PheoSeq-Reference-Cited by-同舟云学术

PheoSeq

Published:2017-07 Issue:4 Volume:19 Page:575-588
ISSN:1525-1578
Container-title:The Journal of Molecular Diagnostics
language:en
Short-container-title:The Journal of Molecular Diagnostics

Author:

Currás-Freixes Maria,Piñeiro-Yañez Elena,Montero-Conde Cristina,Apellániz-Ruiz María,Calsina Bruna,Mancikova Veronika,Remacha Laura,Richter Susan,Ercolino Tonino,Rogowski-Lehmann Natalie^ORCID,Deutschbein Timo,Calatayud María,Guadalix Sonsoles,Álvarez-Escolá Cristina,Lamas Cristina,Aller Javier,Sastre-Marcos Julia,Lázaro Conxi,Galofré Juan C.,Patiño-García Ana,Meoro-Avilés Amparo,Balmaña-Gelpi Judith,De Miguel-Novoa Paz,Balbín Milagros,Matías-Guiu Xavier,Letón Rocío,Inglada-Pérez Lucía,Torres-Pérez Rafael,Roldán-Romero Juan M.,Rodríguez-Antona Cristina,Fliedner Stephanie M.J.,Opocher Giuseppe,Pacak Karel,Korpershoek Esther,de Krijger Ronald R.,Vroonen Laurent,Mannelli Massimo,Fassnacht Martin,Beuschlein Felix,Eisenhofer Graeme,Cascón Alberto,Al-Shahrour Fátima,Robledo Mercedes

Publisher

Elsevier BV

Subject

Molecular Medicine,Pathology and Forensic Medicine

Reference79 articles.

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2. Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity;Dahia;Nat Rev Cancer,2014

3. Paraganglioma and phaeochromocytoma: from genetics to personalized medicine;Favier;Nat Rev Endocrinol,2015

4. Germ-line PHD1 and PHD2 mutations detected in patients with pheochromocytoma/paraganglioma-polycythemia;Yang;J Mol Med (Berl),2014

5. Whole-exome sequencing identifies MDH2 as a new familial 354 paraganglioma gene;Cascón;J Natl Cancer Inst,2015

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4. Patient Sex and Origin Influence Distribution of Driver Genes and Clinical Presentation of Paraganglioma;Journal of the Endocrine Society;2024-02-29

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