Artigos e Materiais de Revistas Científicas - LIM/42

Artigos e Materiais de Revistas Científicas - LIM/42

 

A coleção de Artigos e Materiais de Revistas Científicas engloba artigos originais, artigos de revisão, artigos de atualização, artigos técnicos, relatos de experiências, resenhas, ensaios, editoriais, cartas ao editor, debates, notas científicas e técnicas, depoimentos, entrevistas e pontos de vista. Consideram-se como artigos científicos originais os trabalhos redigidos para divulgação de informações e resultados sobre determinada pesquisa científica, publicados em periódico científico após avaliação por outros pesquisadores.

Recent Submissions

  • MACHADO, Marcio Carlos; FRAGOSO, Maria Candida Barisson Vilares; MOREIRA, Ayrton Custodio; BOGUSZEWSKI, Cesar Luiz; NETO, Leonardo Vieira; NAVES, Luciana A.; VILAR, Lucio; ARAUJO, Luiz Antonio de; MUSOLINO, Nina Rosa Castro; MIRANDA, Paulo Augusto C.; CZEPIELEWSKI, Mauro A.; GADELHA, Monica R.; BRONSTEIN, Marcello Delano; RIBEIRO-OLIVEIRA JR., Antonio (SBEM-SOC BRASIL ENDOCRINOLOGIA & METABOLOGIA, RIO DE JANEIRO, RJ, BRAZIL, 2018)
    The treatment objectives for a patient with Cushing's disease (CD) are remission of hypercortisolism, adequate management of co-morbidities, restoration of the hypothalamic-pituitary-adrenal axis, preservation of fertility ...
  • RAMOS, Carolina O.; LATRONICO, Ana C.; CUKIER, Priscilla; MACEDO, Delanie B.; BESSA, Danielle S.; CUNHA-SILVA, Marina; ARNHOLD, Ivo J.; MENDONCA, Berenice B.; BRITO, Vinicius N. (KARGER, BASEL, SWITZERLAND, 2018)
    Background: Hypothalamic hamartoma (HH) represents the commonest cause of organic central precocious puberty (CPP). Follow-up of these patients in adulthood is scarce. Objective: To describe the anthropometric, metabolic, ...
  • CUNHA, Flavia Siqueira; DOMENICE, Sorahia; SIRCILI, Maria Helena Palma; MENDONCA, Berenice Bilharinho de; COSTA, Elaine Maria Frade (HOSPITAL CLINICAS, UNIV SAO PAULO, SAO PAULO, BRAZIL, 2018)
    OBJECTIVE: The ideal dosage of cross-sex hormones remains unknown. The aim of this study was to evaluate the luteinizing hormone, follicle-stimulating hormone, testosterone, estradiol and prolactin levels after low-dose ...
  • BATISTA, Rafael Loch; COSTA, Elaine M. Frade; RODRIGUES, Andresa de Santi; GOMES, Nathalia Lisboa; FARIA JR., Jose Antonio; NISHI, Mirian Y.; ARNHOLD, Ivo Jorge Prado; DOMENICE, Sorahia; MENDONCA, Berenice Bilharinho de (SBEM-SOC BRASIL ENDOCRINOLOGIA & METABOLOGIA, RIO DE JANEIRO, RJ, BRAZIL, 2018)
    Androgenic insensitivity syndrome is the most common cause of disorders of sexual differentiation in 46, XY individuals. It results from alterations in the androgen receptor gene, leading to a frame of hormonal resistance, ...
  • CAMARA-DE-SOUZA, A. B.; TOYOSHIMA, M. T. K.; GIANNELLA, M. L.; FREIRE, D. S.; CAMACHO, C. P.; LOURENCO JR., D. M.; ROCHA, M. S.; BACCHELLA, T.; JUREIDINI, R.; MACHADO, M. C. C.; ALMEIDA, M. Q.; PEREIRA, M. A. A. (ELSEVIER SCIENCE BV, AMSTERDAM, NETHERLANDS, 2018)
    Background/objectives: Insulinoma is a rare pancreatic tumor and, usually, a benign disease but can be a malignant one and, sometimes, a highly aggressive disease. The aim of this study was to determine differences between ...
  • CUNHA-SILVA, M.; BRITO, V. N.; MACEDO, D. B.; BESSA, D. S.; RAMOS, C. O.; LIMA, L. G.; BARROSO, P. S.; ARNHOLD, I. J. P.; SEGALOFF, D. L.; MENDONCA, B. B.; LATRONICO, A. C. (OXFORD UNIV PRESS, OXFORD, ENGLAND, 2018)
    Testotoxicosis is a rare cause of peripheral precocious puberty in boys caused by constitutively activating mutations of the LHCG receptor. Affected males usually have normal gonadotropin profiles and fertility in their ...
  • PONTES, Flavia Sirotheau Correa; LOPES, Marcio Ajudarte; SOUZA, Lucas Lacerda de; REZENDE, Diogo dos Santos da Mata; SANTOS-SILVA, Alan Roger; JORGE JR., Jacks; SILVA, Wagner Gomes da; PIRES, Fabio Ramoa; ROCHA, Andre Caroli; CAMPOS, Wladimir Gushiken de; CALDATO, Milena Coelho Fernandes; MARTIN, Regina Matsunaga; FONSECA, Felipe Paiva; PONTES, Helder Antonio Rebelo (ELSEVIER SCIENCE INC, NEW YORK, USA, 2018)
    Objective. To describe the oral and maxillofacial manifestations of patients diagnosed with chronic kidney disease-mineral and bone disorders. Study Design. Over a 13-year period, clinicopathologic data of patients diagnosed ...
  • PASSAIA, Barbara dos Santos; DIAS, Matheus Henrique; KREMER, Jean Lucas; ANTONINI, Sonir Roberto Rauber; ALMEIDA, Madson Queiroz de; FRAGOSO, Maria Candida Barisson Villares; LOTFI, Claudimara Ferini Pacicco (FRONTIERS MEDIA SA, LAUSANNE, SWITZERLAND, 2018)
    With recent progress in understanding the pathogenesis of adrenocortical tumors (ACTs), identification of molecular markers to predict their prognosis has become possible. Transcription factor 21 (TCF21)/podocyte-expressed ...
  • HOMMA, Thais K.; KREPISCHI, Ana C. V.; FURUYA, Tatiane K.; HONJO, Rachel S.; MALAQUIAS, Alexsandra C.; BERTOLA, Debora R.; COSTA, Silvia S.; CANTON, Ana P.; ROELA, Rosimeire A.; FREIRE, Bruna L.; KIM, Chong A.; ROSENBERG, Carla; JORGE, Alexander A. L. (KARGER, BASEL, SWITZERLAND, 2018)
    Background/Aims: Genetic imbalances are responsible for many cases of short stature of unknown etiology. This study aims to identify recurrent pathogenic copy number variants (CNVs) in patients with syndromic short stature ...
  • FREIRE, Bruna L.; HOMMA, Thais K.; FUNARI, Mariana F. A.; LERARIO, Antonio M.; LEAL, Aline M.; VELLOSO, Elvira D. R. P.; MALAQUIAS, Alexsandra C.; JORGE, Alexander A. L. (ELSEVIER SCIENCE BV, AMSTERDAM, NETHERLANDS, 2018)
    Background: Fanconi Anemia (FA) is a rare and heterogeneous genetic syndrome. It is associated with short stature, bone marrow failure, high predisposition to cancer, microcephaly and congenital malformation. Many genes ...
  • CORREA, Fernanda A.; BIANCHI, Paulo H. M.; FRANCA, Marcela M.; OTTO, Aline P.; RODRIGUES, Rodrigo J. M.; EJZENBERG, Dani; SERAFINI, Paulo C.; BARACAT, Edmundo Chada; FRANCISCO, Rossana P. V.; BRITO, Vinicius N.; ARNHOLD, Ivo J. P.; MENDONCA, Berenice B.; CARVALHO, Luciani R. (ENDOCRINE SOC, WASHINGTON, USA, 2017)
    Context: Women with hypopituitarism have lower pregnancy rates after ovulation induction. Associated pituitary hormone deficiencies might play a role in this poorer outcome. Objective: We evaluated fertility treatment and ...
  • PETROLI, Reginaldo J.; HIORT, Olaf; STRUVE, Dagmar; GESING, Julia K.; SOARDI, Fernanda C.; SPINOLA-CASTRO, Angela M.; MELO, Karla; ARNHOLD, Ivo J. Prado; MACIEL-GUERRA, Andrea T.; GUERRA-JUNIOR, Gil; WERNER, Ralf; MELLO, Maricilda P. de (KARGER, BASEL, SWITZERLAND, 2017)
    Androgens are responsible for the development and maintenance of male sex characteristics. Dysfunctions in androgen action due to mutations in the androgen receptor gene (AR) can lead to androgen insensitivity syndrome ...
  • CAVALCANTE, Isadora P.; NISHI, Mirian; ZERBINI, Maria Claudia N.; ALMEIDA, Madson Q.; BRONDANI, Vania B.; BOTELHO, Maria Luiza Anhaia de Arruda; TANNO, Fabio Y.; SROUGI, Victor; CHAMBO, Jose Luis; MENDONCA, Berenice B.; BERTHERAT, Jerome; LOTFI, Claudimara F. P.; FRAGOSO, Maria Candida B. V. (ELSEVIER IRELAND LTD, CLARE, IRELAND, 2018)
    The participation of aberrant receptors and intra-adrenal ACTH in hyperplastic tissue are considered mechanisms that regulate hypercortisolism in PMAH. Additionally, germline ARMC5 mutations have been described as the most ...
  • VASQUES, Gabriela A.; FUNARI, Mariana F. A.; FERREIRA, Frederico M.; AZA-CARMONA, Miriam; SENTCHORDI-MONTANE, Lucia; BARRAZA-GARCIA, Jimena; LERARIO, Antonio M.; YAMAMOTO, Guilherme L.; NASLAVSKY, Michel S.; DUARTE, Yeda A. O.; BERTOLA, Debora R.; HEATH, Karen E.; JORGE, Alexander A. L. (OXFORD UNIV PRESS INC, CARY, USA, 2018)
    Context: Genetic evaluation has been recognized as an important tool to elucidate the causes of growth disorders. Objective: To investigate the cause of short stature and to determine the phenotype of patients with IHH ...
  • BATISTA, Rafael Loch; RODRIGUES, Andresa De Santi; MACHADO, Aline Zamboni; NISHI, Mirian Yumie; CUNHA, Flavia Siqueira; SILVA, Rosana Barbosa; COSTA, Elaine M. F.; MENDONCA, Berenice B.; DOMENICE, Sorahia (WALTER DE GRUYTER GMBH, BERLIN, GERMANY, 2018)
    Background: Androgen insensitivity syndrome (AIS) is the most frequent etiology of 46, XY disorders of sex development (DSDs), and it is an X-linked disorder caused by mutations in the androgen receptor (AR) gene. AIS ...
  • MADEIRA, Joao Lo; NISHI, Mirian Y.; NAKAGUMA, Marilena; BENEDETTI, Anna F.; BISCOTTO, Isabela Peixoto; FERNANDES, Thamiris; PEQUENO, Thiago; FIGUEIREDO, Thalita; FRANCA, Marcela M.; CORREA, Fernanda A.; OTTO, Aline P.; ABRAO, Milena; MIRAS, Mirta B.; SANTOS, Silvana; JORGE, Alexander A. L.; COSTALONGA, Everlayny F.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P.; CARVALHO, Luciani R. (WILEY, HOBOKEN, USA, 2017)
    BackgroundMutations in PROP1, HESX1 and LHX3 are associated with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP). ObjectiveTo identify mutations in PROP1, HESX1 and LHX3 in a large ...
  • COOLS, M.; WOLFFENBUTTEL, K. P.; HERSMUS, R.; MENDONCA, B. B.; KAPROVA, J.; DROP, S. L. S.; STOOP, H.; GILLIS, A. J. M.; OOSTERHUIS, J. W.; COSTA, E. M. F.; DOMENICE, S.; NISHI, M. Y.; WUNSCH, L.; QUIGLEY, C. A.; T'SJOEN, G.; LOOIJENGA, L. H. J. (OXFORD UNIV PRESS, OXFORD, ENGLAND, 2017)
    STUDY QUESTION: What is the prevalence of malignant testicular germ cell tumors (TGCT) and its precursors, (pre-) germ cell neoplasia in situ (GCNIS), in late teenagers and adults who have androgen insensitivity syndrome ...
  • CORREA, Fernanda A.; JORGE, Alexander A. L.; NAKAGUMA, Marilena; CANTON, Ana P. M.; COSTA, Silvia S.; FUNARI, Mariana F.; LERARIO, Antonio M.; FRANCA, Marcela M.; CARVALHO, Luciani R.; KREPISCHI, Ana C. V.; ARNHOLD, Ivo J. P.; ROSENBERG, Carla; MENDONCA, Berenice B. (WILEY, HOBOKEN, USA, 2018)
    ObjectivesThe aetiology of congenital hypopituitarism (CH) is unknown in most patients. Rare copy number variants (CNVs) have been implicated as the cause of genetic syndromes with previously unknown aetiology. Our aim was ...
  • FRANCA, M. M.; FUNARI, M. F. A.; NISHI, M. Y.; NARCIZO, A. M.; DOMENICE, S.; COSTA, E. M. F.; LERARIO, A. M.; MENDONCA, B. B. (WILEY, HOBOKEN, USA, 2018)
    Targeted massively parallel sequencing (TMPS) has been used in genetic diagnosis for Mendelian disorders. In the past few years, the TMPS has identified new and already described genes associated with primary ovarian ...
  • SROUGI, Victor; BESSA JUNIOR, Jose; TANNO, Fabio Y.; FERREIRA, Amanda M.; HOFF, Ana O.; BEZERRA, Joao E.; ALMEIDA, Cristiane M.; ALMEIDA, Madson Q.; MENDONCA, Berenice B.; NAHAS, William C.; CHAMBO, Jose L.; SROUGI, Miguel; FRAGOSO, Maria C. B. V. (BRAZILIAN SOC UROL, RIO DE JANEIRO, BRAZIL, 2017)
    Purpose: To evaluate the role of ARDT after surgical resection of ACC. Materials and Methods: Records of patients from our institutional ACC database were retrospectively assessed. A paired comparison analysis was used to ...

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