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Results of search for 'au:"Mendonca, B B"', page 5 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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81.
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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82.
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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83.
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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84.
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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85.
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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86.
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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87.
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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88.
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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89.
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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90.
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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91.
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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92.
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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93.
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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94.
Male pseudohermaphroditism due to 5 alpha reductase deficiency associated with gynecomastia.
[electronic resource]
by
Mendonça, B B
Batista, M C
Arnhold, I J
Nicolau, W
Madureira, G
Lando, V S
Kohek, M B
Carvalho, D G
Bloise, W
Producer:
19880418
In:
Revista do Hospital das Clinicas
vol. 42
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95.
The desmopressin stimulation test in the differential diagnosis of Cushing's syndrome.
[electronic resource]
by
Malerbi, D A
Mendonça, B B
Liberman, B
Toledo, S P
Corradini, M C
Cunha-Neto, M B
Fragoso, M C
Wajchenberg, B L
Producer:
19930817
In:
Clinical endocrinology
vol. 38
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96.
Treatment of gonadotropin dependent precocious puberty due to hypothalamic hamartoma with gonadotropin releasing hormone agonist depot.
[electronic resource]
by
de Brito, V N
Latronico, A C
Arnhold, I J
Lo, L S
Domenice, S
Albano, M C
Fragoso, M C
Mendonca, B B
Producer:
19990520
In:
Archives of disease in childhood
vol. 80
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97.
Male pseudohermaphroditism due to steroid 5alpha-reductase 2 deficiency. Diagnosis, psychological evaluation, and management.
[electronic resource]
by
Mendonca, B B
Inacio, M
Costa, E M
Arnhold, I J
Silva, F A
Nicolau, W
Bloise, W
Russel, D W
Wilson, J D
Producer:
19960517
In:
Medicine
vol. 75
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98.
[Cushing syndrome due to ectopic ACTH secretion].
[electronic resource]
by
Mendonça, B B
Madureira, G
Bloise, W
Albergaria, A
Halpern, A
Liberman, B
Villares, S M
Batista, M C
Avancini, V F
Nitterdorfi, C T
Producer:
19900226
In:
Revista paulista de medicina
vol. 107
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99.
Long-term treatment of central precocious puberty with a long-acting analogue of luteinizing hormone release hormone (D-Tryp6-GnRH) in monthly injections. Its possible use in normal puberty.
[electronic resource]
by
Marcondes, J A
Abujamra, A C
Minanni, S L
Mendonca, B B
Nery, M
Lerario, A C
Pereira, M A
Abelin, N
Wajchenberg, B L
Producer:
19930427
In:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
vol. 25
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100.
Clinical and molecular characterization of Brazilian patients with growth hormone gene deletions.
[electronic resource]
by
Arnhold, I J
Osorio, M G
Oliveira, S B
Estefan, V
Kamijo, T
Krishnamani, M R
Cogan, J D
Phillips, J A
Mendonca, B B
Producer:
19981006
In:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas
vol. 31
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