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Degosdisease.org lookup results from http://whois.publicdomainregistry.com server:
- Domain created: 2021-08-27T16:19:33Z
- Domain updated: 2023-10-03T13:00:38Z
- Domain expires: 2024-08-27T16:19:33Z 0 Years, 116 Days left
- Website age: 2 Years, 248 Days
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- handle : NET-192-252-144-0-1
- status : Direct Allocation
- created : 2013-01-31
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Host name | s416.sureserver.com |
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Location | Waltham United States |
Latitude | 42.3972 |
Longitude | -71.2434 |
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Timezone | America/New_York |
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Degos disease - Wikipedia
Degos disease, also known as Köhlmeier-Degos disease or malignant atrophic papulosis, is an extremely rare condition caused by blockage of arteries and veins. Individuals with this condition will develop papules. Those diagnosed with this disease may also develop complications due to impairment of internal organs. The exact underlying mechanism is still unknown, and an effective tre…
En.wikipedia.orgDA: 16 PA: 19 MOZ Rank: 35
Degos Disease - Symptoms, Causes, Treatment | NORD
Aug 7, 2023 Degos disease is an extremely rare disorder, with only about 200 reported cases worldwide. In affected individuals, arteries of smaller diameter become blocked …
Rarediseases.orgDA: 16 PA: 29 MOZ Rank: 46
Diagnosing Degos | For Doctors - Degos Disease
Degos disease (malignant atrophic papulosis) is a rare progressive, small and medium size arterial occluding disease, leading to tissue infarction initially involving the skin and later …
Degosdisease.orgDA: 16 PA: 42 MOZ Rank: 60
An Overview | Information for Doctors - Degos Disease
The Papulosis atrophicans maligna (Köhlmeier-Degos disease) is a very rare illness. It was described for the first time by Köhlmeier in 1941 and documented as a distinct illness by …
Degosdisease.orgDA: 16 PA: 37 MOZ Rank: 56
Degos disease – malignant atrophic papulosis or …
Apr 16, 2015 Degos disease is a very rare syndrome with a rare type of multisystem vasculopathy of unknown cause that affects the skin, gastrointestinal tract, and central …
Ncbi.nlm.nih.govDA: 20 PA: 25 MOZ Rank: 49
Degos disease: a case report and review of the literature
Oct 29, 2020 Degos disease (DD), also called “malignant atrophic papulosis” or “lethal cutaneous and gastrointestinal arteriolar thrombosis,” is a rare occlusive arteriopathy …
Ncbi.nlm.nih.govDA: 20 PA: 25 MOZ Rank: 50
Degos Disease: Background, Pathophysiology, Etiology - Medscape
Dec 10, 2019 Broadly speaking, Degos disease is a vasculopathy or an endovasculitis. It is an occlusive arteriopathy involving small-caliber vessels. Specifically, it is a progressive, …
Emedicine.medscape.comDA: 22 PA: 25 MOZ Rank: 53
Malignant Atrophic Papulosis - StatPearls - NCBI …
Aug 7, 2023 Malignant atrophic papulosis, otherwise known as Kohlmeier–Degos disease or Degos disease, is a rare disorder of thrombo-obliterative vasculopathy affecting the skin, gastrointestinal tract, and …
Ncbi.nlm.nih.govDA: 20 PA: 17 MOZ Rank: 44
Degos Disease - an overview | ScienceDirect Topics
Degos Disease. Degos disease, also known as malignant atrophic papulosis, is an often-fatal disorder characterized by multiple infarcts in the skin and viscera owing to a …
Sciencedirect.comDA: 21 PA: 44 MOZ Rank: 73
Clinical and laboratory prognosticators of atrophic papulosis …
May 6, 2021 Degos Disease, also known as Köhlmeier-Degos disease, was first identified in 1941 and subsequently described as a unique thrombotic microangiopathic entity in …
Ojrd.biomedcentral.comDA: 22 PA: 36 MOZ Rank: 67
Dowling-Degos Disease - StatPearls - NCBI Bookshelf
Aug 16, 2023 Dowling-Degos disease is a rare autosomal dominant disorder characterized by acquired reticular hyperpigmentation in flexural sites. Hyperpigmentation is often recalcitrant to therapy and may lead to …
Ncbi.nlm.nih.govDA: 20 PA: 17 MOZ Rank: 47
Gastrointestinal Kohlmeier–Degos disease: a narrative review
Apr 20, 2022 Introduction Kohlmeier-Degos (K-D) disease is a rare obliterative vasculopathy that can present as a benign cutaneous form or with potentially malignant …
Ojrd.biomedcentral.comDA: 22 PA: 36 MOZ Rank: 69
Dowling-Degos disease | DermNet
Dowling-Degos disease, Reticulate pigmented anomaly, Reticulate pigmented anomaly of flexures, MIM 179850. Authoritative facts from DermNet New Zealand. DermNet provides …
Dermnetnz.orgDA: 13 PA: 29 MOZ Rank: 54
Degos Disease | American Journal of Clinical Pathology | Oxford …
Apr 1, 2011 By using cutaneous endothelial cells as substrate, we observed a distinct band of immunoreactivity corresponding to a molecular weight of 92 kDa. , A similar band of …
Academic.oup.comDA: 16 PA: 31 MOZ Rank: 60
Degos disease: a case report and review of the literature
Oct 29, 2020 Degos disease is a very rare syndrome with multisystem vasculopathy of unknown cause. It can affect the skin, gastrointestinal tract, and central nervous system. …
Jmedicalcasereports.biomedcentral.comDA: 37 PA: 36 MOZ Rank: 87
What is Degos disease? Malignant Atrophic Papulosis, Köhlmeier
Degos disease, also known as malignant atrophic papulosis, is a very rare illness that affects a person’s blood vessels. When cells in the linings of veins and arteries under the skin …
Degosdisease.orgDA: 16 PA: 27 MOZ Rank: 58
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