Results 131 to 140 of about 2,952,556 (266)

Tumoral calcinosis with vitamin D deficiency

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2008
A 50-year-old woman presented with recurrent calcified mass in the left gluteal region. The clinical, radiological, and biochemical profile confirmed the diagnosis of tumoral calcinosis. She also had associated vitamin D deficiency. The patient underwent
Kannan Subramanian   +6 more
doaj  

Improved hypercalcemia after debulking of uremic tumoral calcinosis in a parathyroidectomized patient. [PDF]

open access: yes, 2005
Uremic Tumoral Calcinosis (UTC) is a rare complication of chronic kidney disease on dialysis, characterized by large periarticular calcification. Among some cases, hypercalcemia with no conventional etiologies has been reported.
Bornemann, Michael   +2 more
core  

Tumoral infrapatellar calcinosis

open access: diamond, 2023
Andrea González De Godos   +4 more
openalex   +1 more source

Tumoral calcinosis in an 8-year-old girl: A case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Tumoral Calcinosis is a rare, benign metabolic disorder, characterized by the deposition of calcium phosphate crystals in extra-articular soft tissues.
M. Savadier, N. Maistry, D.S. Harrison
doaj   +1 more source

Tumoral calcinosis: a case report

open access: yesThe Turkish Journal of Pediatrics, 1999
Tumoral calcinosis is a rare disorder with the calcified masses in subcutaneous tissues. We report herein a nine-year-old girl, in whom the calcified lesions bilaterally involved the soft tissues in the anterior part of the knee joint.
I Ozkan   +5 more
doaj  

TUMORAL CALCINOSIS [PDF]

open access: yesAmerican Journal of Roentgenology, 1971
I, Yaghmai, P, Mirbod
openaire   +2 more sources

Pilomatrixoma. Revisión de 179 casos [PDF]

open access: yes, 2016
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  

Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey

open access: yesJCRPE, 2019
Inactivating autosomal recessive mutations in fibroblast growth factor 23 (FGF23), klotho (KL) and polypeptide N-acetylgalactosaminotransferase 3 (GALNT3) genes lead to a rare disorder, hyperphosphatemic familial tumoral calcinosis (HFTC).
Rabia Miray Kışla Ekinci   +6 more
doaj   +1 more source

Rh immunization in ruptured tubal pregnancy.

open access: yesBritish medical journal, 1973
Tuberculous Peritonitis   +39 more
semanticscholar   +1 more source

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