Artículos Publicados por los Socios en el período 2006-2007

Roberto Lanes, Adriana Siviero-Miachon, Fideleff HL ..

Roberto Lanes

  • Gunczler P and Lanes R. Relationship between different fasting-based insulin sensitivity indices in obese children and adolescents. Journal of Pediatric Endocrinology and Metabolism 19:259-265,2006.
  • Lanes R, Soros A, Gunczler P, Paoli M, Carrillo E, Villaroel O and Palacios A. Growth hormone deficiency in adolescence is associated with low serum levels of adiponectin and with an unfavorable serum lipid and lipoprotein profile. Journal of Pediatrics 149:324-329, 2006.
  • Peter Gunczler, Roberto Lanes, Arlette Soros, Livia Verdu, Yolanda Ramon, Beatriz Guevara y Nusen Beer. Coronary artery calcifications, serum lipids and lipoproteins and peripheral inflammatory markers in adolescents and young adults with type 1 diabetes. Journal of Pediatrics 149:320-323, 2006.
  • Lanes R. Cardiovascular risk in growth hormone deficiency. Changes detected with replacement therapy. Endopedonline, Number 13, May 2007, article requested by the editor.

Adriana Siviero-Miachon

  • SIVIERO-MIACHON, A. A. ; SPINOLA-CASTRO, A. M. ; TOSTA-HERNANDEZ, P. D. C. ; LEE, M. L. ; PETRILLI, A. S. . Leptin Assessment in Acute Lymphocytic Leukemia Survivors: Role of Cranial Radiotherapy?. Journal of Pediatric Hematology/Oncology, v. 29, p. 776-782, 2007.
  • MINOTTO, I. ; ABDALA, N. ; SIVIERO-MIACHON, A. A. ; SPINOLA-CASTRO, A. M. ; IMAMURA, P. ; NOGUEIRA, R.G. . Basal Encephalocele Associated with Morning Glory Syndrome: Case Report. Arquivos de Neuro-Psiquiatria, v. 65, p. 988-991, 2007.

Titania Pasqualini

  • Aszpis S, Gottlieb S, Knoblovits P, Pacenza N, Pasqualini T, Rey R, Stewart U J. Revisión: Síndrome de Klinefelter: viejos y nuevos conceptos. Revista Argentina de Endocrinología y Metatabolismo 43: 22-39, 2006.
  • Aszpis Sergio, Gottlieb Silvia, Knoblovits Pablo, Pacenza Néstor, Pasqualini Titania, Rey rodolfo, Stewart Usher Jorge. Sindrome de Klinefelter: viejos y nuevos conceptos. Revista Argentina de Andrología 15 (2): 40-54, 2006.
  • Rey R, Ciaccio M, Suarez M, Boquete H, Martinez A, Jasper H, Rivarola M, Gottlieb S, Sequera A, Azaretzky M, Bengolea SV, Brunetto O, Falkon G, Ferrari P, Pasqualini T. Evaluación diagnóstica del niño y del adolescente sin gónadas palpables. Revista Argentina de Endocrinología y Metatabolismo 43: 40-52, 2006.
  • Pasqualini Titania, Alonso Guillermo, Granillo Elsa, Ruiz Eduardo, Christiansen Silvia, Gallo Guillermo, Mastandrea Claudio Emilio, Rey Rodolfo. Asignación de sexo en un recién nacido con ambigüedad genital y anomalías cromosómicas. Revista Argentina de Andrología 15 (2): 36-39, 2006.
  • Ferreira LV, Souza SAL, Montenegro LR, Arnhold IJP, Pasqualini T, Heinrich JJ, Keselman AC, Mendonça BB, Jorge AAL. Variabilidade do fenótipo de pacientes com Síndrome de Noonan com e sem mutações no gene PTPN11. Arq Bras Endocrinol Metab 51/3: 450-456, 2007
  • Pasqualini Titania, Alonso Guillermo, Tomasini Rosángela, Galich Ana María, Buzzalino Noemí, Fernández Cecilia, Minutolo Carolina, Alba Liliana, Dain Liliana. Congenital Adrenal Hyperplasia: clinical characteristics and genotype in newborn, childhood and adolescense. Medicina 67: 253-261, 2007.
  • Alonso Guillermo, Pasqualini Titania, Busaniche Julio, Ruiz Eduardo, Chemes Héctor. True hermaphroditism in a phenotypic male without ambiguous genitalia: an unusual presentation at puberty. Hormone Research 68: 261-264, 2007.

Dra María Eugenia Escobar

  • ?Síndrome de Rokitansky (agenesia útero-vaginal): aspectos clínicos, diagnósticos y terapéuticos? María Eugenia Escobar, M Gryngarten, G. del Rey, E. Boulgourdjian, A. Keselman, A. Martínez, A Arcari, M. Bou-khair y L. Zuccardi. Archivos Argentinos de Pediatría. 105, 25-31, 2007.
  • ?Acceleration of Luteinizing Hormone pulse frequency in adolescent girls with a history of Central Precocious Puberty with versus without hyperandrogenism? María Eugenia Escobar, María Gabriela Ropelato, María Gabriela Ballerini, Mirta Graciela Gryngarten, María Cecilia García Rudaz, Johannes D Veldhuis, Marta Barontini. Hormone Research 68, 278-285, 2007.

Fideleff HL,

  • Fideleff HL, Boquete H, Giaccio A, Sobrado P; KIMS, Argentine Group. Medium and long-term outcome of growth hormone therapy in growth hormone deficient adults. Medicina (B Aires). 2006;66(4):296-302.
  • Casanueva FF, Molitch ME, Schlechte JA, Abs R, Bonert V, Bronstein MD, Brue T, Cappabianca P, Colao A, Fahlbusch R, Fideleff H, Hadani M, Kelly P, Kleinberg D, Laws E, Marek J, Scanlon M, Sobrinho LG, Wass JA, Giustina A. Guidelines of the Pituitary Society for the diagnosis and management of prolactinomas. Clin Endocrinol (Oxf). 2006 Aug;65(2):265-73.
  • Guerra LN, Miler EA, Moiguer S, Karner M, Orlandi AM, Fideleff H, Burdman JA. Telomerase activity in fine needle aspiration biopsy samples: application to diagnosis of human thyroid carcinoma. Clin Chim Acta. 2006 Aug;370(1-2):180-4. Epub 2006 Mar 6. Erratum in: Clin Chim Acta. 2007 Sep;384(1-2):188.
  • Fideleff HL, Boquete H, Fideleff G, Albornoz L, Lloret SP, Suarez M, Esquifino AI, Honfi M, Cardinali DP. Gender-related differences in urinary 6-sulfatoxymelatonin levels in obese pubertal individuals. J Pineal Res. 2006 Apr;40(3):214-8.

Belgorosky

  • Saraco N, Berensztein E, Sciara M, Davila M.T. G. de, Ciaccio M, Ferraris P, Belgorosky, Rivarola M. High TGFß1, estrogen receptors and aromatase gene expression in a large cell calcifying sertoli cell tumor (LCCSCT). Implications for the mechanism of oncogenesis. Pediatric and Developmental Pathology. 2006, 9: 181-189. Springer New York. ISSN: 1093-5266
  • Chaler E, Travaglino P, Pagani S, Bozzola E, Marino R, Berensztein E, Maceiras M, Tauber M, Rivarola MA, Belgorosky A. GH dose dependency of the serum bio/immuno GH ratio in samples drawn from children during pharmacological tests of GH secretion. Journal of Endocrinological Investigation 2006; 29(2):109-14. The Italian Society of Endocrinology by Editrice Kurtis ? ISSN: 0391-4097
  • Bernasconi A, Marino R, Ribas A, Rossi J, Ciaccio M, Oleastro M, Ornani A, Paz R, Rivarola MA, Zelazko M, Belgorosky A. Characterization of Immunodeficiency in a patient with growth hormone insensitivity secondary to a novel STAT5b gene mutation. Pediatrics 2006; 118(5):e1584-92. Edit.: American Academy of Pediatrics ISSN 0031-4005
  • Chaler EA, Rivarola MA, Guerci B, Ciaccio M, Costanzo M, Travaglino P, Maceiras M, Pagani S, Meazza C, Bozzola E, Barberi S, Bozzola M, Belgorosky A. Differences in serum GH cut-off values for pharmacological tests of GH secretion depend on the serum GH method: clinical validation from the growth velocity score during the first year of treatment. Hormone Research 2006;66(5):231-235. S. Karger AG, Basel. ISSN 0301?0163
  • Berensztein E, Baquedano MS, Gonzalez CR, Saraco NI, Rodríguez J, Ponzio R, Rivarola MA, Belgorosky A. Expression of aromatase, estrogen receptor alpha and beta, androgen receptor and cP450scc, in the human early prepubertal testis. Pediatric Research 2006;60 (6):740-744. ISSN: 0031-3998
  • Herzovich V, Vaiani E, Marino R, Dratler G, Lazzati JM, Tilitzky S, Ramirez P, Iorcansky S, Rivarola MA, Belgorosky A. Unexpected Peripheral Markers of Thyroid Function in a Patient with a Novel Mutation of the MCT8 Thyroid Hormone Transporter Gene. Hormone Research. 2007;67(1):1-6. Karger AG, Basel. ISSN 0301?0163
  • Pagani S, Chaler EA, Radetti G, Travaglino P, Meazza C, Bozzola E, Sessa N, Belgorosky A, Bozzola M. Variations in Biological and Immunological Activity of Growth Hormone during the Neonatal Period. Variations in Biological and Immunological Activity of Growth Hormone during the Neonatal Period.Horm Res. 2007;68(3):145-149. S. Karger AG, Basel. ISSN 0301?0163
  • Rosenfeld RG, Belgorosky A, Camacho-Hubner C, Savage MO, Wit JM, Hwa V. Defects in growth hormone receptor signaling. Trends Endocrinol Metab 18: 134-41. 2007. Elsevier Ltd. ISSN: 1043-2760
  • Baquedano MS, Saraco N, Berensztein E, Pepe C, Bianchini M, Levy E, Goni J, Rivarola MA, Belgorosky A. Identification and developmental changes of aromatase and estrogen receptor expression in prepubertal and pubertal human adrenal tissues. J Clin Endocrinol Metab 92(6): 2215-2222, 2007. The Endocrine Society ISSN: 0021-972X.
  • Mericq V, Ciaccio M, Marino R, Viterbo G, Rivarola MA, Belgorosky A. A new dax-1 mutation in a family with a case of neonatal adrenal insufficiency and a sibling with adrenal hypoplasia and sudden death at 3 years of age . Journal of Pediatric Endocrinology and Metabolism. Freund Publishing House Ltd. ISSN 0334-018X
  • Pepe CM, Saraco NI, Baquedano MS, Guercio G, Vaiani E, Marino R, Pandey AV, Flück Ch E, Rivarola MA, Belgorosky A. The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues. Clin Endocrinol (Oxf). 67(5):698-705, 2007. ISSN:0300-0664
  • Pepe CM, Saraco NI, Baquedano MS, Guercio G, Vaiani E, Berensztein E, Rivarola MA, Belgorosky A. El splicing alternativo del exon 5 de la citocromo P450 aromatasa podría ser un mecanismo de regulación de la producción de estrógenos en humanos. Medicina (Buenos Aires) 67(4):369-73,2007. ISSN 0025-7680
  • Vaiani E, Gil S, Breyter P, Rivarola MA, Belgorosky A. Telarca Precoz. Medicina Infantil XIV (1):50-52,2007. ISSN: 0031-4021.
  • Belgorosky A, Bergadá I, Fideleff H, Miras M. Retraso Puberal. Rev Argentina de Endocrinología y Metabolismo 44,3:187-190, 2007. ISSN: 0326-4610

Mendonca BB

  • GROWTH HORMONE (GH) PHARMACOGENETICS: INFLUENCE OF GH RECEPTOR EXON 3 RETENTION OR DELETION ON FIRST-YEAR GROWTH RESPONSE AND FINAL HEIGHT IN PATIENTS WITH SEVERE GH DEFICIENCY. Jorge AAL, Marchisotti FG, Montenegro LR, Carvalho LR, Mendonca BB, Arnhold IJP, J Clin Endocrinol Metab 2006; 91(3):1076-1080.
  • A SINGLE SOMATIC ACTIVATING ASP578HIS MUTATION OF THE LUTEINIZING HORMONE RECEPTOR CAUSES LEYDIG CELL TUMOUR IN BOYS WITH GONADOTROPIN-INDEPENDENT PRECOCIOUS PUBERTY. d’Alva CB, Brito VN, Palhares HM, Carvalho FM, Arnhold IJ, Mendonca BB, Latronico AC. Clin Endocrinol (Oxf). 2006; 65(3):408-10.
  • COMBINED PITUITARY HORMONE DEFICIENCY (CPHD) DUE TO A COMPLETE PROP1 DELETION. Abrao MG, Leite MV, Carvalho LR, Billerbeck AE, Nishi MY, Barbosa AS, Martin RM, Arnhold IJ, Mendonca BB. Clin Endocrinol (Oxf). 2006; 65(3):294-300.
  • PTPN1 (PROTEIN TYROSINE PHOSPHATASE, NONRECEPTOR TYPE 11) MUTATIONS AND RESPONSE TO GROWTH HORMONE THERAPY IN CHILDREN WITH NOONAN SYNDROME. Ferreira LV, Souza SA, Arnhold IJP, Mendonca BB, Jorge AAL. J Clin Endocrinol Metab. 2006; 91(9):5156-5160.
  • PRECLINICAL DIAGNOSIS OF TESTOTOXICOSIS IN A BOY WITH AN ACTIVATING MUTATION OF THE LUTEINIZING HORMONE RECEPTOR. Teles M, Brito VN, Arnhold IJ, Mendonca BB, Latronico AC. Related. Pediatr Endocrinol Metab. 2006; 19(4):541-544.
  • ALLELIC VARIANTS OF THE GAMMA-AMINOBUTYRIC ACID-A RECEPTOR ALPHA1-SUBUNIT GENE (GABRA1) ARE NOT ASSOCIATED WITH IDIOPATHIC GONADOTROPIN-DEPENDENT PRECOCIOUS PUBERTY IN GIRLS WITH AND WITHOUT ELECTROENCEPHALOGRAPHIC ABNORMALITIES. Brito VN, Mendonca BB, Guilhoto LM, Freitas KC, Arnhold IJ, Latronico AC. J Clin Endocrinol Metab. 2006; 91(6):2432-2436.
  • HORMONAL, PITUITARY MAGNETIC RESONANCE, LHX4 AND HESX1 EVALUATION IN PATIENTS WITH HYPOPITUITARISM AND ECTOPIC POSTERIOR PITUITARY LOBE. Melo ME, Marui S, Carvalho LR, Arnhold IJ, Leite CC, Mendonca BB, Knoepfelmacher M. Clin Endocrinol (Oxf). 2007; 66(1):95-102.
  • SHOX MUTATIONS IN IDIOPATHIC SHORT STATURE AND LERI-WEILL DYSCHONDROSTEOSIS: FREQUENCY AND PHENOTYPIC VARIABILITY. Jorge AA, Souza SC, Nishi MY, Billerbeck AE, Liborio DC, Kim CA, Arnhold IJ, Mendonca BB. Clin Endocrinol (Oxf). 2007; 66(1):130-135.
  • MOLECULAR ANALYSIS OF THE NEUROPEPTIDE Y1 RECEPTOR GENE IN HUMAN IDIOPATHIC GONADOTROPIN-DEPENDENT PRECOCIOUS PUBERTY AND ISOLATED HYPOGONADOTROPIC HYPOGONADISM. Freitas KC, Ryan G, Brito VN, Tao YX, Costa EM, Mendonca BB, Segaloff D, Latronico AC. Fertil Steril. 2007; 87(3):627-634.
  • EXON 3-DELETED GENOTYPE OF GROWTH HORMONE RECEPTOR (GHRD3) POSITIVELY INFLUENCES IGF-1 INCREASE AT GENERATION TEST IN CHILDREN WITH IDIOPATHIC SHORT STATURE. Toyoshima MT, Castroneves LA, Costalonga EF, Mendonca BB, Arnhold IJ, Jorge AA. Clin Endocrinol (Oxf). 2007; 67(4):500-504.

Bachega, T. A. S.

1.- Reproductive Outcome of Women with 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia
C. Moran, R. Azziz, N. Weintrob, S. F. Witchel, V. Rohmer, D. Dewailly, J. A. M. Marcondes, M. Pugeat,P. W. Speiser, D. Pignatelli, B. B. Mendonca, T. A. S. Bachega, H. F. Escobar-Morreale, E. Carmina,F. Fruzzetti, and F. Kelestimur
The Journal of Clinical Endocrinology & Metabolism 91(9):3451?3456
2006

2.- Microconversion between CYP21A2 and CYP21A1P Promoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency
Rogério S. Araújo, Berenice B. Mendonca, Ângela S. Barbosa, Chin J. Lin, José A. M. Marcondes, Ana Elisa C. Billerbeck, and Tânia A. S. S. Bachega
The Journal of Clinical Endocrinology & Metabolism 92(10):4028?4034
2007

3.- ANATOMICAL AND FUNCTIONAL OUTCOMES OF FEMINIZING GENITOPLASTY FOR AMBIGUOUS GENITALIA IN PATIENTS WITH VIRILIZING CONGENITAL ADRENAL HYPERPLASIA
Maria Helena Palma Sircili, Berenice B. de Mendonca, Francisco Tibor Denes, Guiomar Madureira, Tânia Aparecida Sartori Sanchez Bachega, and Frederico Arnaldo de Queiroz e Silva
CLINICS 2006;61(3):209-14

4.- Utilidad del estudio molecular de CYP21A2 en el manejo prenatal de hiperplasia suprarrenal congénita: detección de dos nuevas mutaciones en Chile
Paulina Merino1a, Tania Bachega2, Pablo Céspedes3, León Trejo3, Ana Elisa Billerbeck2, Ethel Codner3.
Rev Méd Chile 2007; 135: 1450-1455

Guimaraes M M

1.- IGF-I, IGFBP-3 and ALS generation test in Turner syndrome q
Andréa Noronha Pessoa de Queiroz, Paulo F. Collett-Solberg *, Monique Esteves Cardoso, Rafaela Cattan Jusan, Mario Vaisman, Mari´lia Martins Guimarãs
Growth Hormone & IGF Research 17 (2007) 254?260

2.- Na Síndrome de Turner a Função Tireoidiana Não Deve Ser Esquecida
MARILIA MARTINS GUIMARÃES
JOÃO GABRIEL H. CORDEIRO
Arq Bras Endocrinol Metab 2007;51/3

3.- Deficiência de Hormônio do Crescimento,Hipotireoidismo e Cromossomo 18 em Anel ?Relato de Caso
Juliana V. Thomas,Daniela F.C. Mezzasalma,Andreza M. Teixeira,Ludmila N.R. Campos,Jorge Luiz Luescher,Izabel C.R. Beserra,Marilia M. Guimarães
Arq Bras Endocrinol Metab 2006;50/5:951-956

4.- Nailfold video capillaroscopy in Turner syndrome: a descriptive study
Videocapilaroscopia na síndrome de Turner: estudo descritivo
Simone C. S. Coelho, Andressa D. Ramos, Virgínia S. Pinheiro, Paulo F. C. Solberg,1 Janaina P. de Faria, Erika C. O. Naliato, Therezinha J. Fernandes, Marília M. Guimarães J Vasc Bras 2007, Vol. 6, Nº 4,325-332

Publicações

Artigos:

  • ?Hypophosphatemic rickets and osteomalacia.? Hamilton Cabral de Menezes Filho, Luiz Cláudio Castro, Durval Damiani. Arq. Bras. Endocrinol. Metab., v.50, p.802-13, 2006.
  • Domingos Malerbi, Durval Damiani, Nélson Rassi, Antônio Roberto Chacra, Edgar D?Avila NIclewicz, Ruy Lyra da Silva Filho, Sérgio Atala Dib. Posição de Consenso da Sociedade Brasileira de Diabetes ? Insulinoterapia intensiva e terapêutica com bombas de insulina. Arq Bras Endocrinol Metab 2006;50/1:125-135.
  • ?Neuroendócrino-imunomodulação: a complexa expressão das respostas integradas ao estresse.? Daniel Damiani, Ully Caroline Fernandes e Souza, Durval Damiani. Pediatria Moderna 2006;XLII (3):105-14.
  • ?Tecido adiposo: ?depósito de gordura? ou um complexo órgão endócrino?? Durval Damiani e Daniel Damiani. Pediatria Moderna 2006;XLII(2):55-66.
  • ?Bomba de infusão de insulina em diabetes mellitus tipo1 ? insulin pump therapy in type 1 diabetes mellitus.? Raphael Del Roio Liberatore Junior e Durval Damiani. J Pediatr (Rio J.) 2006;82:249-54.
  • ?Novel vasopressin type 2 (AVPR2) gene mutations in Brazilian nephrogenic diabetes insipidus patients.? Boson WL, Della Manna T, Damiani D, Miranda DM, Gadelha M, Liberman B, Correa H, Romano Silva MA, Friedman E, Silva FF, Ribeiro PA, De Marco L. Genetic Testing 2006;10(3):157-162.
  • ?Digestive adaptation with intestinal reserve: a neuroendocrine-based operation for morbid obesity.? Santoro S, Malzoni CE, Velhote MC, Milleo FQ, Santoro MA, Klajner S, Damiani D, Maksoud JG. Obes Surg 2006;16:1371-9.

Capítulos:

  • Capítulo ?Hipocalcemia?. Kuperman H, Menezes Filho HC. In: ?Endocrinologia para o pediatra.? Monte, O.; Longui, C.A.; Calliari, L.E.; Kochi, C. São Paulo, Editora Atheneu, p.479-94, 2006.
  • Projeto Diretrizes (AMB/CFM) 4o Volume, 2006. ?Raquitismo Hipofosfatêmico Ligado ao X.? Menezes Filho HC, Correa PHS.
  • Projeto Diretrizes (AMB/CFM) 4o Volume, 2006. ?Baixa estatura por deficiência de hormônio de crescimento: diagnóstico.? Jorge A, Setian N.
  • Projeto Diretrizes (AMB/CFM) 4o Volume, 2006. ?Baixa estatura por deficiência de hormônio de crescimento: tratamento.? Setian N, Jorge A.
  • Diretrizes SBD ? ?Tratamento e acompanhamento do Diabetes Mellitus ? 2006?. Damiani D.
  • Capítulo ?Hiperplasia Congênita das Supra-Renais?. Dichtchekenian V, Menezes Filho HC. In: ?Tratado de Pediatria?. Lopez, F.ª; Campos Júnior, D. Barueri ? SP, Editora Manole, p.751-60, 2007.
  • Capítulo ?Distúrbios do Metabolismo do Cálcio, Fósforo e do Magnésio?. Menezes Filho HC, Dichtchekenian V. In: ?Tratado de Pediatria?. Lopez, F.A.; Campos Júnior, D. Barueri ? SP, Editora Manole, p.761-7, 2007.
  • Capitulo ?Hipoglicemia? ? Hilton Kuperman e Mário Roberto Hirschheimer ? do livro ?Terapia Intensiva Pediátrica? ? 3ª Edição Werther Brunow de Carvalho, Mário Roberto Hirscheimer, Toshio Matsumoto, Editores, Atheneu 2006, São Paulo, 2006, p 823-48.
  • Participação do Grupo de Trabalho ?Medicamentos Hipoglicemiantes? e da elaboração do ?Protocolo Clínico e Diretrizes Terapêuticas para Diabetes Mellitus do Tipo 1? – Hospital da Clínicas da Faculdade de Medicina da Universidade de São Paulo. Thais Della Manna.
  • Ropelato María Gabriela y ColaboradoresRevisión:
  • Management of a boy with hypogonadism. Rey RA, Bergadá I, Ropelato MG, Gottlieb S. En: Progress in Paediatric Urology. Bajpai M., Gearhart J.P., Mouriquand PDE, Mitra DK, Radhakishanan J, Mathews R, Etker S.(eds), Penwel Publishers Plc, London, Vol 8, 27-46, 2006.Trabajos originales:
  • Time course of the serum gonadotropin surge, inhibins and anti-müllerian hormone (AMH) in normal newborn males during the first month of life. Bergadá I, Milani C, Bedecarrás P, Andreone L, Ropelato MG, Gottlieb S, Bergada C, Campo S, Rey RA. J Clin Endocrinol Metab. 2006; 91:4092-4098.
  • Normal growth spurt and final height despite low levels of all forms of circulating IGF-I in a patient with acid labile subunit deficiency. Domené HM, Martínez AS, Frystyk J, Bengolea SV, Ropelato MG, Scaglia PA, Chen JW, Heuck C, Wolthers OD, Heinrich JJ, Jasper HG. Horm Res (67 (5): 243-249, 2007.
  • Características clínicas, endocrinas y metabólicas de una población argentina de niñas con pubarca prematura?. Escobar María Eugenia, Gryngarten MG, Ballerini MG, Ropelato MG. Revista Argentina de Endocrinología y Metabolismo. 44, 6-16, 2007.
  • Acceleration of LH pulse frequency in adolescent girls with a history of central precocious puberty with versus without hyperandrogenism Escobar ME, Ropelato MG, Ballerini MG, Gryngarten MG, García Rudaz MC, Veldhuis JD, Barontini M.. Horm Res 68:278-285, 2007.
  • Establishment of testicular endocrine function impairment during childhood and puberty in boys with Klinefelter syndrome. Bastida MG, Rey RA., Bergadá I, Bedecarrás P, Andreone L, Del Rey G, Boywitt A, Ropelato MG, Cassinelli H, Arcari A, Campo S, Gottlieb S. Clinical Endocrinology 67:863-870, 2007.
  • Seminiferous tubule function in delayed-onset X-linked adrenal hypoplasia congenita associated with incomplete hypogonadotrophic hypogonadism. Bergadá I, Andreone L, Bedecarrás P, Ropelato MG, Copelli S, Laissue P, Rey R, Campo S. Clinical Endocrinology (Oxf) [Epub ahead of print], 2007.ADAN, L
  • BRANDAO, FR, VICENTE, EJ, DALTRO, CH, SACRAMENTO, M., MOREIRA, A, ADAN, L Bone metabolism is linked to disease duration and metabolic control in type 1 diabetes mellitus. Diabetes Research and Clinical Practice. , v.78, p.334 – 339, 2007.DINIZ-SANTOS, DR, BRANDAO, FR, ADAN, L, MOREIRA, A, VICENTE, EJ, SILVA LR Bone mineralization in young patients with type 1 diabetes mellitus and screening-identified evidence of celiac disease. Digestive Diseases and Sciences. 2007 Oct 16 [Epub ahead of print).
  • OLIVEIRA, A M, OLIVEIRA, A C, ALMEIDA, M S, OLIVEIRA, NB, ADAN, L Influence of the family nucleus on obesity in children from northeastern Brazil: a cross-section study. BMC Public Health (Online). , v.7, p.235, 2007.
  • LADEIA, A M, STEFANELLI, E, LADEIA-FROTA, C, MOREIRA, A, HILTNER, A., ADAN, L Association between elevated serum C-reactive protein and triglyceride levels in young subjects with type 1 diabetes. Diabetes Care. , v.29, p.424 – 426, 2006.
  • TRIVIN, C, SOUBERBIELLE, JC, AUBERTIN, G, LAWSON-BODY, E, ADAN, L, BRAUNER, R Diagnosis of idiopathic growth hormone deficiency: contributions of data on the acid-labile subunit, insulin-like growth factor (IGF)-I and-II, and IGF binding protein-3. Journal of Pediatric Endocrinology and Metabolism. , v.19, p.481 – 489, 2006.
  • PONTES, A. A. N., ADAN, L Interferência do iodo e alimentos bociogênicos no aparecimento e evolução das tireopatias. Revista Brasileira de Ciências da Saúde. , v.10, p.81 – 86, 2006.
  • LADEIA, A M, ADAN, L, COUTO-SILVA, A. C., HILTNER, A., GUIMARÃES, A Lipid profile correlates with glycemic control in young patients with type 1 diabetes mellitus. Preventive Cardiology. , v.9, p.82 – 88, 2006.
  • AGUIAR, A L, COUTO-SILVA, A. C., VICENTE, EJ, FREITAS, I, CRUZ, T, ADAN, L Weight evolution in girls treated for idiopathic central precocious puberty with GnRH analogues. Journal of Pediatric Endocrinology and Metabolism. , v.19, p.1327 – 1334, 2006.

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