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Bouchemal N, Ouss L, Brassier A, Barbier V, Gobin S, Hubert L, Diagnosis and phenotypic assessment of trimethylaminuria, and its treatment with riboflavin: 1H NMR spectroscopy and genetic testing10.1186/s13023-019-1174-6 [Google Scholar] [CrossRef] [25]

This evidence demonstrates wide variation in KD formula selections and corresponding treatment outcomes, which suggests that the selection of a specific KD treatment for patients should be based on the patients circumstances, and individual family genetic background, as well as the expertise guiding patients adherance

Metab Brain Dis 29:1936 Morris G, Anderson G, Maes M (2017a) Hypothalamic-pituitary-adrenal hypofunction in myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS) as a consequence of activated immune-inflammatory and oxidative and nitrosative pathways