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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 6631453)

  • 21. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.
    Harding AE
    Brain; 1982 Mar; 105(Pt 1):1-28. PubMed ID: 7066668
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Marinesco-Sjögren syndrome. Report of an autopsy.
    Mahloudji M; Amirhakimi GH; Haghighi P; Khodadoust AA
    Brain; 1972; 95(4):675-80. PubMed ID: 4647150
    [No Abstract]   [Full Text] [Related]  

  • 23. [An autopsy case of hereditary ataxia (hereditary spastic ataxia)].
    Yagishita S; Nakano T; Iwabuchi K; Sakai H
    No To Shinkei; 1985 Jun; 37(6):603-9. PubMed ID: 4041292
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Familial form of cutaneous epitheliomatosis with complex neurological characteristics similar to hereditary spinocerebellar degeneration. Apropos of 4 cases including one case with anatomo-clinical description].
    Chateau R; Tommasi M; Groslambert R; Perret J; Pasquier B
    Rev Neurol (Paris); 1975 Jun; 131(6):387-406. PubMed ID: 1209055
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Platal myoclonus associated with cerevellar neoplasm in von Recklinghausen's disease (a clinicopathologic study).
    Haberland C; Brumlik J
    Psychiatr Neurol (Basel); 1967; 154(4):209-29. PubMed ID: 4969498
    [No Abstract]   [Full Text] [Related]  

  • 26. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
    Lance JW
    Adv Neurol; 1986; 43():33-55. PubMed ID: 3080851
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cerebellar efferent fibers around the dentate nucleus. Pathological anatomy in olivo-ponto-cerebellar and dentato-pallido-luysian atrophy.
    Koga M; Nagara H; Tateishi J
    Acta Neuropathol; 1987; 73(4):403-5. PubMed ID: 3475929
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Autopsy case of a family with hereditary ataxia].
    Fujimoto S; Tsuchimoto K; Inoue K; Nakamura K; Kanda M
    No To Shinkei; 1976 Mar; 28(3):255-61. PubMed ID: 1036048
    [No Abstract]   [Full Text] [Related]  

  • 29. [Olivo-ponto-cerebellar atrophy (a clinico-morphologic and biochemical study of one case)].
    Drobysheva NA; Grushina AG; Kut'lina VA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(12):1793-8. PubMed ID: 4450909
    [No Abstract]   [Full Text] [Related]  

  • 30. Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report.
    Teive HA; Munhoz RP; Muzzio JA; Scola RH; Kay CK; Raskin S; Werneck LC; Bruhn H
    Mov Disord; 2008 Jun; 23(8):1191-2. PubMed ID: 18412280
    [No Abstract]   [Full Text] [Related]  

  • 31. Superficial hemosiderosis of the central nervous system.
    Kott E; Bechar M; Bornstein B; Askenasy HM; Sandbank U
    Acta Neurochir (Wien); 1966; 14(3):287-98. PubMed ID: 5298356
    [No Abstract]   [Full Text] [Related]  

  • 32. Neuropathologic findings in idiopathic opsoclonus and myoclonus. Their similarity to those in paraneoplastic cerebellar cortical degeneration.
    Hunter S; Kooistra C
    J Clin Neuroophthalmol; 1986 Dec; 6(4):236-41. PubMed ID: 2947929
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Opsoclonus-myoclonus syndrome: correlation of radiographic and pathological observations.
    Tuchman RF; Alvarez LA; Kantrowitz AB; Moser FG; Llena J; Moshé SL
    Neuroradiology; 1989; 31(3):250-2. PubMed ID: 2779775
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.
    Berciano J; García A; Infante J
    Handb Clin Neurol; 2013; 115():907-32. PubMed ID: 23931821
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Olivopontocerebellar atrophy. A review of 117 cases.
    Berciano J
    J Neurol Sci; 1982 Feb; 53(2):253-72. PubMed ID: 7057212
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Magnetic resonance imaging in hereditary and idiopathic ataxia.
    Wüllner U; Klockgether T; Petersen D; Naegele T; Dichgans J
    Neurology; 1993 Feb; 43(2):318-25. PubMed ID: 8437696
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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]  

  • 38. [Dominantly inherited type of cerebellar ataxia].
    Becker PE; Sabuncu N; Hopf HC
    Z Neurol; 1971 Apr; 199(1):116-39. PubMed ID: 4102742
    [No Abstract]   [Full Text] [Related]  

  • 39. Opsoclonus, myoclonus, ataxia, and encephalopathy in adults with cancer: a distinct paraneoplastic syndrome.
    Anderson NE; Budde-Steffen C; Rosenblum MK; Graus F; Ford D; Synek BJ; Posner JB
    Medicine (Baltimore); 1988 Mar; 67(2):100-9. PubMed ID: 3352511
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Proton MR spectroscopy of the cerebellum and pons in patients with degenerative ataxia.
    Mascalchi M; Cosottini M; Lolli F; Salvi F; Tessa C; Macucci M; Tosetti M; Plasmati R; Ferlini A; Tassinari CA; Villari N
    Radiology; 2002 May; 223(2):371-8. PubMed ID: 11997539
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.