VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW

The steadily growing interest in studying of endocrine genetics is driven not only by the search for new pathologies but also by the most pressing need to develop methods for early diagnosis, treatment and management of patients. Though 20% of all the patients with von Hippel-Lindau syndrome do not...

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Hlavní autoři:	I. I. Larina, N. M. Platonova, E. A. Troshina, A. A. Roslyakova, D. G. Belzevich, L. S. Selivanova, M. Yu. Ukina, L. V. Nikankina, N. M. Malysheva, A. N. Tyulpakov, L. D. Kovalevich
Médium:	Artigo
Jazyk:	Russo
Vydáno:	SINAPS LLC 2019-05-01
Edice:	Архивъ внутренней медицины
Témata:	facomatosis von hippel-lindau syndrome pheochromocytoma hemangioblastoma vhl
On-line přístup:	https://www.medarhive.ru/jour/article/view/924
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