Challenges in treating children with optic pathway gliomas: an 18-year experience from a middle-income country
Ramírez-Melo, Jorge Luis, Moreira, Daniel C, Orozco-Alvarado, Ana Luisa, Sánchez-Zubieta, Fernando, Navarro-Martín Del Campo, Regina M
Published in Frontiers in oncology (13.02.2024)
Published in Frontiers in oncology (13.02.2024)
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Resources for the practice of pediatric neuro-oncology in Mexico: a cross-sectional evaluation
Arce-Cabrera, Daniela, Escamilla-Asiain, Gabriela, Nájera-Castillo, Melisa F., Navarro-Martín del Campo, Regina M., Ortiz-Azpilcueta, Mariana, Pantoja-Guillén, Francisco J., Arreguín González, Farina E., Zapata-Sosa, Imelda, Lugo-Juárez, Jocelyn Z., Santillán Cortéz, Daniel, Morales-La Madrid, Andrés, Moreira, Daniel C., Benito-Reséndiz, Alma E.
Published in Frontiers in oncology (21.06.2024)
Published in Frontiers in oncology (21.06.2024)
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Journal 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
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
Published in Cells (Basel, Switzerland) (05.04.2019)
Published in Cells (Basel, Switzerland) (05.04.2019)
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Journal Article
Symptomatic intracranial hypertension and prolonged hypocalcemia following treatment of Paget’s disease of the skull with zoledronic acid
Ferraz-de-Souza, Bruno, Martin, Regina M., Correa, Pedro Henrique S.
Published in Journal of bone and mineral metabolism (01.05.2013)
Published in Journal of bone and mineral metabolism (01.05.2013)
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Journal Article
46,XY disorder of sex development (DSD) due to 17β-hydroxysteroid dehydrogenase type 3 deficiency
Mendonca, Berenice B., Gomes, Nathalia Lisboa, Costa, Elaine M.F., Inacio, Marlene, Martin, Regina M., Nishi, Mirian Y., Carvalho, Filomena Marino, Tibor, Francisco Denes, Domenice, Sorahia
Published in The Journal of steroid biochemistry and molecular biology (01.01.2017)
Published in The Journal of steroid biochemistry and molecular biology (01.01.2017)
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Journal Article
Nephrocalcinosis and kidney function in children and adults with X-linked hypophosphatemia: baseline results from a large longitudinal study
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
Published in Journal of bone and mineral research (16.08.2024)
Published in Journal of bone and mineral research (16.08.2024)
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Journal Article
Successful Live Birth in a Woman With 17α-Hydroxylase Deficiency Through IVF Frozen-Thawed Embryo Transfer
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
Published in The journal of clinical endocrinology and metabolism (01.02.2016)
Published in The journal of clinical endocrinology and metabolism (01.02.2016)
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Journal Article
Potential Effects of Alendronate on Fibroblast Growth Factor 23 Levels and Effective Control of Hypercalciuria in an Adult with Jansen's Metaphyseal Chondrodysplasia
Onuchic, Laura, Ferraz-de-Souza, Bruno, Mendonca, Berenice B, Correa, Pedro Henrique S, Martin, Regina M
Published in The journal of clinical endocrinology and metabolism (01.04.2012)
Published in The journal of clinical endocrinology and metabolism (01.04.2012)
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Journal Article
Comprehensive Genetic Analysis of 128 Candidate Genes in a Cohort With Idiopathic, Severe, or Familial Osteoporosis
Rocha-Braz, Manuela G M, França, Monica M, Fernandes, Adriana M, Lerario, Antonio M, Zanardo, Evelin A, de Santana, Lucas S, Kulikowski, Leslie D, Martin, Regina M, Mendonca, Berenice B, Ferraz-de-Souza, Bruno
Published in Journal of the Endocrine Society (01.12.2020)
Published in Journal of the Endocrine Society (01.12.2020)
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Journal Article
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD)
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
Published in European journal of endocrinology (01.08.2016)
Published in European journal of endocrinology (01.08.2016)
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Journal Article
Bridging the Gap in Access to Care for Children With CNS Tumors Worldwide
Moreira, Daniel C, Rajagopal, Revathi, Navarro-Martin Del Campo, Regina M, Polanco, Ana C, Alcasabas, Ana Patricia, Arredondo-Navarro, Luis A, Campos, Danny, Casavilca-Zambrano, Sandro, Diaz Coronado, Rosdali Yesenia, Faizal, Nor, Ganesan, Dharmendra, Hamid, Syed Ahmer, Khan, Rafeah, Khu, Kathleen, Loh, Jasmin, Lukban, Marissa, Negreiros, Tatiana, Pineda, Estuardo, Yaqoob, Nausheen, Zia, Nida, Gajjar, Amar, Rodriguez-Galindo, Carlos, Qaddoumi, Ibrahim
Published in JCO global oncology (01.04.2020)
Published in JCO global oncology (01.04.2020)
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Journal Article
Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene
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.
Published in Human molecular genetics (01.11.2007)
Published in Human molecular genetics (01.11.2007)
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Journal Article
P450c17 Deficiency in Brazilian Patients: Biochemical Diagnosis through Progesterone Levels Confirmed by CYP17 Genotyping
Martin, Regina M, Lin, Chin J, Costa, Elaine M. F, de Oliveira, Maria Leocadia, Carrilho, Alexandre, Villar, Heloisa, Longui, Carlos A, Mendonca, Berenice B
Published in The journal of clinical endocrinology and metabolism (01.12.2003)
Published in The journal of clinical endocrinology and metabolism (01.12.2003)
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Journal 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
Melo, Karla F. S, Martin, Regina M, Costa, Elaine M. F, Carvalho, Filomena M, Jorge, Alexander A, Arnhold, Ivo J. P, Mendonca, Berenice B
Published in The journal of clinical endocrinology and metabolism (01.06.2002)
Published in The journal of clinical endocrinology and metabolism (01.06.2002)
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Journal Article
Origin of an Ovarian Steroid Cell Tumor Causing Isosexual Pseudoprecocious Puberty Demonstrated by the Expression of Adrenal Steroidogenic Enzymes and Adrenocorticotropin Receptor
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
Published in The journal of clinical endocrinology and metabolism (01.03.2000)
Published in The journal of clinical endocrinology and metabolism (01.03.2000)
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Journal Article
Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings
Martin, Regina M, Lin, Chin J, Nishi, Mirian Y, Billerbeck, Ana Elisa C, Latronico, Ana Claudia, Russell, David W, Mendonca, Berenice B
Published in The journal of clinical endocrinology and metabolism (01.07.2003)
Published in The journal of clinical endocrinology and metabolism (01.07.2003)
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Journal Article
46,XY disorder of sex development (DSD) due to 17ß-hydroxysteroid dehydrogenase type 3 deficiency
Mendonca, Berenice B, Gomes, Nathalia Lisboa, Costa, Elaine MF, Inacio, Marlene, Martin, Regina M, Nishi, Mirian Y, Carvalho, Filomena Marino, Tibor, Francisco Denes, Domenice, Sorahia
Published in The Journal of steroid biochemistry and molecular biology (01.01.2017)
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Published in The Journal of steroid biochemistry and molecular biology (01.01.2017)
Journal Article
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD)
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
Published in European journal of endocrinology (01.08.2016)
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Published in European journal of endocrinology (01.08.2016)
Journal Article