Molecular theranostics: principles, challenges and controversies
Molecular theranostics offers a powerful tool to drive precision medicine in nuclear oncology. While theranostics is not a new principle in nuclear medicine, recent advances in instrumentation and radiopharmacy have driven a reinvigoration and a broader suite of applications.
Geoffrey Currie
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Impaired central sensitivity to thyroid hormones is associated with increased liver fibrosis degree in the euthyroid population. [PDF]
Li Y, Huang J, Wang F, Gan H.
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Hypersscretion of ACTH growth hormone and prolactin in a patient with pituitary adenoma [PDF]
Fink, R. +3 more
core +1 more source
Reduced prevalence of periodontitis in antidepressant users: Findings from a large‐scale US sample
Abstract Background Periodontitis and major depression disorder have been shown to have a bidirectional association. However, the impact of antidepressants, the primary pharmacological treatment for depression, on periodontal health remains unclear.
María Martínez +3 more
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Impaired sensitivity to thyroid hormones is associated with frailty in older patients with cardiometabolic disease. [PDF]
Kodera R +9 more
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Abstract Objectives Functional constipation (FC) is common in children with comorbid neurodevelopmental disorders (NDD) and its optimal treatment may be challenged by adherence and medication tolerability issues in this population. We assessed the efficacy and safety of linaclotide in pediatric patients with FC and NDD.
Hannibal Person +9 more
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The mechanisms, epidemiology, and clinical implications of thyroid hormones and age-related macular degeneration: a narrative review. [PDF]
Zhang X, Wang Z, Li Z, Zhan Z.
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Abstract Objectives This study aims to quantify the levels of relaxin 2 (RLX2), oxytocin (OXT), and insulin‐like peptide 3 (INSL3) in colostrum (postpartum days 1–5, Visit 1) and mature breast milk (postpartum days 21–35, Visit 2), and to evaluate their associations with neonatal growth outcomes.
Hakan Doneray +3 more
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Association between thyroid hormones and diabetic kidney disease in euthyroid type 2 diabetes mellitus patients. [PDF]
Liu J +10 more
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Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno +7 more
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