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Show new changes starting from 18:41, 10 August 2020
   
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10 August 2020

     18:04  Occupations‎‎ (2 changes | history) . . (+83,011). . [Prab‎ (2×)]
     
18:04 (cur | prev) . . (+73,639). . Prab (talk | contribs) (Tag: 2017 source edit)
     
18:00 (cur | prev) . . (+9,372). . Prab (talk | contribs) (Tag: 2017 source edit)
     17:51  Sandbox‎‎ (3 changes | history) . . (+20,939). . [Prab‎ (3×)]
     
17:51 (cur | prev) . . (+29,421). . Prab (talk | contribs) (Tag: 2017 source edit)
     
17:28 (cur | prev) . . (+14,959). . Prab (talk | contribs) (Tag: 2017 source edit)
     
17:28 (cur | prev) . . (-23,441). . Prab (talk | contribs) (Blanked the page) (Tags: Blanking, Visual edit)
     16:30  (Import log). . [Prab‎ (21×)]
     
16:30 . . Prab (talk | contribs) imported 8p23.1 duplication syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 7q11.23 duplication syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 6th nerve palsy by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 5p deletion syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 5 alpha reductase deficiency by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 49,XXXXY by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 48,XXYY syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 47,XYY syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 3q29 microdeletion syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 3C syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 3 beta hydroxysteroid dehydrogenase deficiency by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 2q37 deletion syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 21 hydroxylase deficiency by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 2,8 dihydroxyadenine urolithiasis by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 1q21.1 microdeletion by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 1p36 deletion syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 18p by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 18 trisomy by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 17q21.31 microdeletion syndrome by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 17 alpha hydroxylase deficiency by file upload (1 revision) ‎
     
16:30 . . Prab (talk | contribs) imported 11 beta hydroxylase deficiency by file upload (1 revision) ‎
N    12:45  Hemochromatosis type 3‎ (diff | hist) . . (+55). . Deepika vegiraju (talk | contribs) (Redirected page to Hemochromatosis) (Tags: New redirect, 2017 source edit)
     12:42  Templates‎ (diff | hist) . . (+42). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
N    12:34  Category:Red blood cell disorders‎ (diff | hist) . . (+171). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    12:34  Category:Iron metabolism‎ (diff | hist) . . (+153). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    12:34  Hemochromatosis type 2‎ (diff | hist) . . (+5,714). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Juvenile hemochromatosis; Hemochromatosis juvenile; Iron overload disease juvenile; Juvenile hereditary hemochromatosis Hemochromatosis type 2 is a diseas...") (Tag: 2017 source edit)
N    11:24  Category:Abnormal clinical and laboratory findings for blood‎ (diff | hist) . . (+225). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    11:24  Category:Inborn errors of metal metabolism‎ (diff | hist) . . (+189). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    11:24  Hemochromatosis - Not a rare disease‎ (diff | hist) . . (+9,596). . Deepika vegiraju (talk | contribs) (Created page with "Hemochromatosis is a disease in which too much iron builds up in the body. This is also called '''iron overload'''. Accumulation of iron in the organs is toxic and can cause o...") (Tag: 2017 source edit)
N    06:52  Heinz body anemias‎ (diff | hist) . . (+529). . Deepika vegiraju (talk | contribs) (Created page with "This is a form of nonspherocytic hemolytic anemia of Dacie type I (in vitro autohemolysis is not corrected by added glucose). After splenectomy, which has little benef...") (Tag: 2017 source edit)
     06:43  Hashimoto-Pritzker syndrome‎ (diff | hist) . . (+2,486). . Deepika vegiraju (talk | contribs) (Removed redirect to Congenital self-healing reticulohistiocytosis) (Tags: Removed redirect, 2017 source edit)
     06:28  Granulomatous slack skin‎ (diff | hist) . . (+1,100). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
N    03:19  Glycoprotein VI deficiency‎ (diff | hist) . . (+3,759). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Bleeding diathesis due to glycoprotein VI deficiency; Platelet-type bleeding disorder-11; BDPLT11; Bleeding diathesis due to a collagen receptor defect; GP...") (Tag: 2017 source edit)
     02:48  Rare diseases‎‎ (3 changes | history) . . (+10,250). . [Prab‎ (3×)]
     
02:48 (cur | prev) . . (+14,772). . Prab (talk | contribs) (Tag: 2017 source edit)
     
02:47 (cur | prev) . . (-14,772). . Prab (talk | contribs) (Tag: 2017 source edit)
     
02:46 (cur | prev) . . (+10,250). . Prab (talk | contribs) (Tag: 2017 source edit)
     02:25  Glossary of ophthalmology‎ (diff | hist) . . (+44,948). . Prab (talk | contribs) (Tag: 2017 source edit)

9 August 2020

     15:16  Glycogen storage disease type 7‎ (diff | hist) . . (+6,363). . Deepika vegiraju (talk | contribs) (Removed redirect to Phosphofructokinase deficiency) (Tags: Removed redirect, 2017 source edit)
N    14:54  Glycogen storage disease type 12‎ (diff | hist) . . (+573). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' GSD12; Glycogen storage disease 12; Aldolase A deficiency; Red cell aldolase deficiency; Aldolase deficiency red cell; Aldoa deficiency Glycogen storage d...") (Tag: 2017 source edit)
N    14:48  Glutamate formiminotransferase deficiency‎ (diff | hist) . . (+3,485). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Formiminotransferase deficiency syndrome; Formiminoglutamicaciduria (FIGLU-uria); Formiminoglutamic acidemia; Arakawa syndrome 1 Glutamate formiminotransfe...") (Tag: 2017 source edit)
N    10:44  Glucocorticoid remediable aldosteronism‎ (diff | hist) . . (+2,732). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Familial hyperaldosteronism type 1; Hyperaldosteronism, familial type 1; Dexamethasone sensitive hypertension; Glucocorticoid sensitive hypertension Glucoc...") (Tag: 2017 source edit)
     10:19  Giant platelet syndrome‎ (diff | hist) . . (+6,395). . Deepika vegiraju (talk | contribs) (Removed redirect to Giant platelet disorder) (Tags: Removed redirect, 2017 source edit)
N    09:54  Genuine diffuse phlebectasia‎ (diff | hist) . . (+715). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Bockenheimer syndrome Genuine diffuse phlebectasia or Bockenheimer's syndrome is a very rare condition characterized by an extensive venous [[malformation]...") (Tag: 2017 source edit)
N    09:40  Fibromuscular dysplasia - Not a rare disease‎ (diff | hist) . . (+3,283). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Fibromuscular dysplasia of arteries; FMD Fibromuscular dysplasia (FMD) is a condition characterized by abnormal development or growth of cells in the walls...") (Tag: 2017 source edit)
N    09:11  Fetal and neonatal alloimmune thrombocytopenia‎ (diff | hist) . . (+4,070). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' NAIT Fetal and neonatal alloimmune thrombocytopenia (NAIT) is a blood disorder that affects pregnant women and their babies. == '''Epidemiology''' == NAIT...") (Tag: 2017 source edit)