Related references
Note: Only part of the references are listed.Severe 5,10-methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia
A. Perna et al.
EUROPEAN JOURNAL OF NEUROLOGY (2018)
Adolescence/adult onset MTHFR deficiency may manifest as isolated and treatable distinct neuro-psychiatric syndromes
Ana Gales et al.
ORPHANET JOURNAL OF RARE DISEASES (2018)
Insights into Severe 5,10-Methylenetetrahydrofolate Reductase Deficiency: Molecular Genetic and Enzymatic Characterization of 76 Patients
Patricie Burda et al.
HUMAN MUTATION (2015)
Survival and Psychomotor Development With Early Betaine Treatment in Patients With Severe Methylenetetrahydrofolate Reductase Deficiency
Eugene F. Diekman et al.
JAMA NEUROLOGY (2014)
Severe Methylenetetrahydrofolate Reductase Deficiency Clinical Clues to a Potentially Treatable Cause of Adult-Onset Hereditary Spastic Paraplegia
Alexander Lossos et al.
JAMA NEUROLOGY (2014)
A Common Left Occipito-Temporal Dysfunction in Developmental Dyslexia and Acquired Letter-By-Letter Reading?
Fabio Richlan et al.
PLOS ONE (2010)
Differential Patterns of Cognitive Decline in Anterior and Posterior White Matter Hyperintensity Progression
Maria J. Marquine et al.
STROKE (2010)
Psychosis, paraplegia and coma revealing methylenetetrahydrofolate reductase deficiency in a 56-year-old woman
J. M. Michot et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2008)
Letter-by-letter acquired dyslexia is due to the serial encoding of letters
K Rayner et al.
PSYCHOLOGICAL SCIENCE (2005)
Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD-responsive mutation
S Sibani et al.
HUMAN MUTATION (2003)
MR findings in subacute combined degeneration of the spinal cord: A case of reversible cervical myelopathy
B Ravina et al.
AMERICAN JOURNAL OF ROENTGENOLOGY (2000)