Rebecca Ann Flint BSW
Social Worker
375 APPLE TREE DR IONIA MI, 48846About
Rebecca Ann Flint BSW is a top Social Worker in IONIA, MI. With a passion for the field and an unwavering commitment to their specialty, Rebecca Ann Flint BSW is an expert in changing the lives of their patients for the better. Through their designated cause and expertise in the field, Rebecca Ann Flint BSW is a prime example of a true leader in health care. As a leader and expert in their field, Rebecca Ann Flint BSW is passionate about enhancing patient quality of life. They embody the values of communication, safety, and trust when dealing directly with patients. In IONIA, MI, Rebecca Ann Flint BSW is a true asset to their field and dedicated to the profession of medicine.
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Expert Publications
Data provided by the National Library of Medicine- A single external enzyme confers alternative NADH:ubiquinone oxidoreductase activity in Yarrowia lipolytica.
- Properties of the common inhibitor-binding domain in mitochondrial NADH-dehydrogenase (complex I).
- Binding of detergents and inhibitors to bovine complex I - a novel purification procedure for bovine complex I retaining full inhibitor sensitivity.
- Three molecules of ubiquinone bind specifically to mitochondrial cytochrome bc1 complex.
- 3-Ureidopropionate contributes to the neuropathology of 3-ureidopropionase deficiency and severe propionic aciduria: a hypothesis.
- Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiency.
- Animal models for glutaryl-CoA dehydrogenase deficiency.
- S-Acetylglutathione normalizes intracellular glutathione content in cultured fibroblasts from patients with glutathione synthetase deficiency.
- Methylmalonic acid--an endogenous toxin?
- Measurement of bile acid CoA esters by high-performance liquid chromatography-electrospray ionisation tandem mass spectrometry (HPLC-ESI-MS/MS).
- Massive insulin secretion in response to anaerobic exercise in exercise-induced hyperinsulinism.
- Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).
- Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblasts.
- Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice).
- Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approach.
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