Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
about
Spontaneous rupture of adrenal pheochromocytoma in a patient with Von Recklinghausen's disease.Presenting signs and symptoms of pheochromocytoma in pediatric-aged patients.When to look for Von Hippel-Lindau disease in gastroenteropancreatic neuroendocrine tumors?Retinal capillary hemangiomas and von Hippel-Lindau disease.Paragangliomas/Pheochromocytomas: clinically oriented genetic testingMutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.Fluorine-18-fluorodihydroxyphenylalanine Positron-emission Tomography Scans of Neuroendocrine Tumors (Carcinoids and Pheochromocytomas).From childhood migraine headache to pheochromocytoma.Sporadic endocrine tumours and their relationship to the hereditary endocrine neoplasia syndromes.Hereditary paraganglioma targets diverse paraganglia.Modifiers of risk of hereditary breast and ovarian cancer.Pheochromocytoma: the expanding genetic differential diagnosis.Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing.Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma.Undiagnosed giant cystic pheochromocytoma: A case report.Malignancy in pheochromocytomas.Updated and new perspectives on diagnosis, prognosis, and therapy of malignant pheochromocytoma/paraganglioma.Pheochromocytoma - update on disease management.The molecular basis of von Hippel-Lindau diseasePheochromocytoma and paraganglioma.Overexpression of ERBB-2 was more frequently detected in malignant than benign pheochromocytomas by multiplex ligation-dependent probe amplification and immunohistochemistry.Classification and management of cervical paragangliomas.Clinical use of laboratory tests for the identification of secondary forms of arterial hypertension.Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.Clinical features of paraganglioma syndromes.Pheochromocytoma of the pancreas: A report of three cases and a literature reviewLeu-M1 immunoreactivity and phaeochromocytoma.Partial adrenalectomy minimizes the need for long-term hormone replacement in pediatric patients with pheochromocytoma and von Hippel-Lindau syndrome.Hypoxia-inducible factor signaling in pheochromocytoma: turning the rudder in the right direction.The long-term outcomes of radiosurgery for intracranial hemangioblastomas.PET/CT imaging of neuroendocrine tumors with (68)Gallium-labeled somatostatin analogues: An overview and single institutional experience from India.Malignant pheochromocytomas and paragangliomas: a diagnostic challenge.Neurogenic tumors of soft tissue.Nervous system involvement in von Hippel-Lindau disease: pathology and mechanisms.Stereotactic radiosurgery in hemangioblastoma: Experience over 14 years.Diagnosis and management of hereditary paraganglioma syndrome due to the F933>X67 SDHD mutation.Precision medicine in pheochromocytoma and paraganglioma: current and future concepts.A vascular mass in the neck.Von Hippel-Lindau disease: a single gene, several hereditary tumors.Persistent Hiccups-An Unusual Presentation of Bilateral Pheochromocytoma without Syndromic Association: A Case Report.
P2860
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P2860
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
description
1993 nî lūn-bûn
@nan
1993 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@ast
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@en
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@nl
type
label
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@ast
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@en
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@nl
prefLabel
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@ast
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@en
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@nl
P2093
P1476
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
@en
P2093
Neumann HP
P304
P356
10.1056/NEJM199311183292103
P407
P577
1993-11-01T00:00:00Z