R. Kastally

发表

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K-dependent coagulation factor deficiency.

J. Rosa, K. Berkner, R. Shtofman, 2006, Blood.

Compound heterozygosity of novel missense mutations in the γ-carboxylase gene causes hereditary combined vitamin K-dependent coagulation factor deficiency

K. Berkner, R. Shtofman, D. Darghouth, 2006 .

Hepatitis C core antibody detection in acute hepatitis and cirrhosis patients from Tunisia.

P. Coursaget, R. Kastally, B. Simpson, 1992, Pathologie-biologie.

HB Tunis [α2β2124(H2) PRO→SER], A New β Chain Variant Identified by HPLC

Y. Blouquit, J. Rosa, N. Arous, 1988 .

High risk genotypes for celiac disease.

M. Babron, F. Clerget-Darpoux, J. Eliaou, 1994, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

High interferon titer and defective NK‐cell activity in the circulation of nasopharyngeal carcinoma patients

R. Oueslati, R. Kastally, M. Cammoun, 1989, International journal of cancer.

Prevalence of hepatitis C virus infection in Africa: anti-HCV antibodies in the general population and in patients suffering from cirrhosis or primary liver cancer.

B. Yvonnet, P. Coursaget, J. Chiron, 1990, Research in virology.

Etiology of acute sporadic hepatitis in adults in Senegal and Tunisia.

P. Coursaget, D. Leboulleux, M. Ndao, 1995, Scandinavian journal of infectious diseases.

Familial clustering of hepatitis B virus infections and prevention of perinatal transmission by immunization with a reduced number of doses in an area of intermediate endemicity (Tunisia).

P. Coursaget, B. Fritzell, N. Boukhris, 1994, Vaccine.

First observation of Hb Montgomery [alpha 48(CD6)Leu----Arg] in Tunisia.

F. Galactéros, J. Rosa, N. Arous, 1988, Hemoglobin.

Hemoglobin Beirut [α2β2126(H4)Val→Ala] in an Algerian Family

Y. Blouquit, F. Galactéros, J. Rosa, 1986 .

Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyria.

C. Beaumont, H. de Verneuil, Y. Nordmann, 1984, American journal of human genetics.

[Neonatal screening of G6PD deficiency in Tunisia].

M. Ouederni, M. Chahed, S. Kacem, 2010, Archives de l'Institut Pasteur de Tunis.

Presence of in vivo‐activated t‐cells expressing hla‐dr molecules and il‐2 receptors in peripheral blood of patients with nasopharyngeal carcinoma

R. Ellouz, H. Kammoun, R. Kastally, 1987, International journal of cancer.

[Homocystinuria. A type with vascular thrombosis and factor VII deficiency].

R. Kastally, R. Benosman, S. Karoui, 1986, Archives francaises de pediatrie.

Incidence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Tunisian populations.

R. Rosa, A. Mrad, Y. Gharbi, 1989, Nouvelle revue francaise d'hematologie.