Results 161 to 170 of about 24,454 (211)

Coexistence of acromegaly and raised intracranial pressure: insights from a rare case report and literature review. [PDF]

BMC Neurol
Hanifa H, Mandili Y, Olabi S, Hababeh MN, Alchaar E, Mahouk MA, Okdah S, Qashqash M, Hamouda AR, Rashid R, Atrachan L, Sheikha N, Alhoesh O, Samhouri MR, Alkhani AA, Alsamarrai O.   +15 more
europepmc   +1 more source

Automatic acromegaly detection using deep learning on hand images: a multicenter observational study.

J Clin Endocrinol Metab
Ohmachi Y, Nishio M, Abe I, Kobayashi K, Iida T, Shirakawa M, Nagata Y, Takeuchi K, Taguchi A, Kinoshita Y, Fukuhara N, Nishioka H, Tahara S, Fujio S, Ogura T, Kurosaki M, Hada Y, Susa S, Otsuka Y, Otsuka F, Ishida I, Kameda H, Oyama K, Yamada S, Kobatake M, Oi-Yo Y, Fujii G, Tomofuji S, Sasaki Y, Bando H, Yamamoto M, Iguchi G, Motomura Y, Tsujimoto Y, Yamamoto N, Suzuki M, Urai S, Takahashi M, Murakami T, Ogawa W, Fukuoka H.   +40 more
europepmc   +1 more source

Acromegaly diagnosis.

J Clin Endocrinol Metab
Yogi-Morren D, Chanson P.
europepmc   +1 more source

Changing understanding of acromegaly epidemiology and early mortality risk.

J Clin Endocrinol Metab
Esposito D, Johannsson G.
europepmc   +1 more source

The acromegaly patient experience: burden of treatment and quality of life.

J Clin Endocrinol Metab
Geer EB, Sisco J.
europepmc   +1 more source

Acromegaly complications: an update.

J Clin Endocrinol Metab
Giustina A, Fleseriu M.
europepmc   +1 more source

Acromegaly [PDF]

Nature Reviews Disease Primers, 2019
Acromegaly is characterized by increased release of growth hormone and, consequently, insulin-like growth factor I (IGF1), most often by a pituitary adenoma. Prolonged exposure to excess hormone leads to progressive somatic disfigurement and a wide range of systemic manifestations that are associated with increased mortality. Although considered a rare
Philippe Chanson, Andrea Giustina, Annamaria Colao   +2 more
exaly   +10 more sources

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Acromegaly

Pituitary, 2006
Acromegaly is a slowly progressive disease characterized by 30% increase of mortality rate for cardiovascular disease, respiratory complications and malignancies. The estimated prevalence of the disease is 40 cases/1000000 population with 3-4 new cases/1000000 population per year.
M. Scacchi, F. Cavagnini
openaire   +2 more sources

ACROMEGALY

Clinical Endocrinology, 1987
SUMMARY A personal series of 256 cases of acromegaly/gigantism seen over a 20‐year period from 1963 is described. The insidious nature of the condition resulted in delay in diagnosis which was often made by a doctor when seeing the patient for an unrelated problem.
openaire   +4 more sources