Results 81 to 90 of about 1,223 (121)

Prevalence and genetics of "de novo" MEN2 syndromes.

J Clin Endocrinol Metab
Casalini R, Romei C, Bottici V, Cappagli V, Tascini V, Matrone A, Prete A, Ciampi R, Ramone T, Elisei R.   +9 more
europepmc   +1 more source

<i>RET</i> Gene Alterations in Clinical Practice: A Comprehensive Review and Database Update. [PDF]

Genes (Basel)
Ricciardi Tenore C, Tulli E, Perrucci A, Bertozzi R, Fortuna L, Maneri G, Santonocito C, Urbani A, De Bonis M, Minucci A.   +9 more
europepmc   +1 more source

Pheochromocytomas and Paragangliomas. [PDF]

Endocrinol Metab Clin North Am
Alkaissi H, Taieb D, Ghayee HK.
europepmc   +1 more source

Kinome profiling reveals pathogenic variant specific protein signalling networks in MEN2 children with Medullary Thyroid Cancer. [PDF]

NPJ Precis Oncol
Rix B, Chauhan R, Masoumi Z, Grönroos E, Brain CE, Ogunbiyi OK, Swarbrick K, Swanton C, Bonnet D, Kurzawinski TR, Izatt L, McDonald NQ, Grey W.   +12 more
europepmc   +1 more source

Bilateral pheochromocytoma: case series and review of treatment strategies based on genetic mutations. [PDF]

Transl Androl Urol
Katsumi K, Ito K, Yanagisawa T, Yamashiro K, Maeda M, Takiguchi Y, Takahashi K, Kasai K, Miki J, Kimura T, Furuta N.   +10 more
europepmc   +1 more source

A Rare Case of Acromegaly and Prolactinoma in MEN4 Caused by a CDKN1B Mutation. [PDF]

AACE Endocrinol Diabetes
Yuke L, Hongxing W, Huiwen T, Jianwei L, Yerong Y.   +4 more
europepmc   +1 more source

Subepithelial Lesions of the Ocular Surface: A Review. [PDF]

Curr Ophthalmol Rep
Najdawi W, Li WJ, De Arrigunaga S, Amer MM, Galor A, Karp CL.   +5 more
europepmc   +1 more source

Clinicopathologic features of allied disorders of Hirschsprung disease and status update.

World J Gastrointest Surg
Lu M.
europepmc   +1 more source

Multiple endocrine neoplasia type 2B (MEN2B) diagnosis: a case report. [PDF]

AME Case Rep
Tuckumantel MS, Altomari IC, Galvani CM, Thomaz ALA, Madurro LCC, Latorre L, Neto GVA, Amira BV, Cestari C, Neto SS.   +9 more
europepmc   +1 more source

Phenotype-driven cascade screening in a Syrian family with clinically consistent multiple endocrine neoplasia type 2A. [PDF]

JCEM Case Rep
Hraib M, Alturun M, Al Kheder T, Alonainy F.   +3 more
europepmc   +1 more source