Results 11 to 20 of about 5,641 (192)

Primeras y sumario

open access: yesGestión y Análisis de Políticas Públicas, 2015
Índice Revista GAPP, número 14.
Revista GAPP
doaj   +9 more sources

Desautorización

open access: yesGestión y Análisis de Políticas Públicas, 2015
La revista Gestión y Análisis de Políticas Públicas (GAPP), en aplicación de las recomendaciones de los comités internacionales de ética sobre publicaciones académicas, ha decidido proceder a la desautorización formal del siguiente artículo: Herrera ...
Revista GAPP
doaj   +5 more sources

Recensiones

open access: yesGestión y Análisis de Políticas Públicas, 2016
Stiglitz, Joseph y Greenwald, Bruce G. La creación de una sociedad del aprendizaje. La Esfera de los Libros, Madrid, 2016 (Miguel Anxo Bastos Boubeta). Fontaine, Guillaume. El análisis de políticas públicas. Conceptos, teorías y métodos.
Revista GAPP
doaj   +9 more sources

Malignant Potential of Temporal Bone Paragangliomas With Reference to GAPP System

open access: yesLaryngoscope Investigative Otolaryngology
Objectives To evaluate the temporal bone paragangliomas (so‐called glomus tumors, TB‐PGLs) via the Grading System for Adrenal Pheochromocytoma and Paraganglioma (GAPP) and succinate dehydrogenase subunit B (SDHB) immunohistochemistry, and to discuss ...
Noritaka Komune   +10 more
doaj   +2 more sources

Olenellus baileyi Gapp & Lieberman, 2014, sp. nov.

open access: yes, 2014
Olenellus baileyi sp. nov. Fig. 1.3, 1.6 Type material. Holotype PWNHC-2013.23.1. Paratype KUMIP 355554. Likely from the Olenellus zone or Waucoban Series, Dyeran stage, sensu Webster (2011a, b) and Webster et al. (2011), early Cambrian, Sekwi Formation, Mackenzie Mountains, Northwest Territories, Canada, but occurring from Section 4 in float ...
Gapp, I. Wesley, Lieberman, Bruce S.
openaire   +3 more sources

Who can safely discontinue lifelong follow-up among patients with sporadic pheochromocytoma and paraganglioma? [PDF]

open access: yesJ Intern Med
Abstract Background Current guidelines recommend at least 10 years of follow‐up for all pheochromocytoma and paraganglioma (PPGL) patients and lifelong monitoring for high‐risk individuals. Nonetheless, data identifying patients who may not require routine lifelong follow‐up are scarce. Methods Among 999 patients with PPGL, 703 who were non‐metastatic,
Park MJ   +15 more
europepmc   +2 more sources

Mesonacis wileyi Gapp & Lieberman, 2014, sp. nov.

open access: yes, 2014
Mesonacis wileyi sp. nov. Fig. 4 Type material. Holotype KUMIP 355550. Paratypes KUMIP 355551 and PWNHC-2013.23.4-5. Olenellus zone or Waucoban Series, Dyeran stage, sensu Webster (2011a, b) and Webster et al. (2011), early Cambrian, Sekwi Formation, Mackenzie Mountains, Northwest Territories, Canada, Section 4, 430– 435m above the base of section ...
Gapp, I. Wesley, Lieberman, Bruce S.
openaire   +3 more sources

Mummaspis delgadoae Gapp & Lieberman, 2014, sp. nov.

open access: yes, 2014
Published as part of Gapp, I. Wesley & Lieberman, Bruce S., 2014, New olenelloid trilobites from the Northwest Territories, Canada, pp. 479-498 in Zootaxa 3866 (4) on pages 492-494, DOI: 10.11646/zootaxa.3866.4.2, http://zenodo.org/record ...
Gapp, I. Wesley, Lieberman, Bruce S.
openaire   +3 more sources

Elliptocephala jaredi Gapp & Lieberman, 2014, sp. nov.

open access: yes, 2014
Elliptocephala jaredi sp. nov. Fig. 1.1, 1.2, 1.4, 1.5 Type material. Holotype KUMIP 355534. Paratypes KUMIP 355535-355544 and PWNHC-2013.23.6-16. Etymology. In honour of Jared Lieberman, son of BSL. Diagnosis. LA contacts anterior cephalic margin; LA approximately 1.5 times combined length of LO and L1; glabellar furrows not conjoined; S3 strongly ...
Gapp, I. Wesley, Lieberman, Bruce S.
openaire   +2 more sources

Two Cases of Hereditary Paraganglioma-Pheochromocytoma Syndrome in Siblings, Caused by a Novel Succinate Dehydrogenase Complex Subunit D Variant. [PDF]

open access: yesIJU Case Rep
ABSTRACT Introduction Pheochromocytomas and paragangliomas are increasingly recognized as hereditary malignancies, with ~30%–40% of cases involving germline variants. We report a familial case of hereditary pheochromocytoma‐paraganglioma syndrome caused by a novel variant in the SDHD gene.
Nakamura R   +9 more
europepmc   +2 more sources

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