(Q50473046)

14 March 2018

title

Causes of hemolysis in neonates with extreme hyperbilirubinemia. (English)

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14 March 2018

bilirubin metabolic disorder

main subject

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R D Christensen

1

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14 March 2018

R H Nussenzveig

2

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14 March 2018

H M Yaish

3

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14 March 2018

E Henry

4

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14 March 2018

L D Eggert

5

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14 March 2018

A M Agarwal

6

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14 March 2018

publication date

24 April 2014

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14 March 2018

published in

Journal of Perinatology

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14 March 2018

volume

34

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14 March 2018

issue

8

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14 March 2018

page(s)

616-619

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14 March 2018

https://scigraph.springernature.com/pub.10.1038/jp.2014.68

exact match

0 references

cites work

Toward understanding kernicterus: a challenge to improve the management of jaundiced newborns

1 reference

12 December 2020

Urgent clinical need for accurate and precise bilirubin measurements in the United States to prevent kernicterus

1 reference

12 December 2020

Reduction of severe hyperbilirubinemia after institution of predischarge bilirubin screening

1 reference

12 December 2020

The erythrocyte indices of neonates, defined using data from over 12,000 patients in a multihospital health care system

1 reference

12 December 2020

Neonatal hemolytic jaundice: morphologic features of erythrocytes that will help you diagnose the underlying condition

1 reference

12 December 2020

Acute kernicterus in a neonate with O/B blood group incompatibility and a mutation in SLC4A1.

1 reference

12 December 2020

(TA)n UGT 1A1 Promoter Polymorphism: A Crucial Factor in the Pathophysiology of Jaundice in G-6-PD Deficient Neonates

1 reference

12 December 2020

Neonatal death suspected to be from sepsis was found to be kernicterus with G6PD deficiency

1 reference

12 December 2020

Imbalance between production and conjugation of bilirubin: a fundamental concept in the mechanism of neonatal jaundice

1 reference

12 December 2020

Understanding neonatal jaundice: a perspective on causation

1 reference

12 December 2020

Coexpression of gene polymorphisms involved in bilirubin production and metabolism

1 reference

12 December 2020

Hereditary spherocytosis in neonates with hyperbilirubinemia.

1 reference

12 December 2020

The effect of instituting a prehospital-discharge newborn bilirubin screening program in an 18-hospital health system

1 reference

12 December 2020

Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system.

1 reference

12 December 2020

Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.

1 reference

12 December 2020

Should we screen newborns for glucose-6-phosphate dehydrogenase deficiency in the United States?

1 reference

12 December 2020

Kernicterus Associated with Hereditary Spherocytosis and UGT1A1 Promoter Polymorphism

1 reference

12 December 2020

Clinical report from the pilot USA Kernicterus Registry (1992 to 2004).

1 reference

12 December 2020

Complex multifactorial nature of significant hyperbilirubinemia in neonates

1 reference

12 December 2020

A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine

1 reference

12 December 2020

Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis

1 reference

12 December 2020

The contribution of hemolysis to early jaundice in normal newborns

1 reference

12 December 2020

Identifiers

DOI

10.1038/JP.2014.68

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14 March 2018

PubMed ID

24762414

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14 March 2018