Results 81 to 90 of about 625 (116)

Radial Nerve Palsy Caused by Desmoid-Type Fibromatosis: A Case Report and Review of the Literature. [PDF]

Cureus
Iwanaga R, Mihara A, Sakai T, Muramatsu K, Hashimoto T.   +4 more
europepmc   +1 more source

Cutaneous soft tissue tumors in the 5th edition of the World Health Organization classification of skin tumors: key updates and new entities. [PDF]

J Pathol Transl Med
Choi JH.
europepmc   +1 more source

Infantile Systemic Hyalinosis: A Case Report with a Brief Review. [PDF]

Indian Dermatol Online J
Sangwan P, Shreya K, Rout AN, Jaladi HC.
europepmc   +1 more source

A Pelvic Mass in a Young Patient With Crohn's Disease. [PDF]

ACG Case Rep J
Evers CD, Ravindran A, Rosenblum F, Weber F.   +3 more
europepmc   +1 more source

Desmoid-type fibromatosis in an uncommon location: A case report of shoulder involvement misdiagnosed as rhabdomyosarcoma. [PDF]

Int J Surg Case Rep
Limaiem F, Gharbi MA, Boujelbene N, Triki R, Romdhane KB, Bouzidi R.   +5 more
europepmc   +1 more source

Primary nasopharyngeal Kaposi's sarcoma without cutaneous manifestations: a case report. [PDF]

J Med Case Rep
Lugina EL, Ernesti ZM, Nundu EL, Mlole AT, Tupa F, StanleyNoah H, Mwita CJ, Mosha IJ, Iddy S, Kahesa CA, Ngalamika O, Wood C, Mwaiselage JD, Lidenge SJ.   +13 more
europepmc   +1 more source

Infantile systemic Hyalinosis in a 6-month-old male: identification of homozygous ANTXR2 gene mutation. [PDF]

Oxf Med Case Reports
Moshfegh F, Hosseinzade Z, Javanbakht M, Javid A, Mozaffari M.   +4 more
europepmc   +1 more source

Symptomatic Plantar Osteochondroma of the Third Metatarsal With Toe Flexion Deformity: A Case Report. [PDF]

Cureus
Al Kholaki S, Nader F, Bassil GF, Missaoui Z.   +3 more
europepmc   +1 more source

Dynamic S-acylation controls CMG2 maturation, extracellular matrix regulation, and anthrax toxin entry

Abrami L, Blaskovic S, Joliot O, Mercier V, Kunz B, Mesquita FS, van der Goot FG.   +6 more
europepmc   +1 more source

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Hyaline fibromatosis of Hoffa’s fat pad in a patient with a mild type of hyaline fibromatosis syndrome

Skeletal Radiology, 2013
Hyaline fibromatosis syndrome (HFS) is a rare, homozygous, autosomal recessive disease, characterized by deposition of hyaline material in skin and other organs, resulting in esthetic problems, disability, and potential life-threatening complications.
Duncan E Meuffels, Edwin H G Oei, Van Leenders Geert J L H   +2 more
exaly   +4 more sources