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T. Chellali
Observed names:
T Chellali,
Thouraya Chellali
Institutions:
Hôpital Necker-Enfants Malades,
Hôpital Mustapha Pacha,
Laboratoire d'hématologie
Observed institutions:
Hôpital Necker-Enfants Malades,
Hôpital Mustapha Pacha,
Laboratoire d'hématologie
OpenAlex ID:
A5085130572
Severe hypofibrinogenemia associated with bilateral ischemic necrosis of toes and fingers
1995
·
O. Chafa
, T. Chellali
, et al.
·
Blood Coagulation & Fibrinolysis
·
45
Behçet Syndrome Associated with Protein S Deficiency
1992
·
O Chafa
, A M Fischer
, et al.
·
Thrombosis and Haemostasis
·
42
Hemostasis and pregnancy
1990
·
F. Meriane
, A. Cheikh
, et al.
·
Fibrinolysis and Proteolysis
·
6
Screening for mutations in factor VIII gene using the single-strand conformation polymorphism
1995
·
Khédoudja Nafa
, Farida Meriane
, et al.
·
Human Mutation
386 Inherited deficiency of protein S in an algerian family with recurrent venous thrombosis
1988
·
O. Chafa
, A.M. Fisher
, et al.
·
Fibrinolysis and Proteolysis
416 The coagulation-fibrinolysis in the patients with prosthetic heart valves
1988
·
F. Mériane
, T. Chellali
, et al.
·
Fibrinolysis and Proteolysis
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Works count:
6
Citation count:
93
H-index:
3
I10-index:
2
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