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Results 11-20 of 41 (Search time: 0.003 seconds).
Issue DateTitleAuthor(s)
2014Congenital Hypopituitarism: Stem Cell Accumulation in Mutants with Developmental Arrest and Depletion in Mutants with HyperplasiaCHANG, Claudia Veiga; ARAUJO, Ricardo Viera; CIRQUEIRA, Cinthya Santos; PARFIENIUK, Agata; GUZZO, Mariana F.; BENEDETTI, Anna Flavia F.; SOARES, Ibere C.; MILLAN, Maria Ines Perez; CAMPER, Sally Ann; CARVALHO, Luciani R. S.
2014Unique Effects of PROP1 and POU1F1 on Pituitary Progenitor Development, Proliferation and DifferentiationMILIAN, Maria Ines Perez; BRINKMEIER, Michelle L.; CHANG, Claudia Veiga; CARVALHO, Luciani R. S.; CAMPER, Sally Ann
2014Analysis of GNAS Defects in 28 Patients with Pseudohypoparathyroidism or Pseudopseudohypoparathyroidism and Correlation with the PhenotypeREIS, Mariana Tenorio Antunes; FERRAZ-DE-SOUZA, Bruno; NISHI, Mirian Yumie; AYAKIAN, Amaryllis; CORREA, Pedro Henrique S.; MARTIN, Regina M.
2014Congenital Hypopituitarism: Stem Cell Accumulation in Mutants with Developmental Arrest and Depletion in Mutants with HyperplasiaCHANG, Claudia Veiga; ARAUJO, Ricardo Viera; CIRQUEIRA, Cinthya Santos; PARFIENIUK, Agata; GUZZO, Mariana F.; BENEDETTI, Anna Flavia F.; SOARES, Ibere C.; MILLAN, Maria Ines Perez; CAMPER, Sally Ann; CARVALHO, Luciani R. S.
2014Apparently Sporadic Central Precocious Puberty Is Caused By Paternally Inherited Mutations in the Imprinted MKRN3 GeneABREU, Ana Paula; MACEDO, Delanie B.; REIS, Ana Claudia Silva; MONTENEGRO, Luciana Ribeiro; DAUBER, Andrew; BENEDUZZI, Diane; CULIER, Priscilla; SILVEIRA, Leticia Gontijo; TELES, Milena Gurgel; CARROLL, Rona S.; GUERRA, Gil; GUARAGNA FILHO, Guilherme; GUCEV, Zoran Spasico; ARNHOLD, Ivo J. P.; CASTRO, Margaret; MOREIRA, Ayrton Custodio; MARTINELLI, Carlos Eduardo; HIRSCHHORN, Joel N.; MENDONASA, Berenice Bilharinho; BRITO, Vinicius N.; ANTONINI, Sonir Roberto; KAISER, Ursula B.; LATRONICO, Ana Claudia
2014A Novel OTX2 Mutation, p.H230L, Causes Hypopituitarism with Incomplete Penetrance: Exome Sequencing to Identify Modifier GenesFOYOUZI, Nastaran; CAMPER, Sally Ann; MOREIRA, Michele; FRANCA, Marcela M.; OTTO, Aline P.; CORREA, Fernanda de Azevedo; ARNHOLD, Ivo J. P.; MENDONCA, Berenice B.; MA, Qianyi; LI, Jun Z.; FANG, Qing; CARVALHO, Luciani R. S.
2014Inherited Digenic Missense Variants in FGFR2 and MAP3K1 Genes in Two Siblings with 46,XY Partial Gonadal DysgenesisMACHADO, Aline Zamboni; NISHI, Mirian Yumie; COSTA, Elaine Maria Frade; MENDONCA, Berenice B.; DOMENICE, Sorahia
2014Gene Identification in Patients with Hypopituitarism: Next Generation Exome Sequencing ExperienceFANG, Qing; ARNHOLD, Ivo J. P.; BENEDETTI, Anna Flavia F.; MENDONAA, Berenice Bilharinho; BRUE, Thierry; CARVALHO, Luciani R. S.; CASTINETTI, Frederic; CORREA, Fernanda de Azevedo; LI, Jun Z.; MA, Qianyi; REYNAUD, Rachel; CAMPER, Sally Ann
2014High Frequency of Subclinical Cushing's Syndrome in the Inherited Autosomal Dominant Primary Macronodular Adrenal Hyperplasia Due to ARMC5 MutationsALENCAR, Guilherme Asmar; ALMEIDA, Madson Q.; LERARIO, Antonio Marcondes; RESENDE, Gabriela; NISHI, Mirian Yumie; PEREIRA, Maria Adelaide Albergaria; MENDONCA, Berenice B.; FRAGOSO, Maria Candida B. V.
2014Improving the Effectiveness of CAH Newborn Screening Adjusting 17OHP Levels According to Degree of Prematurity and Age at Sample CollectionCARYALHO, Daniel Fiordelisio de; HAYASHI, Giselle Yuri; FAURE, Claudia; VALLEJOS, Carla Gabriella; BRITO, Vinicius N.; MENDONCA, Berenice B.; BACHEGA, Tania A.