Results 231 to 240 of about 57,573 (289)

Perianal Rhabdomyosarcoma Mimicking Perianal Abscess: Case Report and Literature Review. [PDF]

Case Rep Oncol
Shamohammadi M, Mohammadtaheri B, Abbasi Garavand A, Madankan A, Mousavie SH, Panahi M.   +5 more
europepmc   +1 more source

The Approximate Subcutaneous LD₅₀ and Associated Lesions Induced by Ivalin, Extracted and Purified from <i>Geigeria aspera</i> Harv., in Sprague-Dawley Rats. [PDF]

Molecules
Locke S, Botha C, Clift S, Lensink A.
europepmc   +1 more source

Primary Renal Fibrosarcoma with Massive Tumor Size and Inferior Vena Cava Extension Mimicking Renal Cell Carcinoma: A Rare Case Report. [PDF]

J Kidney Cancer VHL
Rathore K, Mehra K, Yadav M, Kaushal D, Joshi D, Madhavan K, Shrivastava N, Chandana.   +7 more
europepmc   +1 more source

Duodenal leiomyoma: a case report of upper gastrointestinal hemorrhage from a giant duodenal tumor. [PDF]

Int J Surg Case Rep
MacKenzie M, MacKenzie B, Kwan AY, Chen CH, Yap WW, MacKenzie S.   +5 more
europepmc   +1 more source

Clinical features analysis of inflammatory myofibroblastic tumors of the retroperitoneal and genitourinary system. [PDF]

BMC Urol
Huang Q, Ding M, Huang Y, Lian X, Xie Y, Wang T, Chen B, Chen Y.   +7 more
europepmc   +1 more source

Rare primary pleomorphic rhabdomyosarcoma of the thyroid gland with lung and adrenal metastases: a case report and literature review. [PDF]

Front Oncol
Altabbouche R, Musiał J, Jałocha-Kaczka A, Dziki Ł, Maryńczak K, Kaczka K.   +5 more
europepmc   +1 more source

A nipple-like lesion: A case report of leiomyosarcoma on the back. [PDF]

SAGE Open Med Case Rep
DeBiasio C, Dhawan J, Nakonechny Q, Glassman SJ.   +3 more
europepmc   +1 more source

Directed Cell Self-Assembly to Form Tendon and Muscle Models for Studying Early Stages of Musculoskeletal Tissue Formation. [PDF]

J Biomech Eng
Stephenson TR, Marchus CR, Clair AG, Lama MM, Wieber PJ, Schiele NR.   +5 more
europepmc   +1 more source

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Desmin-related myopathy

Clinical Genetics, 2010
Desmin-related myopathy (DRM) is an autosomally inherited skeletal and cardiac myopathy, mainly caused by dominant mutations in the desmin gene (DES). We provide (i) a literature review on DRM, including clinical manifestations, inheritance, molecular genetics, myopathology and management and (ii) a meta-analysis of reported DES mutation carriers ...
van Spaendonck-Zwarts, K. Y., van Hessem, L., Jongbloed, J. D. H., de Walle, H. E. K., Capetanaki, Y., van der Kooi, A. J., van Langen, I. M., van den Berg, M. P., van Tintelen, J. P.   +8 more
openaire   +3 more sources

Desmin myopathy with cardiomyopathy

Acta Neuropathologica, 1995
We report a case of abnormal desmin accumulation within the muscle of a 30-year-old female with a 2-year history of cardiomyopathy and axial muscle weakness. Serum creatine kinase was normal. A quadriceps muscle biopsy revealed pink hyaline inclusions, which stained for acid phosphatase and with PAS and were present in both fibre types.
C H, Cameron, M, Mirakhur, I V, Allen
openaire   +2 more sources