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au.\*:("MENDONCA, Berenice B")

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The laparoscopic management of intersex patients : the preferred approachDENES, Francisco T; COCUZZA, Marcelo A. S; SCHNEIDER-MONTEIRO, Edison D et al.BJU international (Papier). 2005, Vol 95, Num 6, pp 863-867, issn 1464-4096, 5 p.Article

Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR geneMENDONCA, Berenice B; LEITE, Maristela V; DE CASTRO, Margaret et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 4, pp 1805-1809, issn 0021-972XArticle

Potential Effects of Alendronate on Fibroblast Growth Factor 23 Levels and Effective Control of Hypercalciuria in an Adult with Jansen's Metaphyseal ChondrodysplasiaONUCHIC, Laura; FERRAZ-DE-SOUZA, Bruno; MENDONCA, Berenice B et al.The Journal of clinical endocrinology and metabolism. 2012, Vol 97, Num 4, pp 1098-1103, issn 0021-972X, 6 p.Article

The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase DeficiencyGOMES, Larissa G; NINGWU HUANG; AGRAWAL, Vishal et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 7, pp 2913-2916, issn 0021-972X, 4 p.Article

The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH analogue therapy not restored by dihydrotestosterone administrationJORGE, Alexander A. L; SOUZA, Silvia C. A. L; ARNHOLD, Ivo J. P et al.Clinical endocrinology (Oxford. Print). 2004, Vol 60, Num 1, pp 36-40, issn 0300-0664, 5 p.Article

Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH reception gene. EditorialJORGE, Alexander A; SOUZA, Silvia C; ARNHOLD, Ivo J et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 2, pp 466-472, issn 0021-972XArticle

Absence of mutations involving the lim homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis : Hormones and reproductive healthOTTOLENGHI, Chris; MOREIRA-FILHO, Carlos; MENDONCA, Berenice B et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 6, pp 2465-2469, issn 0021-972XArticle

Genotyping of the type II 3β-hydroxysteroid dehydrogenase gene (HSD3B2) in women with hirsutism and elevated ACTH-stimulated Δ5-steroidsMARUI, Suemi; RUSSELL, Alan J; PAULA, Francisco J. A et al.Fertility and sterility. 2000, Vol 74, Num 3, pp 553-557, issn 0015-0282Article

Extraadrenal 21-Hydroxylation by CYP2C19 and CYP3A4 : Effect on 21-Hydroxylase DeficiencyGOMES, Larissa G; NINGWU HUANG; AGRAWAL, Vishal et al.The Journal of clinical endocrinology and metabolism. 2009, Vol 94, Num 1, pp 89-95, issn 0021-972X, 7 p.Article

PTPN11 (protein tyrosine phosphatase, nonreceptor type 11) mutations and response to growth hormone therapy in children with Noonan syndromeFERREIRA, Lize V; SOUZA, Silvia A. L; ARNHOLD, Ivo J. P et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 9, pp 5156-5160, issn 0021-972X, 5 p.Article

Surgery for adrenal tumours with thrombus in the supra-diaphragmatic infra-atrial inferior vena cava, with no cardiopulmonary bypassLUCON, Antonio M; MACHADO, Marcel C. C; PEREIRA, Maria A. A et al.BJU international (Papier). 2004, Vol 94, Num 1, pp 70-73, issn 1464-4096, 4 p.Article

Detection of Y-specific sequences in 122 patients with Turner syndrome: Nested PCR is not a reliable methodNISHI, Mirian Y; DOMENICE, Sorahia; MEDEIROS, Maria Aparecida et al.American journal of medical genetics. 2002, Vol 107, Num 4, pp 299-305, issn 0148-7299Article

Combined expression of BUB1B, DLGAP5, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patientsFRAGOSO, Maria Candida B. V; QUEIROZ ALMEIDA, Madson; LUCON, Antonio M et al.European journal of endocrinology. 2012, Vol 166, Num 1, pp 61-67, issn 0804-4643, 7 p.Article

Exon 3-deleted genotype of growth hormone receptor (GHRd3) positively influences IGF 1 increase at generation test in children with idiopathic short statureTOYOSHIMA, Marcos T. K; CASTRONEVES, Luciana A; COSTALONGA, Everlayny F et al.Clinical endocrinology (Oxford. Print). 2007, Vol 67, Num 4, pp 500-504, issn 0300-0664, 5 p.Article

A meiotic recombination in a new isolated familial somatotropinoma kindredLUCCIO-CAMELO, Douglas C; UNE, Karina N; GADELHA, Monica R et al.European journal of endocrinology. 2004, Vol 150, Num 5, pp 643-648, issn 0804-4643, 6 p.Article

Expression of Insulin-Like Growth Factor-II and Its Receptor in Pediatric and Adult Adrenocortical TumorsALMEIDA, Madson Q; BARISSON VILLARES FRAGOSO, Maria Candida; MENDONCA, Berenice B et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 9, pp 3524-3531, issn 0021-972X, 8 p.Article

Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndromeFLÜCK, Christa E; TAJIMA, Toshihro; PANDEY, Amit V et al.Nature genetics. 2004, Vol 36, Num 3, pp 228-230, issn 1061-4036, 3 p.Article

Growth Standards of Patients With Noonan and Noonan-Like Syndromes With Mutations in the RAS/MAPK PathwayMALAQUIAS, Alexsandra C; BRASIL, Amanda S; PEREIRA, Alexandre C et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 11, pp 2700-2706, issn 1552-4825, 7 p.Article

Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing DeficiencyTRARBACH, Ericka B; ABREU, Ana Paula; LATRONICO, Ana Claudia et al.The Journal of clinical endocrinology and metabolism. 2010, Vol 95, Num 7, pp 3491-3496, issn 0021-972X, 6 p.Article

Novel Mutations in CYP11B1 Gene Leading to 11β-Hydroxylase Deficiency in Brazilian PatientsSOARDI, Fernanda C; PENACHIONI, Junia Y; JUSTO, Giselle Z et al.The Journal of clinical endocrinology and metabolism. 2009, Vol 94, Num 9, pp 3481-3485, issn 0021-972X, 5 p.Article

Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patientsFERREIRA, Lize V; SOUZA, Silvia C. A. L; MONTENEGRO, Luciana R et al.Clinical endocrinology (Oxford. Print). 2008, Vol 69, Num 3, pp 426-431, issn 0300-0664, 6 p.Article

The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor geneROCHA, Rosana O; BILLERBECK, Ana Elisa C; PINTO, Emilia M et al.Clinical endocrinology (Oxford. Print). 2008, Vol 68, Num 2, pp 226-232, issn 0300-0664, 7 p.Article

Microconversion between CYP21A2 and CYP21A1P promoter regions causes the nonclassical form of 21-hydroxylase deficiencyARAUJO, Rogério S; MENDONCA, Berenice B; BARBOSA, Angela S et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 10, pp 4028-4034, issn 0021-972X, 7 p.Article

Familial hyperestrogenism in both sexes: Clinical, hormonal, and molecular studies of two siblingsMARTIN, Regina M; LIN, Chin J; NISHI, Mirian Y et al.The Journal of clinical endocrinology and metabolism. 2003, Vol 88, Num 7, pp 3027-3034, issn 0021-972X, 8 p.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 : The impact of the human genome on endocrinology: Special featuresMELO, Karla F. S; MARTIN, Regina M; COSTA, Elaine M. F et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 6, pp 2500-2505, issn 0021-972XArticle

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