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Results 1-10 of 29 (Search time: 0.087 seconds).
| Issue Date | Title | Author(s) |
|---|---|---|
| 2018 | Comparison of Ga-68 PET/CT to Other Imaging Studies in Medullary Thyroid Cancer: Superiority in Detecting Bone Metastases | CASTRONEVES, Luciana Audi; COURA FILHO, George; FREITAS, Ricardo Miguel Costa de; SALLES, Raphael; MOYSES, Raquel Ajub; LOPEZ, Rossana Veronica Mendoza; PEREIRA, Maria Adelaide Albergaria; TAVARES, Marcos Roberto; JORGE, Alexander Augusto de Lima; BUCHPIGUEL, Carlos Alberto; HOFF, Ana Oliveira |
| 2019 | Genetic Evidence of the Association of DEAH-Box Helicase 37 Defects With 46,XY Gonadal Dysgenesis Spectrum | SILVA, Thatiana Evilen da; GOMES, Nathalia Lisboa; LERARIO, Antonio Marcondes; KEEGAN, Catherine Elizabeth; NISHI, Mirian Yumi; CARVALHO, Filomena Marino; VILAIN, Eric; BARSEGHYAN, Hayk; MARTINEZ-AGUAYO, Alejandro; FORCLAZ, Maria Veronica; PAPAZIAN, Regina; PAULA, Leila Cristina Pedroso de; COSTA, Eduardo Correa; CARVALHO, Luciani Renata; JORGE, Alexander Augusto Lima; ELIAS, Felipe Martins; MITCHELL, Rod; COSTA, Elaine Maria Frade; MENDONCA, Berenice Bilharinho; DOMENICE, Sorahia |
| 2018 | A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation | HUSSAIN, Iram; PATNI, Nivedita; UEDA, Masako; SORKINA, Ekaterina; VALERIO, Cynthia M.; COCHRAN, Elaine; BROWN, Rebecca J.; PEEDEN, Joseph; TIKHONOVICH, Yulia; TIULPAKOV, Anatoly; STENDER, Sarah R. S.; KLOUDA, Elisabeth; TAYEH, Marwan K.; INNIS, Jeffrey W.; MEYER, Anders; LAL, Priti; GODOY-MATOS, Amelio F.; TELES, Milena G.; ADAMS-HUET, Beverley; RADER, Daniel J.; HEGELE, Robert A.; ORAL, Elif A.; GARG, Abhimanyu |
| 2018 | IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy | 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. |
| 2017 | Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations | GKOUROGIANNI, Alexandra; ANDREW, Melissa; TYZINSKI, Leah; CROCKER, Melissa; DOUGLAS, Jessica; DUNBAR, Nancy; FAIRCHILD, Jan; FUNARI, Mariana F. A.; HEATH, Karen E.; JORGE, Alexander A. L.; KURTZMAN, Tracey; LAFRANCHI, Stephen; LALANI, Seema; LEBL, Jan; LIN, Yuezhen; LOS, Evan; NEWBERN, Dorothee; NOWAK, Catherine; OLSON, Micah; POPOVIC, Jadranka; PRUHOVA, Stepanka; ELBLOVA, Lenka; QUINTOS, Jose Bernardo; SEGERLUND, Emma; SENTCHORDI, Lucia; SHINAWI, Marwan; STATTIN, Eva-Lena; SWARTZ, Jonathan; ANGEL, Ariadna Gonzalez del; CUELLAR, Sinhue Diaz; HOSONO, Hidekazu; SANCHEZ-LARA, Pedro A.; HWA, Vivian; BARON, Jeffrey; NILSSON, Ola; DAUBER, Andrew |
| 2011 | MiR-1 Is a Tumor Suppressor in Thyroid Carcinogenesis Targeting CCND2, CXCR4, and SDF-1 alpha | LEONE, Vincenza; D'ANGELO, Daniela; RUBIO, Ileana; FREITAS, Paula Mussnich de; FEDERICO, Antonella; COLAMAIO, Marianna; PALLANTE, Pierlorenzo; MEDEIROS-NETO, Geraldo; FUSCO, Alfredo |
| 2014 | Pasireotide Versus Octreotide in Acromegaly: A Head-to-Head Superiority Study | COLAO, A.; BRONSTEIN, M. D.; FREDA, P.; GU, F.; SHEN, C. -C.; GADELHA, M.; FLESERIU, M.; LELY, A. J. van der; FARRALL, A. J.; RESENDIZ, K. Hermosillo; RUFFIN, M.; CHEN, Y.; SHEPPARD, M. |
| 2014 | Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 | MACEDO, Delanie B.; ABREU, Ana Paula; REIS, Ana Claudia S.; MONTENEGRO, Luciana R.; DAUBER, Andrew; BENEDUZZI, Daiane; CUKIER, Priscilla; SILVEIRA, Leticia F. G.; TELES, Milena G.; CARROLL, Rona S.; GUERRA JUNIOR, Gil; GUARAGNA FILHO, Guilherme; GUCEV, Zoran; ARNHOLD, Ivo J. P.; CASTRO, Margaret de; MOREIRA, Ayrton C.; MARTINELLI JR., Carlos Eduardo; HIRSCHHORN, Joel N.; MENDONCA, Berenice B.; BRITO, Vinicius N.; ANTONINI, Sonir R.; KAISER, Ursula B.; LATRONICO, Ana Claudia |
| 2014 | Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: The Influence of a SOCS2 Polymorphism | BRAZ, Adriana F.; COSTALONGA, Everlayny F.; TRARBACH, Ericka B.; SCALCO, Renata C.; MALAQUIAS, Alexsandra C.; GUERRA-JUNIOR, Gil; ANTONINI, Sonir R. R.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P.; JORGE, Alexander A. L. |
| 2015 | Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation | TOLEDO, Sergio P. A.; LOURENCO JR., Delmar M.; SEKIYA, Tomoko; LUCON, Antonio M.; BAENA, Marcos E. S.; CASTRO, Claudio C.; BORTOLOTTO, Luiz A.; ZERBINI, Maria C. N.; SIQUEIRA, Sheila A. C.; TOLEDO, Rodrigo A.; DAHIA, Patricia L. M. |