MeSH tree: C05.116.132
An AI can accurately diagnose a rare endocrinological condition just by analyzing pictures of the back of the hand and the clenched fist. The privacy-conscious achievement by Kobe University holds promise for establishing ...
Feb 27, 2026
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The journal Pituitary has highlighted research led by Manel Puig, head of the Endocrine, Thyroid and Obesity Research Group at the Germans Trias i Pujol Research Institute (IGTP), which explores the potential of AI and machine ...
Oct 30, 2025
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People with the rare growth hormone disorder acromegaly have a significantly higher risk of developing various types of cancer, often at ages younger than typically seen in the general population, according to a study presented ...
Jul 15, 2025
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New research has taken a significant step in terms of research and care for acromegaly, a rare disease caused by an excess of growth hormone secretion, which occurs in over 99% of cases due to a generally benign pituitary ...
Aug 13, 2024
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For newborns with congenital hypothyroidism, early diagnosis spells the difference between a normal, healthy life and lifelong disability.
May 8, 2023
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Babies undergo a newborn screening test for inherited metabolic disorders within seven days of birth. The test checks for risk factors such as hypothyroidism, phenylketonuria and maple syrup urine disease, which can lead ...
Jan 19, 2023
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Newborn screening (NBS) and management of congenital hypothyroidism is addressed in a clinical report published online Dec. 19 in Pediatrics.
Dec 20, 2022
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