Hershfield MS - Search Results

1

Response to: 'Total adenosine deaminase highly correlated with adenosine deaminase 2 activity in serum' by Gao et al.

Lee PY, Huang Z, Hershfield MS, Nigrovic PA. Lee PY, et al. Among authors: hershfield ms. Ann Rheum Dis. 2022 Feb;81(2):e31. doi: 10.1136/annrheumdis-2020-217055. Epub 2020 Feb 13. Ann Rheum Dis. 2022. PMID: 32054602 No abstract available.

2

IgG antibody response to polyethylene glycol-modified adenosine deaminase in patients with adenosine deaminase deficiency.

Chaffee S, Mary A, Stiehm ER, Girault D, Fischer A, Hershfield MS. Chaffee S, et al. Among authors: hershfield ms. J Clin Invest. 1992 May;89(5):1643-51. doi: 10.1172/JCI115761. J Clin Invest. 1992. PMID: 1569204 Free PMC article.

3

PEG-ADA replacement therapy for adenosine deaminase deficiency: an update after 8.5 years.

Hershfield MS. Hershfield MS. Clin Immunol Immunopathol. 1995 Sep;76(3 Pt 2):S228-32. doi: 10.1016/s0090-1229(95)90306-2. Clin Immunol Immunopathol. 1995. PMID: 7554473 Clinical Trial.

4

Enzyme replacement therapy of adenosine deaminase deficiency with polyethylene glycol-modified adenosine deaminase (PEG-ADA).

Hershfield MS. Hershfield MS. Immunodeficiency. 1993;4(1-4):93-7. Immunodeficiency. 1993. PMID: 8167743 Review. No abstract available.

5

Clinical expression, genetics and therapy of adenosine deaminase (ADA) deficiency.

Hershfield MS, Arredondo-Vega FX, Santisteban I. Hershfield MS, et al. J Inherit Metab Dis. 1997 Jun;20(2):179-85. doi: 10.1023/a:1005300621350. J Inherit Metab Dis. 1997. PMID: 9211190 Review.

6

Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles.

Arredondo-Vega FX, Santisteban I, Daniels S, Toutain S, Hershfield MS. Arredondo-Vega FX, et al. Among authors: hershfield ms. Am J Hum Genet. 1998 Oct;63(4):1049-59. doi: 10.1086/302054. Am J Hum Genet. 1998. PMID: 9758612 Free PMC article.

7

Adenosine deaminase deficiency: clinical expression, molecular basis, and therapy.

Hershfield MS. Hershfield MS. Semin Hematol. 1998 Oct;35(4):291-8. Semin Hematol. 1998. PMID: 9801258 Review.

8

E. coli expression system for identifying folding mutations of human adenosine deaminase.

Santisteban I, Arredondo-Vega FX, Daniels S, Hershfield MS. Santisteban I, et al. Among authors: hershfield ms. Methods Mol Biol. 2003;232:175-82. doi: 10.1385/1-59259-394-1:175. Methods Mol Biol. 2003. PMID: 12840549 No abstract available.

9

A 24-Year Enzyme Replacement Therapy in an Adenosine-deaminase-Deficient Patient.

Tartibi HM, Hershfield MS, Bahna SL. Tartibi HM, et al. Among authors: hershfield ms. Pediatrics. 2016 Jan;137(1). doi: 10.1542/peds.2015-2169. Epub 2015 Dec 18. Pediatrics. 2016. PMID: 26684479

10

Disrupted N-linked glycosylation as a disease mechanism in deficiency of ADA2.

Lee PY, Huang Y, Zhou Q, Schnappauf O, Hershfield MS, Li Y, Ganson NJ, Sampaio Moura N, Delmonte OM, Stone SS, Rivkin MJ, Pai SY, Lyons T, Sundel RP, Hsu VW, Notarangelo LD, Aksentijevich I, Nigrovic PA. Lee PY, et al. Among authors: hershfield ms. J Allergy Clin Immunol. 2018 Oct;142(4):1363-1365.e8. doi: 10.1016/j.jaci.2018.05.038. Epub 2018 Jun 21. J Allergy Clin Immunol. 2018. PMID: 29936104 Free PMC article.

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