Girot R - Search Results

1

High adenosine deaminase level among healthy probands of Diamond Blackfan anemia (DBA) cosegregates with the DBA gene region on chromosome 19q13. The DBA Working Group of Société d'Immunologie Pédiatrique (SHIP).

Willig TN, Pérignon JL, Gustavsson P, Gane P, Draptchinskaya N, Testard H, Girot R, Debré M, Stéphan JL, Chenel C, Cartron JP, Dahl N, Tchernia G. Willig TN, et al. Among authors: girot r. Blood. 1998 Dec 1;92(11):4422-7. Blood. 1998. PMID: 9834249 Free article.

2

Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anemia patients. DBA group of Société d'Hématologie et d'Immunologie Pédiatrique (SHIP), Gesellshaft für Pädiatrische Onkologie und Hämatologie (GPOH), and the European Society for Pediatric Hematology and Immunology (ESPHI).

Willig TN, Niemeyer CM, Leblanc T, Tiemann C, Robert A, Budde J, Lambiliotte A, Kohne E, Souillet G, Eber S, Stephan JL, Girot R, Bordigoni P, Cornu G, Blanche S, Guillard JM, Mohandas N, Tchernia G. Willig TN, et al. Among authors: girot r. Pediatr Res. 1999 Nov;46(5):553-61. doi: 10.1203/00006450-199911000-00011. Pediatr Res. 1999. PMID: 10541318

3

Donor for BMT with haemoglobin H disease.

Peltier JY, Girault D, Debre M, Galacteros F, Fischer A, Girot R. Peltier JY, et al. Among authors: girot r. Bone Marrow Transplant. 1993 Jul;12(1):81-4. Bone Marrow Transplant. 1993. PMID: 8374539

4

[Thalassemia major manifested by megaloblastic anemia caused by folate deficiency].

Danel P, Girot R, Tchernia G. Danel P, et al. Among authors: girot r. Arch Fr Pediatr. 1983 Dec;40(10):799-801. Arch Fr Pediatr. 1983. PMID: 6673685 French.

5

Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients. The French Study Group on Sickle Cell Disease.

Maier-Redelsperger M, de Montalembert M, Flahault A, Neonato MG, Ducrocq R, Masson MP, Girot R, Elion J. Maier-Redelsperger M, et al. Among authors: girot r. Blood. 1998 Jun 15;91(12):4472-9. Blood. 1998. PMID: 9616141 Free article.

6

Hereditary orotic aciduria: a defect of pyrimidine metabolism with cellular immunodeficiency.

Girot R, Durandy A, Perignon JL, Griscelli C. Girot R, et al. Birth Defects Orig Artic Ser. 1983;19(3):313-6. Birth Defects Orig Artic Ser. 1983. PMID: 6606448 No abstract available.

7

Strong association between a new marker of hemolysis and glomerulopathy in sickle cell anemia.

Maier-Redelsperger M, Lévy P, Lionnet F, Stankovic K, Haymann JP, Lefèvre G, Avellino V, Perol JP, Girot R, Elion J. Maier-Redelsperger M, et al. Among authors: girot r. Blood Cells Mol Dis. 2010 Dec 15;45(4):289-92. doi: 10.1016/j.bcmd.2010.08.001. Epub 2010 Sep 15. Blood Cells Mol Dis. 2010. PMID: 20833087

8

[Autoimmune hemolytic anemia complicating homozygotic beta- thalassemia].

Fonty E, Cartron J, Gire R, Girot R. Fonty E, et al. Among authors: girot r. Arch Fr Pediatr. 1986 Apr;43(4):261-2. Arch Fr Pediatr. 1986. PMID: 3767588 French.

9

Natural history of GBV-C/hepatitis G virus infection through the follow-up of GBV-C/hepatitis G virus-infected blood donors and recipients studied by RNA polymerase chain reaction and anti-E2 serology.

Lefrère JJ, Loiseau P, Maury J, Lasserre J, Mariotti M, Ravera N, Lerable J, Lefèvre G, Morand-Joubert L, Girot R. Lefrère JJ, et al. Among authors: girot r. Blood. 1997 Nov 1;90(9):3776-80. Blood. 1997. PMID: 9345065 Free article.

10

Natural history of the TT virus infection through follow-up of TTV DNA-positive multiple-transfused patients.

Lefrère JJ, Roudot-Thoraval F, Lefrère F, Kanfer A, Mariotti M, Lerable J, Thauvin M, Lefèvre G, Rouger P, Girot R. Lefrère JJ, et al. Among authors: girot r. Blood. 2000 Jan 1;95(1):347-51. Blood. 2000. PMID: 10607723 Free article.

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