Mattei JF - Search Results

1

Outcome of a school screening programme for carriers of haemoglobin disease.

Lena-Russo D, Badens C, Aubinaud M, Merono F, Paolasso C, Martini N, Mattei JF. Lena-Russo D, et al. Among authors: mattei jf. J Med Screen. 2002;9(2):67-9. doi: 10.1136/jms.9.2.67. J Med Screen. 2002. PMID: 12133925

2

[Genetic hemoglobin diseases. Prevention at centers for family planning and education of maternal-child protection in Marseille].

Lena-Russo D, Erny N, Serradimigni F, Badens C, Aubinaud M, Merono F, Paolasso C, Mattei JF, Giraud F. Lena-Russo D, et al. Among authors: mattei jf. Presse Med. 1996 Feb 3;25(4):151-3. Presse Med. 1996. PMID: 8728899 French.

3

[Glucose-6-phosphate dehydrogenase et neonatal jaundice].

Badens C, Leclaire M, Collomb J, Auquier P, Soyer P, Michel G, Mattei JF, Lena-Russo D. Badens C, et al. Among authors: mattei jf. Presse Med. 2001 Mar 24;30(11):524-6. Presse Med. 2001. PMID: 11317924 French.

4

Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian population.

Badens C, Martinez di Montemuros F, Thuret I, Michel G, Mattei JF, Cappellini MD, Lena-Russo D. Badens C, et al. Among authors: mattei jf. Hematol J. 2000;1(4):264-8. doi: 10.1038/sj.thj.6200042. Hematol J. 2000. PMID: 11920200

5

Characterization of a new polymorphism, IVS-I-108 (T-->C), and a new beta-thalassemia mutation, -27 (A-->T), discovered in the course of a prenatal diagnosis.

Badens C, Jassim N, Martini N, Mattei JF, Elion J, Lena-Russo D. Badens C, et al. Among authors: mattei jf. Hemoglobin. 1999 Nov;23(4):339-44. doi: 10.3109/03630269909090749. Hemoglobin. 1999. PMID: 10569722

6

A novel polymorphism 3' to the beta-globin gene.

Badens C, Merghoub T, Lena-Russo D, Labie D, Elion J, Mattei JF. Badens C, et al. Among authors: mattei jf. Hemoglobin. 1998 Jul;22(4):387-90. doi: 10.3109/03630269809071534. Hemoglobin. 1998. PMID: 9730370 No abstract available.

7

Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene.

Badens C, Thuret I, Michel G, Krawczak M, Mattei JF, Lena-Russo D, Labie D, Elion J. Badens C, et al. Among authors: mattei jf. Hum Mutat. 1996;8(1):89-92. doi: 10.1002/(SICI)1098-1004(1996)8:1<89::AID-HUMU16>3.0.CO;2-N. Hum Mutat. 1996. PMID: 8807345 No abstract available.

8

[Molecular biology in genetic counseling of Duchenne and Becker myopathy].

Philip N, Voelckel MA, Girardot L, Lambert JC, Moncla A, Mattei JF, Giraud F. Philip N, et al. Among authors: mattei jf. Pediatrie. 1992;47(12):821-8. Pediatrie. 1992. PMID: 1338927 French.

9

Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling.

Moncla A, Malzac P, Livet MO, Voelckel MA, Mancini J, Delaroziere JC, Philip N, Mattei JF. Moncla A, et al. Among authors: mattei jf. J Med Genet. 1999 Jul;36(7):554-60. J Med Genet. 1999. PMID: 10424818 Free PMC article.

10

[Medicine facing the challenge of genetics: from singular workshop to public health].

Mattei JF. Mattei JF. Bull Acad Natl Med. 1996 Jun-Jul;180(6):1303-9; discussion 1309-14. Bull Acad Natl Med. 1996. PMID: 8991611 French.

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