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Journal Abstract Search

106 related items for PubMed ID: 1559789

  • 1. Benign monomelic amyotrophy: description of a patient with a focal motor neuron disorder.
    Di Bella P, Logullo F, Tulli D, Ragno M, Scarpelli M.
    Ital J Neurol Sci; 1992 Feb; 13(1):84. PubMed ID: 1559789
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  • 2. Familial monomelic amyotrophy: a case report from India.
    Nalini A, Lokesh L, Ratnavalli E.
    J Neurol Sci; 2004 May 15; 220(1-2):95-8. PubMed ID: 15140613
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  • 4. Absence of cognitive, behavioral, or emotional dysfunction in progressive muscular atrophy.
    Wicks P, Abrahams S, Leigh PN, Williams T, Goldstein LH.
    Neurology; 2006 Nov 14; 67(9):1718-9. PubMed ID: 17101922
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  • 5. Neuroimage: monomelic amyotrophy.
    Sethi PK, Khandelwal D, Thukral R, Sethi NK, Torgovnick J.
    Eur Neurol; 2006 Nov 14; 56(4):261. PubMed ID: 17077640
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  • 7. Long-term follow-up of monomelic amyotrophy of the upper limb.
    Gourie-Devi M.
    Arch Neurol; 2010 Apr 14; 67(4):517; author reply 517-8. PubMed ID: 20385925
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  • 8. [Lower motor neuron diseases with predominantly upper limbs affection: are they independent forms or atypical variants of amyotrophic lateral sclerosis?].
    Stuchevskaia TR, Kazakov VM, Rudenko DI, Posokhina OV, Skoromets AA.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2006 Apr 14; 106(1):14-20. PubMed ID: 16457128
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  • 12. [Hereditary distal motor neuropathy due to mutation of BSCL2].
    Rafael M, Lacerda C, Goncalves E, Rocha S.
    Rev Neurol; 2017 Jan 01; 64(1):45-47. PubMed ID: 28000912
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  • 14. Sympathetic skin response in monomelic amyotrophy.
    Gourie-Devi M, Nalini A.
    Acta Neurol Scand; 2001 Sep 01; 104(3):162-6. PubMed ID: 11551236
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  • 15. Monomelic amyotrophy is not always benign: a case report.
    Moglia C, Calvo A, Cammarosano S, Ilardi A, Canosa A, Gallo S, Bersano E, Chiò A.
    Amyotroph Lateral Scler; 2011 Jul 01; 12(4):307-8. PubMed ID: 21344999
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  • 19. Motor neuropathies and lower motor neuron syndromes.
    Verschueren A.
    Rev Neurol (Paris); 2017 May 01; 173(5):320-325. PubMed ID: 28434507
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  • 20. Reverse split hand syndrome: Dissociated intrinsic hand muscle atrophy pattern in Hirayama disease/brachial monomelic amyotrophy.
    Singh RJ, Preethish-Kumar V, Polavarapu K, Vengalil S, Prasad C, Nalini A.
    Amyotroph Lateral Scler Frontotemporal Degener; 2017 Feb 01; 18(1-2):10-16. PubMed ID: 27575868
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