Schved JF - Search Results

1

Global sequencing approach for characterizing the molecular background of hereditary iron disorders.

Cunat S, Giansily-Blaizot M, Bismuth M, Blanc F, Dereure O, Larrey D, Quellec AL, Pouderoux P, Rose C, Raingeard I, Renard E, Schved JF, Aguilar-Martinez P; CHU Montpellier AOI 2004 Working Group. Cunat S, et al. Among authors: schved jf. Clin Chem. 2007 Dec;53(12):2060-9. doi: 10.1373/clinchem.2007.090605. Epub 2007 Oct 19. Clin Chem. 2007. PMID: 17951290

2

Autoantibody to plasma fibrinopeptide A in a patient with a severe acquired haemorrhagic syndrome.

Gris JC, Schved JF, Branger B, Aguilar-Martinez P, Vécina F, Oulès R, Sarlat C, Fourcade J. Gris JC, et al. Among authors: schved jf. Blood Coagul Fibrinolysis. 1992 Oct;3(5):519-29. doi: 10.1097/00001721-199210000-00002. Blood Coagul Fibrinolysis. 1992. PMID: 1450318

3

Impaired fibrinolytic capacity and early recurrent spontaneous abortion.

Gris JC, Schved JF, Neveu S, Mares P, Aguilar-Martinez P, Dupaigne D. Gris JC, et al. Among authors: schved jf. BMJ. 1990 Jun 9;300(6738):1500. doi: 10.1136/bmj.300.6738.1500. BMJ. 1990. PMID: 2115385 Free PMC article. No abstract available.

4

Impaired fibrinolytic capacity in patients with inflammatory bowel disease.

Gris JC, Schved JF, Raffanel C, Dubois A, Aguilar-Martinez P, Arnaud A, Sanchez N, Sarlat C, Balmès JL. Gris JC, et al. Among authors: schved jf. Thromb Haemost. 1990 Jun 28;63(3):472-5. Thromb Haemost. 1990. PMID: 2119529

5

Direct carrier detection for severe haemophilia A: application to families with no available affected male.

Maugard C, Aguilar-Martinez P, Schved JF, Biron C, Gris JC, Demaille J, Claustres M. Maugard C, et al. Among authors: schved jf. Genet Couns. 1995;6(2):109-12. Genet Couns. 1995. PMID: 7546452

6

DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory.

Aguilar-Martinez P, Fabre N, Navarro R, Schved JF, Gris JC, Romey MC, Demaille J, Claustres M. Aguilar-Martinez P, et al. Among authors: schved jf. Genet Couns. 1993;4(4):311-9. Genet Couns. 1993. PMID: 7906519

7

Factor IX gene mutations causing haemophilia B: comparison of SSC screening versus systematic DNA sequencing and diagnostic applications.

Aguilar-Martinez P, Romey MC, Schved JF, Gris JC, Demaille J, Claustres M. Aguilar-Martinez P, et al. Among authors: schved jf. Hum Genet. 1994 Sep;94(3):287-90. doi: 10.1007/BF00208285. Hum Genet. 1994. PMID: 8076946

8

A novel mutation (Val-373 to Glu) in the catalytic domain of factor IX, resulting in moderately/severe hemophilia B in a southern French patient.

Aguilar-Martinez P, Romey MC, Gris JC, Schved JF, Demaille J, Claustres M. Aguilar-Martinez P, et al. Among authors: schved jf. Hum Mutat. 1994;3(2):156-8. doi: 10.1002/humu.1380030211. Hum Mutat. 1994. PMID: 8199596 No abstract available.

9

Comparison of the protein and DNA approaches for the characterization of a beta-globin chain variant, hemoglobin Cocody [beta 21 (B3) Asp--->Asn], in a Caucasian patient.

Aguilar-Martinez P, Galacteros F, Schved JF, Blouquit Y, Gris JC, Demaille J, Claustres M. Aguilar-Martinez P, et al. Among authors: schved jf. Ann Hematol. 1993 May;66(5):269-72. doi: 10.1007/BF01738480. Ann Hematol. 1993. PMID: 8507722

10

A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome.

Aguilar-Martinez P, Biron C, Masmejean C, Jeanjean P, Schved JF. Aguilar-Martinez P, et al. Among authors: schved jf. Blood. 1996 Sep 1;88(5):1895. Blood. 1996. PMID: 8781450 Free article. No abstract available.

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