The pathogenesis of hydrocephalus in inborn errors of the single carbon transfer pathway

Neuropediatrics

Volumn 32, Issue 6, 2001, Pages 335-336

  Rossi, Andrea ^a   Biancheri, R ^a   Tortori Donati, P ^a  

^a G GASLINI INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

COBALAMIN; HOMOCYSTEINE; S ADENOSYLMETHIONINE;

CEREBROSPINAL FLUID FLOW; HOMOCYSTINURIA; HUMAN; HYDROCEPHALUS; HYPERHOMOCYSTEINEMIA; INBORN ERROR OF METABOLISM; LETTER; METHYLMALONIC ACIDURIA; PATHOPHYSIOLOGY; PRIORITY JOURNAL;

CEREBROSPINAL FLUID; HOMOCYSTINURIA; HUMANS; HYDROCEPHALUS; INFANT; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); METHYLMALONIC ACID; OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; VITAMIN B 12 DEFICIENCY;

EID: 0035716173     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-20411     Document Type: Letter

References (3)

1. Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiency
2. The pathogenesis and hemodynamics of hydrocephalus. Proposal for a new understanding
3. Early-onset combined methylmalonic aciduria and homocystinuria: Neuroradiologic findings