Articles
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Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A28
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NMDA receptor dependent anti-diabetic effects
Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A26 -
A novel mutation in the PAX8 promoter region causes permanent congenital hypothyroidism in a patient with Down’s Syndrome
Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A24 -
Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism are both ATP1A3-related disorders
Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A15 -
Uncovering common pathogenic transcriptional dysregulations in Silver-Russell syndrome
Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A13 -
Connexin 37 and Connexin 43 genotypes in correlation to cytokines in induced sputum and blood in cystic fibrosis (CF)
Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A11 -
MIRIS – an adequate method to measure fortified breast milk?
Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A9 -
Molecular and Cellular Pediatrics
No abstract.
Citation: Molecular and Cellular Pediatrics 2014 1:4 -
Monogenic forms of childhood obesity due to mutations in the leptin gene
Congenital leptin deficiency is a rare autosomal recessive monogenic obesity syndrome caused by mutations in the leptin gene. This review describes the molecular and cellular characteristics of the eight disti...
Citation: Molecular and Cellular Pediatrics 2014 1:3 -
Perinatal programming - myths, fact, and future of research
Perinatal programming, i.e., the (epigenetic) modification of (genetic) functions throughout lifetime, suffers from the notion of premature theories and difficult and extensive research strategies.
Citation: Molecular and Cellular Pediatrics 2014 1:2 -
The quest for fragile X biomarkers
Fragile X is the most common form of inherited intellectual disability and the leading known genetic cause of autism. There is currently no cure or approved medication for fragile X although various drugs targ...
Citation: Molecular and Cellular Pediatrics 2014 1:1
- ISSN: 2194-7791 (electronic)