Toumi Nel H - Search Results

1

Screening for deep venous thrombosis after idiopathic scoliosis surgery in children: a pilot study.

Kaabachi O, Alkaissi A, Koubaa W, Aloui N, Toumi Nel H. Kaabachi O, et al. Among authors: toumi nel h. Paediatr Anaesth. 2010 Feb;20(2):144-9. doi: 10.1111/j.1460-9592.2009.03237.x. Paediatr Anaesth. 2010. PMID: 20078811

2

Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association.

Laouini N, Bibi A, Ammar H, Kazdaghli K, Ouali F, Othmani R, Amdouni S, Haloui S, Sahli CA, Jouini L, Hadj Fredj S, Siala H, Ben Romdhane N, Toumi NE, Fattoum S, Messsaoud T. Laouini N, et al. Mol Biol Rep. 2013 Feb;40(2):851-6. doi: 10.1007/s11033-012-2124-8. Epub 2012 Oct 14. Mol Biol Rep. 2013. PMID: 23065279

3

Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion.

Amri Y, Dabboubi R, Mghaieth F, Zili M, Messaoud T, Casini A, De Moerloose P, Toumi NEH. Amri Y, et al. Haemophilia. 2020 Jul;26(4):e194-e197. doi: 10.1111/hae.13974. Epub 2020 Mar 23. Haemophilia. 2020. PMID: 32202028 No abstract available.

4

Thrombosis in congenital deficiencies of AT III, protein C or protein S: a study of 44 children.

Toumi NH, Khaldi F, Ben Becheur S, Hammou A, Bouttière B, Sampol J, Boukef K. Toumi NH, et al. Hematol Cell Ther. 1997 Dec;39(6):295-9. doi: 10.1007/s00282-997-0295-x. Hematol Cell Ther. 1997. PMID: 9497888

5

[Deficiencies of physiological coagulation inhibitors in children with venous thromboses of the lower limbs. Prospective study of 6 cases].

Khaldi F, Toumi NH, Ben Jaballah N, Zriba S, Ben Naceur B. Khaldi F, et al. Ann Pediatr (Paris). 1993 Jun;40(6):348-52. Ann Pediatr (Paris). 1993. PMID: 8352495 French.

6

Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients.

Jouini L, Sahli CA, Laaouini N, Ouali F, Ben Youssef I, Dakhlaoui B, Othmeni R, Ouennich F, Hadj Fredj S, Siala H, Becher M, Toumi NE, Fattoum S, Hafsia R, Bibi A, Messaoud T. Jouini L, et al. Mol Biol Rep. 2013 Nov;40(11):6205-12. doi: 10.1007/s11033-013-2732-y. Epub 2013 Sep 25. Mol Biol Rep. 2013. PMID: 24065537

7

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia.

Sahli CA, Bibi A, Ouali F, Fredj SH, Dakhlaoui B, Othmani R, Laouini N, Jouini L, Ouenniche F, Siala H, Touhami I, Becher M, Fattoum S, Toumi Nel H, Messaoud T. Sahli CA, et al. Among authors: toumi nel h. Clin Chem Lab Med. 2013 Nov;51(11):2115-24. doi: 10.1515/cclm-2013-0354. Clin Chem Lab Med. 2013. PMID: 23800659

8

Molecular identification of Gd A- and Gd B- G6PD deficient variants by ARMS-PCR in a Tunisian population.

Haloui S, Laouini N, Sahli CA, Daboubi R, Becher M, Jouini L, Kazdaghli K, Tinsa F, Cherif S, Khemiri M, Fredj SH, Othmani R, Ouali F, Siala H, Toumi Nel H, Barsaoui S, Bibi A, Messaoud T. Haloui S, et al. Among authors: toumi nel h. Ann Biol Clin (Paris). 2016 Mar-Apr;74(2):219-26. doi: 10.1684/abc.2016.1123. Ann Biol Clin (Paris). 2016. PMID: 27029726 Free article.

9

Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications.

Amri Y, Kallel C, Becheur M, Dabboubi R, Elloumi M, Belaaj H, Kammoun S, Messaoud T, de Moerloose P, Toumi Nel H. Amri Y, et al. Among authors: toumi nel h. Clin Chim Acta. 2016 Sep 1;460:55-62. doi: 10.1016/j.cca.2016.06.024. Epub 2016 Jun 22. Clin Chim Acta. 2016. PMID: 27343352

10

Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.

Amri Y, Toumi Nel H, Hadj Fredj S, de Moerloose P. Amri Y, et al. Among authors: toumi nel h. Thromb Res. 2016 Jul;143:11-6. doi: 10.1016/j.thromres.2016.04.016. Epub 2016 Apr 27. Thromb Res. 2016. PMID: 27164460

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