Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report. - Wikidata - wikimedia - TriplyDB

Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

http://www.wikidata.org/entity/Q37735985

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Leptomeningeal disease: current diagnostic and therapeutic strategies.Remarkable efficacy of temozolomide for relapsed spinal myxopapillary ependymoma with multiple recurrence and cerebrospinal dissemination: a case report and literature review.

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Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

http://www.wikidata.org/entity/Q37735985

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 27 January 2017

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

@en

Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

@nl

type

label

Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

@en

Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

@nl

prefLabel

Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

@en

Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

@nl

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2016.10.SPINE16948

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Journal of Neurosurgery-Spine

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Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.

@en

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Adam L Cohen

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Cheryl A Palmer

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Joshua D Schiffman

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Karen L Salzman

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Marjan Champine

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Meic H Schmidt

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Nick Thomson

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15 YEARS OF PARAGANGLIOMA: Imaging and imaging-based treatment of pheochromocytoma and paraganglioma

Resveratrol protects against global cerebral ischemic injury in gerbils.

External beam radiation therapy in treatment of malignant pheochromocytoma and paraganglioma.

Treatment of malignant pheochromocytoma.

The size of the primary tumor and age at initial diagnosis are independent predictors of the metastatic behavior and survival of patients with SDHB-related pheochromocytoma and paraganglioma: a retrospective cohort study

Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.

External beam radiation therapy (EBRT) for patients with malignant pheochromocytoma and non-head and -neck paraganglioma: combination with 131I-MIBG.

Potential therapeutic target for malignant paragangliomas: ATP synthase on the surface of paraganglioma cells

The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer

18F-FLT PET/CT in the Evaluation of Pheochromocytomas and Paragangliomas: A Pilot Study.

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