Hershfield MS - Search Results

1

Long-term outcomes after gene therapy for adenosine deaminase severe combined immune deficiency.

Reinhardt B, Habib O, Shaw KL, Garabedian E, Carbonaro-Sarracino DA, Terrazas D, Fernandez BC, De Oliveira S, Moore TB, Ikeda AK, Engel BC, Podsakoff GM, Hollis RP, Fernandes A, Jackson C, Shupien S, Mishra S, Davila A, Mottahedeh J, Vitomirov A, Meng W, Rosenfeld AM, Roche AM, Hokama P, Reddy S, Everett J, Wang X, Luning Prak ET, Cornetta K, Hershfield MS, Sokolic R, De Ravin SS, Malech HL, Bushman FD, Candotti F, Kohn DB. Reinhardt B, et al. Among authors: hershfield ms. Blood. 2021 Oct 14;138(15):1304-1316. doi: 10.1182/blood.2020010260. Blood. 2021. PMID: 33974038 Free PMC article. Clinical Trial.

2

Antibody responses to bacteriophage phi X174 in patients with adenosine deaminase deficiency.

Ochs HD, Buckley RH, Kobayashi RH, Kobayashi AL, Sorensen RU, Douglas SD, Hamilton BL, Hershfield MS. Ochs HD, et al. Among authors: hershfield ms. Blood. 1992 Sep 1;80(5):1163-71. Blood. 1992. PMID: 1387561 Free 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

PEG-ADA: an alternative to haploidentical bone marrow transplantation and an adjunct to gene therapy for adenosine deaminase deficiency.

Hershfield MS. Hershfield MS. Hum Mutat. 1995;5(2):107-12. doi: 10.1002/humu.1380050202. Hum Mutat. 1995. PMID: 7749407 Review.

5

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.

6

Correct splicing despite mutation of the invariant first nucleotide of a 5' splice site: a possible basis for disparate clinical phenotypes in siblings with adenosine deaminase deficiency.

Arredondo-Vega FX, Santisteban I, Kelly S, Schlossman CM, Umetsu DT, Hershfield MS. Arredondo-Vega FX, et al. Among authors: hershfield ms. Am J Hum Genet. 1994 May;54(5):820-30. Am J Hum Genet. 1994. PMID: 8178821 Free PMC article.

7

A homozygous 5 base-pair deletion in exon 10 of the adenosine deaminase (ADA) gene in a child with severe combined immunodeficiency and very low levels of ADA mRNA and protein.

Gossage DL, Norby-Slycord CJ, Hershfield MS, Markert ML. Gossage DL, et al. Among authors: hershfield ms. Hum Mol Genet. 1993 Sep;2(9):1493-4. doi: 10.1093/hmg/2.9.1493. Hum Mol Genet. 1993. PMID: 8242080 No abstract available.

8

T lymphocyte ontogeny in adenosine deaminase-deficient severe combined immune deficiency after treatment with polyethylene glycol-modified adenosine deaminase.

Weinberg K, Hershfield MS, Bastian J, Kohn D, Sender L, Parkman R, Lenarsky C. Weinberg K, et al. Among authors: hershfield ms. J Clin Invest. 1993 Aug;92(2):596-602. doi: 10.1172/JCI116626. J Clin Invest. 1993. PMID: 8349799 Free PMC article.

9

Enzyme replacement therapy with polyethylene glycol-adenosine deaminase in adenosine deaminase deficiency: overview and case reports of three patients, including two now receiving gene therapy.

Hershfield MS, Chaffee S, Sorensen RU. Hershfield MS, et al. Pediatr Res. 1993 Jan;33(1 Suppl):S42-7; discussion S47-8. doi: 10.1203/00006450-199305001-00236. Pediatr Res. 1993. PMID: 8433874 Review.

10

Suppression of an antibody to adenosine-deaminase (ADA) in an ADA-deficient patient receiving polyethylene glycol modified adenosine deaminase.

Chun JD, Lee N, Kobayashi RH, Chaffee S, Hershfield MS, Stiehm ER. Chun JD, et al. Among authors: hershfield ms. Ann Allergy. 1993 Jun;70(6):462-6. Ann Allergy. 1993. PMID: 8507039

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