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Novel factor V C2-domain mutation (R2074H) in two families with factor V deficiency and bleeding

Thrombosis and haemostasis, 2002-02, Vol.87 (2), p.294-299

2002

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Cytokine and immunoglobulin production by PWM-stimulated peripheral and tumor-infiltrating lymphocytes of undifferentiated nasopharyngeal carcinoma (NPC) patients

BMC cancer, 2004-09, Vol.4 (1), p.68-68, Article 68

2004

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Occurrence of the αI 22 Arg→His (CGT→CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis

British journal of haematology, 1991-05, Vol.78 (1), p.108-113

1991

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Neonatal screening of G6PD deficiency in Tunisia

Archives de l'Institut Pasteur de Tunis, 2010, Vol.87 (1-2), p.69

2010

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

International journal of cancer, 1989-04, Vol.43 (4), p.543-548

1989

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Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

Blood, 1989-08, Vol.74 (2), p.828-832

1989

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Spectrin Tunis (αI/78): A New αI Variant That Causes Asymptomatic Hereditary Elliptocytosis in the Heterozygous State

Blood, 1988-02, Vol.71 (2), p.508-511

1988

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

International journal of cancer, 1987-06, Vol.39 (6), p.663-669

1987

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Hemoglobin Athens‐Georgia [α2 β2 40(C6)Arg→Lys] in association with β0‐thalassemia in Tunisia

American journal of hematology, 1989-10, Vol.32 (2), p.117-122

1989

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Hemoglobin Athens-Georgia [alpha 2 beta 2 40(C6)Arg----Lys] in association with beta 0-thalassemia in Tunisia

American journal of hematology, 1989-10, Vol.32 (2), p.117-122

1989

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

Pathologie biologie (Paris), 1992-06, Vol.40 (6), p.646-648

1992

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

Hemoglobin, 1988, Vol.12 (1), p.23-30

1988

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First Observation of HB Montgomery [α48(CDb)LEU→ARG] in Tunisia

Hemoglobin, 1988, Vol.12 (1), p.67-70

1988

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Porphyrie hépato-érythrocytaire chez deux sœurs jumelles

Annales de dermatologie et de vénéréologie, 1985, Vol.112 (5), p.453-456

1985

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SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in trans

The Journal of clinical investigation, 1991-06, Vol.87 (6), p.2169-2177

1991

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Infection par le virus de l'hépatite B dans les centres d'hémodialyse en Tunisie

La Presse médicale (1983), 1984-09, Vol.13 (32)

1984

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

Hemoglobin, 1986, Vol.10 (6), p.651-654

1986

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Familial clustering of hepatitis B virus infections and prevention of perinatal transmission by immunization with a reduced number of doses in an area

Vaccine, 1994, Vol.12 (3), p.275-278

1994

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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)

Vaccine, 1994, Vol.12 (3), p.275-278

1994

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High risk genotypes for celiac disease

Comptes rendus de l'Académie des sciences, Série III, Sciences de la vie, 1994-10, Vol.317 (10), p.931

1994

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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

Research in virology (Paris), 1990-07, Vol.141 (4), p.449-454

1990

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Association of heterozygote drepanocytosis and G6PD deficiency: apropos of a case

Tunisie Medicale, 1995-10, Vol.73 (10), p.415

1995

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

Nouvelle revue francaise d'hematologie, 1989, Vol.31 (3), p.189

1989

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

American journal of human genetics, 1984-05, Vol.36 (3), p.613-622

1984

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Low expression allele αLELY of red cell spectrin is associated with mutations in exon 40 (αV/41 polymorphism) and intron 45 and with partial skipping of exon 46

The Journal of clinical investigation, 1993-05, Vol.91 (5), p.2091-2096

1993

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Novel factor V C2-domain mutation (R2074H) in two families with factor V deficiency and bleeding

Cytokine and immunoglobulin production by PWM-stimulated peripheral and tumor-infiltrating lymphocytes of undifferentiated nasopharyngeal carcinoma (NPC) patients

Occurrence of the αI 22 Arg→His (CGT→CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis

Neonatal screening of G6PD deficiency in Tunisia

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

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

Spectrin Tunis (αI/78): A New αI Variant That Causes Asymptomatic Hereditary Elliptocytosis in the Heterozygous State

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

Hemoglobin Athens‐Georgia [α2 β2 40(C6)Arg→Lys] in association with β0‐thalassemia in Tunisia

Hemoglobin Athens-Georgia [alpha 2 beta 2 40(C6)Arg----Lys] in association with beta 0-thalassemia in Tunisia

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

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

First Observation of HB Montgomery [α48(CDb)LEU→ARG] in Tunisia

Porphyrie hépato-érythrocytaire chez deux sœurs jumelles

SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in trans

Infection par le virus de l'hépatite B dans les centres d'hémodialyse en Tunisie

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

Familial clustering of hepatitis B virus infections and prevention of perinatal transmission by immunization with a reduced number of doses in an area

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)

High risk genotypes for celiac disease

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

Association of heterozygote drepanocytosis and G6PD deficiency: apropos of a case

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

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

Low expression allele αLELY of red cell spectrin is associated with mutations in exon 40 (αV/41 polymorphism) and intron 45 and with partial skipping of exon 46

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