| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Raluca Badila, Simina Mustatea, Sandra Neamtu, Corina Roma. Successful Target Temperature Management After Cardiac Arrest: A Case Report and a Review of the Literature. Cureus. vol 16. issue 8. 2024-09-30. PMID:39347325. |
magnetic resonance imaging showed late hypoxic leukoencephalopathy with a level of the white matter of the semioval centers, radiating corona, splenium corpus callosum, and internal capsular posterior arm with extension to the cerebral peduncles. |
2024-09-30 |
2024-10-02 |
Not clear |
| Teresa Macheda, Margaret R Andres, Lydia Sanders, Kelly N Roberts, Ryan K Shahidehpour, Josh M Morganti, Adam D Bachstette. Old Age Exacerbates White Matter Neuroinflammation and Cognitive Deficits Following Closed-Head Injury, Particularly in Female Mice. Neurotrauma reports. vol 5. issue 1. 2024-08-26. PMID:39184175. |
we assessed the righting reflex, body weight, behavior (radial arm water maze and active avoidance), and inflammation (gfap, iba1, cd45) in the neocortex, corpus callosum, and hippocampus. |
2024-08-26 |
2024-08-28 |
mouse |
| Elvio Della Giustina, Alessandro Iodice, Carlotta Spagnoli, Simona Giovannini, Daniele Frattini, Carlo Fusco, Giuseppe Gobbi, Marcella Zollino, Giovanni Ner. "Minimal" holoprosencephaly in a 14q deletion syndrome patient. American journal of medical genetics. Part A. vol 173. issue 12. 2018-03-21. PMID:29136354. |
we report on a patient with terminal deletion of the long arm of chromosome 14 displaying brain interhemispheric fusion limited to the midline anterior frontal cortex associated with hypoplastic corpus callosum and incomplete rotation of the left hippocampus in a clinical setting of motor and intellectual disability with poor language, and social behavior abnormalities with aggressiveness. |
2018-03-21 |
2023-08-13 |
Not clear |
| Jill Campbell Stewart, Pritha Dewanjee, George Tran, Erin Burke Quinlan, Lucy Dodakian, Alison McKenzie, Jill See, Steven C Crame. Role of corpus callosum integrity in arm function differs based on motor severity after stroke. NeuroImage. Clinical. vol 14. 2017-11-07. PMID:28348955. |
role of corpus callosum integrity in arm function differs based on motor severity after stroke. |
2017-11-07 |
2023-08-13 |
human |
| Dominik S Westphal, Stephanie Andres, Kirsten I Beitzel, Christine Makowski, Thomas Meitinger, Julia Hoefel. Identification of a de novo microdeletion 1q44 in a patient with hypogenesis of the corpus callosum, seizures and microcephaly - A case report. Gene. vol 616. 2017-05-26. PMID:28336463. |
microdeletion 1q44 on the long arm of chromosome 1 leads to a phenotype that includes microcephaly, seizure, agenesis or hypogenesis of the corpus callosum, polydactyly, congenital heart defects and severe developmental delay along with characteristic facial dysmorphic signs. |
2017-05-26 |
2023-08-13 |
Not clear |
| S Puvabanditsin, G Herrera-Garcia, N Gengel, K Hussein, M February, J Mayne, R Meht. PARTIAL TRISOMY 4p AND PARTIAL MONOSOMY 13q: CASE REPORT AND A LITERATURE REVIEW. Genetic counseling (Geneva, Switzerland). vol 27. issue 1. 2016-06-07. PMID:27192890. |
we report on a term first born dichorionic-diamniotic twin with deletion of the distal long arm of chromosome 13, partial trisomy of the short arm of chromosome 4, intrauterine growth retardation, and multiple anomalies including microcephaly, colpocephaly, absent corpus callosum, bulbous tip of the nose, large and low set ears, macroglossia, thin upper lip, double outlet right ventricle, atria/ventricular septal defect, cleft mitral valve, pulmonary stenosis, single umbilical artery, multicystic dysplastic left kidney, sacral dimple, anterior displacement of anus, simian creases, abnormal thumb (congenital clasped thumb), overlapping toes, and congenital hypothyroidism. |
2016-06-07 |
2023-08-13 |
Not clear |
| Hafize Sav, Mustafa Altay Atalay, Gonca Demir, Mehmet Akif Ozdemir, Ayse Nedret Ko. Early diagnosis of cerebral aspergillosis with various methods: a case report. Le infezioni in medicina. vol 21. issue 2. 2014-06-30. PMID:23774978. |
upon development of neutropenia and focal seizures in the left arm during implementation of the all treatment protocol, brain mri was performed in the patient and nodular lesions compliant with brain abscess were detected in the frontal lobe, left cerebellum and the cingulate gyrus on the superior aspect of the left corpus callosum. |
2014-06-30 |
2023-08-12 |
Not clear |
| Marina Michelson, Anat Ben-Sasson, Chana Vinkler, Esther Leshinsky-Silver, Ifat Netzer, Ayala Frumkin, Sara Kivity, Tally Lerman-Sagie, Dorit Le. Delineation of the interstitial 6q25 microdeletion syndrome: refinement of the critical causative region. American journal of medical genetics. Part A. vol 158A. issue 6. 2012-09-24. PMID:22585544. |
we report on a boy with global developmental delay, distinct dysmorphic features, dysgenesis of the corpus callosum, limb anomalies, and genital hypoplasia who has a small interstitial deletion of the long arm of chromosome 6 detected by comparative genomic hybridization (cgh). |
2012-09-24 |
2023-08-12 |
Not clear |
| Udo Koehler, Elke Holinski-Feder, Birgit Ertl-Wagner, Juergen Kunz, Arpad von Moers, Hubertus von Voss, Chayim Schell-Apaci. A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum. European journal of pediatrics. vol 169. issue 4. 2010-05-20. PMID:19763616. |
we report another case of a microdeletion with involvement of the nfia gene in the short arm of chromosome 1 (del(1)(p31.3p32.2)) with, amongst other features, hypoplasia of the corpus callosum, ventriculomegaly, and dysmorphic features. |
2010-05-20 |
2023-08-12 |
Not clear |
| Ingrid Witters, Elyes Chabchoub, Joris R Vermeesch, Jean-Pierre Fryn. Submicroscopic distal deletion of the long arm of chromosome 13(13q34) with corpus callosum agenesis. American journal of medical genetics. Part A. vol 149A. issue 8. 2009-09-30. PMID:19610112. |
submicroscopic distal deletion of the long arm of chromosome 13(13q34) with corpus callosum agenesis. |
2009-09-30 |
2023-08-12 |
Not clear |
| B W M van Bon, D A Koolen, R Borgatti, A Magee, S Garcia-Minaur, L Rooms, W Reardon, M Zollino, M C Bonaglia, M De Gregori, F Novara, R Grasso, R Ciccone, H A van Duyvenvoorde, A M Aalbers, R Guerrini, E Fazzi, W M Nillesen, S McCullough, S G Kant, C L Marcelis, R Pfundt, N de Leeuw, D Smeets, E A Sistermans, J M Wit, B C Hamel, H G Brunner, F Kooy, O Zuffardi, B B A de Vrie. Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis. Journal of medical genetics. vol 45. issue 6. 2008-08-11. PMID:18178631. |
patients with a microscopically visible deletion of the distal part of the long arm of chromosome 1 have a recognisable phenotype, including mental retardation, microcephaly, growth retardation, a distinct facial appearance and various midline defects including corpus callosum abnormalities, cardiac, gastro-oesophageal and urogenital defects, as well as various central nervous system anomalies. |
2008-08-11 |
2023-08-12 |
Not clear |
| Dagmar Sternad, Kunlin Wei, Jörn Diedrichsen, Richard B Ivr. Intermanual interactions during initiation and production of rhythmic and discrete movements in individuals lacking a corpus callosum. Experimental brain research. vol 176. issue 4. 2007-07-25. PMID:16917769. |
three individuals lacking a corpus callosum, two due to callosotomy and one agenesis, and three age-matched healthy controls were tested on a bimanual task in which a discrete or rhythmic arm movement was initiated following a visual signal while the other arm produced continuous, rhythmic movements. |
2007-07-25 |
2023-08-12 |
human |
| K Kutsche, W Werner, O Bartsch, A von der Wense, P Meinecke, A Ga. Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of Xp. Cytogenetic and genome research. vol 99. issue 1-4. 2004-01-21. PMID:12900578. |
the patient showed agenesis of the corpus callosum, histiocytoid cardiomyopathy, and lactic acidosis but no microphthalmia, and carried a mosaic subtle inversion of the short arm of the x chromosome in 15% of his peripheral blood lymphocytes, 46,y,inv(x)(p22.13 approximately 22.2p22.32 approximately 22.33)[49]/46,xy[271]. |
2004-01-21 |
2023-08-12 |
Not clear |
| E Marszał, E Jamroz, J Pilch, E Kluczewska, H Jabłecka-Deja, R Krawczy. Agenesis of corpus callosum: clinical description and etiology. Journal of child neurology. vol 15. issue 6. 2000-10-18. PMID:10868784. |
the etiology of agenesis of the corpus callosum has been established in four children: partial trisomy of chromosome 13, partial duplication of the long arm of chromosome 10, aicardi's syndrome, and intracranial bleeding during the fetal period as a result of injury. |
2000-10-18 |
2023-08-12 |
Not clear |
| U Nocentini, N A Borghese, C Caltagirone, L Fadda, F Lacquanit. A callosal disconnection syndrome of vascular origin. Journal of neurosurgical sciences. vol 41. issue 1. 1997-10-21. PMID:9273867. |
to study the after-effects of a selective lesion of the corpus callosum on the capacity in transferring spatial information on arm posture derived from kinesthesia and vision. |
1997-10-21 |
2023-08-12 |
Not clear |
| J P Fryns, A Bonhomme, H Van den Bergh. Nager acrofacial dysostosis. An adult male with severe neurological deficit. Genetic counseling (Geneva, Switzerland). vol 7. issue 2. 1996-12-17. PMID:8831135. |
in addition to the typical maxillofacial dysostosis and the bilateral thumb hypoplasia, he presented a severe neurological syndrome with spastic diplegia, hemiparesis of the left arm, and agenesis of the corpus callosum on ct-scan. |
1996-12-17 |
2023-08-12 |
Not clear |