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Publications by S. A. Newton
CSF 5-Methyltetrahydrofolate Serial Monitoring to Guide Treatment of Congenital Folate Malabsorption Due to Proton-Coupled Folate Transporter (PCFT) Deficiency
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Related publications
Folate Receptor Autoantibodies and Spinal Fluid 5-Methyltetrahydrofolate Deficiency in Rett Syndrome
Neuropediatrics
Medicine
Child Health
Neurology
Pediatrics
Perinatology
The Human Proton-Coupled Folate Transporter: Determination of Conformation and Identification of the Folate-Binding Pocket
Biophysical Journal
Biophysics
Identification of the Amino Acid Residue Responsible for the Myricetin Sensitivity of Human Proton-Coupled Folate Transporter
Scientific Reports
Multidisciplinary
Malabsorption of Folate Polyglutamates in Tropical Sprue
BMJ
Epilepsy and Folate Deficiency.
BMJ
The Clinical Course and Genetic Defect in the PCFT Gene in a 27-Year-Old Woman With Hereditary Folate Malabsorption
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Correction To: Ancestral Folate Promotes Neuronal Regeneration in Serial Generations of Progeny
Molecular Neurobiology
Neuroscience
Neurology
Cellular
Molecular Neuroscience
Folate Deficiency and Neurological Disease.
BMJ
Folate Deficiency in Premature Infants.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
