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Results of search for 'au:"Mendonca, B"', page 5 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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Topics
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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81.
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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82.
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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83.
Texture image analysis in differentiating malignant from benign adrenal cortical tumors in children and adults.
[electronic resource]
by
Shirata, N K
Sredni, S T
Castelo, A
Santinelli, A
Mendonça, B
Montironi, R
Filho, A Longatto
Zerbini, M C N
Producer:
20090930
In:
Anticancer research
vol. 29
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84.
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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85.
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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86.
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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87.
No evidence for oncogenic mutations in the adrenocorticotropin receptor gene in human adrenocortical neoplasms.
[electronic resource]
by
Latronico, A C
Reincke, M
Mendonça, B B
Arai, K
Mora, P
Allolio, B
Wajchenberg, B L
Chrousos, G P
Tsigos, C
Producer:
19950411
In:
The Journal of clinical endocrinology and metabolism
vol. 80
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88.
Brief report: testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene.
[electronic resource]
by
Latronico, A C
Anasti, J
Arnhold, I J
Rapaport, R
Mendonca, B B
Bloise, W
Castro, M
Tsigos, C
Chrousos, G P
Producer:
19960223
In:
The New England journal of medicine
vol. 334
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89.
Real-world impact of glucocorticoid replacement therapy on bone mineral density: retrospective experience of a large single-center CAH cohort spanning 24 years.
[electronic resource]
by
Iervolino, L L
Ferraz-de-Souza, B
Martin, R M
Costa, F C
Miranda, M C
Mendonça, B B
Bachega, T S
Producer:
20210318
In:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
vol. 31
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90.
Clinical and molecular analysis of human reproductive disorders in Brazilian patients.
[electronic resource]
by
Latronico, A C
Costa, E M F
Domenice, S
Correa, R V
Kohek, M B F
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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91.
Diagnosis of prolactinoma in two male-to-female transsexual subjects following high-dose cross-sex hormone therapy.
[electronic resource]
by
Cunha, F S
Domenice, S
Câmara, V L
Sircili, M H P
Gooren, L J G
Mendonça, B B
Costa, E M F
Producer:
20160601
In:
Andrologia
vol. 47
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92.
The effects of spironolactone on testosterone fractions and sex-hormone binding globulin binding capacity in hirsute women.
[electronic resource]
by
Marcondes, J A
Minanni, S L
Luthold, W W
Lerário, A C
Nery, M
Mendonça, B B
Wajchenberg, B L
Kirschner, M A
Producer:
19951222
In:
Journal of endocrinological investigation
vol. 18
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93.
CYP21A2 genotypes do not predict the severity of hyperandrogenic manifestations in the nonclassical form of congenital adrenal hyperplasia.
[electronic resource]
by
Moura-Massari, V O
Bugano, D D G
Marcondes, J A M
Gomes, L G
Mendonca, B B
Bachega, T A S S
Producer:
20131104
In:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
vol. 45
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94.
An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors.
[electronic resource]
by
Latronico, A C
Pinto, E M
Domenice, S
Fragoso, M C
Martin, R M
Zerbini, M C
Lucon, A M
Mendonca, B B
Producer:
20011101
In:
The Journal of clinical endocrinology and metabolism
vol. 86
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95.
21-Hydroxylase deficiency in Brazil.
[electronic resource]
by
Bachega, T A
Billerbeck, A E
Madureira, G
Marcondes, J A
Longui, C A
Leite, M V
Arnhold, I J
Mendonça, B B
Producer:
20001116
In:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas
vol. 33
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96.
A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty.
[electronic resource]
by
Latronico, A C
Anasti, J
Arnhold, I J
Mendonça, B B
Domenice, S
Albano, M C
Zachman, K
Wajchenberg, B L
Tsigos, C
Producer:
19950907
In:
The Journal of clinical endocrinology and metabolism
vol. 80
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97.
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency.
[electronic resource]
by
Bachega, T A
Billerbeck, A E
Madureira, G
Marcondes, J A
Longui, C A
Leite, M V
Arnhold, I J
Mendonca, B B
Producer:
19990111
In:
The Journal of clinical endocrinology and metabolism
vol. 83
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98.
Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue.
[electronic resource]
by
Domenice, S
Nishi, M Y
Billerbeck, A E
Carvalho, F M
Frade, E M
Latronico, A C
Arnhold, I J
Mendonca, B B
Producer:
20010726
In:
Medical science monitor : international medical journal of experimental and clinical research
vol. 7
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99.
Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene.
[electronic resource]
by
Danilovic, D L S
Correa, P H S
Costa, E M F
Melo, K F S
Mendonca, B B
Arnhold, I J P
Producer:
20070606
In:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
vol. 18
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100.
Monensin, virginiamycin, and flavomycin in a no-roughage finishing diet fed to zebu cattle.
[electronic resource]
by
Lemos, B J M
Castro, F G F
Santos, L S
Mendonça, B P C
Couto, V R M
Fernandes, J J R
Producer:
20170419
In:
Journal of animal science
vol. 94
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