DEREGIBUS MARIA; POMPOZZI LUIS; DRA GABRIELA SANSO

Feocromocitoma y paraganglioma en un hospital pediátrico de Argentina. Serie de casos

ARCHIVOS ARGENTINOS DE PEDIATRIA; Lugar: Buenos Aires; Año: 2024 vol. 122 p. 216 - 220

MATHÓ, CECILIA; FERNÁNDEZ, MARÍA CELIA; BONANATA, JENNER; LIU, XIAN-DE; MARTIN, AYELEN; VIEITES, ANA; SANSÓ, GABRIELA; BARONTINI, MARTA; JONASCH, ERIC; COITIÑO, E. LAURA; PENNISI, PATRICIA ALEJANDRA

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

Frontiers in Endocrinology; Año: 2022 vol. 13

CASTRO, SEBASTIÁN; BRUNELLO, FRANCO G.; SANSÓ, GABRIELA; SCAGLIA, PAULA; ESNAOLA AZCOITI, MARÍA; IZQUIERDO, AGUSTÍN; VILLEGAS, FLORENCIA; BERGADÁ, IGNACIO; ROPELATO, MARÍA GABRIELA; MARTÍ, MARCELO A.; REY, RODOLFO A.; GRINSPON, ROMINA P.

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

Frontiers in Pediatrics; Lugar: washington; Año: 2022 vol. 10

GRINSPON, ROMINA P.; CASTRO, SEBASTIÁN; BRUNELLO, FRANCO G.; SANSÓ, GABRIELA; ROPELATO, MARÍA GABRIELA; REY, RODOLFO A.

Diagnosis of male central hypogonadism during childhood

Journal of the Endocrine Society; Lugar: washington; Año: 2021 vol. 5

ARMAIZ-PENA, GUSTAVO; FLORES, SHAHIDA K; CHENG, ZI-MING; ZHANG, XHINGYU; ESQUIVEL, EMMANUEL; POULLARD, NATALIE; VAIDYANATHAN, ANUSHA; LIU, QIANQIAN; MICHALEK, JOEL; SANTILLAN-GOMEZ, ALFREDO A; LISS, MICHAEL; AHMADI, SARA; KATSELNIK, DANIEL; MALDONADO, ENRIQUE; SALGADO, SARIMAR AGOSTO; JIMENEZ, CAMILO; FISHBEIN, LAUREN; HAMIDI, OKSANA; ELSE, TOBIAS; LECHAN, RON; TISCHLER, ART S; BENN, DIANA E; DWIGHT, TRISHA; CLIFTON-BLIGH, RORY; SANSO, GABRIELA; BARONTINI, MARTA; VINCENT, DEEPA; ARONIN, NEIL; BIONDI, BERNADETTE; KOOPS, MAUREEN; BOWHAY-CARNES, ELIZABETH; GIMENEZ-ROQUEPLO, ANNE-PAULE; ALVAREZ-ESLAVA, ANDREA; BRUDER, JAN M; KITANO, MIO; BURNICHON, NELLY; DING, YANLI; DAHIA, PATRICIA L. M

Genotype-phenotype features of germline variants of the TMEM127 pheochromocytoma susceptibility gene: A 10-year update

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; Año: 2021 vol. 106 p. 350 - 364

CASTINETTI, FREDERIC; WAGUESPACK, STEVEN G; MACHENS, ANDREAS; UCHINO, SHINYA; HASSE-LAZAR, KORNELIA; SANSO, GABRIELLA; ELSE, TOBIAS; DVORAKOVA, SARKA; QI, XIAO PING; ELISEI, ROSSELLA; MAIA, ANA LUISA; GLOD, JOHN; LOURENÇO, DELMAR MUNIZ; VALDES, NURIA; MATHIESEN, JES; WOHLLK, NELSON; BANDGAR, TUSHAR R; DRUI, DELPHINE; KORBONITS, MARTA; DRUCE, MARALYN R; BRAIN, CAROLINE; KURZAWINSKI, TOM; PATOCS, ATILA; BUGALHO, MARIA JOAO; LACROIX, ANDRE; CARON, PHILIPPE; FAINSTEIN-DAY, PATRICIA; BORSON CHAZOT, FRANCOISE; KLEIN, MARC; LINKS, THERA P; LETIZIA, CLAUDIO; FUGAZZOLA, LAURA; CHABRE, OLIVIER; CANU, LETIZIA; COHEN, REGIS; TABARIN, ANTOINE; SPEHAR UROIC, ANITA; MAITER, DOMINIQUE; LABOUREAU, SANDRINE; MIAN, CATERINA; PECZKOWSKA, MARIOLA; SEBAG, FREDERIC; BRUE, THIERRY; MIREBEAU-PRUNIER, DELPHINE; LECLERC, LAURENCE; BAUSCH, BIRKE; BERDELOU, AMANDINE; SUKURAI, AKIHIRO; VLCEK, PETR; KRAJEWSKA, JOLANTA; BARONTINI, MARTA; VAZ FERREIRA VARGAS, CARLA; VALERIO, LAURA; CEOLIN, LUCIELI; AKSHINTALA, SRIVANDANA; HOFF, ANA; GODBALLE

Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study

The Lancet Diabetes and Endocrinology; Lugar: Marceille; Año: 2019 vol. 7 p. 213 - 220

IRINA BANCOS; MASSIMILIANO FERRARA; TOBIAS KRAUSS, MD,; THERA P. LINKS; ULRICH WELLNER; ANDREY KVACHENYUK; KARINA VILLAR GÓMEZ DE LAS HERAS; MARINA Y. YUKINA; ROMAN PETROV; GARRETT BULLIVANT; LAURA VON DUECKER; SWATI JADHAV; URSULA PLOECKINGER; STAFFAN WELIN; CAMILLA SCHALIN-JÄNTTI; OLIVER GIMM; MARIJA PFEIFER; JOANNE NGEOW; KORNELIA HASSE-LAZAR; GABRIELA SANSÓ, PHD

Preventive Medicine and Management of von Hippel-Lindau Disease-associated Pancreatic Neuroendocrine Tumors.

ENDOCRINE - RELATED CANCER; Lugar: Bristol; Año: 2018

DRA ANA VIEITES; DRA GABRIELA SANSO; DR IGNACIO BERGADA; DRA MARTA BARONTINI

Feocromocitoma: nuevas perspectivas en diagnóstico y seguimiento

Revista Hospital de Niños Ricardo Gutierrez; Lugar: CABA; Año: 2018 vol. 60

CECILIA MATHÓ , PHD; GABRIELA SANSÓ, PHD; BLANCA DIEZ; ,MARTA BARONTINI, MD,; PATRICIA PENNISI,

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

GENETIC TESTING AND MOLECULAR BIOMARKERS; Lugar: New York; Año: 2016 vol. 20 p. 771 - 776

BIRKE BAUSCH,MD; ULRICH WELLNER, MD,; MATHIEU PEYRE, MD,; CARSTEN C. BOEDEKER,MD; FREDERIK J. HES, MD; ,MARIAGIULIA ANGLANI, MD; JOSE M. DE CAMPOS, MD,; HIROSHI KANNO, MD, PHD; EAMONN R. MAHER, MD,; TOBIAS KRAUSS, MD,; SANSO GABRIELA, PHD; ,MARTA BARONTINI, MD,; P. H. NEUMANN, MD

Characterization of Endolymphatic Sac Tumors and von Hippel-Lindau Disease in the International ELST Registry

HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK; Lugar: New York; Año: 2015

FREDERIC CASTINETTI; XIAO-PING QI; MARTIN K WALZ; ANA LUIZA MAIA; DRA GABRIELA SANSO; HARTMUT P H NEUMANN

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

LANCET; Lugar: Amsterdam; Año: 2014 vol. 15 p. 648 - 655

JORGE L SALAZAR VEGA; DRA GLORIA LEVIN; DRA GABRIELA SANSO; ANA VIEITES; REYNALDO GOMEZ; DRA MARTA BARONTINI

Pheochromocytoma associatedwith pregnancy: unexpected favourable outcome in patients diagnosed after delivery

JOURNAL OF HYPERTENSION; Lugar: Philadelphia; Año: 2014 vol. 32 p. 1458 - 1463

BAUSCH B; URICH WELLNER; DIRK BAUSCH; FRANCESCA SCHIAVI; DRA MARTA BARONTINI; DRA GABRIELA SANSO; HARTMUT P H NEUMANN

Long-Term prognosis of patients with pediatric pheochromocytoma

Endocrine -Related Cancer; Lugar: Bristol; Año: 2014 vol. 21 p. 17 - 25

BAUSCH B; WELLNER U; BAUSCH D; SCHIAVI F; BARONTINI M; SANSO G; WALZ M; PECZKOWSKA; WERYHA G; DALL I; CECCETTO G; BISOGNO G; MOELLER L; BOCKENHAUER

Long Term Prognosis of Patients with Pediatric Pheochromocytoma

NEW ENGLAND JOURNAL OF MEDICINE; Año: 2013

CALIFANO I; CASTRO J; ALICIA LOWENSTEIN; BALZARETTI M; NOVELLI JL; FIGARI M; OLSTEIN G; G SANSÓ; BARONTINI M; *IORCANSKY S; *CABEZON C

CARCINOMA MEDULAR DE TIROIDES: ESTUDIO MULTICÉNTRICO. PRESENTACIÓN Y EVOLUCIÓN EN 219 PACIENTES

REVISTA ARGENTINA DE ENDOCRINOLOGIA Y METABOLISMO; Lugar: Buenos Aires; Año: 2013 vol. 50 p. 1 - 8

FERNANDEZ MC; MARTIN A; VENARA M; DE LUJÁN CALCAGNO M; SANSÓ G; QUINTANA S; CHEMES HE; BARONTINI M; PA PENNISI

OVEREXPRESSION OF THE INSULIN-LIKE GROWTH FACTOR 1 RECEPTOR (IGF-1R) IS ASSOCIATED WITH MALIGNANCY IN FAMILIAL PHEOCHROMOCYTOMAS AND PARAGANGLIOMAS.

CLINICAL ENDOCRINOLOGY; Lugar: Londres; Año: 2013 p. 1001 - 1012

FRANK-RAUE K; RYBICKI LA; ERLIC Z; SCHWEIZER H; WINTER A; MILOS I; TOLEDO SP,; TOLEDO RA; TAVARES MR; ALEVIZAKI M; MIAN C; SIGGELKOW H; HUFNER M; WOHLLK N,; OPOCHER G; DVORAKOVA S; BENDLOVA B; CZETWERTYNSKA M; SKASKO E; BARONTINI M; SANSO G; NEUMANN HP

RISK PROFILES AND PENETRANCE ESTIMATIONS IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A CAUSED BY GERMLINE RET MUTATIONS LOCATED IN EXON 10

HUMAN MUTATION; Lugar: Heidelberg; Año: 2011 vol. 32 p. 51 - 58

: MARTA BARONTINI; GLORIA LEVIN; GABRIELA SANSO

Characteristics of pheochromocytoma in a 4- to 20-year-old population

ANNALS OF THE NEW YORK ACADEMY OF SCIENCES.; Lugar: New York, USA; Año: 2006 vol. 1073 p. 30 - 37

DAHIA PLM; ROSS K,; WRIGHT ME,; HAYASHIDA CY; SANTAGATA S; BARONTINI M; KUNG AL; SANSÓ G; POWERA JA,; TISCHLER A; HODIN R,; HEITRITTER S; MOORE FJR; DLUHY R; SOSA JA; TOLGAY OCAL I; BENN DE; MARSH DJ; ROBINSON BG; SCHNEIDER K; GARBER J; ARUM SM; KORBONITS M; GROSSMAN A; PIGNY P; TOLEDO SPA; NOSÉ V; LI CH; STILES CHD

A HIF1á REGULATORY LOOP LINKS HYPOXIA AND MITOCONDRIAL SIGNALS IN PHEOCHROMOCYTOMAS PLOS GENET.

PLOS GENETICS; Año: 2005 vol. 1 p. 72 - 80

DAHIA PLM; ROSS K,; WRIGHT ME,; HAYASHIDA CY; SANTAGATA S; BARONTINI M; KUNG AL; SANSÓ G; POWERA JA,; TISCHLER A; HODIN R,; HEITRITTER S; MOORE FJR; DLUHY R; SOSA JA; TOLGAY OCAL I; BENN DE; MARSH DJ; ROBINSON BG; SCHNEIDER K; GARBER J; ARUM SM; KORBONITS M; GROSSMAN A; PIGNY P; TOLEDO SPA; NOSÉ V; LI CH; STILES CHD

A HIF1á REGULATORY LOOP LINKS HYPOXIA AND MITOCONDRIAL SIGNALS IN PHEOCHROMOCYTOMAS PLOS GENET.

PLoS Genetics; Año: 2005 vol. 1 p. 72 - 80

GABRIELA SANSÓ; MARIA C GARCÍA RUDAZ; GLORIA LEVIN; MARTA BARONTINI

FAMILIAL ISOLATED PHEOCHROMOCYTOMA PRESENTING A NEW MUTATION IN THE VHL GENE.

AMERICAN JOURNAL OF HYPERTENSION; Año: 2004 vol. 17 p. 1107 - 1111

GABRIELA SANSÓ; HORACIO DOMENÉ; MARIA GARCIA RUDAZ; EDUARDO PUSIOL; ANA K. DE MONDINO; MARIA ROQUE; ALEJANDRO RING; HECTOR PERINETTI; BORIS ELSNER; SONIA IORSCANSKY; MARTA BARONTINI

VERY EARLY DETECTION OF RET PROTO-ONCOGENE MUTATION IS CRUCIAL FOR PREVENTIVE THYROIDECTOMY IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2 CHILDREN.

CANCER; Lugar: New York; Año: 2002 vol. 94 p. 323 - 330