IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain development

Best Practice and Research: Clinical Endocrinology and Metabolism

Volumn 25, Issue 1, 2011, Pages 181-190

  Netchine, Irne ^a,b,c   Azzi, Salah ^a,b,c   Le Bouc, Yves ^a,b,c   Savage, Martin O ^d  

^a ARMAND TROUSSEAU HOSPITAL   (France)

^b INSERM   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

brain development; deafness; fetal growth; IGF I deficiency; IGF I treatment; IGF1 gene; intrauterine growth restriction; microcephaly; short stature; small for gestational age

Indexed keywords

SOMATOMEDIN C;

ARTICLE; BRAIN DEVELOPMENT; CASE REPORT; FETUS GROWTH; GONAD DYSFUNCTION; GROWTH HORMONE DEFICIENCY; HUMAN; INNER EAR; INSULIN RESISTANCE; INTRAUTERINE GROWTH RETARDATION; MICROCEPHALY; MOUSE; NONHUMAN; OBESITY; OSTEOPOROSIS; POSTNATAL GROWTH; PROTEIN BLOOD LEVEL; PROTEIN FUNCTION; PROTEIN POLYMORPHISM;

EID: 79952496635     PISSN: 1521690X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.beem.2010.08.005     Document Type: Review

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