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Growth Hormone Deficiency

open access: yesEndocrines, 2022
Short stature is a common reason for a child to visit the endocrinologist, and can be a variant of normal or secondary to an underlying pathologic cause. Pathologic causes include growth hormone deficiency (GHD), which can be congenital or acquired later.
Colleen O'Neill   +2 more
doaj   +2 more sources

Adult growth hormone deficiency

open access: yesIndian Journal of Endocrinology and Metabolism, 2011
Adult growth hormone deficiency (AGHD) is being recognized increasingly and has been thought to be associated with premature mortality. Pituitary tumors are the commonest cause for AGHD.
Vishal Gupta
doaj   +4 more sources

Effect of growth hormone therapy on Taiwanese children with growth hormone deficiency [PDF]

open access: yesJournal of the Formosan Medical Association, 2012
Human growth hormone (GH) has been successfully used in children with GH deficiency (GHD). However, there are few published data on the effect of GH in Taiwanese children with GHD.
Ying-Hua Huang   +3 more
doaj   +3 more sources

Prevalence of growth hormone deficiency in brain tumor survivors: a systematic review and meta-analysis [PDF]

open access: yesEndocrine Oncology
Objective: To evaluate the prevalence of growth hormone deficiency in patients who underwent cranial irradiation for brain tumors. Methods: Ovid Medline and Embase databases were used for review.
Tatiana Tselovalnikova   +5 more
doaj   +2 more sources

Diagnosing Growth Hormone Deficiency in Adults [PDF]

open access: yesInternational Journal of Endocrinology, 2012
Adult growth hormone (GH) deficiency is a recognised syndrome associated with adverse phenotypic, metabolic, and quality-of-life features which improve in many patients when GH is substituted.
Nigel Glynn, Amar Agha
doaj   +3 more sources

Response to growth hormone according to provocation test results in idiopathic short stature and idiopathic growth hormone deficiency [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2022
Purpose To investigate growth response in children with either idiopathic short stature (ISS) or growth hormone (GH) deficiency (GHD). Methods The data of prepubertal GHD or ISS children treated using recombinant human GH were obtained from the LG Growth
Ju Young Yoon   +9 more
doaj   +1 more source

Growth hormone in growth hormone deficiency [PDF]

open access: yesBMJ, 2002
Papers p 70 With the advent of an unlimited supply of recombinant DNA growth hormonesome 15 years ago endocrinologists and paediatricians hoped that the majorgoal in treating children with growth hormone deficiency—that is, a near normal adult height—would finally be achievable.
Jean-Claude Carel   +2 more
openaire   +5 more sources

Growth Hormone Deficiency [PDF]

open access: yesAnnals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1987
Growth hormone deficiency is relative, not absolute. Conventional stimulation tests of hGH release do not recognise some children who will benefit from hGH treatment and it is probably justified, at this point, undertaking a six month trial of hGH in all short children who are growing slowly (less than 4 cm/yr).
openaire   +6 more sources

Prolyl Endopeptidase-like Deficiency Associated with Growth Hormone Deficiency

open access: yesJCRPE, 2023
Prolyl endopeptidase-like (PREPL) deficiency (MIM#616224) is a rare congenital disorder characterised by neonatal hypotonia and feeding difficulties, growth hormone (GH) deficiency and hypergonadotropic hypogonadism.
Laura Sayol-Torres   +5 more
doaj   +1 more source

Cushing disease due to a somatic USP8 mutation in a patient with evolving pituitary hormone deficiencies due to a germline GH1 splicing variant

open access: yesArchives of Endocrinology and Metabolism, 2022
SUMMARY We present the unique case of an adult Brazilian woman with severe short stature due to growth hormone deficiency with a heterozygous G to T substitution in the donor splice site of intron 3 of the growth hormone 1 (GH1) gene (c.291+1G>T).
Julia Haddad Labello   +8 more
doaj   +1 more source

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