Nussenzveig RH - Search Results

1

Development of a rapid multiplex PCR assay for identification of the three common Hemoglobin-Lepore variants (Boston-Washington, Baltimore, and Hollandia) and identification of a new Lepore variant.

Nussenzveig RH, Vanhille DL, Hussey D, Reading NS, Agarwal AM. Nussenzveig RH, et al. Am J Hematol. 2012 Oct;87(10):E74-5. doi: 10.1002/ajh.23304. Epub 2012 Aug 1. Am J Hematol. 2012. PMID: 23001912 Free article. No abstract available.

2

Commentary.

Agarwal AM, Nussenzveig R. Agarwal AM, et al. Clin Chem. 2012 Feb;58(2):335-6. doi: 10.1373/clinchem.2011.175844. Clin Chem. 2012. PMID: 22287664 No abstract available.

3

Detection of JAK2 mutations in paraffin marrow biopsies by high resolution melting analysis: identification of L611S alone and in cis with V617F in polycythemia vera.

Nussenzveig RH, Burjanivova T, Salama ME, Ogilvie NW, Marcinek J, Plank L, Agarwal AM, Perkins SL, Prchal JT. Nussenzveig RH, et al. Leuk Lymphoma. 2012 Dec;53(12):2479-86. doi: 10.3109/10428194.2012.697562. Epub 2012 Jul 9. Leuk Lymphoma. 2012. PMID: 22642932

4

Best practices for use of the HEMOX analyzer in the clinical laboratory: quality control determination and choice of anticoagulant.

Vanhille DL, Nussenzveig RH, Glezos C, Perkins S, Agarwal AM. Vanhille DL, et al. Among authors: nussenzveig rh. Lab Hematol. 2012 Sep;18(3):17-9. doi: 10.1532/LH96.12001. Lab Hematol. 2012. PMID: 23000486

5

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: nussenzveig rh. Pediatrics. 2013 Aug;132(2):e531-4. doi: 10.1542/peds.2012-3799. Epub 2013 Jul 22. Pediatrics. 2013. PMID: 23878048

6

Identification of one or two α-globin gene deletions by isoelectric focusing electrophoresis.

Agarwal AM, Nussenzveig RH, Hoke C, Lorey TS, Greene DN. Agarwal AM, et al. Among authors: nussenzveig rh. Am J Clin Pathol. 2013 Sep;140(3):301-5. doi: 10.1309/AJCPF4UIJKH3EOBY. Am J Clin Pathol. 2013. PMID: 23955447

7

Novel exon 2 α spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct α spectrin defects.

Swierczek S, Agarwal AM, Naidoo K, Lorenzo FR, Whisenant J, Nussenzveig RH, Agarwal N, Coetzer TL, Prchal JT. Swierczek S, et al. Among authors: nussenzveig rh. Haematologica. 2013 Dec;98(12):1972-9. doi: 10.3324/haematol.2013.086629. Epub 2013 Sep 27. Haematologica. 2013. PMID: 24077844 Free PMC article.

8

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: nussenzveig rh. Neonatology. 2014;105(1):1-4. doi: 10.1159/000354884. Epub 2013 Oct 31. Neonatology. 2014. PMID: 24193021

9

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: nussenzveig rh. J Perinatol. 2014 Aug;34(8):616-9. doi: 10.1038/jp.2014.68. Epub 2014 Apr 24. J Perinatol. 2014. PMID: 24762414

10

Deparaffinization with mineral oil: a simple procedure for extraction of high-quality DNA from archival formalin-fixed paraffin-embedded samples.

Heikal N, Nussenzveig RH, Agarwal AM. Heikal N, et al. Among authors: nussenzveig rh. Appl Immunohistochem Mol Morphol. 2014 Sep;22(8):623-6. doi: 10.1097/PAI.0b013e3182a77bfe. Appl Immunohistochem Mol Morphol. 2014. PMID: 24897067

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