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Results of search for 'au:"Mendonca, B B"', page 4 of 7
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Authors
Arnhold, I J
Arnhold, I J P
Bachega, T A
Batista, M C
Billerbeck, A E
Bloise, W
Brito, V N
Costa, E M
Domenice, S
Fragoso, M C
Latronico, A C
Lucon, A M
Madureira, G
Marcondes, J A
Mendonca, B B
Mendonça, B B
Nicolau, W
Wajchenberg, B L
Wilson, J D
de Mendonça, B B
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Topics
Adolescent
Adrenal Hyperplasia, Congenital
Adrenocorticotropic Hormone
Adult
Child
Child, Preschool
Disorders of Sex Development
Female
Humans
Male
Middle Aged
Mutation
Polymerase Chain Reaction
Puberty, Precocious
Testosterone
blood
deficiency
diagnosis
genetics
metabolism
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Your search returned 139 results.
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61.
Normal expression of the serologically defined H-Y antigen in Leydig cell hypoplasia.
[electronic resource]
by
Arnhold, I J
Mendonça, B B
Bisi, H
Russo, F O
Nicolau, W
Bloise, W
Moreira-Filho, C A
Producer:
19890106
In:
The Journal of urology
vol. 140
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62.
Women with steroid 5 alpha-reductase 2 deficiency have normal concentrations of plasma 5 alpha-dihydroprogesterone during the luteal phase.
[electronic resource]
by
Milewich, L
Mendonca, B B
Arnhold, I
Wallace, A M
Donaldson, M D
Wilson, J D
Russell, D W
Producer:
19951228
In:
The Journal of clinical endocrinology and metabolism
vol. 80
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63.
Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects.
[electronic resource]
by
Kwok, C
Tyler-Smith, C
Mendonca, B B
Hughes, I
Berkovitz, G D
Goodfellow, P N
Hawkins, J R
Producer:
19961203
In:
Journal of medical genetics
vol. 33
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64.
Ectopic adrenocorticotropic hormone syndrome.
[electronic resource]
by
Wajchenberg, B L
Mendonca, B B
Liberman, B
Pereira, M A
Carneiro, P C
Wakamatsu, A
Kirschner, M A
Producer:
19950511
In:
Endocrine reviews
vol. 15
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65.
Mutations in the type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls.
[electronic resource]
by
Marui, S
Castro, M
Latronico, A C
Elias, L L
Arnhold, I J
Moreira, A C
Mendonca, B B
Producer:
20000421
In:
Clinical endocrinology
vol. 52
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66.
Natural mutagenesis study of the human steroid 5 alpha-reductase 2 isozyme.
[electronic resource]
by
Wigley, W C
Prihoda, J S
Mowszowicz, I
Mendonca, B B
New, M I
Wilson, J D
Russell, D W
Producer:
19940328
In:
Biochemistry
vol. 33
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67.
Calcium-dependent protein kinase-C activity in human adrenocortical neoplasms, hyperplastic adrenals, and normal adrenocortical tissue.
[electronic resource]
by
Latronico, A C
Mendonça, B B
Bianco, A C
Villares, S M
Lucon, M A
Nicolau, W
Wajchenberg, B L
Producer:
19941006
In:
The Journal of clinical endocrinology and metabolism
vol. 79
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68.
[Macrosomia, macrocrania and motor disorders in childhood, Sotos syndrome (McKusick 11755): report of 7 cases and review of clinical aspects of 198 reported cases].
[electronic resource]
by
Moretti-Ferreira, D
Koiffmann, C P
Wajntal, A
Diament, A J
De Mendonça, B B
Mattieli, J
Saldanha, P H
Producer:
19920527
In:
Arquivos de neuro-psiquiatria
vol. 49
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69.
Zinc: an inhibitor of prolactin (PRL) secretion in humans.
[electronic resource]
by
Brandão Néto, J
de Mendonça, B B
Shuhama, T
Marchini, J S
Madureira, G
Pimenta, W P
Tornero, M T
Producer:
19890901
In:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
vol. 21
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70.
Adrenal nodules in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: regression after adequate hormonal control.
[electronic resource]
by
Giacaglia, L R
Mendonca, B B
Madureira, G
Melo, K F
Suslik, C A
Arnhold, I J
Bachega, T A
Producer:
20010906
In:
Journal of pediatric endocrinology & metabolism : JPEM
vol. 14
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71.
GAPO syndrome (McKusick 23074)--a connective tissue disorder: report on two affected sibs and on the pathologic findings in the older.
[electronic resource]
by
Wajntal, A
Koiffmann, C P
Mendonça, B B
Epps-Quaglia, D
Sotto, M N
Rati, P B
Opitz, J M
Producer:
19910110
In:
American journal of medical genetics
vol. 37
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72.
A virilizing Leydig cell tumor of the ovary associated with stromal hyperplasia under gonadotropin control.
[electronic resource]
by
Marcondes, J A
Nery, M
Mendonça, B B
Hayashida, S A
Halbe, H W
Carvalho, F M
Wajchenberg, B L
Producer:
19980409
In:
Journal of endocrinological investigation
vol. 20
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73.
Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions.
[electronic resource]
by
Arnhold, I J
Oliveira, S B
Osorio, M G
Carrilho, A J
Nicolau, W
Bianco, A C
Mendonca, B B
Producer:
20000915
In:
Journal of endocrinological investigation
vol. 23
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74.
High frequency of novel germline mutations in the VHL gene in the heterogeneous population of Brazil.
[electronic resource]
by
Rocha, J C C
Silva, R L A
Mendonça, B B
Marui, S
Simpson, A J G
Camargo, A A
Producer:
20030318
In:
Journal of medical genetics
vol. 40
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75.
Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients.
[electronic resource]
by
Domenice, S
Corrêa, R V
Costa, E M F
Nishi, M Y
Vilain, E
Arnhold, I J P
Mendonca, B B
Producer:
20040719
In:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas
vol. 37
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76.
Male pseudohermaphroditism due to nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency: gender role change and absence of gynecomastia at puberty.
[electronic resource]
by
Mendonca, B B
Bloise, W
Arnhold, I J
Batista, M C
Toledo, S P
Drummond, M C
Nicolau, W
Mattar, E
Producer:
19880220
In:
Journal of steroid biochemistry
vol. 28
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77.
A study of patients with Nelson's syndrome.
[electronic resource]
by
Pereira, M A
Halpern, A
Salgado, L R
Mendonça, B B
Nery, M
Liberman, B
Streeten, D H
Wajchenberg, B L
Producer:
19990111
In:
Clinical endocrinology
vol. 49
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78.
Prepubertal male pseudohermaphroditism due to 17-ketosteroid reductase deficiency: diagnostic value of a hCG test and lack of HLA association.
[electronic resource]
by
Arnhold, I J
Mendonça, B B
Diaz, J A
Nogueira, C
Batista, M C
Madureira, G
Oliveira, D
Nicolau, W
Bloise, W
Producer:
19881003
In:
Journal of endocrinological investigation
vol. 11
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79.
Protocol for rapid fetal sex determination in chorionic villus through polimerase chain reaction.
[electronic resource]
by
Domenice, S
Billerbeck, A E
Rocha, R O
Nishi, M Y
Medeiros, M A
Bachega, T A
Budunki, V
Mendonca, B B
Producer:
19981027
In:
Revista do Hospital das Clinicas
vol. 53
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80.
No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failure.
[electronic resource]
by
da Fonte Kohek, M B
Batista, M C
Russell, A J
Vass, K
Giacaglia, L R
Mendonca, B B
Latronico, A C
Producer:
19981009
In:
Fertility and sterility
vol. 70
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