Dangers of Vitamin Deficiency During Pregnancy
Frontiers | Newborn Screening for Methylmalonic Acidemia in a Chinese Population: Molecular Genetic Confirmation and Genotype Phenotype Correlations
Screening for Methylmalonic and Propionic Acidemia: Clinical Outcomes and Follow-Up Recommendations
Investigation of the Relationship Between Maternal & Neonatal Vitamin B12 Deficiency and Neonatal Hyperbilirubinemia: A Pros
Cobalamin C defect: natural history, pathophysiology, and treatment | SpringerLink
Homocystinuria diagnosis and management: it is not all classical | Journal of Clinical Pathology
Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists | Orphanet Journal of Rare Diseases | Full Text
IJNS | Free Full-Text | Vitamin B12 Deficiency (Un-)Detected Using Newborn Screening in Norway
Cobalamin C Deficiency - EyeWiki
Successful intrauterine treatment of a patient with cobalamin C defect - ScienceDirect
Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity | Pediatric Nephrology
Vitamin B12 deficiency | MedLink Neurology
Molecular picture of cobalamin C/D defects before and after newborn screening era
Outcomes of patients with cobalamin C deficiency: A single center experience - Bourque - 2021 - JIMD Reports - Wiley Online Library
Mason, Cobalamin C Deficiency, Age 7 – Organic Acidemia Association
Analysis of 70 patients with hydrocephalus due to cobalamin C deficiency | Neurology
Vitamin B12 Deficiency: an Update for the General Paediatrician
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
Mild Neonatal Hypoxia Exacerbates the Effects of Vitamin-Deficient Diet on Homocysteine Metabolism in Rats | Pediatric Research
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
![Figure 2. [Testing algorithm to confirm the...]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK1328/bin/cbl-Image002.jpg "Figure 2. [Testing algorithm to confirm the...]. - GeneReviews® - NCBI Bookshelf")
Figure 2. [Testing algorithm to confirm the...]. - GeneReviews® - NCBI Bookshelf
Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns | Orphanet Journal of Rare Diseases | Full Text
![PDF] Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell Loss. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/fff4b6fbab740b0a9e6fac3cd24eb21f3f64da34/4-Figure1-1.png "PDF] Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell Loss. | Semantic Scholar")
PDF] Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell Loss. | Semantic Scholar
Cobalamin C Deficiency - EyeWiki
