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 *

123 related articles for article (PubMed ID: 8836504)

  • 21. Intractable epilepsy with ring chromosome 20 syndrome treated with vagal nerve stimulation: case report and review of the literature.
    Chawla J; Sucholeiki R; Jones C; Silver K
    J Child Neurol; 2002 Oct; 17(10):778-80. PubMed ID: 12546436
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Malignant refractory epilepsy in identical twins mosaic for a supernumerary ring chromosome 19.
    Shahwan A; Green AJ; Carey A; Stallings RL; O'Flaherty OC; King MD
    Epilepsia; 2004 Aug; 45(8):997-1000. PubMed ID: 15270770
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Epilepsy in patient with structural autosomal abnormality].
    Sugama S; Atsukawa K; Kusano K; Akatsuka A; Ochiai Y; Tsuzura S; Maekawa K
    No To Hattatsu; 1994 Nov; 26(6):486-92. PubMed ID: 7803078
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromosome 20 ring: a chromosomal disorder associated with a particular electroclinical pattern.
    Canevini MP; Sgro V; Zuffardi O; Canger R; Carrozzo R; Rossi E; Ledbetter D; Minicucci F; Vignoli A; Piazzini A; Guidolin L; Saltarelli A; dalla Bernardina B
    Epilepsia; 1998 Sep; 39(9):942-51. PubMed ID: 9738673
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Ring chromosome 22: a case report.
    Severien C; Felix S; Bartholomé K
    Klin Padiatr; 1991; 203(6):467-9. PubMed ID: 1721941
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Ring chromosome 15 syndrome in an adult female.
    Matsuishi T; Yamada Y; Endo K; Sakai H; Fukushima Y
    J Intellect Disabil Res; 1996 Oct; 40 ( Pt 5)():478-80. PubMed ID: 8906535
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Total corpus callosotomy for epileptic spasms after acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) in a case with tuberous sclerosis complex.
    Okanishi T; Fujimoto A; Motoi H; Kanai S; Nishimura M; Yamazoe T; Takagi A; Yamamoto T; Enoki H
    Brain Dev; 2017 May; 39(5):431-434. PubMed ID: 27923529
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Proximal trisomy 19q. Interstitial deletion and ring chromosome derived from 19q].
    Klein F; Schuck D; Noël B; Stoessel J; Vibert M
    Pediatrie; 1989; 44(9):717-20. PubMed ID: 2622712
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [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]  

  • 31. Epilepsy and chromosome 18 abnormalities: A review.
    Verrotti A; Carelli A; di Genova L; Striano P
    Seizure; 2015 Nov; 32():78-83. PubMed ID: 26552569
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Prenatal diagnosis of 3 cases of ring G chromosomes: one 21 and two 22, one of which was de novo].
    Crusi A; Engel E
    Ann Genet; 1986; 29(4):253-60. PubMed ID: 3495227
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotype.
    Ozkinay FF; Akisü M; Kültürsay N; Oral R; Tansug N; Sapmaz G
    Clin Genet; 1996 Sep; 50(3):145-8. PubMed ID: 8946113
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Ring chromosome 7 and sacral agenesis.
    Rodríguez L; Sanchís A; Villa A; Cánovas A; Peris S; Estívalis M; Pons S; Martínez-Frías ML
    Am J Med Genet; 2000 Sep; 94(1):52-8. PubMed ID: 10982483
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Analysis of ring chromosome 9 syndrome with fluorescence in situ hybridization].
    Ye ZC; Zhu XY; Zhao R; He XY; Zhang HJ; Li LP; Zhu YM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):559-62. PubMed ID: 20931537
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ring chromosome 14 with localization-related epilepsy: three cases.
    Morimoto M; Usuku T; Tanaka M; Otabe O; Nishimura A; Ochi M; Takeuchi Y; Yoshioka H; Sugimoto T
    Epilepsia; 2003 Sep; 44(9):1245-9. PubMed ID: 12919399
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [r14 syndrome without major dysmorphism].
    de Blois MC; Caille B; Rethoré MO; Dufier JL; Lejeune J
    Ann Genet; 1990; 33(3):155-8. PubMed ID: 2288460
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Abnormal myelination in a patient with ring chromosome 18.
    Nakayama J; Hamano K; Shimakura Y; Iwasaki N; Nakahara C; Imoto N; Kobayashi K; Arinami T; Hamaguchi H
    Neuropediatrics; 1997 Dec; 28(6):335-7. PubMed ID: 9453033
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Description of a case of ring chromosome 21 and pericentric inversion of Y chromosome].
    Ponzio G; Carozzi F; Dragone E; Spada A; Brignone S; De Marchi M; Carbonara A
    Pathologica; 1983; 75 Suppl():276-9. PubMed ID: 6680430
    [No Abstract]   [Full Text] [Related]  

  • 40. An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects.
    Rao A; O'Donnell S; Bain N; Meldrum C; Shorter D; Goel H
    Eur J Med Genet; 2014 Feb; 57(2-3):65-70. PubMed ID: 24462883
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.