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Items: 1 to 20 of 57


Giant occipital meningohydroencephalocele in an adult: Another historical case in neural tube defects.

Coulibaly O, Sogoba Y, Kanikomo D, Dama M, Camara MA, Diallo O.

Neurochirurgie. 2016 Aug;62(4):223-5. doi: 10.1016/j.neuchi.2016.04.002. Epub 2016 Jul 4.


Delayed intracerebral and subdural hematomas after ventriculo-peritoneal shunt in a child: A case report and review of the literature.

Coulibaly O, Dama M, Diallo O, Li G, Sogoba Y, Kanikomo D.

Neurochirurgie. 2016 Apr;62(2):105-7. doi: 10.1016/j.neuchi.2016.01.003. Epub 2016 Apr 28. Review.


[Abdominal pain and fever with urinary symptoms].

Tiemtoré-Kambou BMA, Napon AM, Diallo O, Gnoumou A, Lougué-Sorgho LC, Cissé R.

Rev Med Brux. 2016;37(6):498-500. French.


International trends in health science librarianship part 15: West Africa (Ghana, Nigeria, Senegal).

Sulemani SB, Afarikumah E, Aggrey SB, Ajuwon GA, Diallo O.

Health Info Libr J. 2015 Sep;32(3):241-6. doi: 10.1111/hir.12109.


Urinary tract infection with Corynebacterium aurimucosum after urethroplasty stricture of the urethra: a case report.

Lo S, Thiam I, Fall B, Ba-Diallo A, Diallo OF, Diagne R, Dia ML, Ka R, Sarr AM, Sow AI.

J Med Case Rep. 2015 Jul 14;9:156. doi: 10.1186/s13256-015-0638-0.


Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population.

Zhou S, Xiong L, Xie P, Ambalavanan A, Bourassa CV, Dionne-Laporte A, Spiegelman D, Turcotte Gauthier M, Henrion E, Diallo O, Dion PA, Rouleau GA.

PLoS One. 2015 May 26;10(5):e0128255. doi: 10.1371/journal.pone.0128255. eCollection 2015.


Loss-of-function de novo mutations play an important role in severe human neural tube defects.

Lemay P, Guyot MC, Tremblay É, Dionne-Laporte A, Spiegelman D, Henrion É, Diallo O, De Marco P, Merello E, Massicotte C, Désilets V, Michaud JL, Rouleau GA, Capra V, Kibar Z.

J Med Genet. 2015 Jul;52(7):493-7. doi: 10.1136/jmedgenet-2015-103027. Epub 2015 Mar 24.


[Neurological complications of infective endocarditis in Burkina Faso. Clinical features, management and evolutionary profile].

Yaméogo NV, Seghda A, Kagambèga LJ, Diallo O, Millogo GR, Toguyéni BJ, Samadoulougou AK, Niakara A, Simporé J, Zabsonré P.

Ann Cardiol Angeiol (Paris). 2015 Apr;64(2):81-6. doi: 10.1016/j.ancard.2015.01.012. Epub 2015 Feb 7. French.


Isolated aortic valvular and pulmonary involvement during essential eosinophilia.

Yaméogo NV, Diallo O, Kagambèga LJ, Seghda A, Sanou F, Millogo GR, Toguyéni BJ, Samadoulougou AK, Zabsonré P.

Ann Cardiol Angeiol (Paris). 2016 Feb;65(1):54-7. doi: 10.1016/j.ancard.2015.01.008. Epub 2015 Jan 19.


De novo mutations in moderate or severe intellectual disability.

Hamdan FF, Srour M, Capo-Chichi JM, Daoud H, Nassif C, Patry L, Massicotte C, Ambalavanan A, Spiegelman D, Diallo O, Henrion E, Dionne-Laporte A, Fougerat A, Pshezhetsky AV, Venkateswaran S, Rouleau GA, Michaud JL.

PLoS Genet. 2014 Oct 30;10(10):e1004772. doi: 10.1371/journal.pgen.1004772. eCollection 2014 Oct.


[Management of brain abscesses in era of computed tomography in sub-Saharan Africa: a review of 112 cases].

Kabré A, Zabsonré S, Diallo O, Cissé R.

Neurochirurgie. 2014 Oct;60(5):249-53. doi: 10.1016/j.neuchi.2014.06.011. Epub 2014 Sep 20. Review. French.


Child abdominal tumour in tropical context: think about schistosomiasis!

Napon AM, Bandré E, Nikiéma Z, Diallo O, Ouédraogo I, Kaboret SD, Lougué Sorgho LC, Alfidja A, Boyer L.

Afr J Paediatr Surg. 2014 Apr-Jun;11(2):194-5. doi: 10.4103/0189-6725.132838.


Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.

Landouré G, Zhu PP, Lourenço CM, Johnson JO, Toro C, Bricceno KV, Rinaldi C, Meilleur KG, Sangaré M, Diallo O, Pierson TM, Ishiura H, Tsuji S, Hein N, Fink JK, Stoll M, Nicholson G, Gonzalez MA, Speziani F, Dürr A, Stevanin G, Biesecker LG; NIH Intramural Sequencing Center., Accardi J, Landis DM, Gahl WA, Traynor BJ, Marques W Jr, Züchner S, Blackstone C, Fischbeck KH, Burnett BG.

Hum Mutat. 2013 Oct;34(10):1357-60. doi: 10.1002/humu.22378. Epub 2013 Aug 12.


[Management of end-stage kidney failure: a challenge for the countries of sub-Saharan Africa example of mineral and bone disorders in Burkina Faso].

Coulibaly G, Kaboré GE, Diallo O, Ouédraogo DD, Fessi H, Ronco P, Zabsonré P, Lengani A.

Med Sante Trop. 2013 May 1;23(2):193-6. doi: 10.1684/mst.2013.0178. French.


[Vitamin D-deficiency rickets: a case report from Burkina Faso].

Sagna Y, Ouédraogo DD, Dao F, Diallo O, Tiéno H, Guira O, Traoré LO, Yanogo AR, Drabo YJ.

Med Sante Trop. 2013 Jan-Mar;23(1):104-7. doi: 10.1684/mst.2013.0144. French.


[Cervico-facial traumatic injuries at the Donka national hospital of the teaching hospital of Conakry].

Diallo OR, Camara SA, Diallo A, Bah AT, Kane BT, Camara AD, Cherif F.

Mali Med. 2012;27(1):1-5. French.


A candidate gene for autoimmune myasthenia gravis.

Landouré G, Knight MA, Stanescu H, Taye AA, Shi Y, Diallo O, Johnson JO, Hernandez D, Traynor BJ, Biesecker LG; NIH Intramural Sequencing Center., Elkahloun A, Rinaldi C, Vincent A, Willcox N, Kleta R, Fischbeck KH, Burnett BG.

Neurology. 2012 Jul 24;79(4):342-7. Epub 2012 Jun 27.


Exome sequencing identifies a novel TRPV4 mutation in a CMT2C family.

Landouré G, Sullivan JM, Johnson JO, Munns CH, Shi Y, Diallo O, Gibbs JR, Gaudet R, Ludlow CL, Fischbeck KH, Traynor BJ, Burnett BG, Sumner CJ.

Neurology. 2012 Jul 10;79(2):192-4. doi: 10.1212/WNL.0b013e31825f04b2. Epub 2012 Jun 6. No abstract available.


[Use of SMS to ask mothers to come to vaccination sessions in Bobo-Dioulasso].

Diallo O, Schlumberger M, Sanou C, Dicko H, Aplogan A, Drabo F.

Bull Soc Pathol Exot. 2012 Oct;105(4):291-5. doi: 10.1007/s13149-012-0236-y. Epub 2012 Jun 5. French.


Rheumatoid arthritis in Burkina Faso: clinical and serological profiles.

Ouédraogo DD, Singbo J, Diallo O, Sawadogo SA, Tiéno H, Drabo YJ.

Clin Rheumatol. 2011 Dec;30(12):1617-21. doi: 10.1007/s10067-011-1831-1. Epub 2011 Sep 2.


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