Yaish HM - Search Results

1

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

Christensen RD, Yaish HM, Nussenzveig RH, Reading NS, Agarwal AM, Eggert LD, Prchal JT. Christensen RD, et al. Among authors: yaish hm. Pediatrics. 2013 Aug;132(2):e531-4. doi: 10.1542/peds.2012-3799. Epub 2013 Jul 22. Pediatrics. 2013. PMID: 23878048

2

Three Novel Spectrin Variants in Jaundiced Neonates.

Christensen RD, Agarwal AM, Yaish HM, Reading NS, O'Brien EA, Prchal JT. Christensen RD, et al. Among authors: yaish hm. Clin Pediatr (Phila). 2018 Jan;57(1):19-26. doi: 10.1177/0009922816687326. Epub 2017 Jan 15. Clin Pediatr (Phila). 2018. PMID: 28090778

3

Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis.

Christensen RD, Nussenzveig RH, Reading NS, Agarwal AM, Prchal JT, Yaish HM. Christensen RD, et al. Among authors: yaish hm. Neonatology. 2014;105(1):1-4. doi: 10.1159/000354884. Epub 2013 Oct 31. Neonatology. 2014. PMID: 24193021

4

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

Christensen RD, Yaish HM, Wiedmeier SE, Reading NS, Pysher TJ, Palmer CA, Prchal JT. Christensen RD, et al. Among authors: yaish hm. Pediatrics. 2013 Dec;132(6):e1694-8. doi: 10.1542/peds.2013-1030. Epub 2013 Nov 11. Pediatrics. 2013. PMID: 24218468

5

A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.

Christensen RD, Yaish HM, Gallagher PG. Christensen RD, et al. Among authors: yaish hm. Pediatrics. 2015 Jun;135(6):1107-14. doi: 10.1542/peds.2014-3516. Pediatrics. 2015. PMID: 26009624 Free PMC article. Review.

6

Prolonged phototherapy needed for a neonate with four mutations in genes involved in bilirubin production and metabolism.

Christensen R, Nussenzveig R, Eldridge B, Agarwal A, Yaish H. Christensen R, et al. J Neonatal Perinatal Med. 2015 Mar 10. doi: 10.3233/NPM-15814065. Online ahead of print. J Neonatal Perinatal Med. 2015. PMID: 25758003

7

A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency.

Yaish HM, Christensen RD, Agarwal A. Yaish HM, et al. J Perinatol. 2013 May;33(5):404-6. doi: 10.1038/jp.2012.67. J Perinatol. 2013. PMID: 23624969

8

Causes of hemolysis in neonates with extreme hyperbilirubinemia.

Christensen RD, Nussenzveig RH, Yaish HM, Henry E, Eggert LD, Agarwal AM. Christensen RD, et al. Among authors: yaish hm. J Perinatol. 2014 Aug;34(8):616-9. doi: 10.1038/jp.2014.68. Epub 2014 Apr 24. J Perinatol. 2014. PMID: 24762414

9

Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants.

Christensen RD, Agarwal AM, Nussenzveig RH, Heikal N, Liew MA, Yaish HM. Christensen RD, et al. Among authors: yaish hm. J Perinatol. 2015 May;35(5):357-61. doi: 10.1038/jp.2014.202. Epub 2014 Nov 6. J Perinatol. 2015. PMID: 25357094

10

Siblings with severe pyruvate kinase deficiency and a complex genotype.

Christensen RD, Yaish HM, Nussenzveig RH, Agarwal AM. Christensen RD, et al. Among authors: yaish hm. Am J Med Genet A. 2016 Sep;170(9):2449-52. doi: 10.1002/ajmg.a.37828. Epub 2016 Jun 29. Am J Med Genet A. 2016. PMID: 27354418

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