Dumez Y - Search Results

1

Prenatal testing for inherited immune deficiencies by fetal blood sampling.

Durandy A, Oury C, Griscelli C, Dumez Y, Oury JF, Henrion R. Durandy A, et al. Among authors: dumez y. Prenat Diagn. 1982 Apr;2(2):109-13. doi: 10.1002/pd.1970020206. Prenat Diagn. 1982. PMID: 7145836

2

Prenatal diagnosis of severe combined immunodeficiency with defective synthesis of HLA molecules.

Durandy A, Cerf-Bensussan N, Dumez Y, Griscelli C. Durandy A, et al. Among authors: dumez y. Prenat Diagn. 1987;7(1):27-34. doi: 10.1002/pd.1970070106. Prenat Diagn. 1987. PMID: 3823004

3

Antenatal diagnosis of severe combined immunodeficiency from fetal cord blood.

Durandy A, Griscelli C, Dumez Y, Oury JF, Henrion R, Briard ML, Frezal J. Durandy A, et al. Among authors: dumez y. Lancet. 1982 Apr 10;1(8276):852-3. doi: 10.1016/s0140-6736(82)91898-0. Lancet. 1982. PMID: 6122078 No abstract available.

4

Prenatal diagnosis of severe combined immunodeficiency.

Durandy A, Dumez Y, Guy-Grand D, Oury C, Henrion R, Griscelli C. Durandy A, et al. Among authors: dumez y. J Pediatr. 1982 Dec;101(6):995-7. doi: 10.1016/s0022-3476(82)80029-2. J Pediatr. 1982. PMID: 6982968 No abstract available.

5

Microvillar enzyme assays in amniotic fluid and fetal tissues at different stages of development.

Muller F, Oury JF, Dumez Y, Boué J, Boué A. Muller F, et al. Among authors: dumez y. Prenat Diagn. 1988 Mar;8(3):189-98. doi: 10.1002/pd.1970080305. Prenat Diagn. 1988. PMID: 2897684

6

Prenatal diagnosis of chronic granulomatous disease (CGD) in four high risk male fetuses.

Huu TP, Dumez Y, Marquetty C, Durandy A, Boue J, Hakim J. Huu TP, et al. Among authors: dumez y. Prenat Diagn. 1987 May;7(4):253-60. doi: 10.1002/pd.1970070405. Prenat Diagn. 1987. PMID: 3588543

7

[Prenatal diagnosis of severe hereditary immunologic deficiencies].

Durandy A, Dumez Y, Griscelli C. Durandy A, et al. Among authors: dumez y. Arch Fr Pediatr. 1985 Mar;42(3):163-7. Arch Fr Pediatr. 1985. PMID: 4004478 French.

8

Prenatal diagnosis of mucolipidosis type II on first-trimester amniotic fluid.

Poenaru L, Mezard C, Akli S, Oury JF, Dumez Y, Boue J. Poenaru L, et al. Among authors: dumez y. Prenat Diagn. 1990 Apr;10(4):231-5. doi: 10.1002/pd.1970100404. Prenat Diagn. 1990. PMID: 1973293

9

Early prenatal diagnosis of inherited severe immunodeficiencies linked to enzyme deficiencies.

Pérignon JL, Durandy A, Peter MO, Freycon F, Dumez Y, Griscelli C. Pérignon JL, et al. Among authors: dumez y. J Pediatr. 1987 Oct;111(4):595-8. doi: 10.1016/s0022-3476(87)80129-4. J Pediatr. 1987. PMID: 3116192 No abstract available.

10

Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experience.

Chadefaux-Vekemans B, Rabier D, Cadoudal N, Lescoat A, Chabli A, Aupetit J, Dumez Y, Oury JF. Chadefaux-Vekemans B, et al. Among authors: dumez y. Prenat Diagn. 2006 Sep;26(9):814-8. doi: 10.1002/pd.1509. Prenat Diagn. 2006. PMID: 16821251

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