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Leptin

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Diagnostic Approach to Genetic Obesity in Children: From Pathophysiology to Precision Medicine
Leptin
Prenatal and postnatal choline supplementation alters metabolic dysfunction-associated steatohepatitis (MASH) phenotypes in offspring exposed to maternal obesity and following a western diet into adulthood: A preliminary study.
Leptin
Immune disturbances cluster around specific depressive phenotypes under conditions of structural adversity
Leptin
Atypical energy-related symptoms define biologically distinct subtypes of major depressive disorder
Leptin
Association of leptin gene polymorphisms (rs791620 and rs7799039) with rheumatoid arthritis susceptibility and clinical manifestations: a case-control study.
Leptin
Genetic susceptibility to obesity-related asthma and its modulation by sequelae of obesity
Leptin
Inhibition of protein tyrosine phosphatase PTP1B function ameliorates pathophysiological deficits in Rett Syndrome
Leptin
Novel MFN2 compound heterozygote genotype in a patient with multiple symmetric lipomatosis and metabolic dysfunction.
Leptin
Genotype-Phenotype Spectrum of Non-Syndromic Monogenic Obesity in a National Paediatric Cohort.
Leptin
Genetic variability in the leptin-melanocortin pathway and its role in weight loss.
Leptin

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