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 *

78 related articles for article (PubMed ID: 4651694)

  • 1. [Genetic factors in epilepsy].
    Vucenović V; Radojicić B; Hadzi-Antonović O
    Neuropsihijatrija; 1972; 20(2):207-11. PubMed ID: 4651694
    [No Abstract]   [Full Text] [Related]  

  • 2. [Epilepsy in chromosome aberrations].
    Bahi-Buisson N; Ville D; Eisermann M; Plouin P; Kaminska A; Chiron C
    Arch Pediatr; 2005 Apr; 12(4):449-58. PubMed ID: 15808438
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Electro-clinical phenotypes of chromosome disorders associated with epilepsy in the absence of dysmorphism.
    Macleod S; Mallik A; Tolmie JL; Stephenson JB; O'Regan ME; Zuberi SM
    Brain Dev; 2005 Mar; 27(2):118-24. PubMed ID: 15668051
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosome imbalances associated with epilepsy.
    Schinzel A; Niedrist D
    Am J Med Genet; 2001; 106(2):119-24. PubMed ID: 11579431
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosomal disorders associated with epilepsy.
    Battaglia A; Guerrini R
    Epileptic Disord; 2005 Sep; 7(3):181-92. PubMed ID: 16162426
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Contribution to the study of the Kleine-Levin syndrome in early childhood].
    Lamote de Grignon C; Fernandez Alvarez E
    Rev Neuropsychiatr Infant; 1967; 15(4):365-72. PubMed ID: 5247106
    [No Abstract]   [Full Text] [Related]  

  • 7. [Microcephaly with epilepsy. Supernumerary chromosome in 21].
    Marobbio C
    Minerva Med; 1966 Jun; 57(47):2189-91. PubMed ID: 5939918
    [No Abstract]   [Full Text] [Related]  

  • 8. [Chromosome investigations in epilepsy (chromosome-conditioned convulsive diseases)].
    Koch G
    Folia Clin Int (Barc); 1965 Jun; 15(6):296-300. PubMed ID: 5845418
    [No Abstract]   [Full Text] [Related]  

  • 9. [Complex neuro-ectodermic dysplasia associated with oligophrenia, spastic paraplegia, epilepsy, cataract and congenital ichthyosis. Nosological discussion].
    Boudouresques J; Khalil R; Vigouroux RA; Poncet M; Bille J
    Acta Neurol Psychiatr Belg; 1969 Apr; 69(4):241-8. PubMed ID: 4982215
    [No Abstract]   [Full Text] [Related]  

  • 10. [Genetic molecular basis of epilepsy].
    Serratosa JM
    Rev Neurol; 1995; 23(124):1290-1. PubMed ID: 8556635
    [No Abstract]   [Full Text] [Related]  

  • 11. Medical genetics and adoption.
    Schultz AL; Motulsky AG
    Child Welfare; 1971 Jan; 50(1):4-17. PubMed ID: 5170811
    [No Abstract]   [Full Text] [Related]  

  • 12. Epilepsy and deletion syndromes of chromosome 18: do not forget the short arm!
    Cerminara C; Lo Castro A; D'Argenzio L; Galasso C; Curatolo P
    Epilepsia; 2008 Oct; 49(10):1813-4. PubMed ID: 18973629
    [No Abstract]   [Full Text] [Related]  

  • 13. [Preventive aspects of genetic counselling (author's transl)].
    Klein D
    Schweiz Rundsch Med Prax; 1980 Nov; 69(46):1710-21. PubMed ID: 7022437
    [No Abstract]   [Full Text] [Related]  

  • 14. Molecular basis of inherited epilepsy.
    George AL
    Arch Neurol; 2004 Apr; 61(4):473-8. PubMed ID: 15096393
    [No Abstract]   [Full Text] [Related]  

  • 15. [Familial brain disease with presence of a small metacentric extra chromosome].
    Frezza M; Perona G; Vettore L; De Sandre G
    Folia Hered Pathol (Milano); 1966 Jul; 15(3):107-14. PubMed ID: 5995932
    [No Abstract]   [Full Text] [Related]  

  • 16. [A case of Rud's syndrome].
    Loza-Tulimowska M
    Pol Tyg Lek; 1971 Mar; 26(9):314-5. PubMed ID: 5550672
    [No Abstract]   [Full Text] [Related]  

  • 17. Inv dup (15): is the electroclinical phenotype helpful for this challenging clinical diagnosis?
    Valente KD; Freitas A; Fridman C; Varela M; Silva AE; Fett AC; Koiffmann CP
    Clin Neurophysiol; 2006 Apr; 117(4):803-9. PubMed ID: 16495142
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosomal abnormality at 6p25.1-25.3 identifies a susceptibility locus for hypothalamic hamartoma associated with epilepsy.
    Kerrigan JF; Kruer MC; Corneveaux J; Panganiban CB; Itty A; Reiman D; Ng YT; Stephan DA; Craig DW
    Epilepsy Res; 2007 Jun; 75(1):70-3. PubMed ID: 17512701
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Rud's syndrome. Case report].
    Bourgeois J; Vittori F
    Lyon Med; 1972 Jun; 227(11):1143-6. PubMed ID: 5080074
    [No Abstract]   [Full Text] [Related]  

  • 20. [2 cases of triplo-X with epileptic seizure].
    Takei H; Asaka A; Kurihara T
    No To Shinkei; 1969 May; 21(5):523-32. PubMed ID: 5394316
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.