Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
Search Results
2 results
Results by year
Filters applied: . Clear all
Quoted phrase not found in phrase index: "Periarticular subcutaneous nodules"
Page 1
Clinical and genetic analysis of idiopathic normophosphatemic tumoral calcinosis in 19 patients.
J Endocrinol Invest. 2020 Feb;43(2):173-183. doi: 10.1007/s40618-019-01097-4. Epub 2019 Sep 18.
J Endocrinol Invest. 2020.
PMID: 31535357
PURPOSE: Tumoral calcinosis is a rare clinicopathological entity characterized by ectopic soft-tissue calcification, typically periarticular. Normophosphatemic tumoral calcinosis is seldom reported in East Asian populations, and the preoperative diagnosis is often elusive. …
PURPOSE: Tumoral calcinosis is a rare clinicopathological entity characterized by ectopic soft-tissue calcification, typically periarticu …
Bone marrow transplantation for infantile ceramidase deficiency (Farber disease).
Yeager AM, Uhas KA, Coles CD, Davis PC, Krause WL, Moser HW.
Yeager AM, et al.
Bone Marrow Transplant. 2000 Aug;26(3):357-63. doi: 10.1038/sj.bmt.1702489.
Bone Marrow Transplant. 2000.
PMID: 10967581
Infantile ceramidase deficiency (Farber disease) is an uncommon, progressive lysosomal storage disease characterized by multiple ceramide-containing nodules (lipogranulomata) in the subcutaneous tissue and upper aerodigestive tract, painful periarticular swel …
Infantile ceramidase deficiency (Farber disease) is an uncommon, progressive lysosomal storage disease characterized by multiple ceramide-co …
Item in Clipboard
Cite
Cite