Cerebral folate deficiency

Journal of Inherited Metabolic Disease

Volumn 33, Issue 5, 2010, Pages 563-570

  Hyland, Keith ^a   Shoffner, John ^a   Heales, Simon J ^b  

^a Medical Neurogenetics   (United States)

^b GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

5 METHYLTETRAHYDROFOLIC ACID; AUTOANTIBODY; FOLATE RECEPTOR; FOLIC ACID; FOLINATE CALCIUM; FOLINIC ACID; RECEPTOR ANTIBODY;

AICARDI GOUTIERES SYNDROME; CEREBELLAR ATAXIA; CEREBRAL FOLIC ACID DEFICIENCY; CEREBROSPINAL FLUID ANALYSIS; CEREBROSPINAL FLUID LEVEL; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DYSKINESIA; GENE MUTATION; HUMAN; IRRITABILITY; METABOLIC DISORDER; NEUROLOGIC DISEASE; PERCEPTION DEAFNESS; PSYCHOMOTOR RETARDATION; RECEPTOR GENE; RETT SYNDROME; REVIEW; SLEEP DISORDER; VISUAL DISORDER;

ADMINISTRATION, ORAL; AUTOANTIBODIES; BRAIN DISEASES; DIETARY SUPPLEMENTS; FOLATE RECEPTOR 1; FOLIC ACID DEFICIENCY; FOLIC ACID TRANSPORTERS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LEUCOVORIN; MUTATION; RISK FACTORS; TETRAHYDROFOLATES; TREATMENT OUTCOME;

EID: 77957602102     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-010-9159-6     Document Type: Review

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