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Challenges in treating children with optic pathway gliomas: an 18-year experience from a middle-income country.
Published in:
Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2024.1329729
By:
- Luis Ramírez-Melo, Jorge;
- Moreira, Daniel C.;
- Luisa Orozco-Alvarado, Ana;
- Sánchez-Zubieta, Fernando;
- Navarro-Martín del Campo, Regina M.
Publication type:
Article
Successful Live Birth in a Woman With 17α-Hydroxylase Deficiency Through IVF Frozen-Thawed Embryo Transfer.
Published in:
2016
By:
- Bianchi, Paulo Homem de Mello;
- Gouveia, Gabriela Romanenghi Fanti Carvalho Araujo;
- Costa, Elaine M Frade;
- Domenice, Sorahia;
- Martin, Regina M;
- de Carvalho, Luciane Carneiro;
- Pelaes, Tatiana;
- Inacio, Marlene;
- Codarin, Rodrigo Rocha;
- Sator de Faria, Maria Beatriz;
- Francisco, Rossana Pulcineli Vieira;
- Baracat, Edmund Chada;
- Serafini, Paulo César;
- Mendonca, Berenice B
Publication type:
journal article
P450c17 deficiency in Brazilian patients: biochemical diagnosis through progesterone levels confirmed by CYP17 genotyping.
Published in:
2003
By:
- Martin, Regina M.;
- Lin, Chin J.;
- Costa, Elaine M. F.;
- de Oliveira, Maria Leocadia;
- Carrilho, Alexandre;
- Villar, Heloisa;
- Longui, Carlos A.;
- Mendonca, Berenice B.
Publication type:
journal article
Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3027, doi. 10.1210/jc.2002-021780
By:
- MARTIN, REGINA M.;
- LIN, CHIN J.;
- NISHI, MIRIAN Y.;
- BILLERBECK, ANA ELISA C.;
- LATRONICO, ANA CLAUDIA;
- RUSSELL, DAVID W.;
- MENDONCA, BERENICE B.
Publication type:
Article
Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3027, doi. 10.1210/jc.2002-021780
By:
- MARTIN, REGINA M.;
- LIN, CHIN J.;
- NISHI, MIRIAN Y.;
- BILLERBECK, ANA ELISA C.;
- LATRONICO, ANA CLAUDIA;
- RUSSELL, DAVID W.;
- MENDONCA, BERENICE B.
Publication type:
Article
An Unusual Phenotype of Frasier Syndrome due to IVS9 +4C>T Mutation in the WT1 Gene: Predominantly Male Ambiguous Genitalia and Absence of Gonadal Dysgenesis.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 6, p. 2500, doi. 10.1210/jcem.87.6.8521
By:
- MELO, KARLA F. S.;
- MARTIN, REGINA M.;
- COSTA, ELAINE M. F.;
- CARVALHO, FILOMENA M.;
- JORGE, ALEXANDER A.;
- ARNHOLD, IVO J. P.;
- MENDONCA, BERENICE B.
Publication type:
Article
Origin of an Ovarian Steroid Cell Tumor Causing Isosexual Pseudoprecocious Puberty Demonstrated by the Expression of Adrenal Steroidogenic Enzymes and Adrenocorticotropin Receptor.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 3, p. 1211, doi. 10.1210/jcem.85.3.6454
By:
- LIN, CHIN J.;
- JORGE, ALEXANDER A. L.;
- LATRONICO, ANA CLAUDIA;
- MARUI, SUEMI;
- FRAGOSO, MARIA CANDIDA V.;
- MARTIN, REGINA M.;
- CARVALHO, FILOMENA M.;
- ARNHOLD, IVO J. P.;
- MENDONCA, BERENICE B.
Publication type:
Article
Comprehensive Genetic Analysis of 128 Candidate Genes in a Cohort With Idiopathic, Severe, or Familial Osteoporosis.
Published in:
Journal of the Endocrine Society, 2020, v. 4, n. 12, p. 1, doi. 10.1210/jendso/bvaa148
By:
- Rocha-Braz, Manuela G M;
- França, Monica M;
- Fernandes, Adriana M;
- Lerario, Antonio M;
- Zanardo, Evelin A;
- Santana, Lucas S de;
- Kulikowski, Leslie D;
- Martin, Regina M;
- Mendonca, Berenice B;
- Ferraz-de-Souza, Bruno
Publication type:
Article
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).
Published in:
European Journal of Endocrinology, 2016, v. 175, n. 2, p. K7, doi. 10.1530/EJE-15-0149
By:
- Madeira, João L. O.;
- Jorge, Alexander A. L.;
- Martin, Regina M.;
- Montenegro, Luciana R.;
- Franca, Marcela M.;
- Costalonga, Everlayny F.;
- Correa, Fernanda A.;
- Otto, Aline P.;
- Arnhold, Ivo J. P.;
- Freitas, Helayne S.;
- Machado, Ubiratan F.;
- Mendonca, Berenice B.;
- Carvalho, Luciani R.
Publication type:
Article
Resources for the practice of pediatric neuro-oncology in Mexico: a cross-sectional evaluation.
Published in:
Frontiers in Oncology, 2024, p. 01, doi. 10.3389/fonc.2024.1330705
By:
- Arce-Cabrera, Daniela;
- Escamilla-Asiain, Gabriela;
- Nájera-Castillo, Melisa F.;
- Navarro-Martín Del Campo, Regina M.;
- Ortiz-Azpilcueta, Mariana;
- Pantoja-Guillén, Francisco J.;
- González, Farina E. Arreguín;
- Zapata-Sosa, Imelda;
- Lugo-Juárez, Jocelyn Z.;
- Cortéz, Daniel Santillán;
- Madrid, Andrés Morales-La;
- Moreira, Daniel C.;
- Benito-Reséndiz, Alma E.
Publication type:
Article
Transcriptomic Response to 1,25-Dihydroxyvitamin D in Human Fibroblasts with or without a Functional Vitamin D Receptor (VDR): Novel Target Genes and Insights into VDR Basal Transcriptional Activity.
Published in:
Cells (2073-4409), 2019, v. 8, n. 4, p. 318, doi. 10.3390/cells8040318
By:
- Costa, Pedro L. F.;
- França, Monica M.;
- Katayama, Maria L.;
- Carneiro, Eduardo T.;
- Martin, Regina M.;
- Folgueira, Maria A. K.;
- Latronico, Ana C.;
- Ferraz-de-Souza, Bruno
Publication type:
Article
Assessment of the role of transcript for GATA-4 as a marker of unfavorable outcome in human adrenocortical neoplasms.
Published in:
BMC Endocrine Disorders, 2004, v. 4, p. 3, doi. 10.1186/1472-6823-4-3
By:
- Barbosa, Angela S.;
- Giacaglia, Luciano R.;
- Martin, Regina M.;
- Mendonca, Berenice B.;
- Lin, Chin J.
Publication type:
Article
Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 21, p. 2529, doi. 10.1093/hmg/ddm145
By:
- Demura, Masashi;
- Martin, Regina M.;
- Shozu, Makio;
- Sebastian, Siby;
- Takayama, Kazuto;
- Hsu, Wei-Tong;
- Schultz, Roger A.;
- Neely, Kirk;
- Bryant, Michael;
- Mendonca, Berenice B.;
- Hanaki, Keiichi;
- Kanzaki, Susumu;
- Rhoads, David B.;
- Misra, Madhusmita;
- Bulun, Serdar E.
Publication type:
Article
Nephrocalcinosis and kidney function in children and adults with X-linked hypophosphatemia: baseline results from a large longitudinal study.
Published in:
Journal of Bone & Mineral Research, 2024, v. 39, n. 10, p. 1493, doi. 10.1093/jbmr/zjae127
By:
- Portale, Anthony A;
- Ward, Leanne;
- Dahir, Kathryn;
- Florenzano, Pablo;
- Ing, Steven W;
- Jan de Beur, Suzanne M;
- Martin, Regina M;
- Meza-Martinez, Adriana I;
- Paloian, Neil;
- Ashraf, Ambika;
- Dixon, Bradley P;
- Khan, Aliya;
- Langman, Craig;
- Chen, Angel;
- Wang, Christine;
- Roberts, Mary Scott;
- Tandon, P K;
- Bedrosian, Camille;
- Imel, Erik A
Publication type:
Article

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