G. Sansó

发表

A HIF1α Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas

Sandro Santagata, Marta Barontini, Gabriela Sanso, 2005, PLoS genetics.

Overexpression of the insulin‐like growth factor 1 receptor (IGF‐1R) is associated with malignancy in familial pheochromocytomas and paragangliomas

M. Calcagno, P. Pennisi, M. Barontini, 2013, Clinical endocrinology.

Familial isolated pheochromocytoma presenting a new mutation in the von Hippel-Lindau gene.

M. Barontini, G. Sansó, G. Levin, 2004, American journal of hypertension.

Delayed Puberty Due to a WDR11 Truncation at Its N-Terminal Domain Leading to a Mild Form of Ciliopathy Presenting With Dissociated Central Hypogonadism: Case Report

R. Rey, I. Bergadá, Marcelo Martí, 2022, Frontiers in Pediatrics.

Diagnosis of Male Central Hypogonadism During Childhood

F. Brunello, R. Rey, M. Ropelato, 2021, Journal of the Endocrine Society.

Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study.

T. Zelinka, C. Eng, J. Plukker, 2014, The Lancet. Oncology.

VHL Germline Mutations in Argentinian Patients with Clinical Diagnoses or Single Typical Manifestations of Type 1 von Hippel-Lindau Disease.

P. Pennisi, M. Barontini, G. Sansó, 2016, Genetic testing and molecular biomarkers.

Very early detection of RET proto‐oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children

H. Domené, M. Barontini, G. Sansó, 2002, Cancer.

Characterization of endolymphatic sac tumors and von Hippel–Lindau disease in the International Endolymphatic Sac Tumor Registry

S. Richard, C. Eng, T. Krauss, 2016, Head & neck.

VHL-P138R and VHL-L163R Novel Variants: Mechanisms of VHL Pathogenicity Involving HIF-Dependent and HIF-Independent Actions

E. Jonasch, Xian-de Liu, E. Coitiño, 2022, Frontiers in Endocrinology.

Preventive medicine of von Hippel-Lindau disease-associated pancreatic neuroendocrine tumors.

H. Amthauer, E. Jonasch, W. Young, 2018, Endocrine-related cancer.

Long-term prognosis of patients with pediatric pheochromocytoma.

C. Eng, K. Schmid, K. Rácz, 2013, Endocrine-related cancer.

Genotype-phenotype features of germline variants of the TMEM127 pheochromocytoma susceptibility gene: a ten-year update.

A. Tischler, T. Dwight, J. Michalek, 2020, The Journal of clinical endocrinology and metabolism.

A HIF1-alpha Regulatory Loop Links Hypoxiaand Mitochondrial Signals in Pheochromocytomas

Andrew L. Kung, Sandro Santagata, James F. Powers, 2005 .

Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10

Martin Fassnacht, Marta Barontini, Gabriela Sanso, 2011, Human mutation.

Characteristics of Pheochromocytoma in a 4‐ to 20‐Year‐Old Population

Marta Barontini, Gabriela Sanso, Gloria Levin, 2006, Annals of the New York Academy of Sciences.

Pheochromocytoma associated with pregnancy: unexpected favourable outcome in patients diagnosed after delivery

M. Barontini, G. Sansó, G. Levin, 2014, Journal of hypertension.

The C105fs114X Is the Prevalent Thyrotropin Beta-Subunit Gene Mutation in Argentinean Patients with Congenital Central Hypothyroidism

J. Heinrich, L. Gruñeiro-Papendieck, A. Chiesa, 2004, Hormone Research in Paediatrics.

Pheochromocytoma and paraganglioma at a children's hospital in Argentina. A case series.

G. Sansó, L. Pompozzi, María I Deregibus, 2023, Archivos argentinos de pediatria.