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- Publications
- Influence
Abnormal Umbilical Cord Coiling Is Associated with Adverse Perinatal Outcomes
- G. Machin, J. Ackerman, E. Gilbert-Barness
- Medicine
- Pediatric and developmental pathology : the…
- 1 September 2000
The normal umbilical cord coil index is one coil/5 cm, i.e., 0.2 ± 0.1 coils completed per cm. We report the frequency and clinical correlations of abnormally coiled cords among 1329 cases referred… Expand
Potter's pathology of the fetus and infant
- E. Gilbert-Barness, E. Potter
- Medicine
- 1996
Potters Atlas of Fetal and Infant Pathology will address all aspects of foetal and infant pathology including complicated pregnancies, placental pathology, prenatal diagnosis of abnormalities,… Expand
- 204
- 7
Time to Heal: American Medical Education From the Turn of the Century to the Era of Managed Care
- E. Gilbert-Barness
- Medicine
- 1 March 2001
Obesity: Genetic, molecular, and environmental aspects
- L. Barness, J. Opitz, E. Gilbert-Barness
- Medicine
- American journal of medical genetics. Part A
- 15 December 2007
Obesity has emerged as one of the most serious public health concerns in the 21st century. Obese children tend to become obese adults. The dramatic rise in pediatric obesity closely parallels the… Expand
Teratogenic causes of malformations.
- E. Gilbert-Barness
- Biology, Medicine
- Annals of clinical and laboratory science
- 20 March 2010
Crucial morphogenetic processes during the blastogenesis period, which extends throughout the first 4 wk of development, from fertilization until the end of the gastrulation stage (days 27 to 28… Expand
Potter's pathology of the fetus, infant and child
- E. Gilbert-Barness, R. Kapur, L. L. Oligny, J. Siebert, E. L. Potter
- Medicine
- 2007
The first edition of this book updated Dr Potter’s original text and filled an important niche when it arrived in 1997, serving as one of the few general reference textbooks that dealt with neonatal… Expand
- 128
- 4
Multiple meningiomas, craniofacial hyperostosis and retinal abnormalities in Proteus syndrome.
- E. Gilbert-Barness, M. Cohen, J. Opitz
- Medicine
- American journal of medical genetics
- 31 July 2000
Because clinical evidence suggests that Proteus syndrome may be caused by a somatic mutation during early development, resulting in mosaicism, the possible types of abnormalities and their clinical… Expand
A SPECTRUM OF PHENOTYPICAL EXPRESSION OF NEU-LAXOVA SYNDROME: Three Case Reports and a Review of the Literature
- Wendy L. Coto-Puckett, E. Gilbert-Barness, C. Steelman, T. Stuart, Haynes B. Robinson, Bahig M. Shehata
- Medicine
- Fetal and pediatric pathology
- 1 March 2010
Neu-Laxova syndrome is a rare autosomal recessive disorder characterized by severe intra-uterine growth restriction, extreme microcephaly, marked edema with skin restriction, ichthyosis, craniofacial… Expand
Review: Metabolic cardiomyopathy and conduction system defects in children.
- E. Gilbert-Barness
- Biology, Medicine
- Annals of clinical and laboratory science
- 2004
Metabolic cardiomyopathies include amino acid, lipid and mitochondrial disorders, as well as storage diseases. A number of metabolic disorders are associated with both myopathy and cardiomyopathy.… Expand
HUTCHINSON-GILFORD PROGERIA SYNDROME: A PATHOLOGIC STUDY
- J. Ackerman, E. Gilbert-Barness
- Biology, Medicine
- Pediatric pathology & molecular medicine
- 1 January 2002
Hutchinson-Gilford progeria syndrome is an extremely rare condition with features of premature and accelerated aging. The pattern of inheritance is unclear, although both autosomal recessive and… Expand