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Journal Abstract Search

155 related items for PubMed ID: 31113566

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  • 3. Investigation of Cerebellar Abiotrophy (CA), Lavender Foal Syndrome (LFS), and Severe Combined Immunodeficiency (SCID) Variants in a Cohort of Three MENA Region Horse Breeds.
    Ayad A, Almarzook S, Besseboua O, Aissanou S, Piórkowska K, Musiał AD, Stefaniuk-Szmukier M, Ropka-Molik K.
    Genes (Basel); 2021 Nov 26; 12(12):. PubMed ID: 34946842
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  • 6. The frequency of the equine cerebellar abiotrophy mutation in non-Arabian horse breeds.
    Brault LS, Penedo MC.
    Equine Vet J; 2011 Nov 26; 43(6):727-31. PubMed ID: 21496100
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  • 8. Inheritance of cerebellar abiotrophy in Arabians.
    Brault LS, Famula TR, Penedo MC.
    Am J Vet Res; 2011 Jul 26; 72(7):940-4. PubMed ID: 21728855
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  • 10. Evidence for origin of lavender foal syndrome among Egyptian Arabian horses in Egypt.
    AbouEl Ela NH, El Araby IE, Saleh AA, Abd El-Fattah AH, Hagag NM, Brooks SA, Radwan MA, Kalbfleisch T.
    Equine Vet J; 2023 May 26; 55(3):487-493. PubMed ID: 35665534
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  • 12. Genetics of Equine Neurologic Disease.
    Edwards L, Finno CJ.
    Vet Clin North Am Equine Pract; 2020 Aug 26; 36(2):255-272. PubMed ID: 32654782
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  • 13. Profiling of genetic markers useful for breeding decision in Selle Francais horse.
    Ayad A, Besseboua O, Aissanou S, Stefaniuk-Szmukier M, Piórkowska K, Musiał AD, Długosz B, Kozłowska A, Ropka-Molik K.
    J Equine Vet Sci; 2022 Sep 26; 116():104059. PubMed ID: 35777576
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  • 16. Whole-genome SNP association in the horse: identification of a deletion in myosin Va responsible for Lavender Foal Syndrome.
    Brooks SA, Gabreski N, Miller D, Brisbin A, Brown HE, Streeter C, Mezey J, Cook D, Antczak DF.
    PLoS Genet; 2010 Apr 15; 6(4):e1000909. PubMed ID: 20419149
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  • 17. [Severe combined immunodefiency disease (SCID) in the Arabian horse].
    Don-van't Slot HP, van der Kolk JH.
    Tijdschr Diergeneeskd; 2000 Oct 01; 125(19):577-81. PubMed ID: 11042889
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  • 18. Mapping of equine cerebellar abiotrophy to ECA2 and identification of a potential causative mutation affecting expression of MUTYH.
    Brault LS, Cooper CA, Famula TR, Murray JD, Penedo MC.
    Genomics; 2011 Feb 01; 97(2):121-9. PubMed ID: 21126570
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  • 19. Foal immunodeficiency syndrome: carrier testing has markedly reduced disease incidence.
    Carter SD, Fox-Clipsham LY, Christley R, Swinburne J.
    Vet Rec; 2013 Apr 13; 172(15):398. PubMed ID: 23486505
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  • 20. Immune reconstitution prevents continuous equine infectious anemia virus replication in an Arabian foal with severe combined immunodeficiency: lessons for control of lentiviruses.
    Mealey RH, Fraser DG, Oaks JL, Cantor GH, McGuire TC.
    Clin Immunol; 2001 Nov 13; 101(2):237-47. PubMed ID: 11683583
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