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Show new changes starting from 18:10, 9 August 2020
   
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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)
N    08:38  Familial thoracic aortic aneurysm and dissection‎ (diff | hist) . . (+7,825). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Familial TAAD; Familial aortic aneurysm; Familial thoracic aortic aneurysm; Annuloaortic ectasia; Familial aortic dissection; Familial thoracic aortic aneur...") (Tag: 2017 source edit)
N    06:40  Category:Disorders of sclera and cornea‎ (diff | hist) . . (+183). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    06:40  Familial LCAT deficiency‎ (diff | hist) . . (+5,312). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' FLD Norum disease Complete LCAT deficiency familial lecithin-cholesterol acyltransferase deficiency FLD LCAT deficiency lecithin acyltransferase deficiency...") (Tag: 2017 source edit)
N    05:12  Glossary of drinks‎ (diff | hist) . . (+196,541). . Prab (talk | contribs) (Created page with "* '''aaron burr''' -  United States politician who served as vice president under Jefferson; he mortally wounded his political rival Alexander Hamilton in a duel and fled...") (Tag: 2017 source edit)
     05:11  Drink‎ (diff | hist) . . (+52). . Prab (talk | contribs) (Tag: 2017 source edit)
     05:10  Energy drinks‎ (diff | hist) . . (+17). . Prab (talk | contribs) (Tag: Visual edit)
     03:42  Foods A-Z‎ (diff | hist) . . (+223,904). . Prab (talk | contribs) (Tag: 2017 source edit)
     03:39  Glossary of foods‎ (diff | hist) . . (-426). . Prab (talk | contribs) (Tag: Visual edit)
N    03:23  Edible plants‎‎ (2 changes | history) . . (+109,315). . [Prab‎ (2×)]
     
03:23 (cur | prev) . . (-115). . Prab (talk | contribs) (Tag: 2017 source edit)
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03:22 (cur | prev) . . (+109,430). . Prab (talk | contribs) (Created page with "* '''accessory fruit''' -  fruit containing much fleshy tissue besides that of the ripened ovary; as apple or strawberry * '''achene''' -  small dry indehiscent fru...") (Tag: 2017 source edit)
     02:44  Glossary of fruits‎ (diff | hist) . . (+87,770). . Prab (talk | contribs) (Tag: 2017 source edit)
     02:41  Fruit‎‎ (2 changes | history) . . (+26). . [Prab‎ (2×)]
     
02:41 (cur | prev) . . (+1). . Prab (talk | contribs) (Related pages) (Tag: 2017 source edit)
     
02:41 (cur | prev) . . (+25). . Prab (talk | contribs) (Related pages) (Tag: 2017 source edit)
N    02:20  Familial hyperthyroidism due to mutations in TSH receptor‎ (diff | hist) . . (+1,216). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Familial non-immune hyperthyroidism; Nonautoimmune hyperthyroidism; Resistance to thyroid stimulating hormone A rare hyperthyroidism characterized by m...") (Tag: 2017 source edit)
     01:50  Glossary of vegetables‎ (diff | hist) . . (+14,858). . Prab (talk | contribs) (Tag: 2017 source edit)
     00:47  Diets‎ (diff | hist) . . (+152,731). . Prab (talk | contribs) (Tag: 2017 source edit)

8 August 2020

N    15:21  Category:Blood proteins‎ (diff | hist) . . (+151). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    15:21  Factor V Leiden thrombophilia - Not a rare disease‎ (diff | hist) . . (+6,457). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Hereditary resistance to activated protein C; APC resistance, Leiden type Factor V Leiden thrombophilia is an inherited disorder of blood clotting. Factor V...") (Tag: 2017 source edit)
     12:34  Factor V deficiency‎ (diff | hist) . . (+4,684). . Deepika vegiraju (talk | contribs) (Removed redirect to Factor V) (Tags: Removed redirect, 2017 source edit)
N    11:01  Category:Encyclopedia‎ (diff | hist) . . (+147). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    11:01  Medical encyclopedia‎ (diff | hist) . . (+206,767). . Prab (talk | contribs) (Created page with "An encyclopedia of medicine. * '''abasia''' - noun inability to walk * '''abdomen''' - noun the region of the body of a vertebrate between the thorax and the...") (Tag: 2017 source edit)
N    10:16  Extranodal nasal NK/T cell lymphoma‎ (diff | hist) . . (+987). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' NK/T-cell lymphoma; Angiocentric T-cell lymphoma; Lethal midline granuloma; NKTCL; Nasal T/natural killer-cell lymphoma Extranodal nasal NK/T cell lymphom...") (Tag: 2017 source edit)
     10:14 (User creation log) . . User account Techpluggedbg (talk | contribs) was created ‎
     10:07  Medical terminology‎ (diff | hist) . . (+40,146). . Prab (talk | contribs) (Tag: 2017 source edit)
     09:43  Evans syndrome‎ (diff | hist) . . (+6,272). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
     07:03  Erythema elevatum diutinum‎ (diff | hist) . . (+3,471). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
N    06:33  Category:Syndromes in animals‎ (diff | hist) . . (+163). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    06:33  Category:Collagen disease‎ (diff | hist) . . (+155). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    06:33  Ehlers-Danlos syndrome‎ (diff | hist) . . (+12,624). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' FN abnormality; Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality; EDS10 (formerly); Ehlers-Danlos syndrome, type X (formerly);...") (Tag: 2017 source edit)
N    05:39  Ehlers-Danlos syndrome, dysfibronectinemic type‎ (diff | hist) . . (+61). . Deepika vegiraju (talk | contribs) (Redirected page to Ehlers-Danlos syndrome) (Tags: New redirect, 2017 source edit)
N    05:32  Dyskeratosis congenita X-linked‎ (diff | hist) . . (+61). . Deepika vegiraju (talk | contribs) (Redirected page to Dyskeratosis congenita) (Tags: New redirect, 2017 source edit)
N    05:30  Dyskeratosis congenita autosomal recessive‎ (diff | hist) . . (+61). . Deepika vegiraju (talk | contribs) (Redirected page to Dyskeratosis congenita) (Tags: New redirect, 2017 source edit)
N    05:28  Dyskeratosis congenita autosomal dominant‎ (diff | hist) . . (+61). . Deepika vegiraju (talk | contribs) (Redirected page to Dyskeratosis congenita) (Tags: New redirect, 2017 source edit)
N    03:13  Diamond-Blackfan anemia 3‎‎ (2 changes | history) . . (+62). . [Deepika vegiraju‎ (2×)]
     
03:13 (cur | prev) . . (+1). . Deepika vegiraju (talk | contribs) (Changed redirect target from Diamond-Blakfan anemia to Diamond-Blackfan anemia) (Tags: Redirect target changed, 2017 source edit)
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02:34 (cur | prev) . . (+61). . Deepika vegiraju (talk | contribs) (Redirected page to Diamond-Blakfan anemia) (Tags: New redirect, 2017 source edit)
N    02:32  Diamond-Blackfan anemia 2‎ (diff | hist) . . (+62). . Deepika vegiraju (talk | contribs) (Redirected page to Diamond-Blackfan anemia) (Tags: New redirect, 2017 source edit)
N    02:29  Category:Disorders of synthesis of DNA, RNA, and proteins‎ (diff | hist) . . (+219). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    02:29  Category:Ribosomopathy‎ (diff | hist) . . (+149). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
     02:29  Diamond-Blackfan anemia‎ (diff | hist) . . (+9,351). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)

7 August 2020

N    16:18  Dehydrated hereditary stomatocytosis‎ (diff | hist) . . (+6,176). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Desiccytosis hereditary; Xerocytosis hereditary; Hereditary xerocytosis Dehydrated hereditary stomatocytosis (DHS) is a rare hemolytic anemia charac...") (Tag: 2017 source edit)
N    15:47  Deafness-lymphedema-leukemia syndrome‎ (diff | hist) . . (+4,776). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Emberger syndrome; Lymphedema, primary, with myelodysplasia Deafness-lymphedema-leukemia syndrome is a very rare genetic disorder characterized by swelling...") (Tag: 2017 source edit)
N    02:17  Cystic medial necrosis of aorta‎ (diff | hist) . . (+672). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Erdheim cystic medial necrosis of aorta; Erdheim disease Familial aortic dissection is the term used to describe rupture of the aortic wall at the level of...") (Tag: 2017 source edit)