Medical Wikipedia : The Medical Encyclopedia
All public logs
Jump to navigation
Jump to search
Combined display of all available logs of Medical Wikipedia. You can narrow down the view by selecting a log type, the username (case-sensitive), or the affected page (also case-sensitive).
(newest | oldest) View (newer 50 | older 50) (20 | 50 | 100 | 250 | 500)- 13:20, 21 February 2022 Wisedane talk contribs created page Category:Internal Medicine (Created blank page)
- 09:50, 21 February 2022 Medical Wikipedia talk contribs created page Haptocorrin (Created page with "== What are the other names of Haptocorrin? == Haptocorrin also known as * Transcobalamin-1 * Cobalophilin * R-Protein * R-Factor == What is the Essential function of haptocorrin? == Function of haptocorrin - protection of the acid-sensitive vitamin B12 while it moves through the stomach. == What is the structure of haptocorrin? == * It is a glycoprotein == How the haptocorrin is secreted? == * Produced by -salivary glands * Produced in response to ingestion of...") Tag: Visual edit
- 19:27, 19 February 2022 Wisedane talk contribs created page Homocystinuria (Created page with "<nowiki>= HOMOCYSTINURIA =</nowiki> These are a series of inborn errors of metabolism that are characterized by increased homocysteine levels in blood and urine. These are autosomal recessive disorders and are seen in 1 in 200,000 births. Normal homocysteine level in blood is 5–15 micromol/L. It can rise to 50-100 times the normal level in diseases. Moderate increase is seen in aged people, vitamin B12 or B6 deficiency, smokers and alcoholics and also in hypothy...") Tag: Visual edit
- 07:05, 18 February 2022 Medical Wikipedia talk contribs created page Phenylketonuria (Created page with "<hr> == PHENYLKETONURIA == It is an inborn error of metabolism caused by defective phenylalanine metabolism. It is of 5 types: Type 1, classic phenylketonuria: Due to deficiency of phenylalanine hydroxylase.<hr> Type 2 and type 3: Due to deficiency of Dihydrobiopterin reductase (chromosome 4).<hr> Type 4 and type 5: Due to defective Dihydrobiopterin biosynthesis.<hr> It is an autosomal recessive disorder caused by mutation in short arm of chromosome 12. Frequency of p...")
- 09:55, 4 February 2022 Wisedane talk contribs changed group membership for Medical Wikipedia from (none) to administrator
- 09:47, 4 February 2022 User account Medical Wikipedia talk contribs was created by Wisedane talk contribs
- 09:23, 4 February 2022 Wisedane talk contribs protected Main Page [Edit=Allow only administrators] (indefinite) [Move=Allow only administrators] (indefinite) (hist)
- 14:18, 3 February 2022 Wisedane talk contribs created page MediaWiki:Sidebar (Created page with " * navigation ** medicalwikipedia.org|Medical Wikipedia ** medicalwikipedia.com|Medical Wikipedia ** medicineoutlines.com|Medicine Outlines ** medicinequestionbank.com|Medicine Question Bank ** mainpage|mainpage-description ** recentchanges-url|recentchanges ** randompage-url|randompage ** helppage|help-mediawiki * SEARCH * TOOLBOX * LANGUAGES")
- 04:56, 3 February 2022 MediaWiki default talk contribs created page Main Page