Research Resource: Transcriptional Profiling Reveals Different Pseudohypoxic Signatures in SDHB and VHL-Related PheochromocytomasElena López‐Jiménez, Alberto Cascón, Agnieszka Maliszewska et al.|Molecular Endocrinology|2010Cited by 211
Head and Neck Paragangliomas in Von Hippel-Lindau Disease and Multiple Endocrine Neoplasia Type 2Carsten C. Boedeker, Hartmut P.H. Neumann, Zoran Erlic et al.|The Journal of Clinical Endocrinology & Metabolism|2009Cited by 128
Loss of the actin regulator HSPC300 results in clear cell renal cell carcinoma protection in Von Hippel-Lindau patientsAlberto Cascón, Mercedes Robledo, Beatriz Escobar et al.|Human Mutation|2007Cited by 46
<i>SDHC</i> mutation in an elderly patient without familial antecedentsElena López‐Jiménez, Alberto Cascón, José M. de Campos et al.|Clinical Endocrinology|2008Cited by 40
Genetic characterization and structural analysis of VHL Spanish families to define genotype–phenotype correlationsSergio Ruiz‐Llorente, Mercedes Robledo, Jerónimo Bravo et al.|Human Mutation|2004Cited by 33