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

Journal Abstract Search


109 related items for PubMed ID: 4184168

  • 21. [Progressive myoclonus epilepsy in two siblings and 5 cases with dyssynergia cerebellaris myoclonica in several generations of a kinship, a clinical and genetic study].
    Diebold K, Kastner M, Penin H.
    Nervenarzt; 1974 Nov; 45(11):595-601. PubMed ID: 4217888
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. [Clinical and polyphysiographic findings in a case of familial myoclonic syndrome].
    Quattrini A, Dellantonio R, Scarpino O, Paggi A.
    Riv Neurol; 1978 Nov; 48(6):717-22. PubMed ID: 741169
    [No Abstract] [Full Text] [Related]

  • 31. [Clinico-electrophysiologic correlations in myoclonus epilepsy].
    Grinkevich OV, Beĭn BM.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1970 Nov; 70(9):1316-21. PubMed ID: 5511111
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. [Unusual familial association of epilepsy, myoclonus and muscular atrophy. Case report].
    D'Ecclesia G, Scorrano V, Bernardini C, Poli V.
    Riv Neurol; 1985 Nov; 55(5):313-6. PubMed ID: 4081538
    [Abstract] [Full Text] [Related]

  • 35. [Familial progressive myoclonus epilepsy, of a dominant heredity: clinical and biological study of a family].
    Castaigne P, Cambier J, Brunet P, Schuller E, Chemaly R.
    Encephale; 1967 Nov; 56(4):285-307. PubMed ID: 6057414
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. [Familial progressive myoclonus epilepsy (Unverricht/Lundborg)].
    Herbst A.
    Psychiatr Neurol Med Psychol Beih; 1967 Nov; 6():18-39. PubMed ID: 5006319
    [No Abstract] [Full Text] [Related]

  • 39. [Familial myoclonia epileptica of the Unverricht type; clinical, electroencephalographical and anatomical].
    DE AJURIAGUERRA J, SIGWALD J, PIOT C.
    Presse Med (1893); 1954 Dec 25; 62(86):1813-6. PubMed ID: 13237126
    [No Abstract] [Full Text] [Related]

  • 40. [A case of familial myoclonus showing extremely benign clinical course].
    Nagayama S, Kishikawa H, Yukitake M, Matsui M, Kuroda Y.
    Rinsho Shinkeigaku; 1998 May 25; 38(5):430-4. PubMed ID: 9805989
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 6.