© 2018 SSIEMAim: To explore the clinical presentation, course, treatment and impact of early treatment in patients with remethylation disorders from the European Network and Registry for Homocystinurias and Methylation Defects (E-HOD) international web-based registry. Results: This review comprises 238 patients (cobalamin C defect n = 161; methylenetetrahydrofolate reductase deficiency n = 50; cobalamin G defect n = 11; cobalamin E defect n = 10; cobalamin D defect n = 5; and cobalamin J defect n = 1) from 47 centres for whom the E-HOD registry includes, as a minimum, data on medical history and enrolment visit. The duration of observation was 127 patient years. In 181 clinically diagnosed patients, the median age at presentation was 30 ...
BACKGROUND: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
BACKGROUND: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
Background: The cobalamin E (cblE) (MTRR, methionine synthase reductase) and cobalamin G (cblG) (MTR...
AIM: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
AIM: To explore the clinical presentation, course, treatment and impact of early treatment in pa...
AIM: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
To explore the clinical presentation, course, treatment and impact of early treatment in patients wi...
AIM: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
To explore the clinical presentation, course, treatment and impact of early treatment in patients wi...
Aim: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
Aim: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
Background: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
PMC Free: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203859/Background: Remethylation defects...
PMC Free: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203859/Background: Remethylation defects...
Background: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
BACKGROUND: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
BACKGROUND: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
Background: The cobalamin E (cblE) (MTRR, methionine synthase reductase) and cobalamin G (cblG) (MTR...
AIM: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
AIM: To explore the clinical presentation, course, treatment and impact of early treatment in pa...
AIM: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
To explore the clinical presentation, course, treatment and impact of early treatment in patients wi...
AIM: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
To explore the clinical presentation, course, treatment and impact of early treatment in patients wi...
Aim: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
Aim: To explore the clinical presentation, course, treatment and impact of early treatment in patien...
Background: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
PMC Free: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203859/Background: Remethylation defects...
PMC Free: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203859/Background: Remethylation defects...
Background: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
BACKGROUND: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
BACKGROUND: Remethylation defects are rare inherited disorders in which impaired remethylation of ho...
Background: The cobalamin E (cblE) (MTRR, methionine synthase reductase) and cobalamin G (cblG) (MTR...