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Hormonal Replacement in Hypopituitarism in Adults: An Endocrine Society Clinical Practice Guideline
Journal of Clinical Endocrinology and Metabolism, 2016 Maria Fleseriu +2 more
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Insights into non-classic and emerging causes of hypopituitarism
Nature Reviews Endocrinology, 2020Flavia Prodam +2 more
exaly +2 more sources
Approach to a case with an unusual cause of hypopituitarism.
Journal of Clinical Endocrinology and Metabolism, 2022Hypopituitarism refers to insufficiency of one or more hormones of the pituitary and can be due to myriad causes. The clinical and radiological spectrum of the condition is heterogeneous, based on the age, gender, clinical setting and/or other past ...
L. Das, P. Dutta
semanticscholar +1 more source
The Lancet, 2007
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. Current research has refined the diagnosis of hypopituitarism. Identification of growth
SCHNEIDER HJ +4 more
openaire +6 more sources
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. Current research has refined the diagnosis of hypopituitarism. Identification of growth
SCHNEIDER HJ +4 more
openaire +6 more sources
Pituitary, 2006
Hypopituitarism is the partial or complete insufficiency of anterior pituitary hormone secretion and may result from pituitary or hypothalamic disease. The reported incidence (12-42 new cases per million per year) and prevalence (300-455 per million) is probably underestimated if its occurrence after brain injuries (30-70% of cases) is considered ...
P. Ascoli, F. Cavagnini
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Hypopituitarism is the partial or complete insufficiency of anterior pituitary hormone secretion and may result from pituitary or hypothalamic disease. The reported incidence (12-42 new cases per million per year) and prevalence (300-455 per million) is probably underestimated if its occurrence after brain injuries (30-70% of cases) is considered ...
P. Ascoli, F. Cavagnini
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Human Molecular Genetics, 2017 Congenital hypopituitarism (CH) is characterized by the deficiency of one or more pituitary hormones and can present alone or in association with complex disorders.
Maria Lillina Vignola +2 more
exaly +2 more sources
Endocrine Practice, 1995
Spontaneous recovery of pituitary function in patients with hypopituitarism is rare. We report the case of a 30-year-old man in whom hypopituitarism and sudden onset of bilateral hearing loss developed after a viral infection. No evidence of a mass lesion was detected on computed tomography or magnetic resonance imaging of the pituitary gland.
G H, Tan, W F, Young
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Spontaneous recovery of pituitary function in patients with hypopituitarism is rare. We report the case of a 30-year-old man in whom hypopituitarism and sudden onset of bilateral hearing loss developed after a viral infection. No evidence of a mass lesion was detected on computed tomography or magnetic resonance imaging of the pituitary gland.
G H, Tan, W F, Young
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Skull Base, 2020
BACKGROUND Hypopituitarism is the most frequent complication after pituitary adenoma stereotactic radiosurgery (SRS) and is correlated with increasing radiation to the pituitary gland.
C. Graffeo +5 more
semanticscholar +1 more source
BACKGROUND Hypopituitarism is the most frequent complication after pituitary adenoma stereotactic radiosurgery (SRS) and is correlated with increasing radiation to the pituitary gland.
C. Graffeo +5 more
semanticscholar +1 more source
Clinics in Perinatology, 2018
Mutations of growth hormone genes and pituitary transcription factors account for a small proportion of cases of severe congenital hypopituitarism. Most cases show characteristic MRI findings of pituitary stalk interruption syndrome. Clinical suspicion should prompt assessment of cortisol, free T4, thyroid-stimulating hormone, and growth hormone levels
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Mutations of growth hormone genes and pituitary transcription factors account for a small proportion of cases of severe congenital hypopituitarism. Most cases show characteristic MRI findings of pituitary stalk interruption syndrome. Clinical suspicion should prompt assessment of cortisol, free T4, thyroid-stimulating hormone, and growth hormone levels
openaire +2 more sources
Clinical Endocrinology, 2019
Childhood brain tumour survivors who receive cranial radiotherapy undergo regular surveillance for the development ofhypothalamic‐pituitary (HP) axis dysfunction.
N. Kyriakakis +7 more
semanticscholar +1 more source
Childhood brain tumour survivors who receive cranial radiotherapy undergo regular surveillance for the development ofhypothalamic‐pituitary (HP) axis dysfunction.
N. Kyriakakis +7 more
semanticscholar +1 more source