Plotting Transcutaneous Bilirubin Measurements on Specific Transcutaneous Nomogram Results in Better Prediction of Significant Hyperbilirubinemia in Healthy Term and Near-Term Newborns: A Pilot Study

Neonatology ◽  
2014 ◽  
Vol 105 (4) ◽  
pp. 306-311 ◽  
Author(s):  
I. Mohamed ◽  
A.C. Blanchard ◽  
E. Delvin ◽  
J. Cousineau ◽  
A. Carceller
2011 ◽  
Vol 70 ◽  
pp. 505-505
Author(s):  
S Davidson ◽  
N Ratnavel ◽  
S Mohinuddin ◽  
M F Hird ◽  
A Sinha

PEDIATRICS ◽  
2007 ◽  
Vol 119 (3) ◽  
pp. e659-e665 ◽  
Author(s):  
P. C. Young ◽  
T. S. Glasgow ◽  
X. Li ◽  
G. Guest-Warnick ◽  
G. Stoddard
Keyword(s):  

2010 ◽  
Vol 15 (suppl_A) ◽  
pp. 15A-16A
Author(s):  
A Blanchard ◽  
A Carceller ◽  
J Cousineau ◽  
E Delvin

PEDIATRICS ◽  
2011 ◽  
Vol 128 (3) ◽  
pp. e565-e571 ◽  
Author(s):  
C. M. Draque ◽  
A. Sanudo ◽  
C. de Araujo Peres ◽  
M. F. B. de Almeida

Blood ◽  
1989 ◽  
Vol 74 (4) ◽  
pp. 1409-1414 ◽  
Author(s):  
DH Chui ◽  
WC Mentzer ◽  
M Patterson ◽  
TA Iarocci ◽  
SH Embury ◽  
...  

Abstract A sensitive and specific radioimmunoassay (RIA) for human embryonic zeta-globin chains was used to study normal fetal blood and newborn cord blood as well as cord blood from newborns with alpha-thalassemias. From 17 weeks until 37 weeks of gestation, zeta-globin chains were present in almost all fetal and cord blood samples (0.27% +/- 0.15% in samples of weeks 17 through 30; 0.14% +/- 0.11% in samples of weeks 31 through 37). zeta-Globin chains were present in greater than 80% of cord blood hemolysates from normal, full-term newborns (0.15% +/- 0.11%) as well as from 16 near-term newborns of diabetic mothers (0.13% +/- 0.13%). zeta-Globin chains were not detected in normal infants aged 3 months to 2 years. In cord blood hemolysates from alpha-thalassemic newborns, the levels of zeta-globin chain content varied from very high to undetectable levels. Gene mapping of the zeta-alpha-globin gene cluster was performed in 12 newborns in whom cord blood zeta-globin chains had been determined. Newborns who were carriers of alpha- thalassemia-1 due to the (--SEA/) deletion had very high levels of zeta- globin chains (greater than 1.5%).


2012 ◽  
Vol 97 (Suppl 2) ◽  
pp. A341-A342
Author(s):  
D. Rebelo ◽  
T. Santos ◽  
M. Albuquerque ◽  
G. Oliveira ◽  
T. Rodrigues

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