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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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1
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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2
Cholesteryl ester transfer protein gene : two common mutations and their effect on plasma high-density lipoprotein cholesterol content
Cholesteryl ester transfer protein gene : two common mutations and their effect on plasma high-density lipoprotein cholesterol content
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Cholesteryl ester transfer protein gene : two common mutations and their effect on plasma high-density lipoprotein cholesterol content

AKITA, H ; CHIBA, H ; TSUCHIHASHI, K ; TSUJI, M ; KUMAGAI, M ; MATSUNO, K ; KOBAYASHI, K

Journal of Clinical Endocrinology and Metabolism, 1994-12, Vol.79 (6), p.1615-1618 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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3
Is radiation-induced ovarian failure in rhesus monkeys preventable by luteinizing hormone-releasing hormone agonists ? : preliminary observations
Is radiation-induced ovarian failure in rhesus monkeys preventable by luteinizing hormone-releasing hormone agonists ? : preliminary observations
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Is radiation-induced ovarian failure in rhesus monkeys preventable by luteinizing hormone-releasing hormone agonists ? : preliminary observations

ATAYA, K ; PYDYN, E ; RAMAHI-ATAYA, A ; ORTON, C. G

Journal of Clinical Endocrinology and Metabolism, 1995-03, Vol.80 (3), p.790-795 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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4
A 3-basepair in-frame deletion (ΔLeu999) in exon 17 of the insulin receptor gene in a family with insulin resistance
A 3-basepair in-frame deletion (ΔLeu999) in exon 17 of the insulin receptor gene in a family with insulin resistance
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A 3-basepair in-frame deletion (ΔLeu999) in exon 17 of the insulin receptor gene in a family with insulin resistance

AWATA, T ; MATSUMOTO, C ; MOMOMURA, K ; TAKAHASHI, Y ; ODAWARA, M ; KASUGA, M ; KADOWAKI, T ; IWAMOTO, Y

Journal of Clinical Endocrinology and Metabolism, 1994-12, Vol.79 (6), p.1840-1844 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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5
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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6
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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7
Age and family relationship accentuate the risk of insulin-dependent diabetes mellitus (IDDM) in relatives of patients with IDDM
Age and family relationship accentuate the risk of insulin-dependent diabetes mellitus (IDDM) in relatives of patients with IDDM
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Age and family relationship accentuate the risk of insulin-dependent diabetes mellitus (IDDM) in relatives of patients with IDDM

CANTOR, A. B ; KRISCHER, J. P ; CUTHBERTSON, D. D ; SCHATZ, D. A ; RILEY, W. J ; MALONE, J ; SCHWARTZ, S ; QUATTRIN, T ; MACLAREN, N. K

Journal of Clinical Endocrinology and Metabolism, 1995-12, Vol.80 (12), p.3739-3743 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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8
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency : a clinical research center study
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency : a clinical research center study
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A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency : a clinical research center study

COGAN, J. D ; RAMEL, B ; LEHTO, M ; PHILLIPS, J. III ; PRINCE, M ; BLIZZARD, R. M ; DE RAVEL, T. J. L ; BRAMMERT, M ; GROOP, L

Journal of Clinical Endocrinology and Metabolism, 1995-12, Vol.80 (12), p.3591-3595 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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9
A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom)
A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom)
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A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom)

CONTE, F. A ; GRUMBACH, M. M ; ITO, Y ; FISHER, C. R ; SIMPSON, E. R

Journal of Clinical Endocrinology and Metabolism, 1994-06, Vol.78 (6), p.1287-1292 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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10
Lack of an independent association between the human leukocyte antigen allele DQA10501 and Graves' disease
Lack of an independent association between the human leukocyte antigen allele DQA10501 and Graves' disease
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Lack of an independent association between the human leukocyte antigen allele DQA10501 and Graves' disease

CUDDIHY, R. M ; BAHN, R. S

Journal of Clinical Endocrinology and Metabolism, 1996-02, Vol.81 (2), p.847-849 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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