MMA+HCU (Methylmalonic Acidemia with Homocystinuria) – newbornscreening.info
Vitamin B12 deficiency | MedLink Neurology
Successful intrauterine treatment of a patient with cobalamin C defect - ScienceDirect
Vitamin B12 Deficiency: an Update for the General Paediatrician
Cobalamin C defect: natural history, pathophysiology, and treatment - Martinelli - 2011 - Journal of Inherited Metabolic Disease - Wiley Online Library
Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity | Pediatric Nephrology
Dangers of Vitamin Deficiency During Pregnancy
Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists | Orphanet Journal of Rare Diseases | Full Text
Molecular picture of cobalamin C/D defects before and after newborn screening era
Mild Neonatal Hypoxia Exacerbates the Effects of Vitamin-Deficient Diet on Homocysteine Metabolism in Rats | Pediatric Research
Mason, Cobalamin C Deficiency, Age 7 – Organic Acidemia Association
Retinal degeneration occurs in cobalamin C deficiency independent of... | Download Scientific Diagram
Investigation of the Relationship Between Maternal & Neonatal Vitamin B12 Deficiency and Neonatal Hyperbilirubinemia: A Pros
SciELO - Brazil - Three Main Causes of Homocystinuria: CBS, cblC and MTHFR Deficiency. What do they Have in Common? Three Main Causes of Homocystinuria: CBS, cblC and MTHFR Deficiency. What do
Macular changes in cobalamin C are early and progressive and may... | Download Scientific Diagram
Cobalamin C defect: natural history, pathophysiology, and treatment | SpringerLink
Cobalamin deficiency in pregnancy - Konings - 2021 - Clinical Case Reports - Wiley Online Library
Cobalamin C Deficiency - EyeWiki
Cobalamin C Deficiency - EyeWiki
Metabolites | Free Full-Text | Vitamin B12 (Cobalamin): Its Fate from Ingestion to Metabolism with Particular Emphasis on Diagnostic Approaches of Acquired Neonatal/Infantile Deficiency Detected by Newborn Screening
Efficacy of early treatment in patients with cobalamin C disease identified by newborn screening: a 16-year experience | Genetics in Medicine
Clinical and biochemical outcome after hydroxocobalamin dose escalation in a series of patients with cobalamin C deficiency - ScienceDirect
IJNS | Free Full-Text | Vitamin B12 Deficiency (Un-)Detected Using Newborn Screening in Norway
IJNS | Free Full-Text | Vitamin B12 Deficiency (Un-)Detected Using Newborn Screening in Norway
Outcomes of patients with cobalamin C deficiency: A single center experience - Bourque - 2021 - JIMD Reports - Wiley Online Library
Versatile enzymology and heterogeneous phenotypes in cobalamin complementation type C disease - ScienceDirect
Homocystinuria diagnosis and management: it is not all classical | Journal of Clinical Pathology
Frontiers | Biomarkers and Algorithms for the Diagnosis of Vitamin B12 Deficiency