These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

163 related items for PubMed ID: 32654782

  • 1. Genetics of Equine Neurologic Disease.
    Edwards L, Finno CJ.
    Vet Clin North Am Equine Pract; 2020 Aug; 36(2):255-272. PubMed ID: 32654782
    [Abstract] [Full Text] [Related]

  • 2. Genetic screening for cerebellar abiotrophy, severe combined immunodeficiency and lavender foal syndrome in Arabian horses in Poland.
    Bugno-Poniewierska M, Stefaniuk-Szmukier M, -Kajtoch AP, Fornal A, Piórkowska K, Ropka-Molik K.
    Vet J; 2019 Jun; 248():71-73. PubMed ID: 31113566
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. Genetic Testing as a Tool to Identify Horses with or at Risk for Ocular Disorders.
    Bellone RR.
    Vet Clin North Am Equine Pract; 2017 Dec 26; 33(3):627-645. PubMed ID: 29103563
    [Abstract] [Full Text] [Related]

  • 5. Investigation of Known Genetic Mutations of Arabian Horses in Egyptian Arabian Foals with Juvenile Idiopathic Epilepsy.
    Aleman M, Finno CJ, Weich K, Penedo MCT.
    J Vet Intern Med; 2018 Jan 26; 32(1):465-468. PubMed ID: 29171123
    [Abstract] [Full Text] [Related]

  • 6. Congenital hydrocephalus in a Belgian draft horse associated with a nonsense mutation in B3GALNT2.
    Kolb DS, Klein C.
    Can Vet J; 2019 Feb 26; 60(2):197-198. PubMed ID: 30705458
    [Abstract] [Full Text] [Related]

  • 7. The carrier prevalence of severe combined immunodeficiency, lavender foal syndrome and cerebellar abiotrophy in Arabian horses in South Africa.
    Tarr CJ, Thompson PN, Guthrie AJ, Harper CK.
    Equine Vet J; 2014 Jul 26; 46(4):512-4. PubMed ID: 24033554
    [Abstract] [Full Text] [Related]

  • 8. Genetics of Equine Ocular Disease.
    Bellone RR.
    Vet Clin North Am Equine Pract; 2020 Aug 26; 36(2):303-322. PubMed ID: 32654784
    [Abstract] [Full Text] [Related]

  • 9. Genetics of Equine Reproductive Diseases.
    Raudsepp T.
    Vet Clin North Am Equine Pract; 2020 Aug 26; 36(2):395-409. PubMed ID: 32534849
    [Abstract] [Full Text] [Related]

  • 10. [Assessment of hereditary defects and dispositions of the horse under animal welfare aspects].
    Mählmann Ch, Steiger A.
    Schweiz Arch Tierheilkd; 2009 Apr 26; 151(4):153-8. PubMed ID: 19333900
    [Abstract] [Full Text] [Related]

  • 11. 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
    [No Abstract] [Full Text] [Related]

  • 12. Genetic Testing in the Horse.
    Bellone RR, Avila F.
    Vet Clin North Am Equine Pract; 2020 Aug 13; 36(2):211-234. PubMed ID: 32534857
    [Abstract] [Full Text] [Related]

  • 13. Neurologic diseases.
    Adams R, Mayhew IG.
    Vet Clin North Am Equine Pract; 1985 Apr 13; 1(1):209-34. PubMed ID: 3000543
    [Abstract] [Full Text] [Related]

  • 14. Morphometric magnetic resonance imaging and genetic testing in cerebellar abiotrophy in Arabian horses.
    Cavalleri JM, Metzger J, Hellige M, Lampe V, Stuckenschneider K, Tipold A, Beineke A, Becker K, Distl O, Feige K.
    BMC Vet Res; 2013 May 23; 9():105. PubMed ID: 23702154
    [Abstract] [Full Text] [Related]

  • 15. Clinicopathological and pedigree investigation of a novel spinocerebellar neurological disease in juvenile Quarter Horses in North America.
    Willis AT, Dahlgren AR, Woolard KD, Ghosh S, Donnelly CG, de la Concha-Bermejillo A, Pacheco A, Watson KD, Berryhill E, Aleman M, Wensley F, Humphreys S, Whitehead AE, Goldsmith D, Chesen B, Ragsdale J, Tompkins JE, Nash R, Plunkett AH, Qualls HJ, Rodriguez K, Hochanadel D, Miller AD, Finno CJ.
    J Vet Intern Med; 2024 May 23; 38(3):1808-1814. PubMed ID: 38669583
    [Abstract] [Full Text] [Related]

  • 16. Comparative analysis of cytokine gene expression in cerebrospinal fluid of horses without neurologic signs or with selected neurologic disorders.
    Pusterla N, Wilson WD, Conrad PA, Mapes S, Leutenegger CM.
    Am J Vet Res; 2006 Aug 23; 67(8):1433-7. PubMed ID: 16881858
    [Abstract] [Full Text] [Related]

  • 17. A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease.
    Metallinos DL, Bowling AT, Rine J.
    Mamm Genome; 1998 Jun 23; 9(6):426-31. PubMed ID: 9585428
    [Abstract] [Full Text] [Related]

  • 18. An unusual familial neurological syndrome in newborn thoroughbred foals.
    Mayhew IG, Schneiders DH.
    Vet Rec; 1993 Oct 30; 133(18):447-8. PubMed ID: 8291175
    [No Abstract] [Full Text] [Related]

  • 19. A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses.
    Ducro BJ, Schurink A, Bastiaansen JW, Boegheim IJ, van Steenbeek FG, Vos-Loohuis M, Nijman IJ, Monroe GR, Hellinga I, Dibbits BW, Back W, Leegwater PA.
    BMC Genomics; 2015 Oct 09; 16():761. PubMed ID: 26452345
    [Abstract] [Full Text] [Related]

  • 20. The genetics of skeletal muscle disorders in horses.
    Mickelson JR, Valberg SJ.
    Annu Rev Anim Biosci; 2015 Oct 09; 3():197-217. PubMed ID: 25387114
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.