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 *

137 related articles for article (PubMed ID: 4406233)

  • 1. Nosology of congenital non-progressive cerebellar ataxia. Report on six cases in three families.
    Pfeiffer RA; Palm D; Jünemann G; Mandl-Kramer S; Heimann E
    Neuropadiatrie; 1974 Feb; 5(1):91-102. PubMed ID: 4406233
    [No Abstract]   [Full Text] [Related]  

  • 2. [Non-progressive congenital cerebellar ataxia].
    Clement MC; Briard ML; Ponsot G; Arthuis M
    Arch Fr Pediatr; 1984 Dec; 41(10):695-700. PubMed ID: 6532357
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial cerebellar dysarthria and delayed language development. Report of 5 cases in 2 families].
    Petersen U; Kopf-Mehnert C
    Folia Phoniatr (Basel); 1974; 26(2):127-37. PubMed ID: 4845619
    [No Abstract]   [Full Text] [Related]  

  • 4. Cerebellar ataxia.
    Beighton PH
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):246-7. PubMed ID: 5173376
    [No Abstract]   [Full Text] [Related]  

  • 5. [Kinsbourne's disease. Study of four cases (author's transl)].
    Fernández-Alvarez E; Camino A; Pineda M; Bidegaín I
    An Esp Pediatr; 1978; 11(6-7):461-70. PubMed ID: 697215
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cerebellar vermis defect, oligophrenia, congenital ataxia, and hepatic fibrocirrhosis without coloboma and renal abnormalities: report of three cases.
    Coppola G; Vajro P; De Virgiliis S; Ciccimarra E; Boccone L; Pascotto A
    Neuropediatrics; 2002 Aug; 33(4):180-5. PubMed ID: 12368986
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Opsoclonus with acute cerebellar ataxia (cerebellitis of pontine encephalitis) of childhood.
    Kalyanaraman K; Jagannathan K
    Neurol India; 1971 Jun; 19(2):87-91. PubMed ID: 5097255
    [No Abstract]   [Full Text] [Related]  

  • 8. Cerebellar tumors. Clinical analysis and physiopathologic correlations.
    Amici R; Avanzini G; Pacini L
    Monogr Neural Sci; 1976; 4():1-112. PubMed ID: 995137
    [No Abstract]   [Full Text] [Related]  

  • 9. [Cliniconeurological study of 2 cases of Marinesco-Sjögren syndrome in a family].
    Santa T; Araki S; Terao A; Kuroiwa Y
    No To Shinkei; 1969 Jul; 21(7):821-6. PubMed ID: 5820396
    [No Abstract]   [Full Text] [Related]  

  • 10. [The electroretinogram in some congenital anomalies of the optic nerve and of the choroid].
    Mazzantini L; Apollonio A
    G Ital Oftalmol; 1964; 17(6):327-40. PubMed ID: 5868867
    [No Abstract]   [Full Text] [Related]  

  • 11. [3 cases of the Marinesco-Sjögren syndrome].
    Savettieri G; Serra S; Di Rosa AE; Daricello B; Dattola R; Giordano D
    Riv Neurol; 1979; 49(5):374-81. PubMed ID: 399700
    [No Abstract]   [Full Text] [Related]  

  • 12. Eye movements in a familial vestibulocerebellar disorder.
    Harris CM; Walker J; Shawkat F; Wilson J; Russell-Eggitt I
    Neuropediatrics; 1993 Jun; 24(3):117-22. PubMed ID: 8355816
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Marinesco-Sjögren syndrome: polygraphic study of nocturnal sleep.
    Bramanti P; Ricci RM; Benedetto M; Candela L; Bagalà S; Di Perri R
    Acta Neurol (Napoli); 1985 Feb; 7(1):8-13. PubMed ID: 3993461
    [No Abstract]   [Full Text] [Related]  

  • 14. [A case of congenital non-progressive cerebellar ataxia with pigmentary retinal degeneration, fiber type disproportion and hypercreatine kinasemia].
    Yamasaki T; Taniwaki T; Kikuchi H; Araki E; Arakawa K; Iwaki T; Yamada T; Kira J
    Rinsho Shinkeigaku; 1999 Sep; 39(9):925-9. PubMed ID: 10614155
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cerebromotor disturbances in infants and children with brain damage].
    Wilk F
    Wien Med Wochenschr; 1973 Feb; 123(8):118-21. PubMed ID: 4691245
    [No Abstract]   [Full Text] [Related]  

  • 16. [Gillespie syndrome (incomplete aniridia, cerebellar ataxia and oligophrenia)].
    François J; Lentini F
    Klin Monbl Augenheilkd; 1984 Apr; 184(4):313-5. PubMed ID: 6727263
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Joubert syndrome: episodic hyperpnea, abnormal eye movements, retardation and ataxia, associated with dysplasia of the cerebellar vermis.
    Boltshauser E; Isler W
    Neuropadiatrie; 1977 Feb; 8(1):57-66. PubMed ID: 576733
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis.
    Verloes A; Lambotte C
    Am J Med Genet; 1989 Feb; 32(2):227-32. PubMed ID: 2929661
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Hereditary cerebellar aataxia with spinal muscular atrophies].
    Hopf HC; Duensing F; Lowitzsch K; Krönke R
    Z Neurol; 1971; 199(4):344-52. PubMed ID: 4104837
    [No Abstract]   [Full Text] [Related]  

  • 20. Familial periodic ataxia.
    Margolin DI; Nutt JG; Lovrien EW
    Trans Am Neurol Assoc; 1981; 106():53-7. PubMed ID: 7349006
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.