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Results: 1-24 |
Results: 24
Adrenal nodules in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Regression after adequate hormonal control
Authors: Giacaglia, LR Mendonca, BB Madureira, G Melo, KFF Suslik, CA Arnhold, IJP Bachega, TASS
Citation: Lr. Giacaglia et al., Adrenal nodules in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Regression after adequate hormonal control, J PED END M, 14(4), 2001, pp. 415-419
Premature thelarche in girls after growth hormone therapy
Authors: Carvalho, LRS Mimura, LY Arnhold, IJP Mendonca, BB
Citation: Lrs. Carvalho et al., Premature thelarche in girls after growth hormone therapy, J PEDIAT, 138(3), 2001, pp. 448-448
Adrenocorticotropin-dependent precocious puberty of testicular origin in aboy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 gene
Authors: Domenice, S Latronico, AC Brito, VN Arnhold, IJP Kok, F Mendonca, BB
Citation: S. Domenice et al., Adrenocorticotropin-dependent precocious puberty of testicular origin in aboy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 gene, J CLIN END, 86(9), 2001, pp. 4068-4071
Two novel mutations in the gonadotropin-releasing hormone receptor gene inBrazilian patients with hypogonadotropic hypogonadism and normal olfaction
Authors: Costa, EMF Bedecarrats, GY Mendonca, BB Arnhold, IJP Kaiser, UB Latronico, AC
Citation: Emf. Costa et al., Two novel mutations in the gonadotropin-releasing hormone receptor gene inBrazilian patients with hypogonadotropic hypogonadism and normal olfaction, J CLIN END, 86(6), 2001, pp. 2680-2686
Phenotypic variability and origins of mutations in the gene encoding 3 beta-hydroxysteroid dehydrogenase type II
Authors: McCartin, S Russell, AJ Fisher, RA Wallace, AM Arnhold, IJP Mason, JI Varley, J Mendonca, BB Sutcliffe, RG
Citation: S. Mccartin et al., Phenotypic variability and origins of mutations in the gene encoding 3 beta-hydroxysteroid dehydrogenase type II, J MOL ENDOC, 24(1), 2000, pp. 75-82
Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions
Authors: Arnhold, IJP Oliveira, SB Osorio, MGF Carrilho, AJF Nicolau, W Bianco, AC Mendonca, BB
Citation: Ijp. Arnhold et al., Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions, J ENDOC INV, 23(4), 2000, pp. 258-262
The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes
Authors: Latronico, AC Lins, TSS Brito, VN Arnhold, IJP Mendonca, BB
Citation: Ac. Latronico et al., The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes, CLIN ENDOCR, 53(5), 2000, pp. 609-613
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Authors: Bachega, TASS Billerbeck, AEC Marcondes, JAM Madureira, G Arnhold, IJP Mendonca, BB
Citation: Tass. Bachega et al., Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency, CLIN ENDOCR, 52(5), 2000, pp. 601-607
Mutations in the type II 3 beta-hydroxysteroid dehydrogenase (HSD3B2) genecan cause premature pubarche in girls
Authors: Marui, S Castro, M Latronico, AC Elias, LLK Arnhold, IJP Moreira, AC Mendonca, BB
Citation: S. Marui et al., Mutations in the type II 3 beta-hydroxysteroid dehydrogenase (HSD3B2) genecan cause premature pubarche in girls, CLIN ENDOCR, 52(1), 2000, pp. 67-75
21-hydroxylase deficiency in Brazil
Authors: Bachega, TASS Billerbeck, AEC Madureira, G Marcondes, JAM Longui, CA Leite, MV Arnhold, IJP Mendonca, BB
Citation: Tass. Bachega et al., 21-hydroxylase deficiency in Brazil, BRAZ J MED, 33(10), 2000, pp. 1211-1216
Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase 3 deficiency - Diagnosis, psychological evaluation, and management
Authors: Mendonca, BB Inacio, M Arnhold, IJP Costa, EMF Bloise, W Martin, RM Denes, FT Silva, FAQ Andersson, S Lindqvist, A Wilson, JD
Citation: Bb. Mendonca et al., Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase 3 deficiency - Diagnosis, psychological evaluation, and management, MEDICINE, 79(5), 2000, pp. 299-309
Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1
Authors: Osorio, MGF Kopp, P Mauri, S Latronico, AC Mendonca, BB Arnhold, IJP
Citation: Mgf. Osorio et al., Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1, J CLIN END, 85(8), 2000, pp. 2779-2785
Origin of an ovarian steroid cell tumor causing isosexual pseudoprecociouspuberty demonstrated by the expression of adrenal steroidogenic enzymes and adrenocorticotropin receptor
Authors: Lin, CJ Jorge, AAL Latronico, AC Marui, S Fragoso, MCV Martin, RM Carvalho, FM Arnhold, IJP Mendonca, BB
Citation: Cj. Lin et al., Origin of an ovarian steroid cell tumor causing isosexual pseudoprecociouspuberty demonstrated by the expression of adrenal steroidogenic enzymes and adrenocorticotropin receptor, J CLIN END, 85(3), 2000, pp. 1211-1214
Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: A novel constitutively activating mutation in the first transmembrane helix
Authors: Latronico, AC Shinozaki, H Guerra, G Pereira, MAA Marini, SHVL Baptista, MTM Arnhold, IJP Fanelli, F Mendonca, BB Segaloff, DL
Citation: Ac. Latronico et al., Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: A novel constitutively activating mutation in the first transmembrane helix, J CLIN END, 85(12), 2000, pp. 4799-4805
Insulin-like growth factor-I treatment in two children with growth hormonegene deletions
Authors: Arnhold, IJP Oliveira, SB Osorio, MGF Mendonca, BR
Citation: Ijp. Arnhold et al., Insulin-like growth factor-I treatment in two children with growth hormonegene deletions, J PED END M, 12(4), 1999, pp. 499-506
Clinical features of women with resistance to luteinizing hormone
Authors: Arnhold, IJP Latronico, AC Batista, MC Izzo, CR Mendonca, BB
Citation: Ijp. Arnhold et al., Clinical features of women with resistance to luteinizing hormone, CLIN ENDOCR, 51(6), 1999, pp. 701-707
A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency
Authors: Billerbeck, AEC Bachega, TASS Frazzatto, ET Nishi, MY Goldberg, AC Marin, MLC Madureira, G Monte, O Arnhold, IJP Mendonca, BB
Citation: Aec. Billerbeck et al., A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency, J CLIN END, 84(8), 1999, pp. 2870-2872
Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene
Authors: Mendonca, BB Osorio, MGF Latronico, AC Estefan, V Lo, LSS Arnhold, IJP
Citation: Bb. Mendonca et al., Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene, J CLIN END, 84(3), 1999, pp. 942-945
17 beta-hydroxysteroid dehydrogenase 3 deficiency in women
Authors: Mendonca, BB Arnhold, IJP Bloise, W Andersson, S Russell, DW Wilson, JD
Citation: Bb. Mendonca et al., 17 beta-hydroxysteroid dehydrogenase 3 deficiency in women, J CLIN END, 84(2), 1999, pp. 802-804
Diagnostic value of fluorometric assays in the evaluation of precocious puberty
Authors: Brito, VN Batista, MC Borges, MF Latronico, AC Kohek, MBF Thirone, ACP Jorge, BH Arnhold, IJP Mendonca, BB
Citation: Vn. Brito et al., Diagnostic value of fluorometric assays in the evaluation of precocious puberty, J CLIN END, 84(10), 1999, pp. 3539-3544
Menstrual disorders and infertility caused by inactivating mutations of the luteinizing hormone receptor gene
Authors: Arnhold, IJP Latronico, AC Batista, MC Mendonca, BB
Citation: Ijp. Arnhold et al., Menstrual disorders and infertility caused by inactivating mutations of the luteinizing hormone receptor gene, FERT STERIL, 71(4), 1999, pp. 597-601
Treatment of gonadotropin dependent precocious puberty due to hypothalamichamartoma with gonadotropin releasing hormone agonist depot
Authors: de Brito, VN Latronico, AC Arnhold, IJP Lo, LSS Domenice, S Albano, MCC Fragoso, MCBV Mendonca, BB
Citation: Vn. De Brito et al., Treatment of gonadotropin dependent precocious puberty due to hypothalamichamartoma with gonadotropin releasing hormone agonist depot, ARCH DIS CH, 80(3), 1999, pp. 231-234
Low frequency of CYP21B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Authors: Bachega, TASS Billerbeck, AEC Madureira, G Arnhold, IJP Medeiros, MA Marcondes, JAM Longui, CA Nicolau, W Bloise, W Mendonca, BB
Citation: Tass. Bachega et al., Low frequency of CYP21B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency, HUMAN HERED, 49(1), 1999, pp. 9-14
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency
Authors: Bachega, TASS Billerbeck, EC Madureira, G Marcondes, JAM Longui, CA Leite, MV Arnhold, IJP Mendonca, BB
Citation: Tass. Bachega et al., Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency, J CLIN END, 83(12), 1998, pp. 4416-4419
Risultati: 1-24 |