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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

183 related items for PubMed ID: 8684395

  • 21.
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  • 22. Identification of a novel mutation in the APTX gene associated with ataxia-oculomotor apraxia.
    Inlora J, Sailani MR, Khodadadi H, Teymurinezhad A, Takahashi S, Bernstein JA, Garshasbi M, Snyder MP.
    Cold Spring Harb Mol Case Stud; 2017 Nov; 3(6):. PubMed ID: 28652255
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  • 23.
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  • 25. Neuroepithelial cysts in a patient with Joubert syndrome plus renal cysts.
    Marsh SE, Grattan-Smith P, Pereira J, Barkovich AJ, Gleeson JG.
    J Child Neurol; 2004 Mar; 19(3):227-31. PubMed ID: 15119486
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  • 26. Intrafamilial variability in fragile X-associated tremor/ataxia syndrome.
    Peters N, Kamm C, Asmus F, Holinski-Feder E, Kraft E, Dichgans M, Brüning R, Gasser T, Bötzel K.
    Mov Disord; 2006 Jan; 21(1):98-102. PubMed ID: 16124012
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  • 27. [Benign, hereditary, non-progressive chorea--an important differential diagnosis (author's transl)].
    Foerster K, Foerster G.
    Nervenarzt; 1978 Dec; 49(12):724-5. PubMed ID: 153479
    [No Abstract] [Full Text] [Related]

  • 28. Differential diagnosis of Huntington's disease: what the clinician should know.
    Cardoso F.
    Neurodegener Dis Manag; 2014 Dec; 4(1):67-72. PubMed ID: 24640980
    [Abstract] [Full Text] [Related]

  • 29. Late-onset ataxia telangiectasia in two brothers presenting with juvenile resting tremor.
    Hiel JA, Weemaes CM, Smeets DF, Van de Vlasakker CJ, Horstink MW.
    Mov Disord; 1994 Jul; 9(4):460-2. PubMed ID: 7526160
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  • 30. New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes.
    Devos D, Vuillaume I, de Becdelievre A, de Martinville B, Dhaenens CM, Cuvellier JC, Cuisset JM, Vallée L, Lemaitre MP, Bourteel H, Hachulla E, Wallaert B, Destée A, Defebvre L, Sablonnière B.
    Mov Disord; 2006 Dec; 21(12):2237-40. PubMed ID: 17044090
    [Abstract] [Full Text] [Related]

  • 31. Huntington chorea presenting with motor neuron disease.
    Sadeghian H, O'Suilleabhain PE, Battiste J, Elliott JL, Trivedi JR.
    Arch Neurol; 2011 May; 68(5):650-2. PubMed ID: 21555641
    [Abstract] [Full Text] [Related]

  • 32. Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation.
    Nahas SA, Duquette A, Roddier K, Gatti RA, Brais B.
    Neuromuscul Disord; 2007 Dec; 17(11-12):968-9. PubMed ID: 17720498
    [Abstract] [Full Text] [Related]

  • 33. Recessive ataxia with ocular apraxia: review of 22 Portuguese patients.
    Barbot C, Coutinho P, Chorão R, Ferreira C, Barros J, Fineza I, Dias K, Monteiro J, Guimarães A, Mendonça P, do Céu Moreira M, Sequeiros J.
    Arch Neurol; 2001 Feb; 58(2):201-5. PubMed ID: 11176957
    [Abstract] [Full Text] [Related]

  • 34. Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutations.
    Kerber KA, Jen JC, Perlman S, Baloh RW.
    J Neurol Sci; 2005 Nov 15; 238(1-2):41-5. PubMed ID: 16109427
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  • 35.
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  • 36.
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  • 37. Early-onset ataxia with oculomotor apraxia with a novel APTX mutation.
    Ito A, Yamagata T, Mori M, Momoi MY.
    Pediatr Neurol; 2005 Jul 15; 33(1):53-6. PubMed ID: 15876520
    [Abstract] [Full Text] [Related]

  • 38. Atypical clinical presentation of ataxia telangiectasia.
    Willems PJ, Van Roy BC, Kleijer WJ, Van der Kraan M, Martin JJ.
    Am J Med Genet; 1993 Mar 15; 45(6):777-82. PubMed ID: 8456862
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  • 39. Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms.
    Singh R, Macdonell RA, Scheffer IE, Crossland KM, Berkovic SF.
    Epileptic Disord; 1999 Jun 15; 1(2):93-9. PubMed ID: 10937138
    [Abstract] [Full Text] [Related]

  • 40. [Spinocerebellar ataxia type 5 (SCA5)].
    Sasaki H, Tashiro K.
    Ryoikibetsu Shokogun Shirizu; 1999 Jun 15; (27 Pt 2):283-4. PubMed ID: 10434652
    [No Abstract] [Full Text] [Related]

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