Miss Lauren Jane Fonte
Doctor
218 WOODSTREAM DRIVE GRAND ISLAND NY, 14072About
Miss Lauren Jane Fonte is a top Doctor in GRAND ISLAND, NY. With a passion for the field and an unwavering commitment to their specialty, Miss Lauren Jane Fonte is an expert in changing the lives of their patients for the better. Through their designated cause and expertise in the field, Miss Lauren Jane Fonte is a prime example of a true leader in health care. As a leader and expert in their field, Miss Lauren Jane Fonte is passionate about enhancing patient quality of life. They embody the values of communication, safety, and trust when dealing directly with patients. In GRAND ISLAND, NY, Miss Lauren Jane Fonte 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- Maternal plasma homocysteine, placenta status and docosahexaenoic acid concentration in erythrocyte phospholipids of the newborn.
- 4,5-dimethyl-3-hydroxy-2[5H]-furanone (sotolone)--the odour of maple syrup urine disease.
- N-acetylaspartylglutamate in Canavan disease: an adverse effector?
- Reversible dementia in an adolescent with cblC disease: clinical heterogeneity within the same family.
- False diagnosis of maple syrup urine disease owing to ingestion of herbal tea.
- Normal kynurenine metabolism in 2-oxoadipic aciduria.
- Stereodifferentiation of 3-hydroxyisobutyric- and 3-aminoisobutyric acid in human urine by enantioselective multidimensional capillary gas chromatography-mass spectrometry.
- Enantioselective analysis of ketone bodies in patients with beta-ketothiolase deficiency, medium-chain acyl coenzyme A dehydrogenase deficiency and ketonemic vomiting.
- Rapid enantiomeric differentiation of urinary metabolites in a patient with bacterial overgrowth syndrome.
- Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.
- Selective screening for inborn errors of metabolism: the primary care-based model in rural Crete.
- The chemistry of human neonatal femoral epiphyseal cartilage.
- Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase gene.
- Fetal presentation of Morquio disease type A.
- Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probe.
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