Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
Ayse Tosun, Seda Erisen Karaca, Tolga Unuvar, Yakup Yurekli, Cigdem Yenisey, Imran Kurt Omurl. Bone mineral density and vitamin D status in children with epilepsy, cerebral palsy, and cerebral palsy with epilepsy. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. vol 33. issue 1. 2017-03-15. PMID:27757568. |
we aimed to evaluate the relationship between bone mineral density (bmd) disorders and possible risk factors in patients with epilepsy only (eo), cerebral palsy only (cpo), and cerebral palsy-epilepsy (cp + e). |
2017-03-15 |
2023-08-13 |
Not clear |
Thuong T Ha, Lynette G Sadleir, Simone A Mandelstam, Sarah J Paterson, Ingrid E Scheffer, Jozef Gecz, Mark A Corbet. A mutation in COL4A2 causes autosomal dominant porencephaly with cataracts. American journal of medical genetics. Part A. vol 170A. issue 4. 2016-12-13. PMID:26708157. |
mutations in col4a1 are well described and result in brain abnormalities manifesting with severe neurological deficits including cerebral palsy, intellectual disability, and focal epilepsy. |
2016-12-13 |
2023-08-13 |
Not clear |
Ali Al Kaissi, Herbert Kurz, Wolfgang Bock, Gerald Pärtan, Klaus Klaushofer, Rudolf Ganger, Franz Gril. Agenesis of the Corpus Callosum and Skeletal Deformities in Two Unrelated Patients: Analysis via MRI and Radiography. Case reports in orthopedics. vol 2014. 2014-03-04. PMID:24592343. |
mental retardation, mild to severe epilepsy and cerebral palsy often of hemiplegic type are common accompaniments in patients with agenesis/hypoplasia of the corpus callosum. |
2014-03-04 |
2023-08-12 |
Not clear |
Hamdy Na El Tallawy, Wafaa Ma Farghaly, Tarek A Rageh, Ghaydaa A Shehata, Reda Badry, Nabil A Metwally, Esam A El Moselhy, Mahmoud Hassan, Mohamed A Sayed, Ahmed A Waris, Yaser Hamed, Islam Shaaban, Mohamed A Hamed, Mahmoud Raafat Kandi. Door-to-door survey of major neurological disorders (project) in Al Quseir City, Red Sea Governorate, Egypt. Neuropsychiatric disease and treatment. vol 9. 2013-06-10. PMID:23745047. |
the order of frequency of prevalence of the studied neurological disorders was dementia (3.83% for those aged > 60 years), migraine (2.8% for those aged > 8 years), stroke (6.2/1000 for those aged > 20 years), epilepsy (5.5/1000), parkinson's disease (452.1/100,000 for those aged > 40 years), cerebral palsy (3.6/1000 among children < 18 years), spinal cord disorders (63/100,000) dystonia (39.11/100,000), cerebellar ataxia (30.01/100,000), trigeminal neuralgia (28/100,000 for those aged > 37 years), chorea (21.03/100,000), athetosis (15/100,000), and multiple sclerosis (13.74/100,000). |
2013-06-10 |
2023-08-12 |
Not clear |
F H Boot, J J M Pel, H M Evenhuis, J van der Stee. Factors related to impaired visual orienting behavior in children with intellectual disabilities. Research in developmental disabilities. vol 33. issue 5. 2012-10-09. PMID:22564700. |
therefore, the main objective of this study was to investigate possible correlations between the children's characteristics (age, gender, level of id, mobility, gestational age, cerebral palsy, down syndrome, visual acuity, strabismus, nystagmus, and epilepsy), and abnormal visual orienting behavior. |
2012-10-09 |
2023-08-12 |
Not clear |
K Pelc, N Deconinck, A Monier, T Sékhara, J Bormans, B Da. [A new framework for cerebral palsy]. Revue medicale de Bruxelles. vol 27 Spec No. 2011-09-27. PMID:21818891. |
the motor disorders of cerebral palsy are often accompanied by disturbances of sensation, perception, cognition, communication or behaviour, by epilepsy or by secondary musculoskeletal problems (bax et al. |
2011-09-27 |
2023-08-12 |
Not clear |
Katherine Mortati, Barbara Dworetzky, Orrin Devinsk. Marijuana: an effective antiepileptic treatment in partial epilepsy? A case report and review of the literature. Reviews in neurological diseases. vol 4. issue 2. 2007-11-06. PMID:17609644. |
here we present the case of a 45-year-old man with cerebral palsy and epilepsy who showed marked improvement with the use of marijuana. |
2007-11-06 |
2023-08-12 |
Not clear |
Ganeshwaran H Mochid. Cortical malformation and pediatric epilepsy: a molecular genetic approach. Journal of child neurology. vol 20. issue 4. 2005-07-27. PMID:15921229. |
genetic malformations of the cerebral cortex are important causes of neurologic morbidity in children because they are often associated with developmental delay, motor disturbances (cerebral palsy), and epilepsy. |
2005-07-27 |
2023-08-12 |
human |
Yasutaka Murata, Atsuo Itakura, Katsuji Matsuzawa, Akihisa Okumura, Kenji Wakai, Shigehiko Mizutan. Possible antenatal and perinatal related factors in development of cystic periventricular leukomalacia. Brain & development. vol 27. issue 1. 2005-04-29. PMID:15626536. |
cystic periventricular leukomalacia (cpvl), the principal ischemic brain injury in premature infants, is characterized by necrosis of the white matter in the periventricular region and the major neuropathology for spastic motor deficits in cerebral palsy or epilepsy. |
2005-04-29 |
2023-08-12 |
Not clear |
b' Matti Sillanp\\xc3\\xa4\\xc3\\xa. Learning disability: occurrence and long-term consequences in childhood-onset epilepsy. Epilepsy & behavior : E&B. vol 5. issue 6. 2005-02-28. PMID:15582842.' |
in multivariate analysis, mental retardation and subsequent ld were predicted by occurrence of cerebral palsy (odds ratio [or]=3.83; 95% confidence interval [ci]=1.77-8.28, p=0.0006), onset of epilepsy before the age of 6 years (or=3.63, 95% ci=1.57-8.42, p=0.0026), and poor early effect of drug therapy (or=2.78, 95% ci=1.43-5.39, p=0.0025). |
2005-02-28 |
2023-08-12 |
human |
Larry Burd, Tania M Cotsonas-Hassler, John T Martsolf, Jacob Kerbeshia. Recognition and management of fetal alcohol syndrome. Neurotoxicology and teratology. vol 25. issue 6. 2004-01-20. PMID:14624967. |
people with fas have high rates of comorbid conditions: attention deficit hyperactivity disorder (40%), mental retardation (15-20%), learning disorders (25%), speech and language disorders (30%), sensory impairment (30%), cerebral palsy (4%), epilepsy (8-10%). |
2004-01-20 |
2023-08-12 |
Not clear |
M Zucconi, O Brun. Sleep disorders in children with neurologic diseases. Seminars in pediatric neurology. vol 8. issue 4. 2002-05-07. PMID:11768788. |
this article focuses on the following specific neurologic diseases: nocturnal frontal lobe epilepsy and abnormal motor behaviors of epileptic origin, evaluating differential diagnosis with parasomnias; achondroplasia, confirming the crucial role of craniofacial deformity in determining sleep-disordered breathing; neuromuscular diseases, mainly duchenne's muscular dystrophy and myotonic dystrophy; cerebral palsy, evaluating either the features of sleep architecture and the importance of the respiratory problems associated; headaches, confirming the strict relationships with sleep in terms of neurochemical and neurobehavioral substrates; and finally a review on the effectiveness of melatonin for sleep problems in children with neurologic syndromes and mental retardation, blindness, and epilepsy. |
2002-05-07 |
2023-08-12 |
Not clear |
M C Machuca, A Vélez, G Machuca, H L Tormos, E Nieves, P Bullón Fernánde. [Dental treatment under general anesthesia offered at the Hospital Pediátrico Universitario de Puerto Rico during the years 1989-1994]. Puerto Rico health sciences journal. vol 15. issue 4. 1997-06-13. PMID:9190623. |
the mr group was composed of those who presented only mental retardation (42%), cerebral palsy (17%), epilepsy (15%), syndromes (7%), endocrinopathies (7%), hydrocephalus (5%) and other conditions (7%). |
1997-06-13 |
2023-08-12 |
Not clear |
M Thommessen, A Heiberg, B F Kase, S Larsen, G Rii. Feeding problems, height and weight in different groups of disabled children. Acta paediatrica Scandinavica. vol 80. issue 5. 1991-09-18. PMID:1831317. |
retarded growth and feeding problems were common in children with cerebral palsy, mental retardation, congenital heart disease and deaf-blindness, but rare in children with esophagus atresia, cystic fibrosis and epilepsy. |
1991-09-18 |
2023-08-11 |
Not clear |
K Joh, N Usui, S Aizawa, Y Yamaguchi, S Chiba, T Takahashi, Y Muramatsu, S Saka. Focal segmental glomerulosclerosis associated with infantile spasms in five mentally retarded children: a morphological analysis on mesangiolysis. American journal of kidney diseases : the official journal of the National Kidney Foundation. vol 17. issue 5. 1991-06-05. PMID:2024658. |
four of the five children diagnosed as west syndrome, lennox syndrome, or petit mal epilepsy also had cerebral palsy and microcephaly. |
1991-06-05 |
2023-08-11 |
Not clear |
K Joh, N Usui, S Aizawa, Y Yamaguchi, S Chiba, T Takahashi, Y Muramatsu, S Saka. Focal segmental glomerulosclerosis associated with infantile spasms in five mentally retarded children: a morphological analysis on mesangiolysis. American journal of kidney diseases : the official journal of the National Kidney Foundation. vol 17. issue 5. 1991-06-05. PMID:2024658. |
the other patient had petit mal epilepsy without cerebral palsy and microcephaly. |
1991-06-05 |
2023-08-11 |
Not clear |
H Suzuki, M Aihara, K Suga. [Severely retarded children in a defined area of Japan--prevalence rate, associated disabilities and causes]. No to hattatsu = Brain and development. vol 23. issue 1. 1991-03-26. PMID:1825273. |
association of several disabilities was as follows: cerebral palsy 62%, epilepsy 82%, decreased visual acuity 42%, respiratory distress 16%, and feeding difficulty 32%. |
1991-03-26 |
2023-08-11 |
Not clear |
E Fernell, G Hagberg, B Hagber. Infantile hydrocephalus--the impact of enhanced preterm survival. Acta paediatrica Scandinavica. vol 79. issue 11. 1991-02-13. PMID:2267927. |
the outcome in very preterm surviving infants with ih was still alarmingly poor: 78% had cerebral palsy, 72% mental deficiency, and 56% epilepsy. |
1991-02-13 |
2023-08-11 |
Not clear |
J Süssová, Z Seidl, J Fabe. Hemiparetic forms of cerebral palsy in relation to epilepsy and mental retardation. Developmental medicine and child neurology. vol 32. issue 9. 1990-12-07. PMID:2121572. |
fifty-one children with hemiparetic cerebral palsy underwent clinical, eeg and ct examinations to assess mental performance, laterality of cp and incidence of epilepsy, 80 per cent of the children had epileptic abnormalities on eeg, but less than half had clinical signs of epilepsy. |
1990-12-07 |
2023-08-11 |
Not clear |
W Görk. [Indications for studying evoked potentials in childhood. Methods--indications--value]. Klinische Padiatrie. vol 198. issue 6. 1987-03-13. PMID:3807249. |
testing for evoked potentials is indicated in suspected cerebral palsy in infants, in all cases of psychomotor retardation of unknown origin, impairment of vision or hearing, in cases of brain trauma or in suspected brainstem process, lesions of n. opticus or visual projective systems, neurometabolic or degenerative cns disease, phacomatosis, progressive myoclonic epilepsy, ceroidlipofuscinosis jansky-bielschowski, benign partial epilepsy with extreme somatosensory evoked potentials, ramsey-hunt-syndrome and aplasia of the corpus callosum. |
1987-03-13 |
2023-08-11 |
Not clear |