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Quoted phrase not found in phrase index: "Pituitary hormone deficiency, combined, 6"
Page 1
Inducing puberty.
Delemarre EM, Felius B, Delemarre-van de Waal HA. Delemarre EM, et al. Eur J Endocrinol. 2008 Dec;159 Suppl 1:S9-15. doi: 10.1530/EJE-08-0314. Epub 2008 Sep 16. Eur J Endocrinol. 2008. PMID: 18796540 Review.
Puberty is the result of increasing pulsatile secretion of the hypothalamic gonadotropin releasing hormone (GnRH), which stimulates the release of gonadotropins and in turn gonadal activity. ...Sex steroids will induce development of the secondary sex characteristics alone …
Puberty is the result of increasing pulsatile secretion of the hypothalamic gonadotropin releasing hormone (GnRH), which stimulates t …
Diagnosis and Incidence of Congenital Combined Pituitary Hormone Deficiency in Denmark-A National Observational Study.
Jakobsen LK, Jensen RB, Birkebæk NH, Hansen D, Christensen AR, Bjerrum MC, Christesen HT. Jakobsen LK, et al. J Clin Endocrinol Metab. 2023 Sep 18;108(10):2475-2485. doi: 10.1210/clinem/dgad198. J Clin Endocrinol Metab. 2023. PMID: 37043518 Free PMC article.
CONTEXT: Congenital combined pituitary hormone deficiency (cCPHD) is the loss of 2 pituitary hormones caused by congenital factors. ...CONCLUSION: cCPHD had the highest incidence rate and the most hormone deficiencies in tho …
CONTEXT: Congenital combined pituitary hormone deficiency (cCPHD) is the loss of 2 pituitary hormones
Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.
Fang Q, George AS, Brinkmeier ML, Mortensen AH, Gergics P, Cheung LY, Daly AZ, Ajmal A, Pérez Millán MI, Ozel AB, Kitzman JO, Mills RE, Li JZ, Camper SA. Fang Q, et al. Endocr Rev. 2016 Dec;37(6):636-675. doi: 10.1210/er.2016-1101. Epub 2016 Nov 9. Endocr Rev. 2016. PMID: 27828722 Free PMC article. Review.
The genetic basis for combined pituitary hormone deficiency (CPHD) is complex, involving 30 genes in a variety of syndromic and nonsyndromic presentations. Molecular diagnosis of this disorder is valuable for predicting disease progression, avoi …
The genetic basis for combined pituitary hormone deficiency (CPHD) is complex, involving 30 genes in a variety o …
Hyponatremia and antidiuresis syndrome.
Vantyghem MC, Balavoine AS, Wémeau JL, Douillard C. Vantyghem MC, et al. Ann Endocrinol (Paris). 2011 Dec;72(6):500-12. doi: 10.1016/j.ando.2011.10.001. Epub 2011 Nov 25. Ann Endocrinol (Paris). 2011. PMID: 22119069 Review.
Antidiuretic hormone (ADH), or arginine vasopressin (AVP), is primarily regulated through plasma osmolarity, as well as non-osmotic stimuli including blood volume and stress. ...AVP acts via the intermediary of three types of receptors: V1a, or V1, which exerts vasoconstri …
Antidiuretic hormone (ADH), or arginine vasopressin (AVP), is primarily regulated through plasma osmolarity, as well as non-osmotic s …
Stereotactic radiosurgery for acromegaly.
Lee CC, Vance ML, Xu Z, Yen CP, Schlesinger D, Dodson B, Sheehan J. Lee CC, et al. J Clin Endocrinol Metab. 2014 Apr;99(4):1273-81. doi: 10.1210/jc.2013-3743. Epub 2014 Jan 28. J Clin Endocrinol Metab. 2014. PMID: 24471574
New pituitary hormone deficiency occurred in 43 patients (31.6%); two patients (1.5%) developed panhypopituitarism. Corresponding risk factors for new pituitary hormone deficiency were a margin dose > 25 Gy and tumor volume > 2.5 mL …
New pituitary hormone deficiency occurred in 43 patients (31.6%); two patients (1.5%) developed panhypopituitarism. Cor …
Classical and non-classical causes of GH deficiency in the paediatric age.
Di Iorgi N, Morana G, Allegri AE, Napoli F, Gastaldi R, Calcagno A, Patti G, Loche S, Maghnie M. Di Iorgi N, et al. Best Pract Res Clin Endocrinol Metab. 2016 Dec;30(6):705-736. doi: 10.1016/j.beem.2016.11.008. Epub 2016 Nov 24. Best Pract Res Clin Endocrinol Metab. 2016. PMID: 27974186 Review.
Idiopathic, isolated GHD is the most common sporadic form of hypopituitarism. GHD may also occur in combination with other pituitary hormone deficiencies, and is often referred to as hypopituitarism, combined pituitary hormone d
Idiopathic, isolated GHD is the most common sporadic form of hypopituitarism. GHD may also occur in combination with other pituita
Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events.
Diwaker C, Thadani P, Memon SS, Sarathi V, Lila AR, Arya S, Krishnappa B, Karlekar M, Patil VA, Shah N, Bandgar T. Diwaker C, et al. Pituitary. 2022 Aug;25(4):645-652. doi: 10.1007/s11102-022-01243-x. Epub 2022 Jun 24. Pituitary. 2022. PMID: 35749012
We aim to elucidate the predictors of PSIS among patients with growth hormone deficiency (GHD) and perinatal events in PSIS by comparing cohorts of PSIS and genetically proven GHD without PSIS. METHODS: Among 179 GHD patients, 56 PSIS and 70 genetically posit …
We aim to elucidate the predictors of PSIS among patients with growth hormone deficiency (GHD) and perinatal events in …
Growth hormone replacement in adults and bone mineral density: a systematic review and meta-analysis.
Davidson P, Milne R, Chase D, Cooper C. Davidson P, et al. Clin Endocrinol (Oxf). 2004 Jan;60(1):92-8. doi: 10.1111/j.1365-2265.2004.01935.x. Clin Endocrinol (Oxf). 2004. PMID: 14678294 Review.
BACKGROUND: The effect of GH replacement on bone mineral density (BMD) in adults with GH deficiency (GHD) is uncertain. We carried out a systematic review of randomized trials that compared GH to no active treatment, with BMD as an outcome. ...CONCLUSION: There is evidence …
BACKGROUND: The effect of GH replacement on bone mineral density (BMD) in adults with GH deficiency (GHD) is uncertain. We carried ou …
Very long-term sequelae of craniopharyngioma.
Wijnen M, van den Heuvel-Eibrink MM, Janssen JAMJL, Catsman-Berrevoets CE, Michiels EMC, van Veelen-Vincent MC, Dallenga AHG, van den Berge JH, van Rij CM, van der Lely AJ, Neggers SJCMM. Wijnen M, et al. Eur J Endocrinol. 2017 Jun;176(6):755-767. doi: 10.1530/EJE-17-0044. Epub 2017 Mar 21. Eur J Endocrinol. 2017. PMID: 28325825
Initial craniopharyngioma treatment approaches included gross total resection (n = 25), subtotal resection without radiotherapy (n = 44), subtotal resection with radiotherapy (n = 25), cyst aspiration without radiotherapy (n = 8), and (90)Yttrium brachytherapy (n = 21). RESULTS: …
Initial craniopharyngioma treatment approaches included gross total resection (n = 25), subtotal resection without radiotherapy (n = 44), su …
Update on the diagnosis of GH deficiency in adults.
Abs R. Abs R. Eur J Endocrinol. 2003 Apr;148 Suppl 2:S3-8. doi: 10.1530/eje.0.148s003. Eur J Endocrinol. 2003. PMID: 12670294 Review.
GH deficiency (GHD) in adults is associated with considerable morbidity and mortality. ...Suspicion of GHD is also heightened in the presence of other pituitary hormone deficits. Tests for GHD include measurement of the hormone in urine or serum or mea …
GH deficiency (GHD) in adults is associated with considerable morbidity and mortality. ...Suspicion of GHD is also heightened in the …
191 results