Mortality risk after neonatal seizures in very preterm newborns.

abstract：:The ultimate goal for management of patients with cerebral palsy is to help them grow up to become as independent as possible, learn to make their own choices in life, and pursue their own dreams. Optimal mobility is crucial to achieving independence and is also necessary for better health and quality of life in these...

journal_title：Journal of child neurology

authors： Brunstrom JE

更新日期：2001-01-01 00:00:00

abstract：:Visual electrophysiological techniques represent excellent means for assessing retinal, optic pathways and visual cortex function. Electroretinograms, visual evoked potentials, and clinical records of 17 patients with mucopolysaccharidosis registered in the neurophysiological database of our institution were reviewed ...

journal_title：Journal of child neurology

authors： Suppiej A,Rampazzo A,Cappellari A,Traverso A,Tormene AP,Pinello L,Scarpa M

更新日期：2013-10-01 00:00:00

abstract：:Vigabatrin is an antiepileptic drug that results in higher gamma-aminobutyrate levels in the brain and retina. Vigabatrin-induced visual field defects are usually asymptomatic and only detectable by perimetry. Further, perimetry requires good cooperation, and children aged under 10 years cannot do it. Electroretinogra...

journal_title：Journal of child neurology

authors： Bakhshandeh Bali MK,Otaghsara SM,Soltansanjari M,Sadighi N,Nasehi MM,Ashrafi MR,Karimzadeh P,Taghdiri MM,Ghofrani M

更新日期：2014-06-01 00:00:00

abstract：:This study was conducted to determine the occurrence, severity, and risk factors of gingival enlargement in children treated with valproate and other nonvalproate antiepileptic drugs. A cross-sectional study was carried out in which data obtained from 68 epileptic children under treatment were compared with those from...

journal_title：Journal of child neurology

authors： Tan H,Gürbüz T,Dağsuyu IM

更新日期：2004-12-01 00:00:00

abstract：:Past, present, and future research activities in Rett syndrome are described. Studies to this point have failed to define a biologic or chemical marker. It is hoped that heightened activity in this unique syndrome will provide guidance for the diagnosis of this disorder, and with it, better understanding. ...

journal_title：Journal of child neurology

authors： Percy AK

更新日期：1988-01-01 00:00:00

abstract：:Concussion is a known risk in youth soccer, but little is known about subconcussive head impacts. The authors provided a prospective cohort study measuring frequency and magnitude of subconcussive head impacts using accelerometry in a middle school-age soccer tournament, and association between head impacts and change...

journal_title：Journal of child neurology

authors： Chrisman SP,Mac Donald CL,Friedman S,Andre J,Rowhani-Rahbar A,Drescher S,Stein E,Holm M,Evans N,Poliakov AV,Ching RP,Schwien CC,Vavilala MS,Rivara FP

更新日期：2016-07-01 00:00:00

abstract：:Corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus (CRASH syndrome) is an X-linked recessive disorder caused by mutations in the neuronal cell adhesion molecule L1 (LICAM) gene. L1 plays a key role in axon outgrowth and pathfinding during the development of the nervous syste...

journal_title：Journal of child neurology

authors： Sztriha L,Frossard P,Hofstra RM,Verlind E,Nork M

更新日期：2000-04-01 00:00:00

abstract：:We report 10 years' follow-up of the previously described family with a novel mutation of the KCNA1 gene. The family consisted of 3 affected boys (first seen at ages 3, 11, and 12) and their affected mother and asymptomatic father and sister. They clinically presented with diffuse myokymia, muscle cramps, and lower li...

journal_title：Journal of child neurology

authors： Moghimi N,Rosen JB,Jabbari B

更新日期：2013-11-01 00:00:00

abstract：:Paramyotonia congenita in 22 members of Arab (Omani) family is reported. Four generations were affected. All had early onset around 1 year of age, with myotonia and cold intolerance. Age of onset in the index case was at 3 months of age. Six members with the disease were examined and investigated. To our knowledge, th...

journal_title：Journal of child neurology

authors： Koul R,Alfutaisi A,Hira M

更新日期：2010-02-01 00:00:00

abstract：:Maple syrup urine disease is a disorder of branched-chain keto acid metabolism. Three children were diagnosed with the intermediate form of maple syrup urine disease during routine evaluation of mental retardation. Clinical features were characterized by mental retardation, seizures, autistic features, and movement di...

journal_title：Journal of child neurology

authors： Bindu PS,Shehanaz KE,Christopher R,Pal PK,Ravishankar S

更新日期：2007-07-01 00:00:00

abstract：:Two children with isolated congenital anosmia, a rare syndrome of deficient restricted neuronal migration, are presented with early diagnosis confirmed by standardized smell testing and detailed neuroimaging studies. Recognition of this disorder and its spectrum of presentations provides important insights into the mo...

journal_title：Journal of child neurology

authors： Assouline S,Shevell MI,Zatorre RJ,Jones-Gotman M,Schloss MD,Oudjhane K

更新日期：1998-04-01 00:00:00

abstract：:The efficacy of modafinil in comparison with methylphenidate in treatment of pediatric attention-deficit hyperactivity disorder (ADHD) has not been thoroughly investigated. This study compared the effect of modafinil versus methylphenidate on continuous attention task in children with ADHD, using the Test of Variables...

journal_title：Journal of child neurology

authors： Goez HR,Scott O,Nevo N,Bennett-Back O,Zelnik N

更新日期：2012-12-01 00:00:00

abstract：:The purpose of this study was to assess the cognitive development of 27 children with nonhemorrhagic neonatal stroke (occurring within the first 28 days of life). The cognitive evaluation consisted of the Bayley Scales of Infant Development, administered at 12 and/or 24 months poststroke. Compared with the normative s...

journal_title：Journal of child neurology

authors： McLinden A,Baird AD,Westmacott R,Anderson PE,deVeber G

更新日期：2007-09-01 00:00:00

abstract：:There is strong evidence for a loss of habituation during cognitive processing in migraine as measured by P300 and contingent negative variation in adults. Event-related potentials evoked by an oddball paradigm have not yet been studied in children and adolescents suffering from different primary headache types. We re...

journal_title：Journal of child neurology

authors： Evers S,Bauer B,Grotemeyer KH,Kurlemann G,Husstedt IW

更新日期：1998-07-01 00:00:00

abstract：:The authors reviewed the medical records of very low-birth-weight infants admitted from 1998 to 2007 and compared neurodevelopmental outcomes with their previously reported data from 1989 to 1997. The recent group included 824 infants, and the previous group included 471 infants. Neurodevelopmental outcomes were class...

journal_title：Journal of child neurology

authors： Jang DH,Sung IY,Jeon JY,Moon HJ,Kim KS,Kim EA,Lee BS

更新日期：2011-11-01 00:00:00

abstract：:We describe a case of pathologically confirmed Alexander's disease in which serial cranial ultrasound studies demonstrated unique findings of enlarging subependymal cysts with evolving periventricular hyperechogenicity. Computed tomographic scan of the head showed low attenuation of the periventricular white matter an...

journal_title：Journal of child neurology

authors： Hess DC,Fischer AQ,Yaghmai F,Figueroa R,Akamatsu Y

更新日期：1990-07-01 00:00:00

abstract：:We present 12 cases of males with myalgia and cramps and a normal muscle strength examination. All the patients had muscle dystrophin values consistent with Becker muscular dystrophy. Five of the patients had a normal electromyogram, and five had normal light microscopic muscle biopsy results. Of particular note, four...

journal_title：Journal of child neurology

authors： Samaha FJ,Quinlan JG

更新日期：1996-01-01 00:00:00

abstract：:Lissencephaly is a brain malformation manifested by a smooth cerebral surface and caused by incomplete neuronal migration. Clinical sequellae include minor craniofacial changes (bitemporal hollowing, small jaw), severe mental retardation, and other neurological abnormalities. Patients with classical or type I lissence...

journal_title：Journal of child neurology

authors： Pavone L,Gullotta F,Incorpora G,Grasso S,Dobyns WB

更新日期：1990-01-01 00:00:00

abstract：:The objective of this study is to determine the long-term outcome of children with intractable epilepsy who have diffuse cortical hypometabolism on 2-deoxy-2-((18)F)fluoro-D-glucose positron emission tomography (FDG-PET) scans. Seventeen children with intractable epilepsy showing bilateral, diffuse cortical hypometabo...

journal_title：Journal of child neurology

authors： Shandal V,Veenstra AL,Behen M,Sundaram S,Chugani H

更新日期：2012-01-01 00:00:00

abstract：:Maternal intrauterine inflammation has been implicated in the development of periventricular leukomalacia and white matter injury in the neonate. We hypothesized that intrauterine endotoxin administration would lead to microstructural changes in the neonatal rabbit white matter in vivo that could be detected at birth ...

journal_title：Journal of child neurology

authors： Saadani-Makki F,Kannan S,Makki M,Muzik O,Janisse J,Romero R,Chugani D

更新日期：2009-09-01 00:00:00

abstract：:Friedreich ataxia is a progressive degenerative disease with neurologic and cardiac involvement. This study characterizes comorbid medical conditions in a large cohort of patients with Friedreich ataxia. Patient diagnoses were collected in a large natural history study of 641 subjects. Prevalence of diagnoses in the c...

journal_title：Journal of child neurology

authors： Shinnick JE,Schadt K,Strawser C,Wilcox N,Perlman SL,Wilmot GR,Gomez CM,Mathews KD,Yoon G,Zesiewicz T,Hoyle C,Subramony SH,Yiu EM,Delatycki MB,Brocht AF,Farmer JM,Lynch DR

更新日期：2016-08-01 00:00:00

abstract：:We explored child neurologists' attitudes toward taking on the role of health care surrogate for terminally ill children. Physician members of the Child Neurology Society were sent a 16-question survey via email. Of the assumed 1050 recipients, 116 (11%) answered the questionnaire. Most individuals who have been in pr...

journal_title：Journal of child neurology

authors： Weisleder P,Perkins E,McLaughlin A

更新日期：2011-03-01 00:00:00

abstract：:To further delineate the clinical and developmental features of Angelman syndrome, we collected data through three sources of information: (1) physical examinations; (2) laboratory data and family questionnaire data of affected individuals; and (3) literature review. The questionnaire data describes a generally normal...

journal_title：Journal of child neurology

authors： Zori RT,Hendrickson J,Woolven S,Whidden EM,Gray B,Williams CA

更新日期：1992-07-01 00:00:00

abstract：:Seven children between 2 and 15 years of age with cerebral palsy and upper extremity dystonia were enrolled in an open-label, dose-escalation pilot clinical trial of botulinum toxin type B (Myobloc), injected into the biceps and brachioradialis muscles of I or both arms. The primary outcome measure was the change in m...

journal_title：Journal of child neurology

authors： Sanger TD,Kukke SN,Sherman-Levine S

更新日期：2007-01-01 00:00:00

abstract：:A pseudotumoral presentation of acute hemicerebellitis is rare in pediatric age. The authors report a new single case study of a 7-year-old child with pseudotumoral unilateral cerebellitis mimicking an intracranial tumor, which clinically presented itself with signs of intracranial hypertension and mild contralateral ...

journal_title：Journal of child neurology

authors： Alberini E,Vellante V,Zennaro F,Calligaris L,Barbi E,Carrozzi M,Devescovi R

更新日期：2015-03-01 00:00:00

abstract：:We have established the first prospective, collaborative study of spinal muscular atrophy, the second most common neuromuscular disease of childhood. One hundred and forty-one patients have been evaluated on at least four occasions over a 3-year period. The patients have been grouped by age of onset, as well as by fun...

journal_title：Journal of child neurology

authors： Russman BS,Iannacone ST,Buncher CR,Samaha FJ,White M,Perkins B,Zimmerman L,Smith C,Burhans K,Barker L

更新日期：1992-10-01 00:00:00

abstract：AIM:To investigate etiology and prognostic significance of pontine tegmentum lesions accompanying a cluster of acute flaccid myelitis. METHOD:We retrospectively examined patients from 6 centers in Turkey who manifested encephalitis or myelitis associated with dorsal pontine lesions on magnetic resonance imaging (MRI) ...

journal_title：Journal of child neurology

authors： Bastemur M,Gocmen R,Parlak S,Yuksel D,Arslan EA,Okten AY,Iscan A,Ekici B,Anlar B

更新日期：2020-07-01 00:00:00

abstract：:In lieu of traditional training of examiners to identify cerebral palsy on a neurologic examination at age 1 year, we proposed an alternative approach using a multimedia training video and CD-ROM we developed after a two-step validation process. We hypothesized that use of CD-ROM interactive training will lead to reli...

journal_title：Journal of child neurology

authors： Kuban KC,O'Shea M,Allred E,Leviton A,Gilmore H,DuPlessis A,Krishnamoorthy K,Hahn C,Soul J,O'Connor SE,Miller K,Church PT,Keller C,Bream R,Adair R,Miller A,Romano E,Bassan H,Kerkering K,Engelke S,Marshall D,Milow

更新日期：2005-10-01 00:00:00

abstract：:Two children are described who suddenly developed an encephalitic illness with intractable bilateral facial seizures. The seizures subsided over several days, but the children were left with the signs of pseudobulbar palsy and are unable to speak or swallow effectively. Bilateral destructive lesions in the opercular r...

journal_title：Journal of child neurology

authors： Grattan-Smith PJ,Hopkins IJ,Shield LK,Boldt DW

更新日期：1989-04-01 00:00:00

abstract：:Respiratory syncytial virus is a common cause of acute respiratory infection in children. Previous reports have associated respiratory syncytial virus infection and acute neurologic symptoms, including apnea and seizures. This study examined the prevalence of acute neurologic symptoms associated with respiratory syncy...

journal_title：Journal of child neurology

authors： Kho N,Kerrigan JF,Tong T,Browne R,Knilans J

更新日期：2004-11-01 00:00:00