Renal tubular acidosis complicated with hypokalemic periodic paralysis.

abstract：:Eleven children, 4-48 months old, with congenital cyanotic heart defects developed choreoathetoid movements 2-12 days after cardiac surgery with hypothermia and extracorporeal circulation (ECC). The abnormal movements mainly involved the limbs, facial musculature, and tongue, leading to a severe dysphagia. The symptom...

journal_title：Pediatric neurology

authors： Gherpelli JL,Azeka E,Riso A,Atik E,Ebaid M,Barbero-Marcial M

更新日期：1998-08-01 00:00:00

abstract：BACKGROUND:It is well known that febrile seizures are commonly occur in children with exanthem subitum. In this study, we compared the clinical features and backgrounds of patients with complex febrile seizures with and without primary human herpesvirus 6B infection. METHODS:Sixty-two patients were enrolled after expe...

journal_title：Pediatric neurology

authors： Miyake M,Kawamura Y,Hattori F,Miura H,Ishihara N,Yoshikawa T

更新日期：2020-08-01 00:00:00

abstract：:Twelve patients with hereditary motor and sensory neuropathy with the absence of large myelinated fibers have been reported. All of these patients had central nervous system involvement. In this report, we describe the first patient with pure motor and sensory neuropathy with the absence of large myelinated fibers wit...

journal_title：Pediatric neurology

authors： Fukuda M,Morimoto T,Suzuki Y,Kida K,Ohnishi A

更新日期：2000-10-01 00:00:00

abstract：:We investigated the clinical characteristics of children with continuous spike waves during slow-wave sleep syndrome and their treatment response to levetiracetam. Five boys and one girl, diagnosed with epilepsy with continuous spike waves during slow-wave sleep syndrome, were enrolled. Their clinical characteristics,...

journal_title：Pediatric neurology

authors： Wang SB,Weng WC,Fan PC,Lee WT

更新日期：2008-08-01 00:00:00

abstract：BACKGROUND:Neonatal neurocritical care is a growing and rapidly evolving medical subspecialty, with increasing numbers of dedicated multidisciplinary clinical, educational, and research programs established at academic institutions. The growth of these programs has provided trainees in neurology, neonatology, and pedia...

journal_title：Pediatric neurology

authors： Smyser CD,Tam EWY,Chang T,Soul JS,Miller SP,Glass HC

更新日期：2016-10-01 00:00:00

abstract：:The third case of cyclic vomiting syndrome with a large mitochondrial deoxyribonucleic acid rearrangement is described. Multiple neuromuscular anomalies are present that meet the diagnostic criteria for Kearns-Sayre syndrome, as well as severe symmetrical growth retardation. A 3-kilobase mitochondrial deoxyribonucleic...

journal_title：Pediatric neurology

authors： Boles RG,Baldwin EE,Prezant TR

更新日期：2007-02-01 00:00:00

abstract：:A 16-month-old girl with a history of Prader-Willi syndrome and progressive macrocephaly manifested large, bilateral, subdural hemorrhages of differing ages on magnetic resonance imaging. Subsequent evaluation revealed a deficiency of von Willebrand factor, but after repeated evaluations, no conclusive evidence of non...

journal_title：Pediatric neurology

authors： Carr RB,Khanna PC,Saneto RP

更新日期：2012-07-01 00:00:00

abstract：:The relationship between the dose of ACTH and the initial effect was investigated in 41 children with infantile spasms. More than 0.015 mg (0.6 IU)/kg/day of ACTH was needed for a good initial response of seizures and electroencephalographic abnormalities. The relationship between the dose of ACTH and long-term progno...

journal_title：Pediatric neurology

authors： Ito M,Okuno T,Fujii T,Mutoh K,Oguro K,Shiraishi H,Shirasaka Y,Mikawa H

更新日期：1990-07-01 00:00:00

abstract：:A 13-year, 6-month-old female was evaluated for subacute onset of left-sided hemichorea/hemiballismus, with an old, right parietal, cortical, and subcortical stroke as the presumed cause. Treatment with gabapentin was initiated, with good results at 6-month follow-up. Discussion of the differential diagnosis and evalu...

journal_title：Pediatric neurology

authors： Kothare SV,Pollack P,Kulberg AG,Ravin PD

更新日期：2000-01-01 00:00:00

abstract：BACKGROUND:Seizures may cause added harm in neonates with hypoxic-ischemic encephalopathy (HIE). Specific recommendations about seizure treatment in this context are lacking. We sought to determine the scope of practice regarding management of non-status epilepticus electrographic-only seizures in this setting. METHOD...

journal_title：Pediatric neurology

authors： McNally MA,Hartman AL

更新日期：2017-12-01 00:00:00

abstract：BACKGROUND:Transient bulbar palsy without involvement of the facial or extraocular muscles is a rare presentation. It is considered a form of cranial polyneuropathy, a variant of Guillain-Barré syndrome that is related to the autoimmune mechanisms induced by preceding infections or vaccinations. However, drug-induced c...

journal_title：Pediatric neurology

authors： Han TH,Kim DY,Park DW,Moon JH

更新日期：2017-01-01 00:00:00

abstract：BACKGROUND:The identification of a biomarker for sudden unexpected death in epilepsy (SUDEP) has the potential to save lives. Generalized convulsive seizures and postictal generalized suppression on electroencephalography (EEG) most often precede sudden unexpected death in epilepsy (SUDEP) and are potential biomarkers....

journal_title：Pediatric neurology

authors： Okanari K,Otsubo H,Kouzmitcheva E,Rangrej J,Baba S,Ochi A,Okanishi T,Homma Y,Nita DA,Donner EJ

更新日期：2017-11-01 00:00:00

abstract：:Systemic T-cell lymphoma presenting with neurologic symptoms is infrequently reported in immunocompetent children. We investigated the presenting features in all 20 immunocompetent children diagnosed with T-cell lymphoma at our institution from 1992-2004. Four children presented with neurologic features. These finding...

journal_title：Pediatric neurology

authors： Bassuk AG,Mohile NA,Stack C

更新日期：2006-11-01 00:00:00

abstract：:Opsoclonus is a rare childhood ocular motility disorder characterized by irregular, chaotic, involuntary bursts of high amplitude, back-and-forth oscillations of the eyes,without pause intervals. Although this disorder is associated with neuroblastoma and other neural crest tumors, as well as with other neurologic abn...

journal_title：Pediatric neurology

authors： Morad Y,Benyamini OG,Avni I

更新日期：2004-10-01 00:00:00

abstract：:We report a boy 20 months of age with encephalopathy, petechiae, and ethylmalonic aciduria (EPEMA). Other clinical features were severe hypotonia, orthostatic acrocyanosis, and chronic diarrhea. Magnetic resonance imaging (MRI) of the brain demonstrated bilateral lesions in the lenticular and caudate nuclei, periaqued...

journal_title：Pediatric neurology

authors： García-Silva MT,Ribes A,Campos Y,Garavaglia B,Arenas J

更新日期：1997-09-01 00:00:00

abstract：:Three brothers, born to parents who were first cousins, were referred for progressive diffuse dystonia. Initial physical examinations revealed minor dysmorphic features, e.g., bifrontal narrowing, downslanting palpebral fissures, low-set ears, upturned nostrils, and microretrognathia, as well as neurodevelopmental del...

journal_title：Pediatric neurology

authors： Yosunkaya E,Karaca E,Basaran S,Seven M,Yüksel A

更新日期：2010-05-01 00:00:00

abstract：:Amphetamine-derived medications are being prescribed with increasing frequency to younger pediatric patients to treat attention deficit hyperactivity disorder. Although choreiform movements were reported in adults with amphetamine abuse and in those under therapeutic treatment for attention deficit hyperactivity disor...

journal_title：Pediatric neurology

authors： Ford JB,Albertson TE,Owen KP,Sutter ME,McKinney WB

更新日期：2012-09-01 00:00:00

abstract：BACKGROUND:Although cerebral palsy is reported to have a higher prevalence in low-resource settings, there are few studies describing risk factors for cerebral palsy in these settings. A better understanding of the unique risk factors affecting children with cerebral palsy in low-resource settings could optimize both r...

journal_title：Pediatric neurology

authors： Monokwane B,Johnson A,Gambrah-Sampaney C,Khurana E,Baier J,Baranov E,Westmoreland KD,Mazhani L,Steenhoff AP,Bearden DR

更新日期：2017-12-01 00:00:00

abstract：BACKGROUND:Acute flaccid myelitis (AFM) is a rare disease of young children. The typical presentation involves acute-onset flaccid paralysis in one or more extremities with a nonspecific viral prodrome. Long-term outcomes demonstrate that functional recovery plateaus around six to nine months. The purpose of this study...

journal_title：Pediatric neurology

authors： Paziuk TM,Tadley M,Aversano M,Kozin SH,Zlotolow DA

更新日期：2020-10-01 00:00:00

abstract：:Limited data are available on optic neuritis in Asian children. Clinical profiles tend to vary with different races. We aimed to determine the clinical manifestations, visual outcomes, and etiologies of optic neuritis in Malaysian children, and discuss the literature of optic neuritis in Asian children. A retrospectiv...

journal_title：Pediatric neurology

authors： Shatriah I,Adlina AR,Alshaarawi S,Wan-Hitam WH

更新日期：2012-05-01 00:00:00

abstract：BACKGROUND:Abnormalities of early motor development have been reported in autism spectrum disorder, attention-deficit/hyperactivity disorder, intellectual developmental disorder, developmental coordination disorder, and other Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations (ESSENCE). Howe...

journal_title：Pediatric neurology

authors： Hatakenaka Y,Kotani H,Yasumitsu-Lovell K,Suzuki K,Fernell E,Gillberg C

更新日期：2016-01-01 00:00:00

abstract：BACKGROUND:Insomnia and low iron stores are common in children with autism spectrum disorders, and low iron stores have been associated with sleep disturbance. METHODS:We performed a randomized placebo-controlled trial of oral ferrous sulfate to treat insomnia in children with autism spectrum disorders and low normal ...

journal_title：Pediatric neurology

authors： Reynolds AM,Connolly HV,Katz T,Goldman SE,Weiss SK,Halbower AC,Shui AM,Macklin EA,Hyman SL,Malow BA

更新日期：2020-03-01 00:00:00

abstract：:The clinical phenotype of multiple acyl-CoA dehydrogenase deficiency in infancy is characterized by recurrent episodes of hypoketotic hypoglycemia and lipid storage myopathy. Brain damage has been described only as a consequence of severe and protracted hypoglycemia. We describe a child who experienced normal physical...

journal_title：Pediatric neurology

authors： Uziel G,Garavaglia B,Ciceri E,Moroni I,Rimoldi M

更新日期：1995-11-01 00:00:00

abstract：:Epilepsia partialis continua is defined as a spontaneous regular or irregular clonic muscular twitching affecting a limited part of the body, occurring for a minimum of 1 hour and recurring at intervals of less than 10 seconds. Levamisole is used as an immunomodulating medication in patients with recurrent aphthous ul...

journal_title：Pediatric neurology

authors： Aberastury MN,Silva WH,Vaccarezza MM,Maxit C,Agosta G

更新日期：2011-05-01 00:00:00

abstract：:To assess the incidence of postneonatal epilepsy in term infants treated with antiepileptic drugs for neonatal seizure discharges that were detected with amplitude-integrated electroencephalography (aEEG), 206 term infants were monitored using this modality. They received antiepileptic drugs for clinical as well as su...

journal_title：Pediatric neurology

authors： Toet MC,Groenendaal F,Osredkar D,van Huffelen AC,de Vries LS

更新日期：2005-04-01 00:00:00

abstract：:The outcomes of 60 children unconscious for 90 days or longer following acquired brain injury are reported. Eight children who died had remained in persistent vegetative states. As expected, most neurologic improvement occurred within the first year after injury, although some delayed improvements were observed. Outco...

journal_title：Pediatric neurology

authors： Kriel RL,Krach LE,Jones-Saete C

更新日期：1993-09-01 00:00:00

abstract：:We report on the case of a 6-year-old boy with epilepsy involving febrile seizures and unprovoked generalized tonic clonic seizures. Genetic testing revealed a novel de novo mutation in the SCN1A gene (C>T 4786, R1596C). The epilepsy phenotype is within the spectrum of generalized epilepsy with febrile seizures plus. ...

journal_title：Pediatric neurology

authors： Dlugos DJ,Ferraro TN,Buono RJ

更新日期：2007-10-01 00:00:00

abstract：:To evaluate the efficacy and safety of intranasal midazolam in the treatment of autonomic crises in children with familial dysautonomia, intranasal midazolam was administered at the hospital to six patients during nine episodes of autonomic crisis. Treatment was successful in seven of nine episodes of autonomic crisis...

journal_title：Pediatric neurology

authors： Lahat E,Goldman M,Barr J,Bistritzer T,Berkovitch M

更新日期：2000-01-01 00:00:00

abstract：:The present report concerns a vertically human immunodeficiency virus type 1 (HIV-1)-infected 7-year-old child, in whom a neurodegenerative disease occurred after an acute neurologic disorder that was in all likelihood symptomatic of HIV-1 encephalitis. At the steady state the neurologic disease fulfilled the accepted...

journal_title：Pediatric neurology

authors： Angelini L,Zibordi F,Triulzi F,Pinzani R,Plebani A

更新日期：1999-04-01 00:00:00

abstract：:Cerebral perfusion pressure (CPP), believed to be a major determinant of neurologic outcome, was monitored at the bedside of high-risk premature newborns during the first few days of life. Intraventricular hemorrhage was presumed to have occurred in only one of the seven infants and was associated with ventriculomegal...

journal_title：Pediatric neurology

authors： Braun MA,Rosman NP,Gould JB

更新日期：1986-07-01 00:00:00