Results 131 to 140 of about 2,912,781 (218)
Management of Tumoral Calcinosis-A Rare Case Report [PDF]
Dr.ShivalingappaJArakeri . +4 more
openalex +1 more source
First report of hyperphosphatemic familial tumoral calcinosis due to homozygous GALNT3 mutation in a 16-year-old boy [PDF]
Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare disorder HFTC is caused by a loss of function in fibroblast growth factor 23 (FGF23), leading to increased phosphate levels in the body and calcium deposition.
Gupta, Sushil +2 more
core +2 more sources
Renal Abnormalities During Calcinosis Primary Tumor [PDF]
Primary tumour calcinosis is a rare condition of unknown etiopathogeny. They are transmitted in an autosomal dominant or recessive mode and predominate in the black race.
Lenga Loumingou, Ida Aurélie +1 more
core +1 more source
Hyperphosphatemic Familial Tumoral Calcinosis With Galnt3 Mutation: Transient Response to Anti‐Interleukin‐1 Treatments [PDF]
A. Dauchez +5 more
openalex +1 more source
Pilomatrixoma. Revisión de 179 casos [PDF]
Presentamos un estudio sobre 179 casos de Pilomatrixoma recogidos en los archivos del Hospital General 'Vall d'Hebrón' de Barcelona, entre los años 1972 y 1988. Tumoración de presentación pediátrica, cerca del 50% de los casos se han observado en menores
Berini Aytés, Leonardo +3 more
core
Rh immunization in ruptured tubal pregnancy.
Tuberculous Peritonitis +39 more
semanticscholar +1 more source
Genetic diseases resulting from disordered FGF23/klotho biology [PDF]
Econs, Michael J.
core +1 more source
Proceedings 35th Symposium ESVN‐ECVN
Journal of Veterinary Internal Medicine, Volume 39, Issue 2, March/April 2025.
wiley +1 more source
Tumoral calcinosis is an uncommon type of extraosseous calcification characterized by large rubbery or cystic masses containing calcium-phosphate deposits. The condition prevails in the periarticular tissue with preservation of osteoarticular structures.
Mariana Espiga Maioli +4 more
doaj +1 more source

