All public logs
From WikiMSK
Combined display of all available logs of WikiMSK. You can narrow down the view by selecting a log type, the username (case-sensitive), or the affected page (also case-sensitive).
- 20:52, 11 March 2023 Jeremy talk contribs created page Scapular Fractures (Created page with "{{Creative commons not compatible|source=[https://orthopaedia.com/page/Scapular-Fractures]|terms=not for commercial use, but can be modified.|license=[https://creativecommons....")
- 20:31, 11 March 2023 Jeremy talk contribs created page Cervical Spondylotic Amyotrophy (Created page with "{{Stub}} This rare condition refers to unilateral or bilateral upper limb muscle weakness and wasting without significant sensory deficits in the context of cervi...")
- 20:18, 11 March 2023 Jeremy talk contribs created page Non-Compressive Myelopathy (Created page with "{{DDX Box|ddx-title=Non-compressive Myelopathy DDX|ddx-text=*Inflammatory and vasculitis **Primary progressive multiple sclerosis **Neuromyelitis optica **Eale's disease **Sub...") Tag: Visual edit
- 19:59, 11 March 2023 Jeremy talk contribs created page Category:Spinal Cord Disorders (Created page with "Category:Neurology")
- 19:44, 11 March 2023 Jeremy talk contribs created page Template:Myotonia DDX (Created page with "*Myotonic dystrophy **DM type 1 (DMPK) **DM type 2 (CNBP) * Non-dystrophic myotonias ** Chloride channelopathies (CLCN1) *** Thomsen Myotonia Congenit...")
- 15:39, 11 March 2023 Jeremy talk contribs deleted page Category:Neuromuscular Disorders (content before blanking was: "Category:Neurology")
- 15:38, 11 March 2023 Jeremy talk contribs deleted page Category:Peripheral Nerve Entrapments (content before blanking was: "Also known as compressive neuropathies. See Dr Andrea Trescott's publications. ==Videos== <youtube>https://www.youtube.com/watch?v=UTULxC36tjY</youtube> ==Resources== {{PDF|Entrapment neuropathies a contemporary approach.pdf|Entrapment neuropathies, a contemporary approach|caption=Review article by Schmidt et al, 2020}} {{PDF|Nerve entrapments lower leg ankle and foot - McCrory 2002.pdf|Nerve entrapments lower leg ankle and foot|caption=McCrory et al, 2002}} [...")
- 15:34, 11 March 2023 Jeremy talk contribs created page Category:Muscle Disorders (Created page with "Category:Neurology")
- 15:26, 11 March 2023 Jeremy talk contribs created page Category:Polyneuropathies (Created page with "Cateogory:Neurology Category:Concepts")
- 15:23, 11 March 2023 Jeremy talk contribs created page Category:Plexopathies (Created page with "Category:Neurology Category:Concepts")
- 15:20, 11 March 2023 Jeremy talk contribs created page Category:Radiculopathies (Created page with "Category:Neurology Category:Concepts")
- 15:17, 11 March 2023 Jeremy talk contribs created page Category:Mononeuropathies (Created page with "Category:Widespread Category:Neurology")
- 15:38, 10 March 2023 Jeremy talk contribs created page Distal Weakness (Created page with "==Classification== {{family tree/start |summary=Sample 1}} {{family tree | | | | | | | | A01 | | | | | | |A01=Distally Predominant Weakness}} {{family tree | | | | |,|-|-|-|^...")
- 15:06, 10 March 2023 Jeremy talk contribs created page Facioscapulohumeral Dystrophy/Members (Created page with "{{Members page}} {{PDF|Facioscapulohumeral Muscular Dystrophies - Wagner 2019.pdf}}")
- 14:52, 10 March 2023 Jeremy talk contribs created page Facioscapulohumeral Dystrophy (Created page with "Facioscapulohumeral muscular dystrophy (FSHD) is one of the most prevalent forms of muscular dystrophy. The name refers to how FSHD affects muscles of the face (facio), scapul...") Tag: Visual edit
- 13:54, 10 March 2023 Jeremy talk contribs uploaded File:Muscular dystrophy weakness patterns.jpg (From https://commons.wikimedia.org/w/index.php?curid=45826804)
- 13:54, 10 March 2023 Jeremy talk contribs created page File:Muscular dystrophy weakness patterns.jpg (From https://commons.wikimedia.org/w/index.php?curid=45826804)
- 13:49, 10 March 2023 Jeremy talk contribs created page Idiopathic Inflammatory Myopathy (Redirected page to Myositis) Tags: New redirect Visual edit: Switched
- 09:44, 10 March 2023 Jeremy talk contribs uploaded File:Pompe clinical features.jpg (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551719/)
- 09:44, 10 March 2023 Jeremy talk contribs created page File:Pompe clinical features.jpg (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551719/)
- 09:43, 10 March 2023 Jeremy talk contribs uploaded File:Pompe distribution of weakness.jpg (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551719/)
- 09:43, 10 March 2023 Jeremy talk contribs created page File:Pompe distribution of weakness.jpg (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551719/)
- 09:36, 10 March 2023 Jeremy talk contribs uploaded File:Genomic sequencing history.jpg (https://www.mayoclinicproceedings.org/article/S0025-6196(16)30682-6/fulltext)
- 09:36, 10 March 2023 Jeremy talk contribs created page File:Genomic sequencing history.jpg (https://www.mayoclinicproceedings.org/article/S0025-6196(16)30682-6/fulltext)
- 06:27, 10 March 2023 Jeremy talk contribs uploaded File:Gowers sign.jpg
- 06:27, 10 March 2023 Jeremy talk contribs created page File:Gowers sign.jpg
- 06:27, 10 March 2023 Jeremy talk contribs deleted page File:Gowers sign.jpg
- 06:25, 10 March 2023 Jeremy talk contribs uploaded File:EMG neuropathic vs myopathic.jpeg (https://www.intechopen.com/chapters/43488)
- 06:25, 10 March 2023 Jeremy talk contribs created page File:EMG neuropathic vs myopathic.jpeg (https://www.intechopen.com/chapters/43488)
- 06:07, 10 March 2023 Jeremy talk contribs uploaded File:Gowers sign.jpg
- 06:07, 10 March 2023 Jeremy talk contribs created page File:Gowers sign.jpg
- 05:49, 10 March 2023 Jeremy talk contribs created page Proximal Weakness (Created page with "{{Stub}} ==Classification== {{family tree/start |summary=Sample 1}} {{family tree | | | | | | | | A01 | | | | | | |A01=Proximal Weakness}} {{family tree | | | | |,|-|-|-|^|-|...") Tag: Visual edit: Switched
- 07:42, 9 March 2023 Jeremy talk contribs uploaded File:Nondystrophic myotonias - stunnenberg2020.pdf (File uploaded with MsUpload)
- 07:42, 9 March 2023 Jeremy talk contribs created page File:Nondystrophic myotonias - stunnenberg2020.pdf (File uploaded with MsUpload)
- 07:11, 9 March 2023 Jeremy talk contribs created page Myotonia Congenita (Created page with "== Clinical Features == {| class="wikitable" |+Clinical Features of AR vs AD Myotonia Congenita<ref>https://www.ncbi.nlm.nih.gov/books/NBK1355/</ref> ! colspan="1" rowspan="1"...") Tag: Visual edit: Switched
- 21:39, 8 March 2023 Jeremy talk contribs created page Myotonic Dystrophy/Members (Created page with "{{Members subpage}} {{PDF|Myotonic Dystrophy - Hamel 2022.pdf}} {{PDF|Myotonic Muscular Dystrophies - Johnson 2019.pdf}} {{PDF|Myotonic dystrophies - Meola 2013.pdf}}")
- 21:39, 8 March 2023 Jeremy talk contribs uploaded File:Myotonic dystrophies - Meola 2013.pdf (File uploaded with MsUpload)
- 21:39, 8 March 2023 Jeremy talk contribs created page File:Myotonic dystrophies - Meola 2013.pdf (File uploaded with MsUpload)
- 21:20, 8 March 2023 Jeremy talk contribs uploaded File:Myotonic dystrophy patient.JPG (From https://commons.wikimedia.org/wiki/File:Myotonic_dystrophy_patient.JPG)
- 21:20, 8 March 2023 Jeremy talk contribs created page File:Myotonic dystrophy patient.JPG (From https://commons.wikimedia.org/wiki/File:Myotonic_dystrophy_patient.JPG)
- 18:32, 6 March 2023 Jeremy talk contribs created page Myotonic Dystrophy (Created page with "{{Stub}}{{Condition|inheritance=Autosomal dominant|genetics=DMPK (DM1), CNBP/ZNF9 (DM2)}} Myotonic dystrophy is a clinically and genetically heterogenous disorder with two ma...") Tag: Visual edit
- 17:50, 6 March 2023 Jeremy talk contribs created page Charcot Marie Tooth Disease (Created page with "Charcot Marie Tooth (CMT) is a group of diseases that are characterised by a hereditary peripheral motor and sensory polyneuropathy. Patients experience gradual symmetrical w...") Tag: Visual edit
- 14:24, 6 March 2023 Jeremy talk contribs created page Tarui Disease (Created page with "Tarui Disease (also known as Glycogen Storage Disease Type VII) is an autosomal recessive disorder of carbohydrate metabolism characterised by the absence of phosphofructokina...") Tag: Visual edit
- 05:23, 6 March 2023 Jeremy talk contribs created page Pompe Disease (Created page with "Pompe disease is a Lysosomal Storage Disease (LSD), also a type of Glycogen Storage Disease (GSD II), that is caused by a deficiency in acid alph...") Tag: Visual edit
- 21:12, 5 March 2023 Jeremy talk contribs created page Glycogen Storage Diseases (Created page with "{| class="wikitable" |- !GSD type !Deficiency !Key clinical findings !Diagnosis !Therapy |- |GSD 0a |Glycogen synthase 2 |Ketotic hypoglycemia, no hepatomegaly |Liver biopsy a...") Tag: Visual edit
- 19:23, 5 March 2023 Jeremy talk contribs created page Property:Has condition inheritance (Created a property of type Text)
- 19:23, 5 March 2023 Jeremy talk contribs created page Property:Has condition genetics (Created a property of type Text)
- 16:07, 5 March 2023 Jeremy talk contribs uploaded File:Ting Wang 702 Notes 2022.pdf (File uploaded with MsUpload)
- 16:07, 5 March 2023 Jeremy talk contribs created page File:Ting Wang 702 Notes 2022.pdf (File uploaded with MsUpload)
- 17:56, 1 March 2023 Jeremy talk contribs uploaded File:Rare disease NGS approaches - Vinksel 2020.pdf (File uploaded with MsUpload)