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 *

96 related articles for article (PubMed ID: 7803078)

  • 21. Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature.
    Vignoli A; Borgatti R; Peron A; Zucca C; Ballarati L; Bonaglia C; Bellini M; Giordano L; Romaniello R; Bedeschi MF; Epifanio R; Russo S; Caselli R; Giardino D; Darra F; La Briola F; Banderali G; Canevini MP
    Epilepsia; 2012 Jul; 53(7):1146-55. PubMed ID: 22578097
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Epilepsy in a child with ring chromosome 14].
    Midro AT; Zadrozna-Tołwińska B
    Neurol Neurochir Pol; 1993; 27(1):99-104. PubMed ID: 8502366
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
    Buoni S; Zannolli R; Felice CD; Saponari S; Strambi M; Dotti MT; Castrucci E; Corbini L; Orsi A; Hayek J
    Clin Neurophysiol; 2008 Nov; 119(11):2455-8. PubMed ID: 18842453
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12.
    Grosso S; Pucci L; Farnetani M; Di Bartolo RM; Galimberti D; Mostardini R; Anichini C; Balestri M; Morgese G; Balestri P
    J Child Neurol; 2004 Aug; 19(8):604-8. PubMed ID: 15605470
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Relationship between severity of epilepsy and developmental outcome in Angelman syndrome.
    Ohtsuka Y; Kobayashi K; Yoshinaga H; Ogino T; Ohmori I; Ogawa K; Oka E
    Brain Dev; 2005 Mar; 27(2):95-100. PubMed ID: 15668047
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome.
    Curatolo P; Cilio MR; Del Giudice E; Romano A; Gaggero R; Pessagno A
    Neuropediatrics; 1993 Apr; 24(2):77-82. PubMed ID: 8327066
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Ring chromosome 20: an epileptic channel disorder?].
    Serrano-Castro PJ; Aguilar-Castillo MJ; Olivares-Romero J; Jiménez-Machado R; Molina-Aparicio MJ
    Rev Neurol; 2001 Feb 1-15; 32(3):237-41. PubMed ID: 11310277
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum.
    Romaniello R; Marelli S; Giorda R; Bedeschi MF; Bonaglia MC; Arrigoni F; Triulzi F; Bassi MT; Borgatti R
    J Child Neurol; 2017 Jan; 32(1):60-71. PubMed ID: 27683483
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [The evolution of epilepsy in the most common genetic forms with mental retardation (Down's syndrome and the fragile X syndrome)].
    Guerrini R; Dravet C; Ferrari AR; Battaglia A; Mattei MG; Salvadori P; Genton P; Pfanner P
    Pediatr Med Chir; 1993; 15 Suppl 1():19-22. PubMed ID: 8415189
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The genetics of epilepsy.
    Anderson VE; Hauser WA
    Prog Med Genet; 1985; 6():9-52. PubMed ID: 3915368
    [No Abstract]   [Full Text] [Related]  

  • 31. Cryptic chromosome rearrangements in five patients, with normal and/or abnormal karyotypes, associated with mental retardation, autism and/or epilepsy, detected by BAC genome array-CGH.
    Cabras V; Milia A; Montaldo C; Nucaro A
    Prague Med Rep; 2012; 113(4):279-88. PubMed ID: 23249659
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Epilepsy in patients with angelman syndrome caused by deletion of the chromosome 15q11-13.
    Valente KD; Koiffmann CP; Fridman C; Varella M; Kok F; Andrade JQ; Grossmann RM; Marques-Dias MJ
    Arch Neurol; 2006 Jan; 63(1):122-8. PubMed ID: 16401744
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15.
    Takeda Y; Baba A; Nakamura F; Ito M; Honma H; Koyama T
    Seizure; 2000 Mar; 9(2):145-50. PubMed ID: 10845741
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Spectrum of congenital CNS malformations in pediatric epilepsy.
    Sanghvi JP; Rajadhyaksha SB; Ursekar M
    Indian Pediatr; 2004 Aug; 41(8):831-8. PubMed ID: 15347872
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Epilepsy in three children with Wolf-Hirschhorn syndrome].
    Kaciński M; Kostyk E; Kruczek A; Skowronek-Bała B
    Przegl Lek; 2005; 62(11):1298-301. PubMed ID: 16512625
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Agenesis of the corpus callosum in a man with complete mosaic trisomy 8].
    Baverel F; de Recondo J; Rouffet A; Fredy D; Salesses A; Rondot P
    Presse Med; 1985 Apr; 14(14):781-3. PubMed ID: 3158893
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases.
    Di Meglio C; Lesca G; Villeneuve N; Lacoste C; Abidi A; Cacciagli P; Altuzarra C; Roubertie A; Afenjar A; Renaldo-Robin F; Isidor B; Gautier A; Husson M; Cances C; Metreau J; Laroche C; Chouchane M; Ville D; Marignier S; Rougeot C; Lebrun M; de Saint Martin A; Perez A; Riquet A; Badens C; Missirian C; Philip N; Chabrol B; Villard L; Milh M
    Epilepsia; 2015 Dec; 56(12):1931-40. PubMed ID: 26514728
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Familial progressive sensorimotor neuropathy with agenesis of the corpus callosum (Andermann syndrome): a clinical, neuroradiological and histopathological study.
    Deleu D; Bamanikar SA; Muirhead D; Louon A
    Eur Neurol; 1997; 37(2):104-9. PubMed ID: 9058066
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Late onset epileptic spasms is frequent in MECP2 gene duplication: electroclinical features and long-term follow-up of 8 epilepsy patients.
    Caumes R; Boespflug-Tanguy O; Villeneuve N; Lambert L; Delanoe C; Leheup B; Bahi-Buisson N; Auvin S
    Eur J Paediatr Neurol; 2014 Jul; 18(4):475-81. PubMed ID: 24703762
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Cortical dysplasias and epilepsy].
    Peña JA
    Invest Clin; 2000 Mar; 41(1):59-71. PubMed ID: 10758699
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.