Puck JM - Search Results

1

Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 years.

Kwan A, Church JA, Cowan MJ, Agarwal R, Kapoor N, Kohn DB, Lewis DB, McGhee SA, Moore TB, Stiehm ER, Porteus M, Aznar CP, Currier R, Lorey F, Puck JM. Kwan A, et al. Among authors: puck jm. J Allergy Clin Immunol. 2013 Jul;132(1):140-50. doi: 10.1016/j.jaci.2013.04.024. J Allergy Clin Immunol. 2013. PMID: 23810098 Free PMC article.

2

Severe combined immunodeficiency in an infant with multiple congenital abnormalities.

Tangsinmankong N, Day NK, Nelson RP Jr, Puck J, Good RA. Tangsinmankong N, et al. J Allergy Clin Immunol. 1999 Jun;103(6):1222-3. doi: 10.1016/s0091-6749(99)70207-1. J Allergy Clin Immunol. 1999. PMID: 10359914 No abstract available.

3

Severe combined immunodeficiency: new advances in diagnosis and treatment.

Puck JM. Puck JM. Immunol Res. 2007;38(1-3):64-7. doi: 10.1007/s12026-007-0029-8. Immunol Res. 2007. PMID: 17917011

4

Primary immunodeficiency: meeting the challenges.

Shearer WT, Malech HL, Puck JM. Shearer WT, et al. Among authors: puck jm. J Allergy Clin Immunol. 2007 Oct;120(4):753-5. doi: 10.1016/j.jaci.2007.09.002. J Allergy Clin Immunol. 2007. PMID: 17931558 No abstract available.

5

Population-based newborn screening for severe combined immunodeficiency: steps toward implementation.

Puck JM; SCID Newborn Screening Working Group. Puck JM, et al. J Allergy Clin Immunol. 2007 Oct;120(4):760-8. doi: 10.1016/j.jaci.2007.08.043. J Allergy Clin Immunol. 2007. PMID: 17931561

6

Neonatal screening for severe combined immune deficiency.

Puck JM. Puck JM. Curr Opin Allergy Clin Immunol. 2007 Dec;7(6):522-7. doi: 10.1097/ACI.0b013e3282f14a2a. Curr Opin Allergy Clin Immunol. 2007. PMID: 17989529 Review.

7

Mutations causing severe combined immunodeficiency: detection with a custom resequencing microarray.

Lebet T, Chiles R, Hsu AP, Mansfield ES, Warrington JA, Puck JM. Lebet T, et al. Among authors: puck jm. Genet Med. 2008 Aug;10(8):575-85. doi: 10.1097/gim.0b013e31818063bc. Genet Med. 2008. PMID: 18641513

8

The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency.

Shiow LR, Roadcap DW, Paris K, Watson SR, Grigorova IL, Lebet T, An J, Xu Y, Jenne CN, Föger N, Sorensen RU, Goodnow CC, Bear JE, Puck JM, Cyster JG. Shiow LR, et al. Among authors: puck jm. Nat Immunol. 2008 Nov;9(11):1307-15. doi: 10.1038/ni.1662. Epub 2008 Oct 5. Nat Immunol. 2008. PMID: 18836449 Free PMC article.

9

Allogeneic hematopoietic cell transplantation for primary immune deficiency diseases: current status and critical needs.

Griffith LM, Cowan MJ, Kohn DB, Notarangelo LD, Puck JM, Schultz KR, Buckley RH, Eapen M, Kamani NR, O'Reilly RJ, Parkman R, Roifman CM, Sullivan KE, Filipovich AH, Fleisher TA, Shearer WT. Griffith LM, et al. Among authors: puck jm. J Allergy Clin Immunol. 2008 Dec;122(6):1087-96. doi: 10.1016/j.jaci.2008.09.045. Epub 2008 Nov 6. J Allergy Clin Immunol. 2008. PMID: 18992926 Free PMC article.

10

Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a Coronin-1A mutation and a chromosome 16p11.2 deletion.

Shiow LR, Paris K, Akana MC, Cyster JG, Sorensen RU, Puck JM. Shiow LR, et al. Among authors: puck jm. Clin Immunol. 2009 Apr;131(1):24-30. doi: 10.1016/j.clim.2008.11.002. Epub 2008 Dec 20. Clin Immunol. 2009. PMID: 19097825 Free PMC article.

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