Berenice Mendonca

Papers authored by Berenice Mendonca

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2011 Thatiana Evilen da Silva, Mirian Yumie Nishi, Elaine Maria Frade Costa, Regina Matsunaga Martin, Filomena Marino Carvalho, Berenice Bilharinho Mendonca

, Sorahia Domenice

A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys–Drash syndrome

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Daiane Beneduzzi, Anita K. Iyer, Ericka Barbosa Trarbach, Acacio P. Silveira-Neto, Letícia G. Silveira, Leticia Fg Silveira, Cintia Tusset, Kathleen Yip, Berenice B. Mendonça

, Pamela L. Mellon, Ana Claudia Latronico

Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism

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Ef F. Costalonga, Srr R. R. Antonini, G. Guerra-Junior, Rrd R. D. Coletta, Mm M. Franca, Af F. Braz, Bb B. Mendonca

, Ijp J. P. Arnhold, Aal A. L. Jorge

Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and −202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiency

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Lima,Lorena de Oliveira, Brito,Luciana Pinto, Almeida,Madson Queiroz, Fragoso,Maria Candida Barrison Villares, Lorena de Oliveira Lima, Antonio Marcondes Lerario, Guilherme Asmar Alencar, Lerario,Antonio Marcondes, Alencar,Guilherme Asmar, Luciana Pinto Brito, Madson Queiroz Almeida, Sorahia Domenice, Domenice,Sorahia, Latronico,Ana Claudia, Ana Claudia Latronico and 3 other authors

Clinical and molecular aspects of a pediatric metachronous adrenocortical tumor

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Mirian Yumie Nishi, Elaine Maria Frade Costa, Suely Beirão Oliveira, Berenice Bilharinho Mendonca

, Sorahia Domenice

The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants

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Marlene Inacio, Maria Helena P. Sircili, Vinicius N. Brito, Sorahia Domenice, Ari Alves Oliveira-Junior, Ivo J. P. Arnhold, Francisco D. Tibor, Elaine M. F. Costa, Berenice B. Mendonca

46,XY DSD due to 17β-HSD3 Deficiency and 5α-Reductase Type 2 Deficiency

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Ricardo Pp P. Moreira, Alexander Al L. Jorge

, Larissa G. Gomes, Laura C. Kaupert, João Massud Filho, João Massud Filho, Berenice B. Mendonca

, Tânia A. S. S. Bachega

Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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Ricardo Pp P. Moreira, Alexander Al L. Jorge

, Berenice B. Mendonca

, Tânia A. S. S. Bachega

Frequency of genetic polymorphisms of PXR gene in the Brazilian population

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Ivo J. P. Arnhold, Karla Melo

, Marlene Inacio, Elaine M. F. Costa, Sorahia Domenice, Debora Danilovic

, Berenice B. Mendonca

46,XY Disorders of Sex Development (46,XY DSD) due to Androgen Receptor Defects: Androgen Insensitivity Syndrome

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Maíra Pontual Brandão, Elaine Maria Frade Costa, Maki Fukami, Mariza Gerdulo, Natalia P. Pereira, Sorahia Domenice, Tsutomu Ogata, Berenice B. Mendonca

MAMLD1 (Mastermind-Like Domain Containing 1) Homozygous Gain-of-Function Missense Mutation Causing 46,XX Disorder of Sex Development in a Virilized Female

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2010 Marcela M. França, Alexander A. L. Jorge, Luciani R. S. Carvalho, Everlayny F. Costalonga, Gabriela A. Vasques, Claudia C. Leite, Berenice B. Mendonca

, Ivo J. P. Arnhold

Novel Heterozygous Nonsense GLI2 Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly

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Reis,Mariana Tenorio Antunes, Corrêa,Pedro Henrique Silveira, Mariana Tenorio Antunes Reis, Andreina Cattani, Cattani,Andreina, Mendonca,Berenice Bilharinho, Berenice Bilharinho Mendonca

, Pedro Henrique Silveira Corrêa, Regina Matsunaga Martin, Martin,Regina Matsunaga

A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levels

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Luciana Pinto Brito, Antonio Marcondes Lerário, Marcello Delano Bronstein, Iberê Cauduro Soares, Berenice Bilharinho Mendonca

, Maria Candida Barisson Villares Fragoso

Influence of the Fibroblast Growth Factor Receptor 4 Expression and the G388R Functional Polymorphism on Cushing’s Disease Outcome

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Vinicius Nahime Brito, Karina Berger, Berenice Bilharinho Mendonca

Male hypogonadism: childhood diagnosis and future therapies

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Mariana Fa A. Funari, Alexander Al L. Jorge

, Silvia Cal A. L. Souza, Ana Ec C. Billerbeck, Ivo Jp P. Arnhold, Berenice B. Mendonca

, Mirian Y. Nishi

Usefulness of MLPA in the detection of SHOX deletions

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Maria Helena Palma Sircili, Frederico Arnaldo de Queiroz e. Silva, Elaine M. F. Costa, Vinicius N. Brito, Ivo J. P. Arnhold, Francisco Tibor Dénes, Marlene Inacio, Berenice Bilharinho de Mendonca

Long-Term Surgical Outcome of Masculinizing Genitoplasty in Large Cohort of Patients With Disorders of Sex Development

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Silvana M. Lovisolo, Berenice B. Mendonça

, Emilia M. Pinto

, Thais Della Manna, Paulo Hilário N. Saldiva, Maria Cláudia N. Zerbini

Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells

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Milena G. Teles, Ericka Barbosa Trarbach, Sekoni D. Noel, G. Guerra-Junior, Alexander Jorge

, Daiane Beneduzzi, Suzy Drumond Bianco, Abir Mukherjee, Maria Tereza Baptista, Elaine M. Costa, M. De Castro, B. B. Mendonca

, U. B. Kaiser, A. C. Latronico, Others

A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism

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Berenice B. Mendonca

, Elaine M. F. Costa, Alicia Belgorosky, Marco Aurelio Rivarola, Sorahia Domenice

46,XY DSD due to impaired androgen production

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Madson Q. Almeida, Ibere Cauduro Soares, Tamaya C. Ribeiro, Maria Candida Bv V. Fragoso, Lidiane V. Marins, Alda Wakamatsu, Rodrigo A. Ressio, Mirian Y. Nishi, Alexander Al L. Jorge

, Antonio M. Lerario, Venancio A. F. Alves

, Berenice B. Mendonca

, Ana Claudia Latronico, Others

Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults

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Papers authored by Berenice Mendonca