Recent changes

From WikiMD

Track the most recent changes to the wiki on this page.

Recent changes options Show last 50 | 100 | 250 | 500 changes in last 1 | 3 | 7 | 14 | 30 days
Hide registered users | Hide anonymous users | Hide my edits | Hide bots | Hide minor edits
Show new changes starting from 07:09, 15 August 2020
   
Language:
List of abbreviations:
N
This edit created a new page (also see list of new pages)
m
This is a minor edit
b
This edit was performed by a bot
(±123)
The page size changed by this number of bytes

15 August 2020

N    06:42  Lesch Nyhan syndrome‎ (diff | hist) . . (+6,292). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' LNS; HPRT deficiency, complete; Lesch-Nyhan syndrome; Lesch Nyhan disease; Choreoathetosis self-mutilation syndrome; Complete HPRT deficiency complete; Hypo...") (Tag: 2017 source edit)
     04:37  (Import log). . [Prab‎ (21×)]
     
04:37 . . Prab (talk | contribs) imported Template:Citric acid cycle enzymes and ETC by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Nucleotide metabolism enzymes by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Phospholipids by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Non-mevalonate pathway enzymes by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Lipid metabolism enzymes by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Glycolipid and sphingolipid metabolism enzymes by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Eicosanoids by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Cholesterol and steroid metabolism enzymes by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Porphyrin metabolism enzymes by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Urea cycle/sandbox by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Proteinogenic amino acids by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Neurotransmitter metabolism enzymes by file upload (1 revision) ‎
     
04:37 . . Prab (talk | contribs) imported Template:Amino acid metabolism enzymes by file upload (1 revision) ‎
     
04:36 . . Prab (talk | contribs) imported Template:Proteoglycan metabolism enzymes by file upload (1 revision) ‎
     
04:36 . . Prab (talk | contribs) imported Template:Pentose phosphate pathway enzymes by file upload (1 revision) ‎
     
04:36 . . Prab (talk | contribs) imported Template:Glycosaminoglycans by file upload (1 revision) ‎
     
04:36 . . Prab (talk | contribs) imported Template:Glycoprotein metabolism enzymes by file upload (1 revision) ‎
     
04:36 . . Prab (talk | contribs) imported Template:Glycolysis/sandbox by file upload (1 revision) ‎
     
04:36 . . Prab (talk | contribs) imported Template:Glycolysis enzymes by file upload (1 revision) ‎
     
04:36 . . Prab (talk | contribs) imported Template:Glycogenesis and glycogenolysis enzymes by file upload (1 revision) ‎
     
04:36 . . Prab (talk | contribs) imported Template:Fructose and galactose metabolism enzymes by file upload (1 revision) ‎

14 August 2020

N    12:25  Kaposiform lymphangiomatosis‎ (diff | hist) . . (+3,998). . Deepika vegiraju (talk | contribs) (Created page with "Kaposiform lymphangiomatosis (KLA) is a rare type of tumor and vascular malformation that results from the abnormal development of the lymphatic system. The lymphatic...") (Tag: 2017 source edit)
N    10:52  Kaposiform Hemangioendothelioma‎ (diff | hist) . . (+812). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' KH; Congenital cutaneous multifocal kaposiform hemangioendothelioma; KHE; Kaposiform hemangio-endothelioma A rare blood vessel tumor that usually f...") (Tag: 2017 source edit)
N    10:47  Schindler disease‎‎ (2 changes | history) . . (+5,178). . [Deepika vegiraju‎ (2×)]
     
10:47 (cur | prev) . . (+34). . Deepika vegiraju (talk | contribs) (Tag: Visual edit)
N    
10:45 (cur | prev) . . (+5,144). . Deepika vegiraju (talk | contribs) (Created page with "'''Other names:'''alpha-galactosidase B deficiency;alpha-galNAc deficiency, Schindler type;alpha-N-acetylgalactosaminidase deficiency;alpha-NAGA deficiency;angiokeratoma corpo...") (Tag: 2017 source edit)
N    10:45  Category:Glycoprotein metabolism disorders‎ (diff | hist) . . (+189). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    09:29  Juvenile temporal arteritis‎ (diff | hist) . . (+2,308). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Juvenile giant cell arteritis; JGCA; Juvenile cranial arteritis; Juvenile polymyalgia rheumatica; JPMR Juvenile temporal arteritis is a rare form of vasc...") (Tag: 2017 source edit)
N    08:58  Iron-refractory iron deficiency anemia‎ (diff | hist) . . (+5,120). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' IRIDA; IRIDA syndrome; Anemia, hypochromic microcytic, with defect in iron metabolism; Iron-handling disorder, hereditary; Pseudo-iron-deficiency anemia I...") (Tag: 2017 source edit)
     08:38  Templates‎ (diff | hist) . . (+23). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
N    08:37  Category:Genes mutated in mice‎ (diff | hist) . . (+165). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    08:37  Intrinsic factor deficiency‎ (diff | hist) . . (+3,364). . Deepika vegiraju (talk | contribs) (Created page with " '''Other Names:''' IFD; Pernicious anemia, congenital, due to defect of intrinsic factor; Congenital pernicious anemia due to defect of intrinsic factor; Intrinsic factor, co...") (Tag: 2017 source edit)
N    08:14  Internal carotid agenesis‎ (diff | hist) . . (+5,186). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Agenesis of the internal carotid artery; Internal carotid artery agenesis Internal carotid agenesis occurs when one or both of the blood vessels that supply...") (Tag: 2017 source edit)
N    06:58  Inherited bone marrow failure syndromes - Not a rare disease‎ (diff | hist) . . (+1,044). . Deepika vegiraju (talk | contribs) (Created page with "The inherited bone marrow failure syndromes (IBMFS) are a group of rare genetic blood disorders in which there is usually some form of aplastic anemia (failure of the bo...") (Tag: 2017 source edit)

13 August 2020

N    16:42  Inclusion body myopathy 2‎‎ (2 changes | history) . . (+8,701). . [Deepika vegiraju‎ (2×)]
     
16:42 (cur | prev) . . (-4). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
N    
16:41 (cur | prev) . . (+8,705). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' IBM2; Inclusion body myopathy, autosomal recessive; Inclusion body myopathy, quadriceps-sparing; QSM; Hereditary inclusion body myopathy; HIBM; Distal myopa...") (Tag: 2017 source edit)
N    16:04  Imerslund–Gräsbeck syndrome‎ (diff | hist) . . (+5,715). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' IGS; Pernicious anemia, juvenile, due to selective intestinal malabsorption of vitamin B12, with proteinuria; Enterocyte cobalamin malabsorption; Defect of...") (Tag: 2017 source edit)
N    15:42  Category:Leukocytes‎ (diff | hist) . . (+143). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
N    15:42  Idiopathic neutropenia - Not a rare disease‎ (diff | hist) . . (+1,728). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Nonimmune chronic idiopathic neutropenia of adults; NI-CINA Idiopathic neutropenia is an acquired form of '''severe chronic neutropenia '''whose cause is u...") (Tag: 2017 source edit)
N    13:57  Hermansky Pudlak syndrome 2‎‎ (2 changes | history) . . (+1,940). . [Prab‎; Deepika vegiraju‎]
     
13:57 (cur | prev) . . (+539). . Prab (talk | contribs) (Tag: 2017 source edit)
N    
06:41 (cur | prev) . . (+1,401). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' HPS2; Hermansky-Pudlak syndrome 2; Platelet defects and oculocutaneous albinism Hermansky-Pudlak syndrome type 2 (HPS-2) is a type of Hermansky-Pudlak syn...") (Tag: 2017 source edit)
N    11:57  Hypotrichosis–lymphedema–telangiectasia syndrome‎ (diff | hist) . . (+1,919). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' Hypotrichosis lymphedema telangiectasia syndrome; HLTS; Hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome; Hypotrich...") (Tag: 2017 source edit)
N    11:43  Hypofibrinogenemia, familial‎ (diff | hist) . . (+3,634). . Deepika vegiraju (talk | contribs) (Created page with "Familial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen co...") (Tag: 2017 source edit)
     11:22  Hypocomplementemic urticarial vasculitis‎ (diff | hist) . . (+4,836). . Deepika vegiraju (talk | contribs) (Removed redirect to Urticarial vasculitis) (Tags: Removed redirect, 2017 source edit)
     10:15  Hypersensitivity vasculitis‎ (diff | hist) . . (+3,889). . Deepika vegiraju (talk | contribs) (Removed redirect to Cutaneous small-vessel vasculitis) (Tags: Removed redirect, 2017 source edit)
N    09:51  Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency‎ (diff | hist) . . (+529). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' GPI deficiency; PIGM-CDG; Congenital disorder of glycosylation due to PIGM deficiency; Glycosylphosphatidylinositol deficiency A syndrome with combination...") (Tag: 2017 source edit)
N    09:13  Histiocytosis-lymphadenopathy plus syndrome‎ (diff | hist) . . (+7,329). . Deepika vegiraju (talk | contribs) (Created page with "'''Other Names:''' HJCD; Faisalabad histiocytosis; H syndrome; Histiocytosis with joint contractures and sensorineural deafness; SLC29A3 spectrum disorder Histiocytosis-lymp...") (Tag: 2017 source edit)
     07:15  Hermansky-Pudlak syndrome‎‎ (2 changes | history) . . (+8,368). . [Deepika vegiraju‎ (2×)]
     
07:15 (cur | prev) . . (-110). . Deepika vegiraju (talk | contribs) (Tag: 2017 source edit)
     
07:14 (cur | prev) . . (+8,478). . Deepika vegiraju (talk | contribs) (Removed redirect to Hermansky–Pudlak syndrome) (Tags: Removed redirect, 2017 source edit)
N    07:14  Category:Syndromes affecting the lung‎ (diff | hist) . . (+179). . Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)