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Results 1-10 of 13 (Search time: 0.04 seconds).
Issue DateTitleAuthor(s)
2012Advanced prostate cancer as a cause of oncogenic osteomalacia: an underdiagnosed conditionMAK, Milena Perez; SILVA, Veronica Torres da Costa e; MARTIN, Regina Matsunaga; LERARIO, Antonio Marcondes; YU, Luis; HOFF, Paulo Marcelo Gehm; CASTRO JUNIOR, Gilberto de
2013Analysis of the insulin-like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p.Arg511Trp)LEAL, Andrea C.; MONTENEGRO, Luciana R.; SAITO, Renata F.; RIBEIRO, Tamaya C.; COUTINHO, Debora C.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P.; JORGE, Alexander A. L.
2016Pathogenic Copy Number Variants are Frequently Identified in Children with Short Stature of Unknown EtiologyCANTON, Ana; HOMMA, Thais; FURUYA, Tatiane; ROELA, Rosimeire; ARNHOLD, Ivo; JORGE, Alexander
2014Transcriptomic Response to Calcitriol in Human Fibroblasts with or without a Functional Vitamin D ReceptorFERRAZ-DE-SOUZA, Bruno; KATAYAMA, Maria L.; FOLGUEIRA, Maria A. K.; CORREA, Pedro Henrique S.; LATRONICO, Ana Claudia; MARTIN, Regina M.
2014Sorafenib Treatment Improves Refractory Hypercalcemia in a Patient with Metastatic Parathyroid Carcinoma: A Case ReportLERARIO, Antonio M.; MARTIN, Regina M.; HOFF, Ana Oliveira; NAKAGUMA, Marilena; CASTRO, Gilberto; TEIXEIRA, Carlos Henrique; MENEZES, Marcos; DALALIO, Vanessa; MENDONCA, Berenice B.
2018Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown CauseHOMMA, 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.
2020Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li-Fraumeni syndrome)PETRY, Vanessa; BONADIO, Renata Colombo; CAGNACCI, Allyne Queiroz Carneiro; SENNA, Luiz Antonio Leite; CAMPOS, Roberta da Nascimento Galvao; COTTI, Guilherme Cutait; HOFF, Paulo M.; FRAGOSO, Maria Candida Barisson Villares; ESTEVEZ-DIZ, Maria del Pilar
2019Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutationFERREIRA, Amanda Meneses; BRONDANI, Vania Balderrama; HELENA, Vanessa Petry; CHARCHAR, Helaine Laiz Silva; ZERBINI, Maria Claudia Nogueira; LEITE, Luiz Antonio Senna; HOFF, Ana Oliveira; LATRONICO, Ana Claudia; MENDONCA, Berenice Bilharinho; DIZ, Maria Del Pilar Estevez; ALMEIDA, Madson Queiroz de; FRAGOSO, Maria Candida Barisson Villares
2016Good response to long-term therapy with growth hormone in a patient with 9p trisomy syndrome: A case report and review of the literatureCANTON, Ana Pinheiro Machado; NISHI, Mirian Yumie; FURUYA, Tatiane Katsue; ROELA, Rosimeire Aparecida; JORGE, Alexander Augusto Lima
2014Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutationsLONGUINI, Viviane C.; LOURENCO JR., Delmar M.; SEKIYA, Tomoko; MEIRELLES, Osorio; GONCALVES, Tatiana D.; COUTINHO, Flavia L.; FRANCISCO, Guilherme; OSAKI, Luciana H.; CHAMMAS, Roger; ALVES, Venancio A. F.; SIQUEIRA, Sheila A. C.; SCHLESINGER, David; NASLAVSKY, Michel S.; ZATZ, Mayana; DUARTE, Yeda A. O.; LEBRAO, Maria Lucia; GAMA, Patricia; LEE, Misu; MOLATORE, Sara; PEREIRA, Maria Adelaide A.; JALLAD, Raquel S.; BRONSTEIN, Marcello D.; CUNHA-NETO, Malebranche B.; LIBERMAN, Bernardo; FRAGOSO, Maria Candida B. V.; TOLEDO, Sergio P. A.; PELLEGATA, Natalia S.; TOLEDO, Rodrigo A.