Artigos e Materiais de Revistas Científicas - LIM/42
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Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 505
| Issue Date | Title | Author(s) |
|---|---|---|
| 2022 | A Small Supernumerary Xp Marker Chromosome Including Genes NR0B1 and MAGEB Causing Partial Gonadal Dysgenesis and Gonadoblastoma | NISHI, M. Y.; JúNIOR, J. A. D. Faria; KREPISCHI, A. C. V.; MORAES, D. R. De; COSTA, S. S. Da; SILVA, E. S. D. N.; COSTA, E. M. F.; MENDONCA, B. B.; DOMENICE, S. |
| 2022 | WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease | FERRARI, M. T. M.; WATANABE, A.; SILVA, T. E. Da; GOMES, N. L.; BATISTA, R. L.; NISHI, M. Y.; PAULA, L. C. P. De; COSTA, E. C.; COSTA, E. M. F.; CUKIER, P., et al |
| 2022 | Variants in 46,XY DSD-Related Genes in Syndromic and Non-Syndromic Small for Gestational Age Children with Hypospadias | BRAGA, B. L.; GOMES, N. L.; NISHI, M. Y.; FREIRE, B. L.; BATISTA, R. L.; FARIA JUNIOR, J. A. D.; FUNARI, M. F. A.; BENEDETTI, A. F. F.; NARCIZO, A. De Moraes; CARDOSO, L. Cavalca, et al |
| 2023 | A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity | BASTOS, Thais Sibioni Berti; PAULA, Andre Guilherme Portela de; LUZ, Rebeca Bosso dos Santos; GARNIQUE, Anali M. B.; BELO, Marco A. A.; ETO, Silas Fernandes; FERNANDES, Dayanne Carla; FERRARIS, Fausto Klabund; PONTES, Leticia Gomes de; FRANCA, Tabata Takahashi, et al |
| 2024 | ARMC5 controls the degradation of most Pol II subunits, and ARMC5 mutation increases neural tube defect risks in mice and humans | LUO, Hongyu; LAO, Linjiang; AU, Kit Sing; NORTHRUP, Hope; HE, Xiao; FORGET, Diane; GAUTHIER, Marie-Soleil; COULOMBE, Benoit; BOURDEAU, Isabelle; SHI, Wei, et al |
| 2024 | The effect of hormonal secretion on survival in adrenocortical carcinoma: A multi-center study | SADA, Alaa; FOSTER, Trenton R.; AL-WARD, Ruaa; SAWANI, Sahar; CHARCHAR, Helaine; PISHDAD, Reza; BEN-SHLOMO, Anat; DY, Benzon M.; LYDEN, Melanie L.; BERGSLAND, Emily, et al |
| 2023 | Embryonic stem cell factor <i>FOXD3</i> (Genesis) defects in gastrointestinal stromal tumors | FAUCZ, Fabio R.; HORVATH, Anelia D.; ASSIE, Guillaume; ALMEIDA, Madson Q.; SZAREK, Eva; BOIKOS, Sosipatros; ANGELOUSI, Anna; LEVY, Isaac; MARIA, Andrea G.; CHITNIS, Ajay, et al |
| 2023 | Evaluation of pediatric diabetes mellitus after SARS-CoV-2 infection: A long-term prospective case series | FINK, Thais T.; CANTON, Ana P. M.; PEREIRA, Maria Fernanda B.; BAIN, Vera; MATSUO, Olivia; ASTLEY, Camilla; MARQUES, Heloisa H. S.; CORREA-SILVA, Simone; MONTENEGRO, Marilia M.; PALMEIRA, Patricia, et al |
| 2023 | Efficacy of Oral Furosemide Test for Primary Aldosteronism Diagnosis | FREITAS, Thais C.; MACIEL, Ana Alice W.; FAGUNDES, Gustavo F. C.; PETENUCI, Janaina; SANTANA, Lucas S.; GUIMARAES, Augusto G.; FREITAS-CASTRO, Felipe; SROUGI, Victor; TANNO, Fabio Y.; CHAMBO, Jose L., et al |
| 2023 | International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early Adulthood | HOKKEN-KOELEGA, Anita C. S.; STEEN, Manouk van der; BOGUSZEWSKI, Margaret C. S.; CIANFARANI, Stefano; DAHLGREN, Jovanna; HORIKAWA, Reiko; MERICQ, Veronica; RAPAPORT, Robert; ALHERBISH, Abdullah; BRASLAVSKY, Debora, et al |
| 2022 | A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functions | FRANCA, Monica M.; CONDEZO, Yazmine B.; ELZAIAT, Maeva; FELIPE-MEDINA, Natalia; SANCHEZ-SAEZ, Fernando; MUNOZ, Sergio; SAINZ-URRUELA, Raquel; MARTIN-HERVAS, M. Rosario; GARCIA-VALIENTE, Rodrigo; SANCHEZ-MARTIN, Manuel A., et al |
| 2023 | Editorial: A year in review: discussions in cancer endocrinology | ALMEIDA, Madson; SHARIFI-RAD, Javad; VELLA, Veronica |
| 2023 | Adjuvant mitotane versus surveillance in low-grade, localised adrenocortical carcinoma (ADIUVO): an international, multicentre, open-label, randomised, phase 3 trial and observational study | TERZOLO, Massimo; FASSNACHT, Martin; PEROTTI, Paola; LIBE, Rossella; KASTELAN, Darko; LACROIX, Andre; ARLT, Wiebke; HAAK, Harm Reinout; LOLI, Paola; DECOUDIER, Benedicte, et al |
| 2023 | Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study | SCHROEDER, Mariska A. M.; NEACSU, Mihaela; ADRIAANSEN, Bas P. H.; SWEEP, Fred C. G. J.; AHMED, S. Faisal; ALI, Salma R.; BACHEGA, Tania A. S. S.; BARONIO, Federico; BIRKEBAEK, Niels Holtum; BRUIN, Christiaan de, et al |
| 2023 | Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels | MONTENEGRO, Luciana; SERAPHIM, Carlos; TINANO, Flavia; PIOVESAN, Maiara; CANTON, Ana P. M.; MCELREAVEY, Ken; BRABANT, Severine; BORIS, Natalia P.; MAGNUSON, Melissa; CARROLL, Rona S., et al |
| 2023 | Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability | DANTAS, Naiara C. B.; FUNARI, Mariana F. A.; LERARIO, Antonio M.; ANDRADE, Nathalia L. M.; REZENDE, Raissa C.; CELLIN, Laurana P.; ALVES, Cresio; CRISOSTOMO, Lindiane G.; ARNHOLD, Ivo J. P.; MENDONCA, Berenice, et al |
| 2023 | A ""Grasp Heart"" Situation: Managing Heart Failure with Reduced Ejection Fraction in Primary Adrenal Insufficiency | STUMPF, Matheo Augusto Morandi; ALMEIDA, Madson Queiroz |
| 2023 | Evaluation of the trabecular bone score in 35 children and adults with X-linked hypophosphatemic rickets | COLARES NETO, Guido de Paula; PEREIRA, Rosa Maria Rodrigues; ALVARENGA, Jackeline Couto; TAKAYAMA, Liliam; FUNARI, Mariana Ferreira de Assis; MARTIN, Regina Matsunaga |
| 2023 | Homozygous <i>CDH2</i> variant may be associated with hypopituitarism without neurological disorders | FERREIRA, Nathalia G. B. P.; MADEIRA, Joao L. O.; GERGICS, Peter; KERTSZ, Renata; MARQUES, Juliana M.; TRIGUEIRO, Nicholas S. S.; BENEDETTI, Anna Flavia Figueredo; V, Bruna Azevedo; V, Bianca H. Fernandes; BISSEGATTO, Debora D., et al |
| 2023 | Rare variants in the<i> MECP2</i> gene in girls with central precocious puberty: a translational cohort study | CANTON, Ana P. M.; TINANO, Flavia R.; GUASTI, Leonardo; MONTENEGRO, Luciana R.; RYAN, Fiona; SHEARS, Deborah; MELO, Maria Edna de; GOMES, Larissa G.; PIANA, Mariana P.; BRAUNER, Raja, et al |
Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 505
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