Results 111 to 120 of about 26,235 (251)
This case report describes a rare differential diagnosis of soft-tissue infection in a neonate. Fever, pain, inflammation, and acute tenderness in the limb of a neonate signify acute infection or osteomyelitis unless proved otherwise.
A Arora, A Agarwal, S Kumar, SK Gupta
doaj +1 more source
Fibroblast growth factor receptor inhibitor therapy induced calcinosis cutis treated with sodium thiosulfate [PDF]
Justin Qian +7 more
openalex +1 more source
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 8, Page 1009-1012, August 2025.
Edgar Akuffo‐Addo +4 more
wiley +1 more source
Calcinosis in systemic sclerosis: prevalence, clinical picture, management, complications
This literature review summarizes current data on the epidemiology, pathophysiology, diagnosis and treatment of calcinosis cutis in patients with systemic sclerosis (SSc).
Ye.D. Yehudina, I.Yu. Golovach
doaj +1 more source
Hipoparatiroidismo primario idiopático felino. Caso clínico [PDF]
Se describe un caso clínico de hipoparatiroidismo primario idiopático, en un gato macho de 2 años y medio de edad, que se presentó en nuestro hospital con un cuadro de anorexia, temblores, cambio de comportamiento, agresividad y alteraciones neurológicas.
Gil, V. +3 more
core
Calcinosis Cutis at the Tarsus of the Upper Eyelid [PDF]
Calcinosis cutis involves the inappropriate deposition of calcium within the dermis layer of the skin, and is often associated with rheumatoid disease. A 42-year-old woman presented for evaluation of a hard palpable mass on the left upper eyelid.
Boulman +13 more
core +2 more sources
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 8, Page 1009-1012, August 2025.
Edgar Akuffo‐Addo +4 more
wiley +1 more source
A Case of Calcinosis Cutis in a Patient With Sjögren Syndrome
Calcinosis cutis is a challenging, debilitating condition that often is observed in patients with systemic sclerosis or dermatomyositis. However, it is rarely documented in cases of Sjögren syndrome, with only 6 previous cases reported in the medical ...
Arya P.V. Akhila +2 more
doaj +1 more source
The ABCC6 Transporter: A New Player in Biomineralization [PDF]
Pseudoxanthoma elasticum (PXE) is an inherited metabolic disease with autosomal recessive inheritance caused by mutations in the ABCC6 gene. Since the first description of the disease in 1896, alleging a disease involving the elastic fibers, the concept ...
Arányi, Tamás +4 more
core +1 more source
The Journal of Dermatology, Volume 52, Issue 6, Page e430-e480, June 2025.
Yoshihide Asano +27 more
wiley +1 more source

