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10.4103/jnrp.jnrp_100_17 http://scihub22266oqcxt.onion/10.4103/jnrp.jnrp_100_17 C5602264!5602264!28936074     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Neurosci+Rural+Pract 2017 ; 8 (Suppl 1): S66-71 Nephropedia Template TP {{tp|p=28936074|t=2017. Syndromes of Rapidly Progressive Cognitive Decline-Our Experience |pdf=|usr=}}{{28936074}} gab.com Text Syndromes of Rapidly Progressive Cognitive Decline-Our Experience JO: J Neurosci Rural Pract http://www.kidney.de/pget.php?&tw=1&pmid=28936074 #FOAvip Background:: Dementias are fairly slowly progressive degenerative diseases of brain for which treatment options are very less and carry a lot of burden on family and society. A small percentage of them are rapidly progressive and mostly carry a different course outcome. However, there are no definite criteria other than the time line for these patients. Aims:: The aim of this was to identify and categorize the causes and course of rapidly progressive dementias seen in our center. Settings and Design:: Patients who presented with rapid deterioration of cognitive functions within weeks to 1 year between 2011 and December 2016 were evaluated. Patients and Methods:: All patients underwent all mandatory tests for dementia including brain imaging. Complete vasculitis workup, autoimmune encephalitis profile including Voltage Gated Potassium Channel, N-methyl-D-aspartic acid receptor, glutamic acid-decarboxylase, thyroid-peroxidase antibody, cerebrospinal fluid, and other special tests such as duodenal biopsy and paraneoplastic workup were done based on clinical indications. Results and Conclusions:: Out of 144 patients 42 had immune-mediated encephalopathy, 18 had Creutzfeldt-Jakob disease, 3 had Vitamin B12 deficiency, 63 had infection with neurocysticercosis, 7 had tuberculosis, 2 had HIV, 1 had herpes simplex encephalitis, 1 had neurosyphilis, 1 Whipples disease, 1 had Subacute Sclerosing Panencephalitis, 1 had Mass lesion, 3 had Frontotemporal dementia, and 3 had small vessel disease. Good majority of these patients have infective and immune-mediated causes and less number belong to degenerative group. Therefore, caution is needed to look for treatable cause as it carries a different treatment options and outcome. Twit Text FOAVip Syndromes of Rapidly Progressive Cognitive Decline-Our Experience ????J Neurosci Rural Pract http://www.kidney.de/pget.php?&tw=1&pmid=28936074 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28936074 #FOAvip English Wikipedia <ref>{{Cite pmid|28936074}}</ref> Syndromes of Rapidly Progressive Cognitive Decline-Our Experience #MMPMID28936074 Chandra SR; Viswanathan LG; Pai AR; Wahatule R; Alladi S J Neurosci Rural Pract 2017[Aug]; 8 (Suppl 1): S66-71 PMID28936074show ga Background:: Dementias are fairly slowly progressive degenerative diseases of brain for which treatment options are very less and carry a lot of burden on family and society. A small percentage of them are rapidly progressive and mostly carry a different course outcome. However, there are no definite criteria other than the time line for these patients. Aims:: The aim of this was to identify and categorize the causes and course of rapidly progressive dementias seen in our center. Settings and Design:: Patients who presented with rapid deterioration of cognitive functions within weeks to 1 year between 2011 and December 2016 were evaluated. Patients and Methods:: All patients underwent all mandatory tests for dementia including brain imaging. Complete vasculitis workup, autoimmune encephalitis profile including Voltage Gated Potassium Channel, N-methyl-D-aspartic acid receptor, glutamic acid-decarboxylase, thyroid-peroxidase antibody, cerebrospinal fluid, and other special tests such as duodenal biopsy and paraneoplastic workup were done based on clinical indications. Results and Conclusions:: Out of 144 patients 42 had immune-mediated encephalopathy, 18 had Creutzfeldt-Jakob disease, 3 had Vitamin B12 deficiency, 63 had infection with neurocysticercosis, 7 had tuberculosis, 2 had HIV, 1 had herpes simplex encephalitis, 1 had neurosyphilis, 1 Whipples disease, 1 had Subacute Sclerosing Panencephalitis, 1 had Mass lesion, 3 had Frontotemporal dementia, and 3 had small vessel disease. Good majority of these patients have infective and immune-mediated causes and less number belong to degenerative group. Therefore, caution is needed to look for treatable cause as it carries a different treatment options and outcome. äSyndromes of Rapidly Progressive Cognitive Decline-Our Experience (epmc).pdf DeepDyve Pubget Overpricing