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.
561 related articles for article (PubMed ID: 14730948)
21. Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency. Kappeler C; Dhenain M; Phan Dinh Tuy F; Saillour Y; Marty S; Fallet-Bianco C; Souville I; Souil E; Pinard JM; Meyer G; Encha-Razavi F; Volk A; Beldjord C; Chelly J; Francis F J Comp Neurol; 2007 Jan; 500(2):239-54. PubMed ID: 17111359 [TBL] [Abstract][Full Text] [Related]
22. Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene. Caliebe A; Kroes HY; van der Smagt JJ; Martin-Subero JI; Tönnies H; van 't Slot R; Nievelstein RA; Muhle H; Stephani U; Alfke K; Stefanova I; Hellenbroich Y; Gillessen-Kaesbach G; Hochstenbach R; Siebert R; Poot M Eur J Med Genet; 2010; 53(4):179-85. PubMed ID: 20382278 [TBL] [Abstract][Full Text] [Related]
23. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647 [TBL] [Abstract][Full Text] [Related]
24. Morphometric variability of neuroimaging features in children with agenesis of the corpus callosum. Neal JB; Filippi CG; Mayeux R BMC Neurol; 2015 Jul; 15():116. PubMed ID: 26209096 [TBL] [Abstract][Full Text] [Related]
25. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia. Aykut A; Cogulu O; Ekmekci AY; Ozkinay F Genet Couns; 2008; 19(2):237-40. PubMed ID: 18618999 [TBL] [Abstract][Full Text] [Related]
26. The Dandy-Walker variant: a case series of 24 pediatric patients and evaluation of associated anomalies, incidence of hydrocephalus, and developmental outcomes. Sasaki-Adams D; Elbabaa SK; Jewells V; Carter L; Campbell JW; Ritter AM J Neurosurg Pediatr; 2008 Sep; 2(3):194-9. PubMed ID: 18759601 [TBL] [Abstract][Full Text] [Related]
27. Agenesis of the corpus callosum: lessons from humans and mice. Kamnasaran D Clin Invest Med; 2005 Oct; 28(5):267-82. PubMed ID: 16265999 [TBL] [Abstract][Full Text] [Related]
28. Hypoplasia of the cerebellar vermis and corpus callosum in thrombocytopenia with absent radius syndrome on MRI studies. MacDonald MR; Schaefer GB; Olney AH; Patton DF Am J Med Genet; 1994 Mar; 50(1):46-50. PubMed ID: 7512789 [TBL] [Abstract][Full Text] [Related]
29. [Neurocristopathies: a high incidence of cerebral dysgenesis in patients with Hirschsprung's disease]. Carrascosa-Romero MC; Fernández-Córdoba MS; Gonzálvez-Piñera J; Gutiérrez-Junquera C; Pardal-Fernández JM Rev Neurol; 2007 Dec 16-31; 45(12):707-12. PubMed ID: 18075983 [TBL] [Abstract][Full Text] [Related]
30. Lesions of the corpus callosum in children with neurofibromatosis 1. Mimouni-Bloch A; Kornreich L; Kaadan W; Steinberg T; Shuper A Pediatr Neurol; 2008 Jun; 38(6):406-10. PubMed ID: 18486822 [TBL] [Abstract][Full Text] [Related]
31. Dysgenesis of the corpus callosum and associated telencephalic anomalies: MRI. Utsunomiya H; Ogasawara T; Hayashi T; Hashimoto T; Okazaki M Neuroradiology; 1997 Apr; 39(4):302-10. PubMed ID: 9144682 [TBL] [Abstract][Full Text] [Related]
32. [Agenesis of the corpus callosum]. Nielsen LH Ugeskr Laeger; 1995 Feb; 157(6):737-9. PubMed ID: 7701633 [TBL] [Abstract][Full Text] [Related]
33. [Congenital malformations of the brain. 2: Malformations of the corpus callosum and holoprocencephalies]. Rummeny C; Ertl-Wagner B; Reiser MF Radiologe; 2003 Nov; 43(11):925-33. PubMed ID: 14628116 [TBL] [Abstract][Full Text] [Related]
34. Intracranial and extracranial malformations in patients with craniofacial anomalies. Tunçbilek G; Alanay Y; Uzun H; Kayikçioğlu A; Akarsu NA; Benli K J Craniofac Surg; 2010 Sep; 21(5):1460-4. PubMed ID: 20818260 [TBL] [Abstract][Full Text] [Related]
35. Central nervous system anomalies associated with fetal trisomy 18. Chen CP Prenat Diagn; 2005 May; 25(5):419-21. PubMed ID: 15906412 [No Abstract] [Full Text] [Related]
36. Thrombocytopenia-absent radius (tar) syndrome: a case with agenesis of corpus callosum, hypoplasia of cerebellar vermis and horseshoe kidney. Skórka A; Bielicka-Cymermann J; Gieruszczak-Białek D; Korniszewski L Genet Couns; 2005; 16(4):377-82. PubMed ID: 16440880 [TBL] [Abstract][Full Text] [Related]
37. Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome. Cohen MM; Kreiborg S Neurosurg Clin N Am; 1991 Jul; 2(3):565-8. PubMed ID: 1821304 [TBL] [Abstract][Full Text] [Related]
38. [Agenesis of the corpus callosum: modes of manifestation in adults]. Lemesle M; Giroud M; Madinier G; Martin D; Baudouin N; Binnert D; Dumas R Rev Neurol (Paris); 1997 May; 153(4):256-61. PubMed ID: 9296144 [TBL] [Abstract][Full Text] [Related]
39. Magnetic resonance imaging of intracranial malformations in dogs and cats. MacKillop E Vet Radiol Ultrasound; 2011; 52(1 Suppl 1):S42-51. PubMed ID: 21392155 [TBL] [Abstract][Full Text] [Related]
40. Focal lesion in the splenium of the corpus callosum in epileptic patients: antiepileptic drug toxicity? Kim SS; Chang KH; Kim ST; Suh DC; Cheon JE; Jeong SW; Han MH; Lee SK AJNR Am J Neuroradiol; 1999 Jan; 20(1):125-9. PubMed ID: 9974067 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]