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Results: 1 to 20 of 95

Similar articles for PubMed (Select 46025)

1.

Adenosine-deaminase deficiency in a child diagnosed prenatally.

Hirschhorn R, Beratis N, Rosen FS, Parkman R, Stern R, Polmar S.

Lancet. 1975 Jan 11;1(7898):73-5.

PMID:
46025
3.

Severe combined immunodeficiency and adenosine deaminase deficiency.

Parkman R, Gelfand EW, Rosen FS, Sanderson A, Hirschhorn R.

N Engl J Med. 1975 Apr 3;292(14):714-9.

PMID:
1089883
4.

Letter: Severe combined immunodeficiency and adenosine-deaminase deficiency.

Hirschhorn R, Beratis NG.

Lancet. 1973 Nov 24;2(7839):1217-8. No abstract available.

PMID:
4127604
5.

Prenatal diagnosis for adenosine deaminase deficiency.

Ziegler JB, Van der Weyden MB, Lee CH, Daniel A.

J Med Genet. 1981 Apr;18(2):154-6.

6.
7.

Adenosine deaminase deficiency and immunodeficiencies.

Hirschhorn R.

Fed Proc. 1977 Jul;36(8):2166-70.

PMID:
872949
8.

Prenatal detection of a probable heterozygote for ADA deficiency and severe combined immunodeficiency disease using a microradioassay.

Aitken DA, Kleijer WJ, Niermeijer MF, Herbschleb-Voogt E, Galjaard H.

Clin Genet. 1980 Apr;17(4):293-8.

PMID:
7371221
9.
10.

Prenatal exclusion of purine nucleoside phosphorylase deficiency.

Carapella De Luca E, Stegagno M, Dionisi Vici C, Paesano R, Fairbanks LD, Morris GS, Simmonds HA.

Eur J Pediatr. 1986 Apr;145(1-2):51-3.

PMID:
3089796
11.

Adenosine deaminase deficiency.

Hirschhorn R.

Immunodefic Rev. 1990;2(3):175-98. Review.

PMID:
2078332
13.

Severe combined immunodeficiency in a child with a healthy adenosine deaminase deficient mother.

Schmalstieg FC, Mills GC, Tsuda H, Goldman AS.

Pediatr Res. 1983 Dec;17(12):935-40.

PMID:
6606796
15.

Adenosine deaminase deficiency in a child with severe combined immunodeficiency.

Knudsen BB, Dissing J.

Clin Genet. 1973;4(4):344-7. No abstract available.

PMID:
4127044
16.

Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villi.

Aitken DA, Gilmore DH, Frew CA, Ferguson-Smith ME, Carty MJ, Chatfield WR.

J Med Genet. 1986 Feb;23(1):52-4.

17.

Early prenatal diagnosis of the ICF syndrome.

Björck EJ, Bui TH, Wijmenga C, Grandell U, Nordenskjöld M.

Prenat Diagn. 2000 Oct;20(10):828-31.

PMID:
11038463
18.
19.

[Primary immunodeficiencies. Clinical features and variant forms].

Fontán Casariego G.

Allergol Immunopathol (Madr). 2001 May-Jun;29(3):101-7. Review. Spanish.

PMID:
11434882
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