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Results of search for 'au:"Mendonca, B"', page 3 of 8
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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
Carvalho, F M
Domenice, S
Fragoso, M C
Latronico, A C
Liberman, B
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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Adolescent
Adrenal Hyperplasia, Congenital
Adrenocorticotropic Hormone
Adult
Child
Child, Preschool
Disorders of Sex Development
Female
Humans
Infant
Male
Middle Aged
Mutation
Polymerase Chain Reaction
Puberty, Precocious
blood
deficiency
diagnosis
genetics
metabolism
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41.
Pheochromocytoma: study of 50 cases.
[electronic resource]
by
Lucon, A M
Pereira, M A
Mendonça, B B
Halpern, A
Wajchenbeg, B L
Arap, S
Producer:
19970421
In:
The Journal of urology
vol. 157
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42.
Low-dose oral clonidine: effective growth hormone releasing agent in children but not in adolescents.
[electronic resource]
by
Batista, M C
Arnhold, I J
Mendonça, B B
D'Abronzo, F H
Bloise, W
Nicolau, W
Producer:
19871113
In:
The Journal of pediatrics
vol. 111
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43.
Identification of nonclassical 21-hydroxylase deficiency in girls with precocious pubarche.
[electronic resource]
by
Leite, M V
Mendonça, B B
Arnhold, I J
Estefan, V
Nunes, C
Nicolau, W
Bloise, W
Producer:
19910712
In:
Journal of endocrinological investigation
vol. 14
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44.
A novel homozygous nonsense mutations E135* in the type II 3beta-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia. Mutations in brief no. 168. Online.
[electronic resource]
by
Marui, S
Torrealba, I M
Russell, A J
Latronico, A C
Sutcliffe, R G
Mendonca, B B
Producer:
20000118
In:
Human mutation
vol. 12
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45.
Criteria for the cure of acromegaly: comparison between basal growth hormone and somatomedin C plasma concentrations in active and non-active acromegalic patients.
[electronic resource]
by
Giannella-Neto, D
Wajchenberg, B L
Mendonça, B B
Almeida, S F
Macchione, M
Spencer, E M
Producer:
19880609
In:
Journal of endocrinological investigation
vol. 11
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46.
Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene.
[electronic resource]
by
Mendonça, B B
Barbosa, A S
Arnhold, I J
McElreavey, K
Fellous, M
Moreira-Filho, C A
Producer:
19941129
In:
American journal of medical genetics
vol. 52
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47.
Growth hormone receptor messenger ribonucleic acid in normal and pathologic human adrenocortical tissues--an analysis by quantitative polymerase chain reaction technique.
[electronic resource]
by
Lin, C J
Mendonca, B B
Lucon, A M
Guazzelli, I C
Nicolau, W
Villares, S M
Producer:
19970828
In:
The Journal of clinical endocrinology and metabolism
vol. 82
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48.
A novel nonsense mutation in the first zinc finger of the vitamin D receptor causing hereditary 1,25-dihydroxyvitamin D3-resistant rickets.
[electronic resource]
by
Mechica, J B
Leite, M O
Mendonca, B B
Frazzatto, E S
Borelli, A
Latronico, A C
Producer:
19971125
In:
The Journal of clinical endocrinology and metabolism
vol. 82
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49.
Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain.
[electronic resource]
by
Murono, K
Mendonca, B B
Arnhold, I J
Rigon, A C
Migeon, C J
Brown, T R
Producer:
19951214
In:
Human mutation
vol. 6
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50.
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
[electronic resource]
by
Bachega, T A
Billerbeck, A E
Marcondes, J A
Madureira, G
Arnhold, I J
Mendonca, B B
Producer:
20000801
In:
Clinical endocrinology
vol. 52
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51.
Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene.
[electronic resource]
by
Mendonca, B B
Osorio, M G
Latronico, A C
Estefan, V
Lo, L S
Arnhold, I J
Producer:
19990413
In:
The Journal of clinical endocrinology and metabolism
vol. 84
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52.
Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis.
[electronic resource]
by
Ottolenghi, C
Moreira-Filho, C
Mendonça, B B
Barbieri, M
Fellous, M
Berkovitz, G D
McElreavey, K
Producer:
20010705
In:
The Journal of clinical endocrinology and metabolism
vol. 86
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53.
Zinc acutely and temporarily inhibits adrenal cortisol secretion in humans. A preliminary report.
[electronic resource]
by
Brandão-Neto, J
de Mendonça, B B
Shuhama, T
Marchini, J S
Pimenta, W P
Tornero, M T
Producer:
19910220
In:
Biological trace element research
vol. 24
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54.
Spironolactone-reversible rickets associated with 11 beta-hydroxysteroid dehydrogenase deficiency syndrome.
[electronic resource]
by
Batista, M C
Mendonça, B B
Kater, C E
Arnhold, I J
Rocha, A
Nicolau, W
Bloise, W
Producer:
19861229
In:
The Journal of pediatrics
vol. 109
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55.
Hyperandrogenism due to 3 beta-hydroxysteroid dehydrogenase deficiency with accessory adrenocortical tissue: a hormonal and metabolic evaluation.
[electronic resource]
by
Paula, F J
Dick-de-Paula, I
Pontes, A
Schmitt, F C
Mendonça, B B
Foss, M C
Producer:
19950120
In:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas
vol. 27
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56.
Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfaction.
[electronic resource]
by
Costa, E M
Bedecarrats, G Y
Mendonca, B B
Arnhold, I J
Kaiser, U B
Latronico, A C
Producer:
20010705
In:
The Journal of clinical endocrinology and metabolism
vol. 86
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57.
Genotyping of the type II 3beta-hydroxysteroid dehydrogenase gene (HSD3B2) in women with hirsutism and elevated ACTH-stimulated delta(5)-steroids.
[electronic resource]
by
Marui, S
Russell, A J
Paula, F J
Dick-de-Paula, I
Marcondes, J A
Mendonca, B B
Producer:
20001010
In:
Fertility and sterility
vol. 74
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58.
Leydig cell hypoplasia causing male pseudohermaphroditism: case report and review of the literature.
[electronic resource]
by
Arnhold, I J
de Mendonça, B B
Toledo, S P
Madureira, G
Nicolau, W
Bisi, H
Bloise, W
Producer:
19880901
In:
Revista do Hospital das Clinicas
vol. 42
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59.
[Sex reversal in a case of male pseudohermaphroditism (Reifenstein syndrome)].
[electronic resource]
by
Lodovici, O
Salvatore, C A
Bloise, W
Sarmiento, O
Gemperli, R
de Mendonça, B B
Travi, M E
Producer:
19810709
In:
Revista do Hospital das Clinicas
vol. 35
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60.
Ectopic ACTH syndrome caused by pheochromocytoma: computed tomography-guided percutaneous ethanol injection as an alternative treatment.
[electronic resource]
by
Danilovic, D L
Brandão Neto, R A
D'Abronzo, H
Menezes, M R
Lucon, A M
Mendonca, B B
Producer:
20080205
In:
Journal of endocrinological investigation
vol. 30
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