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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1985 1
1989 1
1991 1
1992 1
1993 1
1994 1
1996 4
1997 4
1998 4
1999 4
2000 5
2001 6
2002 5
2003 3
2004 5
2005 6
2006 2
2007 6
2008 5
2009 5
2010 2
2011 6
2012 6
2013 3
2014 4
2015 2
2016 5
2017 5
2018 2
2019 9
2020 6
2021 6
2022 1
2023 3
2024 2

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126 results

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Page 1
Growth Hormone Deficiency: Health and Longevity.
Aguiar-Oliveira MH, Bartke A. Aguiar-Oliveira MH, et al. Endocr Rev. 2019 Apr 1;40(2):575-601. doi: 10.1210/er.2018-00216. Endocr Rev. 2019. PMID: 30576428 Free PMC article. Review.
The important role of GH in the control of mammalian longevity was first deduced from extended longevity of mice with genetic GH deficiency (GHD) or GH resistance. Mice with isolated GHD (IGHD) due to GHRH or GHRH receptor mutations, combined deficiency of GH …
The important role of GH in the control of mammalian longevity was first deduced from extended longevity of mice with genetic GH deficien …
Development of the Pituitary Gland.
Alatzoglou KS, Gregory LC, Dattani MT. Alatzoglou KS, et al. Compr Physiol. 2020 Mar 12;10(2):389-413. doi: 10.1002/cphy.c150043. Compr Physiol. 2020. PMID: 32163208 Review.
The development of the anterior pituitary gland occurs in distinct sequential developmental steps, leading to the formation of a complex organ containing five different cell types secreting six different hormones. ...Abnormalities in any of the steps of pituitary …
The development of the anterior pituitary gland occurs in distinct sequential developmental steps, leading to the formation of a comp …
Hypothyroidism: etiology, diagnosis, and management.
Almandoz JP, Gharib H. Almandoz JP, et al. Med Clin North Am. 2012 Mar;96(2):203-21. doi: 10.1016/j.mcna.2012.01.005. Epub 2012 Feb 14. Med Clin North Am. 2012. PMID: 22443971 Review.
Hypothyroidism is the result of inadequate production of thyroid hormone or inadequate action of thyroid hormone in target tissues. Primary hypothyroidism is the principal manifestation of hypothyroidism, but other causes include central deficiency of thyrotr …
Hypothyroidism is the result of inadequate production of thyroid hormone or inadequate action of thyroid hormone in target tis …
Should Skeletal Maturation Be Manipulated for Extra Height Gain?
Wit JM. Wit JM. Front Endocrinol (Lausanne). 2021 Dec 16;12:812196. doi: 10.3389/fendo.2021.812196. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34975773 Free PMC article. Review.
If rhGH-treated children with growth hormone deficiency or those who were born small-for-gestational age are still short at pubertal onset, co-treatment with a GnRHa for 2-3 years increases AH. ...Administration of letrozole to boys with constitutional delay …
If rhGH-treated children with growth hormone deficiency or those who were born small-for-gestational age are still short at pu …
Overt and subclinical hypothyroidism: who to treat and how.
Khandelwal D, Tandon N. Khandelwal D, et al. Drugs. 2012 Jan 1;72(1):17-33. doi: 10.2165/11598070-000000000-00000. Drugs. 2012. PMID: 22191793 Review.
Hypothyroidism denotes deficient production of thyroid hormone by the thyroid gland and can be primary (abnormality in thyroid gland itself) or secondary/central (as a result of hypothalamic or pituitary disease). ...Limited evidence suggests that treatment o …
Hypothyroidism denotes deficient production of thyroid hormone by the thyroid gland and can be primary (abnormality in thyroid …
Pituitary Hypoplasia.
Gangat M, Radovick S. Gangat M, et al. Endocrinol Metab Clin North Am. 2017 Jun;46(2):247-257. doi: 10.1016/j.ecl.2017.01.003. Epub 2017 Feb 22. Endocrinol Metab Clin North Am. 2017. PMID: 28476222 Review.
This article summarizes pituitary development and function as well as specific mutations of genes encoding the following transcription factors: HESX1, LHX3, LHX4, POU1F1, PROP1, and OTX2. ...
This article summarizes pituitary development and function as well as specific mutations of genes encoding the following transcriptio …
Hypopituitarism.
Schneider HJ, Aimaretti G, Kreitschmann-Andermahr I, Stalla GK, Ghigo E. Schneider HJ, et al. Lancet. 2007 Apr 28;369(9571):1461-1470. doi: 10.1016/S0140-6736(07)60673-4. Lancet. 2007. PMID: 17467517 Review.
Incidence and prevalence of hypopituitarism are estimated to be 4.2 per 100,000 per year and 45.5 per 100,000, respectively. Although the clinical symptoms of this disorder are usually unspecific, it can cause life-threatening events and lead to increased mortality. Curren …
Incidence and prevalence of hypopituitarism are estimated to be 4.2 per 100,000 per year and 45.5 per 100,000, respectively. Although …
Relationship between Iron Deficiency and Thyroid Function: A Systematic Review and Meta-Analysis.
Garofalo V, Condorelli RA, Cannarella R, Aversa A, Calogero AE, La Vignera S. Garofalo V, et al. Nutrients. 2023 Nov 15;15(22):4790. doi: 10.3390/nu15224790. Nutrients. 2023. PMID: 38004184 Free PMC article. Review.
Objective: Iron deficiency (ID) is the most prevalent nutritional deficiency worldwide. ...Quality assessment was performed using Cambridge Quality Checklists. The search strategy included the following combination of Medical Subjects Headings terms and keywo …
Objective: Iron deficiency (ID) is the most prevalent nutritional deficiency worldwide. ...Quality assessment was performed us …
Lutropin alfa.
Dhillon S, Keating GM. Dhillon S, et al. Drugs. 2008;68(11):1529-40. doi: 10.2165/00003495-200868110-00005. Drugs. 2008. PMID: 18627209 Review.
Lutropin alfa is the first and only recombinant human form of luteinizing hormone (LH) developed for use in the stimulation of follicular development. Dose-finding studies revealed a significant dose-dependent increase in the rate of optimal follicular development among wo …
Lutropin alfa is the first and only recombinant human form of luteinizing hormone (LH) developed for use in the stimulation of follic …
Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery.
Correa FA, Nakaguma M, Madeira JLO, Nishi MY, Abrão MG, Jorge AAL, Carvalho LR, Arnhold IJP, Mendonça BB. Correa FA, et al. Arch Endocrinol Metab. 2019 May 13;63(2):167-174. doi: 10.20945/2359-3997000000139. Arch Endocrinol Metab. 2019. PMID: 31090814 Free PMC article. Review.
The first description of patients with combined pituitary hormone deficiencies (CPHD) caused by PROP1 mutations was made 20 years ago. ...PROP1 mutations are the most common cause of autosomal recessive CPHD with a topic posterior pituitary lobe …
The first description of patients with combined pituitary hormone deficiencies (CPHD) caused by PROP1 mutations …
126 results