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Long-term response to olaparib in a patient with metastatic pancreatic cancer associated with hereditary breast and ovarian cancer syndrome.
- Published in:
- Oxford Medical Case Reports, 2022, v. 2022, n. 11, p. 1, doi. 10.1093/omcr/omac124
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- Publication type:
- Article
Bilateral Pheochromocytoma with Germline MAX Variant without Family History.
- Published in:
- 2022
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- Publication type:
- Case Study
Familial Pseudohypoparathyroidism Type IB Associated with an SVA Retrotransposon Insertion in the GNAS Locus.
- Published in:
- Journal of Bone & Mineral Research, 2022, v. 37, n. 10, p. 1850, doi. 10.1002/jbmr.4652
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- Publication type:
- Article
A novel loss-of-function mutation of GATA3 (p.R299Q) in a Japanese family with Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) syndrome.
- Published in:
- BMC Endocrine Disorders, 2015, v. 15, p. 1, doi. 10.1186/s12902-015-0065-7
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- Publication type:
- Article
Successful treatment of Cushing's disease caused by ectopic intracavernous microadenoma.
- Published in:
- 2011
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- Publication type:
- Report
Clinical and Molecular Features of a TSH-Secreting Pituitary Microadenoma.
- Published in:
- Pituitary, 2005, v. 8, n. 2, p. 127, doi. 10.1007/s11102-005-3759-4
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- Publication type:
- Article
A study on traffic management cooperating with IMS in MPLS networks.
- Published in:
- Telecommunication Systems, 2013, v. 52, n. 2, p. 671, doi. 10.1007/s11235-011-9511-7
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- Publication type:
- Article
Prions disturb post-Golgi trafficking of membrane proteins.
- Published in:
- Nature Communications, 2013, v. 4, n. 5, p. 1846, doi. 10.1038/ncomms2873
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- Publication type:
- Article
Endometrial Cancer Diagnosed at an Early Stage during Lynch Syndrome Surveillance: A Case Report.
- Published in:
- Case Reports in Oncology, 2023, v. 16, n. 1, p. 634, doi. 10.1159/000531837
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- Publication type:
- Article
Comparisons of plasma aldosterone and renin data between an automated chemiluminescent immunoanalyzer and conventional radioimmunoassays in the screening and diagnosis of primary aldosteronism.
- Published in:
- PLoS ONE, 2021, v. 15, n. 7, p. 1, doi. 10.1371/journal.pone.0253807
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- Publication type:
- Article
Lack of ACTH and Androgen Receptor Expression in a Giant Adrenal Myelolipoma Associated with 21-hydroxylase Deficiency.
- Published in:
- Endocrine Pathology, 2008, v. 19, n. 2, p. 122, doi. 10.1007/s12022-008-9034-2
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- Publication type:
- Article
A Novel Truncation Mutation of the PRRT2 Gene Resulting in a 16-Amino-Acid Protein Causes Self-inducible Paroxysmal Kinesigenic Dyskinesia.
- Published in:
- Movement Disorders Clinical Practice, 2017, v. 4, n. 4, p. 625, doi. 10.1002/mdc3.12500
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- Publication type:
- Article
Pancreatic cancer risk in diabetic patients using the Japanese Regional Insurance Claims.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-67505-9
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- Publication type:
- Article
Genetic and epigenetic states of the GNAS complex in pseudohypoparathyroidism type Ib using methylation-specific multiplex ligation-dependent probe amplification assay.
- Published in:
- European Journal of Endocrinology, 2013, v. 168, n. 2, p. 169, doi. 10.1530/EJE-12-0548
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- Publication type:
- Article
Resistance to dopamine agonists in prolactinoma is correlated with reduction of dopamine D2receptor long isoform mRNA levels.
- Published in:
- European Journal of Endocrinology, 2012, v. 166, n. 3, p. 383, doi. 10.1530/EJE-11-0656
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- Publication type:
- Article
The impact of equol-producing status in modifying the effect of soya isoflavones on risk factors for CHD: a systematic review of randomised controlled trials.
- Published in:
- Journal of Nutritional Science, 2016, v. 5, p. 1, doi. 10.1017/jns.2016.18
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- Publication type:
- Article
Novel AVPR2 mutation causing partial nephrogenic diabetes insipidus in a Japanese family.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 5, p. 591, doi. 10.1515/jpem-2015-0323
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- Publication type:
- Article
High-dose fludrocortisone therapy was transiently required in a female neonate with 21-hydroxylase deficiency.
- Published in:
- Clinical Pediatric Endocrinology, 2022, v. 31, n. 2, p. 93, doi. 10.1297/cpe.2021-0066
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- Publication type:
- Article
Tumoral calcinosis in a patient with hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome undergoing hemodialysis.
- Published in:
- 2015
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- Publication type:
- Case Study
What Equol Can Do for Human Health?
- Published in:
- Korean Journal of Obesity, 2014, v. 23, n. 1, p. 1, doi. 10.7570/kjo.2014.23.1.1
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- Publication type:
- Article
Functional ovarian cysts in a neonate with classical 21-hydroxylase deficiency: case report and review of the literature.
- Published in:
- 2013
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- Publication type:
- Abstract
Pheochromocytoma with Subclinical Cushing’s Syndrome Caused by Corticomedullary Mixed Tumor of the Adrenal Gland.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 3, p. 746, doi. 10.1210/jc.2008-2013
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- Publication type:
- Article
Antithyroid Drugs Inhibit Thyroid Hormone ReceptorMediated Transcription.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 3, p. 1066, doi. 10.1210/jc.2006-1621
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- Publication type:
- Article
Adiponectin in Anorexia Nervosa and Bulimia Nervosa.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 4, p. 1833, doi. 10.1210/jc.2003-031260
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- Publication type:
- Article
Thyroid Hormone Action Is Disrupted by Bisphenol A as an Antagonist.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 11, p. 5185, doi. 10.1210/jc.2002-020209
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- Publication type:
- Article
Stomach Is a Major Source of Circulating Ghrelin, and Feeding State Determines Plasma Ghrelin-Like Immunoreactivity Levels in Humans.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 10, p. 4753, doi. 10.1210/jcem.86.10.7885
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- Publication type:
- Article
Ghrelin strongly stimulates growth hormone release in humans.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 12, p. 4908, doi. 10.1210/jcem.85.12.7167
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- Publication type:
- Article
Shortened saline infusion test for subtype prediction in primary aldosteronism.
- Published in:
- 2015
- By:
- Publication type:
- Letter
Serum levels of IgG and IgG4 in Hashimoto thyroiditis.
- Published in:
- Endocrine (1355008X), 2014, v. 45, n. 2, p. 236, doi. 10.1007/s12020-013-9988-9
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- Publication type:
- Article
Clinical features of non‐classical 21‐hydroxylase deficiency after normal newborn mass screening.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
P53 gene mutation in an atypical corticotroph adenoma with Cushing's disease.
- Published in:
- 2009
- By:
- Publication type:
- Letter
Parthenogenetic mosaicism: generation via second polar body retention and unmasking of a likely causative PER2 variant for hypersomnia.
- Published in:
- Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01062-0
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- Publication type:
- Article
Histopathological Diagnosis of Primary Aldosteronism Using CYP11B2 Immunohistochemistry.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Aberrant Expression of Thyroid Hormone Receptor β Isoform May Cause Inappropriate Secretion of TSH in a TSH-Secreting Pituitary Adenoma.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 6, p. 948, doi. 10.1210/jc.2010-2496
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- Publication type:
- Article
A case of retinitis pigmentosa homozygous for a rare CNGA1 causal variant.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-84098-9
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- Publication type:
- Article
Hypoparathyroidism-Deafness-Renal Disease Syndrome: The First Case Report from Turkey.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 73
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- Publication type:
- Article
The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Novel tandem germline RET proto-oncogene mutations in a patient with multiple endocrine neoplasia type 2B: Report of a case and a literature review of tandem RET mutations with in silico analysis.
- Published in:
- Head & Neck, 2013, v. 35, n. 12, p. E363, doi. 10.1002/hed.23241
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- Publication type:
- Article
PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Functional Analysis of the Cell-Specific Enhancer in the Human Proopiomelanocortin Gene by β-Galactosidase Histochemical Staining.
- Published in:
- DNA & Cell Biology, 1994, v. 13, n. 7, p. 755, doi. 10.1089/dna.1994.13.755
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- Publication type:
- Article
Isolation of Drosophila CREB-B: A Novel CRE-Binding Protein.
- Published in:
- DNA & Cell Biology, 1993, v. 12, n. 7, p. 589, doi. 10.1089/dna.1993.12.589
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- Publication type:
- Article
Do Differences in Risk Factors Explain the Lower Rates of Coronary Heart Disease in Japanese Versus U.S. Women?
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Asymptomatic Case With MEN1 Slipping Through Genetic Screening by SNV-dependent Allelic Dropout.
- Published in:
- Journal of the Endocrine Society, 2022, v. 6, n. 9, p. 1, doi. 10.1210/jendso/bvac118
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- Publication type:
- Article
ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers.
- Published in:
- Journal of the Endocrine Society, 2019, v. 3, n. 10, p. 1837, doi. 10.1210/js.2019-00210
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- Publication type:
- Article
The Incidence of Gestational Hyperthyroidism and Postpartum Thyroiditis in Treated Patients with Graves' Disease.
- Published in:
- Thyroid, 2007, v. 17, n. 8, p. 767, doi. 10.1089/thy.2007.0003
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- Publication type:
- Article
Effects of lifestyle intervention on weight and metabolic parameters in patients with impaired glucose tolerance related to beta-3 adrenergic receptor gene polymorphism Trp64 Arg( C/ T): Results from the Japan Diabetes Prevention Program.
- Published in:
- Journal of Diabetes Investigation, 2016, v. 7, n. 3, p. 338, doi. 10.1111/jdi.12426
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- Publication type:
- Article
Lung squamous cell carcinoma associated with hypoparathyroidism with sensorineural deafness and renal dysplasia syndrome: a case report.
- Published in:
- OncoTargets & Therapy, 2018, v. 11, p. 1595, doi. 10.2147/OTT.S161420
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- Publication type:
- Article
A case of combined 21‐hydroxylase deficiency and CHARGE syndrome featuring micropenis and cryptorchidism.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 6, p. N.PAG, doi. 10.1002/mgg3.730
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- Publication type:
- Article
Bezafibrate induces hypothyroidism in a patient with resistance to thyroid hormone β due to a G347R variant.
- Published in:
- Clinical Endocrinology, 2022, v. 96, n. 2, p. 236, doi. 10.1111/cen.14591
- By:
- Publication type:
- Article
Chronic kidney disease score for predicting postoperative masked renal insufficiency in patients with primary aldosteronism.
- Published in:
- Clinical Endocrinology, 2014, v. 81, n. 5, p. 665, doi. 10.1111/cen.12497
- By:
- Publication type:
- Article