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Refinado por: Nome da Publicação: Journal Of Clinical Endocrinology And Metabolism remover Nome da Publicação: The Journal Of Clinical Endocrinology And Metabolism remover
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11
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia
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Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia

TONACCHERA, M ; VAN SANDE, J ; CETANI, F ; SWILLENS, S ; SCHVARTZ, C ; WINISZEWSKI, P ; PORTMANN, L ; DUMONT, J. E ; VASSART, G ; PARMA, J

Journal of Clinical Endocrinology and Metabolism, 1996-02, Vol.81 (2), p.547-554 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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12
Nested polymerase chain reaction study of 53 cases with Turner's syndrome : is cytogenetically undetected Y mosaicism common ?
Nested polymerase chain reaction study of 53 cases with Turner's syndrome : is cytogenetically undetected Y mosaicism common ?
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Nested polymerase chain reaction study of 53 cases with Turner's syndrome : is cytogenetically undetected Y mosaicism common ?

BINDER, G ; KOCH, A ; WAJS, E ; RANKE, M. B

Journal of Clinical Endocrinology and Metabolism, 1995-12, Vol.80 (12), p.3532-3536 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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13
Rearrangements at the 11p15 locus and overexpression on insulin-like growth factor-II gene in sporadic adrenocortical tumors
Rearrangements at the 11p15 locus and overexpression on insulin-like growth factor-II gene in sporadic adrenocortical tumors
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Rearrangements at the 11p15 locus and overexpression on insulin-like growth factor-II gene in sporadic adrenocortical tumors

GICQUEL, C ; BERTAGNA, X ; SCHNEID, H ; FRANCILLARD-LEBLOND, M ; LUTON, J.-P ; GIRARD, F ; LE BOUC, Y

Journal of Clinical Endocrinology and Metabolism, 1994-06, Vol.78 (6), p.1444-1453 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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14
Somatic mutations of the ret protooncogene in sporadic medullary thyroid carcinoma are not restricted to exon 16 and are associated with tumor recurrence
Somatic mutations of the ret protooncogene in sporadic medullary thyroid carcinoma are not restricted to exon 16 and are associated with tumor recurrence
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Somatic mutations of the ret protooncogene in sporadic medullary thyroid carcinoma are not restricted to exon 16 and are associated with tumor recurrence

ROMEI, C ; ELISEI, R ; PINCHERA, A ; CECCHERINI, I ; MOLINARO, E ; MANCUSI, F ; MARTINO, E ; ROMEO, G ; PACINI, F

Journal of Clinical Endocrinology and Metabolism, 1996-04, Vol.81 (4), p.1619-1622 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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15
Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene
Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene
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Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene

WILSON, R. C ; JI-QING WEI ; CHENG, K. C ; MERCADO, A. B ; NEW, M. I

Journal of Clinical Endocrinology and Metabolism, 1995-05, Vol.80 (5), p.1635-1640 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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16
Familial hypocalciuric hypercalcemia associated with mutation in the human Ca(2+)-sensing receptor gene
Familial hypocalciuric hypercalcemia associated with mutation in the human Ca(2+)-sensing receptor gene
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Familial hypocalciuric hypercalcemia associated with mutation in the human Ca(2+)-sensing receptor gene

Aida, K ; Koishi, S ; Inoue, M ; Nakazato, M ; Tawata, M ; Onaya, T

Journal of Clinical Endocrinology and Metabolism, 1995-09, Vol.80 (9), p.2594-2598 [Periódico revisado por pares]

United States

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17
A genomic point mutation in the extracellular domain of the thyrotropin receptor in patients with Graves' ophthalmopathy
A genomic point mutation in the extracellular domain of the thyrotropin receptor in patients with Graves' ophthalmopathy
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A genomic point mutation in the extracellular domain of the thyrotropin receptor in patients with Graves' ophthalmopathy

BAHN, R. S ; DUTTON, C. M ; HEUFELDER, A. E ; GOBINDA SARKAR

Journal of Clinical Endocrinology and Metabolism, 1994-02, Vol.78 (2), p.256-260 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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18
Mutated human androgen receptor gene detected in a prostatic cancer patient is also activated by estradiol
Mutated human androgen receptor gene detected in a prostatic cancer patient is also activated by estradiol
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Mutated human androgen receptor gene detected in a prostatic cancer patient is also activated by estradiol

ELO, J. P ; KVIST, L ; LEINONEN, K ; ISOMAA, V ; HENTTU, P ; LUKKARINEN, O ; VIHKO, P

Journal of Clinical Endocrinology and Metabolism, 1995-12, Vol.80 (12), p.3494-3500 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

Sem texto completo

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19
Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor gene
Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor gene
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Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor gene

SCHIPANI, E ; WEINSTEIN, L. S ; VAN DOP, C ; BRICKMAN, A. S ; CRAWFORD, J. D ; POTTS, J. T ; KRONENBERG, H. M ; ABOU-SAMRA, A. B ; SEGRE, G. V ; JÜPPNER, H ; BERGWITZ, C ; IIDA-KLEIN, A ; KONG, X. F ; STUHRMANN, M ; KRUSE, K ; WHYTE, M. P ; MURRAY, T ; SCHMIDTKE, J

Journal of Clinical Endocrinology and Metabolism, 1995-05, Vol.80 (5), p.1611-1621 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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20
The incidence of ophthalmopathy after radioiodine therapy for Graves' disease : prognostic factors and the role of methimazole
The incidence of ophthalmopathy after radioiodine therapy for Graves' disease : prognostic factors and the role of methimazole
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The incidence of ophthalmopathy after radioiodine therapy for Graves' disease : prognostic factors and the role of methimazole

KUNG, A. W. C ; YAU, C. C ; ASHLEY CHENG

Journal of Clinical Endocrinology and Metabolism, 1994-08, Vol.79 (2), p.542-546 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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