&pmid=25610058 #FOAvip Purpose: Congenital cystic pulmonary malformations (CPM) are rare anomalies. The purpose of this study was to present our experience with CPM patients who were surgically treated in our clinic and to discuss our findings along with those from the literature. Materials and Methods:: Surgical treatment was performed on 19 patients under the age of 16 who were diagnosed with CPM in our clinic between January 1995 and December 2008. The diagnoses, ages, gender, symptoms, locations of the lesions, surgical method used, hospitalization times, complications, and the results of all patients were retrospectively evaluated. Results: The distribution of diagnoses was as follows: bronchogenic cyst(s) (BC) - 5 patients; pulmonary sequestration (PS) - 6 patients; congenital lobar emphysema (CLE) - 4 patients; congenital cystic adenomatoid malformation (CCAM) Type I - 3 patients, and PS and CCAM coexistence - 1 patient. All patients underwent resection. No operative mortality occurred. The mean postoperative hospitalization time of the patients was 6.9 days (range 4?17 days). Conslusion: CLE, CCAM, and PS may lead to life-threatening respiratory distress in infants. BC, CCAM, and PS, on the other hand, often progress with recurrent pneumonia in children and adults. Surgery is needed to improve severe symptoms, prevent fatal complications, and establish a histopathological diagnosis. Twit Text FOAVip Congenital Cystic Pulmonary Malformations in Children: Our Experience with 19 Patients ????Eurasian J Med http://www.kidney.de/pget.php?&tw=1&pmid=25610058 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25610058 #FOAvip English Wikipedia <ref>{{Cite pmid|25610058}}</ref> Congenital Cystic Pulmonary Malformations in Children: Our Experience with 19 Patients #MMPMID25610058 Turkyilmaz A; Aydin Y; Erdem AF; Eroglu A; Karaoglanoglu N Eurasian J Med 2009[Apr]; 41 (1): 15-21 PMID25610058show ga Purpose: Congenital cystic pulmonary malformations (CPM) are rare anomalies. The purpose of this study was to present our experience with CPM patients who were surgically treated in our clinic and to discuss our findings along with those from the literature. Materials and Methods:: Surgical treatment was performed on 19 patients under the age of 16 who were diagnosed with CPM in our clinic between January 1995 and December 2008. The diagnoses, ages, gender, symptoms, locations of the lesions, surgical method used, hospitalization times, complications, and the results of all patients were retrospectively evaluated. Results: The distribution of diagnoses was as follows: bronchogenic cyst(s) (BC) - 5 patients; pulmonary sequestration (PS) - 6 patients; congenital lobar emphysema (CLE) - 4 patients; congenital cystic adenomatoid malformation (CCAM) Type I - 3 patients, and PS and CCAM coexistence - 1 patient. All patients underwent resection. No operative mortality occurred. The mean postoperative hospitalization time of the patients was 6.9 days (range 4?17 days). Conslusion: CLE, CCAM, and PS may lead to life-threatening respiratory distress in infants. BC, CCAM, and PS, on the other hand, often progress with recurrent pneumonia in children and adults. Surgery is needed to improve severe symptoms, prevent fatal complications, and establish a histopathological diagnosis. äCongenital Cystic Pulmonary Malformations in Children: Our Experience (epmc).pdf DeepDyve Pubget Overpricing