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Items: 18

1.

Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report.

Amin M, Bakhit Y, Koko M, Ibrahim MOM, Salih MA, Ibrahim M, Seidi OA.

Acta Myol. 2019 Jun 1;38(1):21-24. eCollection 2019 Jun.

PMID:
31309178
2.

Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556.

Cauley ES, Hamed A, Mohamed IN, Elseed M, Martinez S, Yahia A, Abozar F, Abubakr R, Koko M, Elsayed L, Piao X, Salih MA, Manzini MC.

Neurogenetics. 2019 May;20(2):91-98. doi: 10.1007/s10048-019-00577-2. Epub 2019 Apr 13.

PMID:
30982090
3.

Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability.

Liu Y, Schubert J, Sonnenberg L, Helbig KL, Hoei-Hansen CE, Koko M, Rannap M, Lauxmann S, Huq M, Schneider MC, Johannesen KM, Kurlemann G, Gardella E, Becker F, Weber YG, Benda J, Møller RS, Lerche H.

Brain. 2019 Feb 1;142(2):376-390. doi: 10.1093/brain/awy326.

PMID:
30615093
4.

Detarium microcarpum: A novel source of nutrition and medicine: A review.

Hassanin HAM, Koko M, Abdalla M, Mu W, Jiang B.

Food Chem. 2019 Feb 15;274:900-906. doi: 10.1016/j.foodchem.2018.09.070. Epub 2018 Sep 12. Review.

PMID:
30373026
5.

Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report.

Yahia A, Elsayed L, Babai A, Salih MA, El-Sadig SM, Amin M, Koko M, Abubakr R, Idris R, Taha SOMA, Elmalik SA, Brice A, Ahmed AE, Stevanin G.

BMC Neurol. 2018 Oct 23;18(1):175. doi: 10.1186/s12883-018-1180-7.

6.

EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways.

Abdallah MOE, Algizouli UK, Suliman MA, Abdulrahman RA, Koko M, Fessahaye G, Shakir JH, Fahal AH, Elhassan AM, Ibrahim ME, Mohamed HS.

Front Oncol. 2018 Aug 13;8:316. doi: 10.3389/fonc.2018.00316. eCollection 2018.

7.

Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family.

Elsayed LEO, Mohammed IN, Hamed AAA, Elseed MA, Salih MAM, Yahia A, Siddig RA, Amin M, Koko M, Elbashir MI, Ibrahim ME, Brice A, Ahmed AE, Stevanin G.

BMC Med Genet. 2018 May 8;19(1):72. doi: 10.1186/s12881-018-0592-y.

8.

Challenges imposed by minor reference alleles on the identification and reporting of clinical variants from exome data.

Koko M, Abdallah MOE, Amin M, Ibrahim M.

BMC Genomics. 2018 Jan 15;19(1):46. doi: 10.1186/s12864-018-4433-3.

9.

Lactulose production by a thermostable glycoside hydrolase from the hyperthermophilic archaeon Caldivirga maquilingensis IC-167.

Letsididi R, Hassanin HA, Koko MY, Zhang T, Jiang B, Mu W.

J Sci Food Agric. 2018 Feb;98(3):928-937. doi: 10.1002/jsfa.8539. Epub 2017 Aug 28.

PMID:
28703279
10.

Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan.

Elsayed LE, Mohammed IN, Hamed AA, Elseed MA, Johnson A, Mairey M, Mohamed HE, Idris MN, Salih MA, El-Sadig SM, Koko ME, Mohamed AY, Raymond L, Coutelier M, Darios F, Siddig RA, Ahmed AK, Babai AM, Malik HM, Omer ZM, Mohamed EO, Eltahir HB, Magboul NA, Bushara EE, Elnour A, Rahim SM, Alattaya A, Elbashir MI, Ibrahim ME, Durr A, Audhya A, Brice A, Ahmed AE, Stevanin G.

Eur J Hum Genet. 2016 Jan;25(1):100-110. doi: 10.1038/ejhg.2016.108. Epub 2016 Sep 7.

11.

Characterization of a thermostable glycoside hydrolase (CMbg0408) from the hyperthermophilic archaeon Caldivirga maquilingensis IC-167.

Letsididi R, Hassanin HA, Koko MY, Ndayishimiye JB, Zhang T, Jiang B, Stressler T, Fischer L, Mu W.

J Sci Food Agric. 2017 May;97(7):2132-2140. doi: 10.1002/jsfa.8019. Epub 2016 Sep 28.

PMID:
27582034
12.

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease.

Elsayed LE, Drouet V, Usenko T, Mohammed IN, Hamed AA, Elseed MA, Salih MA, Koko ME, Mohamed AY, Siddig RA, Elbashir MI, Ibrahim ME, Durr A, Stevanin G, Lesage S, Ahmed AE, Brice A.

Ann Neurol. 2016 Feb;79(2):335-7. doi: 10.1002/ana.24591. Epub 2016 Jan 19. No abstract available.

PMID:
26703368
13.

Exome sequencing of a colorectal cancer family reveals shared mutation pattern and predisposition circuitry along tumor pathways.

Suleiman SH, Koko ME, Nasir WH, Elfateh O, Elgizouli UK, Abdallah MO, Alfarouk KO, Hussain A, Faisal S, Ibrahim FM, Romano M, Sultan A, Banks L, Newport M, Baralle F, Elhassan AM, Mohamed HS, Ibrahim ME.

Front Genet. 2015 Sep 15;6:288. doi: 10.3389/fgene.2015.00288. eCollection 2015.

14.

Newcastle disease virus in Madagascar: identification of an original genotype possibly deriving from a died out ancestor of genotype IV.

Maminiaina OF, Gil P, Briand FX, Albina E, Keita D, Andriamanivo HR, Chevalier V, Lancelot R, Martinez D, Rakotondravao R, Rajaonarison JJ, Koko M, Andriantsimahavandy AA, Jestin V, Servan de Almeida R.

PLoS One. 2010 Nov 15;5(11):e13987. doi: 10.1371/journal.pone.0013987.

15.

Africa, a reservoir of new virulent strains of Newcastle disease virus?

Servan de Almeida R, Maminiaina OF, Gil P, Hammoumi S, Molia S, Chevalier V, Koko M, Andriamanivo HR, Traoré A, Samaké K, Diarra A, Grillet C, Martinez D, Albina E.

Vaccine. 2009 May 21;27(24):3127-9. doi: 10.1016/j.vaccine.2009.03.076. Epub 2009 Apr 15. No abstract available.

PMID:
19446180
16.

[Epidemiology of Newcastle disease in village poultry farming in Madagascar].

Maminiaina OF, Koko M, Ravaomanana J, Rakotonindrina SJ.

Rev Sci Tech. 2007 Dec;26(3):691-700. French.

17.

Novel 5-aryl-1,3-dihydro-indole-2-thiones. potent, orally active progesterone receptor agonists.

Fensome A, Koko M, Wrobel J, Zhang P, Zhang Z, Cohen J, Lundeen S, Rudnick K, Zhu Y, Winneker R.

Bioorg Med Chem Lett. 2003 Apr 7;13(7):1317-20.

PMID:
12657272
18.

[ELISA for testing swine sera for antibodies against Teschen virus].

Hübschle OJ, Rajanarison I, Koko M, Rakotondramary E, Rasiofomanana P.

Dtsch Tierarztl Wochenschr. 1983 Mar 8;90(3):86-8. German. No abstract available.

PMID:
6301799

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