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International Journal of Laboratory Hematology
|
May 13, 2017
The evaluation of the relevance of thrombin generation and procoagulant activity in thrombotic risk assessment in BCR-ABL-negative myeloproliferative neoplasm patients
H Baccouche, M Ben Jemaa, A Chakroun, et al.
La Tunisie Medicale
|
January 13, 2001
[Costal hydatid cyst (report of 2 cases)]
N Ben Romdhane, S Fenniche, S Bousnina, et al.
La Revue De Medecine Interne
|
August 17, 2010
[Chorea revealing a polycytemia vera]
I Ben Ghorbel, T Ben Salem, M Lamloum, et al.
Pathologie-Biologie
|
August 3, 2010
Evaluation of serum VEGF levels in untreated erythrocytosis patients
C Maktouf, A Bounemra, S Mahjoub, et al.
Journal De Mycologie Medicale
|
March 10, 2018
Disseminated histoplasmosis diagnosed in the bone marrow of an HIV-infected patient: First case imported in Tunisia
N Fakhfakh, R Abdelmlak, S Aissa, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique
|
October 23, 2012
[Pediatric Hodgkin disease in North Tunisia: clinical and therapeutic study]
L Kochbati, F Fdhila, I Belaid, et al.
Bone Marrow Transplantation
|
September 10, 2005
Prevalence of inherited prothrombotic abnormalities and central venous catheter-related thrombosis in haematopoietic stem cell transplants recipients
A Abdelkefi, N Ben Romdhane, A Kriaa, et al.
Bone Marrow Transplantation
|
June 22, 2005
First-line thalidomide-dexamethasone therapy in preparation for autologous stem cell transplantation in young patients (<61 years) with symptomatic multiple myeloma
A Abdelkefi, L Torjman, N Ben Romdhane, et al.
Molecular Biology Reports
|
October 16, 2012
Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association
N Laouini, A Bibi, H Ammar, et al.
Journal of Medical Genetics
|
June 15, 2010
Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia
B Pérez, F Mechinaud, C Galambrun, et al.
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of 2
Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
International Journal of Laboratory Hematology
|
May 13, 2017
The evaluation of the relevance of thrombin generation and procoagulant activity in thrombotic risk assessment in BCR-ABL-negative myeloproliferative neoplasm patients
H Baccouche, M Ben Jemaa, A Chakroun, et al.
La Tunisie Medicale
|
January 13, 2001
[Costal hydatid cyst (report of 2 cases)]
N Ben Romdhane, S Fenniche, S Bousnina, et al.
La Revue De Medecine Interne
|
August 17, 2010
[Chorea revealing a polycytemia vera]
I Ben Ghorbel, T Ben Salem, M Lamloum, et al.
Pathologie-Biologie
|
August 3, 2010
Evaluation of serum VEGF levels in untreated erythrocytosis patients
C Maktouf, A Bounemra, S Mahjoub, et al.
Journal De Mycologie Medicale
|
March 10, 2018
Disseminated histoplasmosis diagnosed in the bone marrow of an HIV-infected patient: First case imported in Tunisia
N Fakhfakh, R Abdelmlak, S Aissa, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique
|
October 23, 2012
[Pediatric Hodgkin disease in North Tunisia: clinical and therapeutic study]
L Kochbati, F Fdhila, I Belaid, et al.
Bone Marrow Transplantation
|
September 10, 2005
Prevalence of inherited prothrombotic abnormalities and central venous catheter-related thrombosis in haematopoietic stem cell transplants recipients
A Abdelkefi, N Ben Romdhane, A Kriaa, et al.
Bone Marrow Transplantation
|
June 22, 2005
First-line thalidomide-dexamethasone therapy in preparation for autologous stem cell transplantation in young patients (<61 years) with symptomatic multiple myeloma
A Abdelkefi, L Torjman, N Ben Romdhane, et al.
Molecular Biology Reports
|
October 16, 2012
Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association
N Laouini, A Bibi, H Ammar, et al.
Journal of Medical Genetics
|
June 15, 2010
Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia
B Pérez, F Mechinaud, C Galambrun, et al.
Page
of 2