CLÉMENT, FLORENCIA; GRINSPON, ROMINA P.; YANKELEVICH, DANIEL; MARTÍN BENÍTEZ, SABRINA; DE LA OSSA SALGADO, MARÍA CAROLINA; ROPELATO, MARÍA GABRIELA; BALLERINI, MARÍA GABRIELA; KESELMAN, ANA C.; BRASLAVSKY, DÉBORA; PENNISI, PATRICIA; BERGADÁ, IGNACIO; FINKIELSTAIN, GABRIELA P.; REY, RODOLFO A.

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Frontiers in Endocrinology; Lugar: Lausanne; Año: 2021 vol. 11

DIMITRI, PAUL; FERNANDEZ-LUQUE, LUIS; BANERJEE, INDRANEEL; BERGADÁ, IGNACIO; CALLIARI, LUIS EDUARDO; DAHLGREN, JOVANNA; DE ARRIBA, ANTONIO; LAPATTO, RISTO; REINEHR, THOMAS; SENNIAPPAN, SENTHIL; THOMAS-TEINTURIER, CÉCILE; TSAI, MENG-CHE; ANUAR ZAINI, AZRIYANTI; BAGHA, MERAT; KOLEDOVA, EKATERINA

An eHealth Framework for Managing Pediatric Growth Disorders and Growth Hormone Therapy

JOURNAL OF MEDICAL INTERNET RESEARCH; Lugar: Lausanne; Año: 2021 vol. 23

VISHNOPOLSKA, SEBASTIAN ALEXIS; MERCOGLIANO, MARIA FLORENCIA; CAMILLETTI, MARIA ANDREA; MORTENSEN, AMANDA HELEN; BRASLAVSKY, DEBORA; KESELMAN, ANA; BERGADÁ, IGNACIO; OLIVIERI, FEDERICO; MIRANDA, LUCAS; MARINO, ROXANA; RAMÍREZ, PABLO; PÉREZ GARRIDO, NATALIA; PATIÑO MEJIA, HELEN; CIACCIO, MARTA; DI PALMA, MARIA ISABEL; BELGOROSKY, ALICIA; MARTÍ, MARCELO ADRIAN; KITZMAN, JACOB OTTO; CAMPER, SALLY ANN; PÉREZ-MILLÁN, MARIA INES

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JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; Año: 2021 vol. 106 p. 1956 - 1976

FINKIELSTAIN, GABRIELA P.; VIEITES, ANA; BERGADÁ, IGNACIO; REY, RODOLFO A.

Disorders of Sex Development of Adrenal Origin

Frontiers in Endocrinology; Lugar: Lausanne; Año: 2021 vol. 12

GERGICS, PETER; SMITH, CATHY; BANDO, HIRONORI; JORGE, ALEXANDER A.L.; ROCKSTROH-LIPPOLD, DENISE; VISHNOPOLSKA, SEBASTIAN A.; CASTINETTI, FREDERIC; MAKSUTOVA, MARIAM; CARVALHO, LUCIANI RENATA SILVEIRA; HOPPMANN, JULIA; MARTÍNEZ MAYER, JULIÁN; ALBAREL, FRÉDÉRIQUE; BRASLAVSKY, DEBORA; KESELMAN, ANA; BERGADÁ, IGNACIO; MARTÍ, MARCELO A.; SAVEANU, ALEXANDRU; BARLIER, ANNE; ABOU JAMRA, RAMI; GUO, MICHAEL H.; DAUBER, ANDREW; NAKAGUMA, MARILENA; MENDONCA, BERENICE B.; JAYAKODY, SAJINI N.; OZEL, A. BILGE; FANG, QING; MA, QIANYI; LI, JUN Z.; BRUE, THIERRY; PÉREZ MILLÁN, MARÍA INES; ARNHOLD, IVO J.P.; PFAEFFLE, ROLAND; KITZMAN, JACOB O.; CAMPER, SALLY A.

High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency

AMERICAN JOURNAL OF HUMAN GENETICS; Año: 2021 vol. 108 p. 1526 - 1539

JULLIEN, NICOLAS; SAVEANU, ALEXANDRU; VERGIER, JULIA; MARQUANT, EMELINE; QUENTIEN, MARIE HELENE; CASTINETTI, FREDERIC; GALON-FAURE, NOÉMIE; BRAUNER, RAJA; MARRAKCHI TURKI, ZINET; TAUBER, MAITÉ; EL KHOLY, MOHAMED; LINGLART, AGNÈS; RODIEN, PATRICE; FEDALA, NORA SOUMEYA; BERGADA, IGNACIO; CORTET-RUDELLI, CHRISTINE; POLAK, MICHEL; NICOLINO, MARC; STUCKENS, CHANTAL; BARLIER, ANNE; BRUE, THIERRY; REYNAUD, RACHEL

Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort

Clinical endocrinology; Año: 2021 vol. 94 p. 277 - 289

FREIRE, ANALÍA V.; ROPELATO, MARÍA G.; PAPENDIECK, PATRICIA; VIEITES, ANA; ELÍAS, EUGENIA; BALLERINI, MARIA G.; RODRIGUEZ, MARÍA E.; BERGADÁ, IGNACIO; CHIESA, ANA

Improving safety in paediatric thyroidectomy by PTH measurements

CLINICAL ENDOCRINOLOGY; Año: 2021 vol. 95 p. 760 - 765

RAMÍREZ, LAURA; SANGUINETI, NORA; SCAGLIA, PAULA; KESELMAN, ANA; BALLERINI, MARÍA GABRIELA; KARABATAS, LILIANA; LANDI, ESTEFANÍA; CASTRO, JULIA; DOMENÉ, SABINA; PENNISI, PATRICIA; JASPER, HÉCTOR; REY, RODOLFO A.; VÁZQUEZ, MARTÍN; DOMENÉ, HORACIO; BERGADÁ, IGNACIO; GUTIÉRREZ, MARIANA

A novel heterozygous STAT5B variant in a patient with short stature and partial growth hormone insensitivity (GHI)

GROWTH HORMONE & IGF RESEARCH : OFFICIAL JOURNAL OF THE GROWTH HORMONE RESEARCH SOCIETY AND THE INTERNATIONAL IGF RESEARCH SOCIETY.; Año: 2020 vol. 50 p. 61 - 70

TORRADO, LIDIA E.; FREIRE, ANALIÁ; MARTÍNEZ, MAYRA; VIEITES, ANA; BERGADÁ, IGNACIO; LÓPEZ, EDUARDO L.; FALLO, AURELIA A.

Exogenous Cushing syndrome due to drug interaction of ritonavir and inhaled fluticasone. Report of three pediatric cases Síndrome de Cushing exógeno por interacción medicamentosa de ritonavir y fluticasona inhalada. Reporte de tres casos pediátricos

ARCHIVOS ARGENTINOS DE PEDIATRIA; Año: 2020 vol. 118 p. 278 - 283

BRASLAVSKY, DÉBORA; SCAGLIAA, PAULA; SANGUINETI, NORA; AZA-CARMONA, MIRIAM; BLANCO, JULIÁN NEVADO; BADIA, PABLO D. LAPUNZINA; FERNÁNDEZ, MARIÁ DEL C.; RUIZ, OLIVIA; CARMONAF, ALEJANDRA; SZLAGO, MARINA; ARBERAS, CLAUDIA; CASSINELLI, HAMILTON; HEATH, KAREN; REY, RODOLFO; BERGADÁ, IGNACIO

Osteoporosis-pseudoglioma Syndrome: A pediatric case of primary osteoporosis Síndrome de osteoporosis-pseudoglioma: A propósito de un caso pediátrico de osteoporosis primaria

ARCHIVOS ARGENTINOS DE PEDIATRIA; Año: 2020 vol. 118 p. 300 - 304

SANGUINETI, NORA; BRASLAVSKY, DEBORA; SCAGLIA, PAULA A.; KESELMAN, ANA; BALLERINI, MARIA G.; ROPELATO, MARIA G.; SUCO, SOFIA; VISHNOPOLSKA, SEBASTIAN; BERENSTEIN, ARIEL J.; JASPER, HÉCTOR; DOMENÉ, HORACIO M.; REY, RODOLFO A.; PÉREZ MILLÁN, MARIA I.; CAMPER, SALLY A.; BERGADÁ, IGNACIO

p.R209H GH1 variant challenges short stature assessment

GROWTH HORMONE & IGF RESEARCH : OFFICIAL JOURNAL OF THE GROWTH HORMONE RESEARCH SOCIETY AND THE INTERNATIONAL IGF RESEARCH SOCIETY.; Año: 2020 vol. 50 p. 23 - 26

GRINSPON, ROMINA P.; BERGADÁ, IGNACIO; REY, RODOLFO A.

Male Hypogonadism and Disorders of Sex Development

Frontiers in Endocrinology; Año: 2020 vol. 11

KESELMAN, ANA CLAUDIA; MARTIN, AYELEN; SCAGLIA, PAULA ALEJANDRA; SANGUINETI, NORA MARÍA; ARMANDO, ROMINA; GUTIÉRREZ, MARIANA; BRASLAVSKY, DÉBORA; BALLERINI, MARÍA GABRIELA; ROPELATO, MARÍA GABRIELA; RAMIREZ, LAURA; LANDI, ESTEFANÍA; DOMENÉ, SABINA; CASTRO, JULIA F; CASSINELLI, HAMILTON; CASALI, BÁRBARA; DEL REY, GRACIELA; BARROS, ÁNGEL CAMPOS; NEVADO BLANCO, JULIÁN; DOMENÉ, HORACIO; JASPER, HÉCTOR; ARBERAS, CLAUDIA; REY, RODOLFO A; LAPUNZINA-BADÍA, PABLO; BERGADÁ, IGNACIO; PENNISI, PATRICIA A

A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency

EUROPEAN JOURNAL OF ENDOCRINOLOGY; Año: 2019 vol. 181 p. 43 - 53

JULLIEN, NICOLAS; ROMANET, PAULINE; PHILIPPON, MÉLANIE; QUENTIEN, MARIE-HÉLÈNE; BECK-PECCOZ, PAOLO; BERGADA, IGNACIO; ODENT, SYLVIE; REYNAUD, RACHEL; BARLIER, ANNE; SAVEANU, ALEXANDRU; BRUE, THIERRY; CASTINETTI, FREDERIC

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

EUROPEAN JOURNAL OF HUMAN GENETICS; Año: 2019 vol. 27 p. 216 - 225

ARCARI, ANDREA J.; FREIRE, ANALIÁ V.; ESCOBAR, MARIÁ E.; BALLERINI, MARIÁ G.; ROPELATO, MARIÁ G.; BERGADÁ, IGNACIO; GRYNGARTEN, MIRTA G.

One-year treatment with gonadotropin-releasing hormone analogues does not affect body mass index, insulin sensitivity or lipid profile in girls with central precocious puberty

JOURNAL OF PEDIATRIC ENDOCRINOLOGY; Año: 2019 vol. 32 p. 181 - 186

GRINSPON, ROMINA P; AROZARENA, MARÍA; PRADA, SILVINA; BARGMAN, GRACIELA; SANZONE, MARÍA; MORALES BAZURTO, MARJORIE; GUTIÉRREZ, MARCELA; BEDECARRÁS, PATRICIA; KANNEMANN, ANA; ELENA, GRACIELA O; GOTTLIEB, SILVIA; BERENSTEIN, ARIEL J; ROPELATO, MARÍA GABRIELA; BERGADÁ, IGNACIO; AVERSA, LUIS A; REY, RODOLFO A

Safety of standardised treatments for haematologic malignancies as regards to testicular endocrine function in children and teenagers

HUMAN REPRODUCTION; Año: 2019 vol. 34 p. 2480 - 2494

GRINSPON, ROMINA P; AROZARENA, MARÍA; PRADA, SILVINA; BARGMAN, GRACIELA; SANZONE, MARÍA; MORALES BAZURTO, MARJORIE; GUTIÉRREZ, MARCELA; BEDECARRÁS, PATRICIA; KANNEMANN, ANA; ELENA, GRACIELA O; GOTTLIEB, SILVIA; BERENSTEIN, ARIEL J; ROPELATO, MARÍA GABRIELA; BERGADÁ, IGNACIO; AVERSA, LUIS A; REY, RODOLFO A

Safety of standardised treatments for haematologic malignancies as regards to testicular endocrine function in children and teenagers

HUMAN REPRODUCTION; Año: 2019 vol. 34 p. 2480 - 2494

BESSA, DANIELLE S.; MACEDO, DELANIE B.; BRITO, VINICIUS N.; FRANÇA, MONICA M.; MONTENEGRO, LUCIANA R.; CUNHA-SILVA, MARINA; SILVEIRA, LETICIA G.; HUMMEL, TIAGO; BERGADÁ, IGNACIO; BRASLAVSKY, DEBORA; ABREU, ANA PAULA; DAUBER, ANDREW; MENDONCA, BERENICE B.; KAISER, URSULA B.; LATRONICO, ANA CLAUDIA

High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic

NEUROENDOCRINOLOGY; Año: 2018 vol. 105 p. 17 - 25

PÉREZ MILLÁN, MARÍA I.; VISHNOPOLSKA, SEBASTIAN A.; DALY, ALEXANDRE Z.; BUSTAMANTE, JUAN P.; SEILICOVICH, ADRIANA; BERGADÁ, IGNACIO; BRASLAVSKY, DÉBORA; KESELMAN, ANA C.; LEMONS, ROSEMARY M.; MORTENSEN, AMANDA H.; MARTI, MARCELO A.; CAMPER, SALLY A.; KITZMAN, JACOB O.

Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism

Molecular Genetics and Genomic Medicine; Año: 2018 vol. 6 p. 514 - 525

CLÉMENT, FLORENCIA; MARTIN, AYELEN; VENARA, MARCELA; DE LUJÁN CALCAGNO, MARIA; MATHÓ, CECILIA; MAGLIO, SILVANA; LOMBARDI, MERCEDES GARCÍA; BERGADÁ, IGNACIO; PENNISI, PATRICIA A

Type 1 IGF Receptor Localization in Paediatric Gliomas: Significant Association with WHO Grading and Clinical Outcome

Hormones and Cancer; Año: 2018 vol. 9 p. 205 - 214

BALLERINI, MARÍA GABRIELA; BRASLAVSKY, DÉBORA; SCAGLIA, PAULA ALEJANDRA; KESELMAN, ANA; RODRÍGUEZ, MARÍA EUGENIA; MARTÍNEZ, ALICIA; FREIRE, ANALÍA VERÓNICA; DOMENÉ, HORACIO MARIO; JASPER, HÉCTOR GUILLERMO; BERGADÁ, IGNACIO; ROPELATO, MARÍA GABRIELA

Circulating IGF-I, IGFBP-3 and the IGF-I/IGFBP-3 Molar Ratio Concentration and Height Outcome in Prepubertal Short Children on rhGH Treatment over Two Years of Therapy

Hormone Research in Paediatrics; Lugar: Basilea; Año: 2017 vol. 88 p. 354 - 363

PRASAD, RATHI; HADJIDEMETRIOU, IRENE; MAHARAJ, AVINAASH; MEIMARIDOU, EIRINI; BUONOCORE, FEDERICA; SALEEM, MOIN; HURCOMBE, JENNY; BIERZYNSKA, AGNIESZKA; BARBAGELATA, ELIANA; BERGADÁ, IGNACIO; CASSINELLI, HAMILTON; DAS, URMI; KRONE, RUTH; HACIHAMDIOGLU, BULENT; SARI, ERKAN; YESILKAYA, EDIZ; STORR, HELEN L.; CLEMENTE, MARIA; FERNANDEZ-CANCIO, MONICA; CAMATS, NURIA; RAM, NANIK; ACHERMANN, JOHN C.; VAN VELDHOVEN, PAUL P.; GUASTI, LEONARDO; BRASLAVSKY, DEBORA; GURAN, TULAY; METHERELL, LOUISE A.

Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome

JOURNAL OF CLINICAL INVESTIGATION; Año: 2017 vol. 127 p. 942 - 953

BRASLAVSKY, DÉBORA; MÉNDEZ, MARIA VIRGINIA; PRIETO, LAURA; KESELMAN, ANA; ENACAN, ROSA; GRUÑEIRO-PAPENDIECK, LAURA; JULLIEN, NICOLAS; SAVENAU, ALEXANDRU; REYNAUD, RACHEL; BRUE, THIERRY; BERGADÁ, IGNACIO; CHIESA, ANA

Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection

Hormone Research in Paediatrics; Lugar: Basilea; Año: 2017 vol. 88 p. 274 - 280

SCAGLIA, PAULA A.; KESELMAN, ANA C.; BRASLAVSKY, DÉBORA; MARTUCCI, LUCÍA C.; KARABATAS, LILIANA M.; DOMENÉ, SABINA; GUTIÉRREZ, MARIANA L.; BALLERINI, MARÍA G.; ROPELATO, MARÍA G.; SPINOLA-CASTRO, ANGELA; SIVIERO-MIACHON, ADRIANA A.; TARTUCI, JULIANA SAITO; RODRÍGUEZ AZRAK, MARÍA SOL; REY, RODOLFO A.; JASPER, HÉCTOR G.; BERGADÁ, IGNACIO; DOMENÉ, HORACIO M.

Characterization of four Latin American families confirms previous findings and reveals novel features of acid-labile subunit deficiency

CLINICAL ENDOCRINOLOGY; Año: 2017 vol. 87 p. 300 - 311

GRINSPON, R; BRASLAVSKY, DÉBORA; CHIESA, A; PAPENDIECK, P; PENNISI, P; CLEMENT, F; VIEITES, A; KESELMAN, A.; GRYNGARTEN, M; FREIRE, A.; BALLERINI, M.G.; REY, R; BERGADÁ, I; DOMENÉ, HORACIO M.

Meeting Reports: 2016 Annual Meeting of the Sociedad Latinoamericana de Endocrinología Pediátrica (SLEP) Buenos Aires, Argentina (November 8-11, 2016), Selected Highlights.

Pediatric endocrinology reviews; Lugar: Netanya; Año: 2017

BERGADÁ, IGNACIO; KESELMAN, ANA; REY, RODOLFO

Juan Jorge Heinrich, MD, PhD, 1937–2016

Hormone Research in Paediatrics; Lugar: Basilea; Año: 2017 vol. 87 p. 423 - 424

BERGADÁ, I; REY, R

In Memoriam: Juan Jorge Heinrich, MD, PhD (1937-2016).

Pediatric endocrinology reviews; Lugar: Netanya; Año: 2017

FORCLAZ, VERÓNICA; MORATO, E; PENNISI, A; FALCO, S; OLSEN, G; RODRIGUEZ, P; PAPAZIAN, R; BERGADÁ, I

Salivary and serum cortisol levels in newborn infants

ARCHIVOS ARGENTINOS DE PEDIATRIA; Lugar: Buenos Aires; Año: 2017 vol. 115

PARDO CAMPOS, M; MUSSO, M; KESELMAN, A.; GRUÑEIRO PAPENDIECK, L; BERGADÁ, I; CHIESA, A

Cognitive profiles of patients with early detected and treated congenital hypothyroidism

ARCHIVOS ARGENTINOS DE PEDIATRIA; Lugar: Buenos Aires; Año: 2017

ARCARI AJ; GRYNGARTEN MG; FREIRE AV; BALLERINI MG; ROPELATO MG; BERGADÁ I; ESCOBAR ME

Body mass index in girls with idiopathic central precocious puberty during and after treatment with GnRH analogues.

Int J Pediatr Endocrinol; Lugar: Londres; Año: 2016

BESSA D; MACEDO DB; BRITO VN; FRANÇA MM; MONTENEGRO LR; SILVA MC; SILVEIRA LG; HUMMEL T; BERGADÁ I; BRASLAVSKY D; ABREU AP; DAUBER A; MENDONCA BB; KAISER UB; LATRONICO AC

High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic.

NEUROENDOCRINOLOGY; Lugar: Basel; Año: 2016

BALLERINI MG; BERGADÁ I; RODRÍGUEZ ME; KESELMAN A; BENGOLEA VS; PIPMAN V; DOMENÉ HM; JASPER HG; ROPELATO MG

Concentración de insulina e índices de insulinosensibilidad en niños y adolescentes sanos

ARCHIVOS ARGENTINOS DE PEDIATRIA; Lugar: Buenos Aires; Año: 2016

BRASLAVSKY, DÉBORA; GRINSPON ROMINA; BALLERINI, M.G.; BEDECARRAS PATRICIA; LORETI N; BASTIDA MG; ROPELATO, M.G.; KESELMAN A; CAMPO STELLA; REY RA; BERGADÁ I

Hypogonadotropic Hypogonadism in Infants with Congenital Hypopituitarism: A Challenge to Diagnose at an Early Stage.

Hormone research in paediatrics; Lugar: Basilea; Año: 2016

FREIRE, A.V.; GRYNGARTEN, M.G.; BALLERINI, M.G.; ARCARI, A.J.; ESCOBAR, M.E.; BERGADÁ, I.; ROPELATO, M.G.

Assessment of estradiol response after depot triptorelin administration in girls with central precocious puberty

Hormone Research in Paediatrics; Lugar: Basilea; Año: 2016

JOUSTRA, S.D.; HEINEN C.A.; SCHOENMAKERS N.; BONOMI, M.; BALLIEUX B.E.; TURGEON M.O.; BERNARD D.J.; FLIERS E.; VAN TROTSENBURG A.S.; LOSEKOOT M.; PERSANI L.; WIT J.M.; BIERMASZ N.R.; PEREIRA A.M.; OOSTDIJK W.; AISENBERG J.; VAN DEN AKKER E.L.; BERGADÁ, I; BOCCA G.; BRASLAVSKY D; CALLEWAERT B.; CUMMINGS E.A.; CUPPEN M.P.; DATTANI M.; DOMENE H M; VAN DER HEYDEN J.C.; VAN HULLE S.; JACOBS M.A.; LINKS T.P.; LUNSHOF L.; MUL D.; NEIJENS F.S.; PEDRO H.F.; SALERNO M.; DE SCHEPPER J.; VOORHOEVE P.G.; ZIDELL A.S.; VAN DER ZWAAG P.A.; ZWAVELING-SOONAWALA N.

IGSF1 deficiency: lessons from an extensive case series and recommendations for clinical management

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; Lugar: Chevy Chase; Año: 2016

CLAIRE ROCHETTE; NICOLAS JULLIEN; ALEXANDRU SAVEANU; EMMANUELLE CALDAGUES; IGNACIO BERGADÁ,; DEBORA BRASLAVSKY; MARIJA PFEIFER; RACHEL REYNAUD; JEAN-PAUL HERMAN; ANNE BARLIER; THIERRY BRUE; ALAIN ENJALBERT; FREDERIC CASTINETTI

Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue

PLOS ONE; Lugar: San Francisco; Año: 2015

PAPENDIECK P; GRUÑEIRO-PAPENDIECK L; VENARA M; ACHA O; COZZANI H; MATEOS F; MAGLIO S; CALCAGNO ML; IGNACIO BERGADÁ,; CHIESA A.

Differentiated Thyroid Cancer in Children: Prevalence and Predictors in a Large Cohort with Thyroid Nodules Followed Prospectively.

JOURNAL OF PEDIATRICS; Año: 2015

FERNANDEZ I; TONIETTI M, ; CAMBEROS MC; IGNACIO BERGADÁ,; SCHENONE A; SZLAGO M; TELLECHEA M; FRETCHTEL G; TRIFONE L; CRESTO JC

Acetyl-L-Carnitine and Nicotinamide for Prevention of Type 1 Diabetes. I-Literature Review which Gave Support to the Treatment. II-Case Report, Evaluation of Five Years Treatment

Immunome Res; Año: 2015

GRINSPON RP; LORETI N; BRASLAVSKY D; VALERI C; SCHTEINGART, H; BALLERINI MG; BEDECARRAS PATRICIA; AMBAO V; GOTTLIEB S; ROPELATO, M.G.; BERGADÁ I; CAMPO SM; REY RA

Spreading the clinical window for diagnosing fetal-onset hypogonadism in boys

Frontiers in Endocrinology; Año: 2014

FREIRE, ANALÍA; ROPELATO, M.G.; BALLERINI MG; ACHA O; BERGADÁ I; GRUÑEIRO PAPENDIECK, L; CHIESA A

Predicting hypocalcemia after thyroidectomy in children

SURGERY.; Lugar: St. Louis; Año: 2014

ABBHIRAMI RAJAGOPAL; BRASLAVSKY D; JAMES T. LU; SOLEDAD KLEPPE; CLEMENT, FLORENCIA; CASSINELLI, H; DAVID S. LIU,; JOSE MIGUEL LIERN; GRACIELA VALLEJO; BERGADÁ I; RICHARD A. GIBBS; PHILLIPE M. CAMPEAU; BRENDAN H. LEE

Exome Sequencing Identifies a Novel Homozygous Mutation in the Phosphate Transporter SLC34A1 in Hypophosphatemia and Nephrocalcinosis

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; Lugar: Chevy Chase; Año: 2014

THOMAS EGGERMANN; GERHARD BINDER; FREDERIC BRIOUDE; EAMONN R. MAHER; PABLO LAPUNZINA; MARIA VITTORIA CUBELLIS; BERGADÁ I; DIRK PRAWITT; MATTHIAS BEGEMANN

CDKN1C mutations: two sides of the same coin

TRENDS IN MOLECULAR MEDICINE; Lugar: Amsterdam; Año: 2014

GRINSPON ROMINA; ANDREONE LUZ; BEDECARRAS PATRICIA; ROPELATO MARIA GABRIELA; REY RODOLFO A; CAMPO STELLA; BERGADA IGNACIO

Male Central Precocious Puberty: Serum Profile of Anti-Müllerian Hormone and Inhibin B before, during, and after Treatment with GnRH Analogue

International Journal of Endocrinology; Lugar: New York; Año: 2013 vol. 2013 p. 1 - 6

BERGADA IGNACIO

Uso de la hormona de crecimiento en niños y adolescentes

MEDICINA (BUENOS AIRES); Lugar: Buenos Aires; Año: 2013 vol. 73 p. 272 - 276

FREIRE, ANALÍA; ESCOBAR, MARÍA EUGENIA; GRYNGARTEN, MIRTA; ARCARI, ANDREA; BALLERINI MG; BERGADÁ, IGNACIO; ROPELATO MARIA GABRIELA

High diagnostic accurency of subcutaneous Triptorelin test with GnRH test for diagnosing central precocious puberty in girls

CLINICAL ENDOCRINOLOGY; Lugar: Londres; Año: 2013 vol. 78 p. 398 - 404

REY RA; GRINSPON RP; GOTTLIEB S; PASQUALINI T; KNOBLOVITS P; ASZPIS S; PACENZA N; STEWART USHER J; BERGADÁ, I; CAMPO SM

Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach

Andrology; Lugar: Los Angeles; Año: 2013

BRASLAVSKY D ; KESELMAN A; CHIESA A; BERGADÁ I

Diagnóstico de endocrinopatía congénita en neonatos con ictericia

ANALES DE PEDIATRIA; Lugar: Madrid; Año: 2012 vol. 76 p. 120 - 126

ARBOLEDA VA; LEE H; PARNAIK R; FLEMING A; BANERJEE A; FERRAZ-DE-SOUZA B; DÉLOT EC; RODRIGUEZ-FERNANDEZ IA; BRASLAVSKY D; BERGADÁ I; DELL'ANGELICA EC; NELSON SF; MARTINEZ-AGOSTO JA; ACHERMANN JC; VILAIN E

Mutations in the PCNA-binding domain of CDKNIC vause IMAGe syndrome

NATURE GENETICS; Lugar: Londres; Año: 2012 p. 788 - 792

GRINSPON RP; LORETI N; BRASLAVSKY D; BEDECARRAS PATRICIA; AMBAO V; GOTTLIEB S; BERGADÁ I; CAMPO SM; REY RA

Sertori cell markers in the diagnosis of paediatric male hypogonadism

JOURNAL OF PEDIATRIC ENDOCRINOLOGY AND METABOLISM; Año: 2012 p. 3 - 11

CHALER EA; BALLERINI MG; LAZZATI JM; MACEIRAS M; FRUSTI M; BERGADÁ I; RIVAROLA MA; BELGOROSKY A; ROPELATO G

Cut-off values of serum growth hormone (GH) in pharmacological stimulation tests (PhT) evaluated in short-statured children using a chemiluminescent immunometric assay (ICMA) calibrated with the International Recombinant Human GH Standard 98/574

CLINICAL CHEMISTRY AND LABORATORY MEDICINE; Lugar: Berlin; Año: 2012 p. 1 - 3

KESELMAN A; SCAGLIA PA; RODRIGUEZ PRIETO MS; BALLERINI MG; RODRIGUEZ ME; ROPELATO MARIA GABRIELA; BERGADA IGNACIO; JASPER HG; DOMENÉ HM

Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus

ARQUIVOS BRASILEIROS DE ENDOCRINOLOGIA E METABOLOGIA; Año: 2012 p. 558 - 563

BRASLAVSKY D; KESELMAN A; GALOPPO M; LEZAMA C; CHIESA A, ; GALOPPO C; BERGADÁ I

Neonatal cholestasis in congenital pituitary hormone deficiency and isolated hypocortisolism: characterization of liver dysfunction and follow-up

ARQUIVOS BRASILEIROS DE ENDOCRINOLOGIA E METABOLOGIA; Año: 2011 vol. 55 p. 622 - 627

BOGUSZEWSKI MC; MERICQ V; BERGADA I; DAMIANI D; BELGOROSKY A, ; GUNCZLER P; ORTIZ T ; LLANO M; DOMENÉ HM; CALZADA-LEÓN R; BLANCO A,; BARRIENTOS M; PROCEL P; LANES R; JARAMILLO O

Latin American consensus: children born small for gestational age

BMC PEDIATRICS; Lugar: Londres; Año: 2011 p. 1 - 10

MARINO R; RAMIREZ P; GALEANO J; PEREZ GARRIDO N; ROCCO C ; CIACCIO M ; WARMAN DM; GUERCIO G; CHALER E; MACEIRAS M; BERGADÁ I; GRYNGARTEN M; BALBI V; PARDES E; RIVAROLA MA; BELGOROSKY A

Steroid 21-hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype-phenotype correlation in a large cohort of patients with congenital adrenal hyperplasia.

CLINICAL ENDOCRINOLOGY; Lugar: Londres; Año: 2011 vol. 75 p. 427 - 435

REY RA; GOTTLIEB S; PASQUALINI T; BASTIDA MG; GRINSPON RP; CAMPO SM; BERGADÁ I

Are Klinefelter boys hypogonadal?

ACTA PAEDIATRICA; Lugar: Londres; Año: 2011 vol. 100 p. 830 - 838

PAPENDIECK P; GRUÑEIRO-PAPENDIECK L; VENARA M; ACHA O; MAGLIO S; BERGADÁ I; CHIESA A

Differentiated thyroid carcinoma: presentation and follow-up in children and

JOURNAL OF PEDIATRIC ENDOCRINOLOGY AND METABOLISM; Año: 2011 vol. 24 p. 743 - 748

LOPEZ AP; FOSCALDI SA ; PEREZ MS, , ; RODRIGUEZ M; TRAVERSA M,; PUCHULU FM, ; BERGADA I; FRECHTEL GD

HNF1 alpha gene coding regions mutations screening, in a Caucasian population clinically characterized as MODY from Argentina..

DIABETES RESEARCH AND CLINICAL PRACTICE; Lugar: Amsterdam; Año: 2011 vol. 91 p. 208 - 212

FARIAS JAVIER; FELEDER ETHEL; GONZALEZ ELISEO; HALABE KARINA; CRISCUOLO MARCELO; BERGADÁ IGNACIO; DIEZ ROBERTO

Relative bioavailability of two drug products of somatropin obtained from either the milk of transgenic cows or bacterial culture.

Hormone research in pædiatrics; Lugar: Basilea; Año: 2010 vol. 73 p. 258 - 264

BERGADÁ I; BLANCO M; KESELMAN A; DOMENE H M; BERGADA C

Tratamiento con hormona de crecimiento en niños menores de 6 años de edad, con talla baja, nacidos pequeños para la edad gestacional

ARCHIVOS ARGENTINOS DE PEDIATRIA; Lugar: Buenos Aires; Año: 2009 vol. 107 p. 410 - 416

LOPEZ AP; FOSCALDI SA; PEREZ MS; KROCHIK G; RODRIGUEZ M; TRAVERSA M; PUCHULU FM; HIRSCHLER V; BERGADA IGNACIO; FRECHTEL GD

Glucokinase gene mutation screening in Argentinean clinically characterized MODY

EXPERIMENTAL CLINICAL ENDOCRINOLOGY & DIABETES; Lugar: Heidelberg ; Año: 2009 vol. 117 p. 391 - 394

LOPEZ AP; FOSCALDI SA; PEREZ MS; KROCHIK G; RODRIGUEZ M; TRAVERSA M; PUCHULU FM; HIRSCHLER V; BERGADA I; FRECHTEL GD

Glucokinase gene mutation screening in Argentinean clinically characterized MODY patients

EXPERIMENTAL CLINICAL ENDOCRINOLOGY & DIABETES; Año: 2008

BERGADÁ I; ANDREONE LUZ; BEDECARRÁS P; ROPELATO MG; COPELLI S; LAISSUE P; REY RA; CAMPO SM

Seminiferous tubule function in delayed-onset X-linked adrenal hypoplasia congenita associated with incomplete hypogonadotrophic hypogonadism

CLINICAL ENDOCRINOLOGY; Lugar: Londres; Año: 2008

BASTIDA MG; REY RA; BERGADÁ I; BEDECARRÁS P; ANDREONE LUZ; DEL REY G; BOYWITT A; ROPELATO MG; CASSINELLI H; ARCARI A; CAMPO SM; GOTTLIEB S

Establishment of testicular endocrine function impairment during childhood and puberty in boys with Klinefelter syndrome

CLINICAL ENDOCRINOLOGY; Lugar: Londres; Año: 2007

ARCARI AJ; BERGADÁ I; REY RA; GOTTLIEB S

Predictive value of anatomical findings and karyotype analysis in the diagnosis of patients with disorders of sexual development

SEXUAL DEVELOPMENT; Lugar: Basel; Año: 2007

BERGADA IGNACIO; MILANI CARLOS; BEDECARRAS PATRICIA; ANDREONE LUZ; ROPELATO MARIA GABRIELA; GOTTLIEB SILVIA; BERGADA CESAR; CAMPO STELLA; REY RODOLFO A

Time Course of the Serum Gonadotropin Surge, Inhibins, and Anti-Mullerian Hormone in Normal Newborn Males during the First Month of Life

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; Año: 2006 vol. 91 p. 4092 - 4098

LAISSUE P; COPELLI S; BERGADÁ I; BERGADA C; BARRIO G; KARABOGA S; WURTZ JM; FELLOUS M; LALLI E; VEITIA RA

Partial defects in transcriptional activity of two novel DAX-1 mutations in childhood onset adrenal hypoplasia congenita

CLINICAL ENDOCRINOLOGY; Lugar: Oxford; Año: 2006 vol. 63 p. 681 - 686

REY RA; CODNER E; IÑÍGUEZ G; BEDECARRÁS P; TRIGO R; OKUMA C; GOTTLIEB S; BERGADÁ, I; CAMPO SM; CASSORLA FG

Low risk of impaired testicular Sertoli and Leydig cell functions in boys with isolated hypospadias

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; Lugar: Chevy Chase; Año: 2005

BERGADÁ I; DEL REY G; LAPUNZINA P; BERGADÁ C; FELLOUS M; COPELLI S

Familial occurrence of the IMAGe association: additional clinical variants and a proposed mode of inheritance

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; Lugar: Chevy Chase; Año: 2005

TRIGO RV; BERGADÁ I; REY RA; BALLERINI MG; BEDECARRÁS P; BERGADÁ C; GOTTLIEB S; CAMPO SM

Altered serum profile of inhibin B, Pro-alphaC and anti-Müllerian hormone in prepubertal and pubertal boys with varicocele

CLINICAL ENDOCRINOLOGY; Lugar: Londres; Año: 2004

BERGADÁ I; AVERSA L; HEINRICH JJ

Peripheral venous thrombosis in children and adolescents with adipsic hypernatremia secondary to hypothalamic tumors

Hormone research in pædiatrics; Lugar: Basilea; Año: 2004

TEPER AM; COLOM AJ; KOFMAN CD; MAFFEY AF; VIDAURRETA SM; BERGADÁ I

Effects of inhaled fluticasone propionate in children less than 2 years old with recurrent wheezing

PEDIATRIC PULMONOLOGY; Lugar: New York; Año: 2004

DARDIS A; MARINO R; BERGADÁ I; ESCOBAR ME; GRYNGARTEN M; RIVAROLA MA; BELGOROSKY A

Analisis molecular de las mutaciones mas frecuentes asociadas a la hiperplasia suprarrenal congenita por deficit de la enzima 21 hidroxilasa

MEDICINA (BUENOS AIRES); Lugar: Buenos Aires; Año: 2001

VENARA M; REY RA; BERGADÁ I; MENDILAHARZU H; CAMPO SM; CHEMES H

Sertoli cell proliferations of the infantile testis: an intratubular form of Sertoli cell tumor?

AMERICAN JOURNAL OF SURGICAL PATHOLOGY; Lugar: Philadelphia; Año: 2001

BERGADÁ I; BERGADÁ C; CAMPO SM

Role of inhibins in childhood and puberty

JOURNAL OF PEDIATRIC ENDOCRINOLOGY; Lugar: Londres; Año: 2001

ROGOFF D; BERGADÁ I; VENARA M; CHEMES H; HEINRICH JJ; BARONTINI M

Intermittent hyperaldosteronism in a child due to an adrenal adenoma

EUROPEAN JOURNAL OF PEDIATRICS; Lugar: Berlin; Año: 2001

ALONSO G; BERGADÁ I; HEINRICH JJ

Resonancia magnética en niños y adolescentes con diabetes insípida central: hallazgos al diagnóstico y durante su seguimiento

ANALES DE PEDIATRIA; Lugar: Madrid; Año: 2000

BERGADÁ I; DEL TORO K; KATZ O; CHEMES H; CAMPO SM

Serum inhibin B concentration in a prepubertal boy with gynecomastia and Peutz-Jeghers syndrome

JOURNAL OF PEDIATRIC ENDOCRINOLOGY; Lugar: Londres; Año: 2000

BERGADÁ I; ROJAS G; ROPELATO G; AYUSO S; BERGADÁ C; CAMPO SM

Sexual dimorphism in circulating monomeric and dimeric inhibins in normal boys and girls from birth to puberty

CLINICAL ENDOCRINOLOGY; Lugar: Londres; Año: 1999

VENARA M; SANCHEZ MARULL R; BERGADÁ I; GAMBONI M; CHEMES H

Functional adrenal cortical tumors in childhood: a study of ploidy, p53-protein and nucleolar organizer regions (AgNORs) as prognostic markers

JOURNAL OF PEDIATRIC ENDOCRINOLOGY; Lugar: Londres; Año: 1998

ROGOFF D; SMOLENICKA Z; BERGADÁ I; VALLEJO G; BARONTINI M; HEINRICH JJ; FERRARI P

The codon 213 of the 11beta-hydroxysteroid dehydrogenase type 2 gene is a hot spot for mutations in apparent mineralocorticoid excess

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; Lugar: Chevy Chase, MD; Año: 1998

CRESTO JC; ABDENUR JP; BERGADÁ I; MARTINO R

Long-term follow up of persistent hyperinsulinaemic hypoglycaemia of infancy

ARCHIVES OF DISEASE IN CHILDHOOD; Lugar: Londres; Año: 1998

BERGADÁ I; VENARA M; MAGLIO S; CIACCIO M; DIEZ B; BERGADÁ C; CHEMES H

Functional adrenal cortical tumors in pediatric patients: a clinicopathologic and immunohistochemical study of a long term follow-up series

CANCER; Lugar: New York; Año: 1996

GRUÑEIRO PAPENDIECK, L; CHIESA, A.; TRIFONE, L; BERGADÁ, I; RAIZMAN, H; BERGADA, C

ALTERACIONES TIROIDEAS EN NIÑOS Y ADOLESCENTES DIABETICOS INSULINODEPENDIENTES

Acta Pediátrica Española; Lugar: Madrid; Año: 1995

BERGADÁ, I; BOULGOURDJIAN, E; HEINRICH JJ; BERGADA, C

POLIDIPSIA PRIMARIA EN LA INFANCIA

Acta Pediátrica Española; Lugar: Madrid; Año: 1992

BERGADÁ I; SUISSA S; DUFRESNE J; SCHIFFRIN A

Severe hypoglycemia in IDDM children

DIABETES CARE; Año: 1989

BERGADÁ I; SCHIFFRIN A; ABU SRAIR H; KAPLAN P; DORNAN J; GOLTZMAN D; HENDY GN

Kenny syndrome: description of additional abnormalities and molecular studies

HUMAN GENETICS.; Lugar: Berlin; Año: 1988