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Items: 30

1.

Strengthening human genetics research in Africa: report of the 9th meeting of the African Society of Human Genetics in Dakar in May 2016.

Ndiaye Diallo R, Gadji M, Hennig BJ, Guèye MV, Gaye A, Diop JPD, Sylla Niang M, Lopez Sall P, Guèye PM, Dem A, Faye O, Dieye A, Cisse A, Sembene M, Ka S, Diop N, Williams SM, Matovu E, Ramesar RS, Wonkam A, Newport M, Rotimi C, Ramsay M.

Glob Health Epidemiol Genom. 2017 Aug 4;2:e10. doi: 10.1017/gheg.2017.3. eCollection 2017.

2.

Challenges in the management of sickle cell disease during pregnancy in Senegal, West Africa.

Faye BF, Kouame KB, Seck M, Diouf AA, Gadji M, Dieng N, Touré SA, Sall A, Toure AO, Diop S.

Hematology. 2018 Jan;23(1):61-64. doi: 10.1080/10245332.2017.1367534. Epub 2017 Aug 28.

PMID:
28846064
3.

Bleeding risk assessment in hemophilia A carriers from Dakar, Senegal.

Seck M, Faye BF, Sall A, Sy D, Touré SA, Dieng N, Guéye YB, Gadji M, Touré AO, Costa C, Lasne D, Rothschild C, Diop S.

Blood Coagul Fibrinolysis. 2017 Dec;28(8):642-645. doi: 10.1097/MBC.0000000000000653.

PMID:
28731872
4.

Efficacy and Safety of Manual Partial Red Cell Exchange in the Management of Severe Complications of Sickle Cell Disease in a Developing Country.

Faye BF, Sow D, Seck M, Dieng N, Toure SA, Gadji M, Senghor AB, Gueye YB, Sy D, Sall A, Dieye TN, Toure AO, Diop S.

Adv Hematol. 2017;2017:3518402. doi: 10.1155/2017/3518402. Epub 2017 May 11.

5.

Molecular diagnosis of haemophilia A in patients from Senegal.

Seck M, Costa C, Faye BF, Sy Bah D, Touré SA, Dieng N, Sall A, Gadji M, Touré AO, Lasne D, Rothschild C, Diop S.

Haemophilia. 2017 May;23(3):e225-e227. doi: 10.1111/hae.13207. Epub 2017 Mar 17. No abstract available.

PMID:
28306216
6.

Pattern of chronic myeloid leukemia in the imatinib era in a Sub-Saharan African setting.

Faye BF, Dieng N, Seck M, Gadji M, Gueye YB, Sy D, Toure SA, Sall A, Toure AO, Dieye TN, Diop S.

Ann Hematol. 2016 Oct;95(10):1603-10. doi: 10.1007/s00277-016-2745-4. Epub 2016 Jul 1.

PMID:
27370991
7.

Characteristics of chronic lymphocytic leukemia in Senegal.

Sall A, Touré AO, Sall FB, Ndour M, Fall S, Sène A, Faye BF, Seck M, Gadji M, Dièye TN, Mathiot C, Reynaud S, Diop S, Raphaël M.

BMC Hematol. 2016 Apr 23;16:10. doi: 10.1186/s12878-016-0051-y. eCollection 2016.

8.

Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations.

Ayub S, Gadji M, Krabchi K, Côté S, Gekas J, Maranda B, Drouin R.

Am J Med Genet A. 2016 Apr;170A(4):896-907. doi: 10.1002/ajmg.a.37428. Epub 2016 Jan 29. Review.

PMID:
26822682
9.

Risk factors for thrombosis in an african population.

Fall AO, Proulle V, Sall A, Mbaye A, Ba PS, Diao M, Seck M, Gadji M, Gning SB, Diop S, Dièye TN, Faye BF, Thiam D, Dreyfus M.

Clin Med Insights Blood Disord. 2014 Apr 10;7:1-6. doi: 10.4137/CMBD.S13401. eCollection 2014.

10.

Antiphospholipid antibodies and systemic scleroderma.

Touré AO, Ly F, Sall A, Diatta A, Gadji M, Seck M, Faye B, Dieye T, Diop S.

Turk J Haematol. 2013 Mar;30(1):32-6. doi: 10.4274/tjh.2012.0059. Epub 2013 Mar 5.

11.

A new der(1;7)(q10;p10) leading to a singular 1p loss in a case of glioblastoma with oligodendroglioma component.

Gadji M, Crous-Tsanaclis AM, Mathieu D, Mai S, Fortin D, Drouin R.

Neuropathology. 2014 Apr;34(2):170-8. doi: 10.1111/neup.12060. Epub 2013 Sep 30.

PMID:
24118308
12.

Profiling three-dimensional nuclear telomeric architecture of myelodysplastic syndromes and acute myeloid leukemia defines patient subgroups.

Gadji M, Adebayo Awe J, Rodrigues P, Kumar R, Houston DS, Klewes L, Dièye TN, Rego EM, Passetto RF, de Oliveira FM, Mai S.

Clin Cancer Res. 2012 Jun 15;18(12):3293-304. doi: 10.1158/1078-0432.CCR-12-0087. Epub 2012 Apr 26.

13.

Efficiency of manual scanning in recovering rare cellular events identified by fluorescence in situ hybridization: simulation of the detection of fetal cells in maternal blood.

Emad A, Ayub S, Samassékou O, Grégoire MC, Gadji M, Ntwari A, Lamoureux J, Hemmings F, Tafas T, Kilpatrick MW, Krabchi K, Drouin R.

J Biomed Biotechnol. 2012;2012:610856. doi: 10.1155/2012/610856. Epub 2012 Mar 8.

14.

Nuclear remodeling as a mechanism for genomic instability in cancer.

Gadji M, Vallente R, Klewes L, Righolt C, Wark L, Kongruttanachok N, Knecht H, Mai S.

Adv Cancer Res. 2011;112:77-126. doi: 10.1016/B978-0-12-387688-1.00004-1. Review.

PMID:
21925302
15.

Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22.

Gadji M, Krabchi K, Langis P, Aboura A, Périgny M, Côté S, Ferland M, Drouin R.

Am J Med Genet A. 2011 Feb;155A(2):430-3. doi: 10.1002/ajmg.a.33654. No abstract available.

PMID:
21271667
16.

Sizing the ends: normal length of human telomeres.

Samassekou O, Gadji M, Drouin R, Yan J.

Ann Anat. 2010 Sep 20;192(5):284-91. doi: 10.1016/j.aanat.2010.07.005. Epub 2010 Aug 6. Review.

PMID:
20732797
17.

Three-dimensional nuclear telomere architecture is associated with differential time to progression and overall survival in glioblastoma patients.

Gadji M, Fortin D, Tsanaclis AM, Garini Y, Katzir N, Wienburg Y, Yan J, Klewes L, Klonisch T, Drouin R, Mai S.

Neoplasia. 2010 Feb;12(2):183-91.

18.

EGF receptor inhibitors in the treatment of glioblastoma multiform: old clinical allies and newly emerging therapeutic concepts.

Gadji M, Crous AM, Fortin D, Krcek J, Torchia M, Mai S, Drouin R, Klonisch T.

Eur J Pharmacol. 2009 Dec 25;625(1-3):23-30. doi: 10.1016/j.ejphar.2009.10.010. Epub 2009 Oct 18. Review.

PMID:
19836372
19.

Is the 1p/19q deletion a diagnostic marker of oligodendrogliomas?

Gadji M, Fortin D, Tsanaclis AM, Drouin R.

Cancer Genet Cytogenet. 2009 Oct;194(1):12-22. doi: 10.1016/j.cancergencyto.2009.05.004.

PMID:
19737649
20.

Application of multi-PRINS to simultaneously identify chromosomes 18, X, and Y in prenatal diagnosis.

Gadji M, Krabchi K, Yan J, Drouin R.

Methods Mol Biol. 2008;444:49-58. doi: 10.1007/978-1-59745-066-9_4.

PMID:
18425471
21.

[Seroprevalence of hepatitis C virus (HCV) in Senegalease blood donors].

Dieye TN, Gadji M, Cisse Y, Diallo TA, Toure Falla O, Diop S, Diallo S, Thiam D, Diakhate L.

Dakar Med. 2006;51(1):47-52. French.

PMID:
16924850
22.

Dual-color PRINS for in situ detection of fetal cells in maternal blood.

Krabchi K, Gadji M, Yan J, Drouin R.

Methods Mol Biol. 2006;334:141-9.

PMID:
16861760
23.

New rapid multicolor PRINS protocol.

Yan J, Gadji M, Krabchi K, Drouin R.

Methods Mol Biol. 2006;334:3-13.

PMID:
16861747
24.

[Dominant negative activity of mutated p53 proteins].

Dridi W, Krabchi K, Gadji M, Lavoie J, Bronsard M, Fetni R, Drouin R.

Med Sci (Paris). 2006 Mar;22(3):301-7. Review. French.

25.

Quantification of all fetal nucleated cells in maternal blood in different cases of aneuploidies.

Krabchi K, Gadji M, Forest JC, Drouin R.

Clin Genet. 2006 Feb;69(2):145-54.

PMID:
16433695
26.

Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniques.

Krabchi K, Gadji M, Samassekou O, Grégoire MC, Forest JC, Drouin R.

Prenat Diagn. 2006 Jan;26(1):28-34.

PMID:
16374897
27.

[Physical performance and thermoregulatory study of subjects with sickle cell trait during a sub-maximal exercise].

Samb A, Kane MO, Ba A, Gadji M, Seck D, Badji L, Sarr FB, Sarr M, Dieng SA, Diakhate EM, Gueye L, Diakhate L, Cisse F, Martineaud JP.

Dakar Med. 2005;50(2):46-51. French.

PMID:
16295755
28.
29.

[Maternal anaemia: effect on the newborn].

Toure-Fall AO, Gadji M, Diop S, Dieye T, Thiam D, Diakhate L.

Dakar Med. 2004;49(3):172-6. French.

PMID:
15776614
30.

[Homozygous drepanocytosis in Dakar: effect of the hemoglobin F level, and sociocultural and economic factors].

Diop S, Cisse M, Toure-Fall AO, Thiam D, Fall K, Gadji M, Diakhaté L.

Dakar Med. 1999;44(2):171-4. French.

PMID:
11963930

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