听力与言语-语言病理学

行为科学

医学伦理学

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  • Clinical efficacy of piracetam in treatment of breath-holding spells.

    abstract::To evaluate the efficacy of piracetam therapy, 76 children with breath-holding spells admitted to the Outpatient Clinic of Dicle University Medical Faculty Paediatrics Department and Bakirköy State Hospital, Paediatrics Department between 1988 and 1990 and 1991 and 1996, respectively, were included in this placebo-con...

    journal_title:Pediatric neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1016/s0887-8994(97)00153-7

    authors: Donma MM

    更新日期:1998-01-01 00:00:00

  • Psychogenic seizures in obsessive-compulsive disorder with poor insight: a case report.

    abstract::Psychogenic seizures or psychogenic nonepileptic seizures occur in various mental disorders. Obsessive-compulsive symptoms can also imitate epileptic partial seizures, but detailed observations of this phenomenon are rare in the literature. A girl of 13 years was referred to the Department of Child Psychiatry because ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)00135-5

    authors: Wolańczyk T,Bryńska A

    更新日期:1998-01-01 00:00:00

  • Bilateral neuropathologic changes in a child with hemimegalencephaly.

    abstract::Evaluation of a 7-month-old girl with developmental delay and intractable seizures revealed hemispheric asymmetry and an enlarged right cerebral hemisphere. Because of a history of seizures refractory to medical therapy, she was admitted for right hemispherectomy, but died of complications of surgery. Postmortem brain...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)00091-x

    authors: Jahan R,Mischel PS,Curran JG,Peacock WJ,Shields DW,Vinters HV

    更新日期:1997-11-01 00:00:00

  • Early expression of proteolipid protein in human fetal and infantile cerebri.

    abstract::Proteolipid protein (PLP) is the major myelin protein of the central nervous system and is widely believed to play an important structural role in maintaining the myelin compaction. We have studied the early developmental changes of PLP with immunohistochemical methods. Our data demonstrate for the first time a compar...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)00099-4

    authors: Iai M,Yamamura T,Takashima S

    更新日期:1997-10-01 00:00:00

  • Neuroimaging in the evaluation of children and adolescents with intractable epilepsy: II. Neuroimaging and pediatric epilepsy surgery.

    abstract::The costs of epilepsy encompass all aspects of life, including medical, educational, and psychosocial. Adults with intractable epilepsy who undergo epilepsy surgery and have seizure-free outcomes still have significant barriers in the attainment of improved quality of life. For this reason, there is increasing interes...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(97)00170-7

    authors: Zupanc ML

    更新日期:1997-09-01 00:00:00

  • Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria.

    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

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)00048-9

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

    更新日期:1997-09-01 00:00:00

  • De novo mutation of Charcot-Marie-Tooth disease type 1A.

    abstract::Charcot-Marie-Tooth disease type 1A (CMT 1A) is an autosomal dominant demyelinating polyneuropathy associated with a 1.5-Mb duplication of the p11.2-p12 region of chromosome 17, including the peripheral myelin protein-22 (PMP-22) gene (CMT 1A duplication). We report a male patient with a de novo CMT 1A diagnosed on cl...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)80670-4

    authors: Tachi N,Kozuka N,Ohya K,Chiba S

    更新日期:1997-07-01 00:00:00

  • Neurophysiological assessment of brain function and maturation. II. A measure of brain dysmaturity in healthy preterm neonates.

    abstract::Severe brain disorders can be expressed as markedly abnormal encephalopathic EEG patterns in neonates who are usually neurologically depressed, with abnormal levels of reactivity and tone. This symptomatic group is now a minority of medically ill neonates as a result of more vigorous fetal and neonatal resuscitative e...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(96)00009-4

    authors: Scher MS

    更新日期:1997-05-01 00:00:00

  • Opsoclonus-myoclonus syndrome with abnormal single photon emission computed tomography imaging.

    abstract::The single photon emission computed tomography (SPECT) findings in 2 patients with opsoclonus-myoclonus syndrome (OMS) who had similar symptoms in the acute stage of the disease are described. In 1 patient with encephalitis, SPECT showed increased blood flow in most of the cerebellum; the highest accumulation of the r...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)00031-3

    authors: Oguro K,Kobayashi J,Aiba H,Hojo H

    更新日期:1997-05-01 00:00:00

  • Evoked potential abnormalities in postoperative patients with biliary atresia.

    abstract::The somatosensory evoked potentials from the lower extremities were measured postoperatively in 15 patients with biliary atresia to investigate whether they were free of neurologic dysfunction. Because long-standing cholestasis causes progressive neuropathy due to malabsorption of vitamin E, the serum vitamin E, D, an...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)00011-8

    authors: Kubota M,Suita S,Kamimura T,Shono K

    更新日期:1997-04-01 00:00:00

  • First U.S. case of adenylosuccinate lyase deficiency with severe hypotonia.

    abstract::Adenylosuccinate lyase (ASL) deficiency is a defect in purine de novo synthesis pathway. The disease has variable clinical presentation involving psychomotor retardation, seizures, hypotonia, and autism. The presence of succinyladenosine and succinylaminoimidazole carboxamide riboside (SAICA riboside) in body fluids c...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)89979-1

    authors: Valik D,Miner PT,Jones JD

    更新日期:1997-04-01 00:00:00

  • Occipital-parietal encephalopathy: a new name for an old syndrome.

    abstract::A boy presented with hypertension, seizures, lethargy, headache, and occipital blindness. He improved with antihypertensive therapy. Other reported children with a similar distinctive clinical condition are compared with adults with a syndrome termed reversible posterior leukoencephalopathy. Because both gray and whit...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(96)00292-5

    authors: Pavlakis SG,Frank Y,Kalina P,Chandra M,Lu D

    更新日期:1997-02-01 00:00:00

  • Expression of the LIS-1 gene product in brain anomalies with a migration disorder.

    abstract::Miller-Dieker syndrome (MDS) is a prototype of brain malformations characterized by abnormal neuronal migration. To clarify the pathomechanisms underlying these anomalies, we performed immunohistochemical studies using specific antibodies against the protein product of LIS-1, the candidate gene responsible for the MDS...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(96)00260-3

    authors: Isumi H,Takashima S,Kakita A,Yamada M,Ikeda K,Mizuguchi M

    更新日期:1997-01-01 00:00:00

  • Muscle pathology and clinical features of the sarcolemmopathies.

    abstract::We report the clinical features and the muscle pathology in 2 patients with congenital muscular dystrophy (CMD) secondary to merosin deficiency and in 2 patients with sarcoglycan (adhalin) deficiency. Electron microscopic examination revealed sarcolemmal defects in non-necrotic muscle fibers in all cases. These pathol...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(96)00265-2

    authors: Fadic R,Waclawik AJ,Lewandoski PJ,Lotz BP

    更新日期:1997-01-01 00:00:00

  • Cockayne syndrome: review of 25 cases.

    abstract::Clinical and laboratory findings of 25 patients with classical Cockayne syndrome (CS) are reviewed. A history of consanguinity was present in 21 patients, and 15 patients had at least 1 affected sibling. Apart from the cardinal features of dwarfism, microcephaly, and mental retardation, the most consistent clinical fe...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(96)00229-9

    authors: Ozdirim E,Topçu M,Ozön A,Cila A

    更新日期:1996-11-01 00:00:00

  • Epilepsy and fragile X gene mutations.

    abstract::We used two strategies to investigate a possible link between predisposition for epilepsy and mutations in the fragile X mental retardation-1 gene. The first entailed performing electroencephalography on 14 patients with an amplification in the fragile X mental retardation-1 gene, and the second involved molecular gen...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(96)00251-2

    authors: Kluger G,Böhm I,Laub MC,Waldenmaier C

    更新日期:1996-11-01 00:00:00

  • Clinical features of developmental disability associated with cerebellar hypoplasia.

    abstract::Sporadic nonsyndromic cerebellar hypoplasia is a radiological diagnosis with clinical features and a relation with developmental disability that are presently not known. Through a retrospective review of a comprehensive standardized computerized database containing more than 2,500 patients examined consecutively by a ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(96)00220-2

    authors: Shevell MI,Majnemer A

    更新日期:1996-10-01 00:00:00

  • Neonatal perifascicular myopathy.

    abstract::Perifascicular atrophy of muscle fibers is generally considered to be a specific feature of autoimmune myopathies, dermatomyositis in particular. We describe a neonate presenting with hypotonia and weakness. A biopsy revealed atrophic and regenerating muscle fibers in a perifascicular distribution, and abnormal alkali...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(96)00127-0

    authors: Nevo Y,Pestronk A

    更新日期:1996-09-01 00:00:00

  • Perturbations of cerebral hemodynamics in Kenyans with cerebral malaria.

    abstract::The mechanisms of death and neurologic sequelae in African children with cerebral malaria are undetermined. Because pathologic features are confined to the cerebral vasculature, perturbations in cerebral hemodynamics may be responsible. We compared the transcranial Doppler findings in 50 children with cerebral malaria...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(96)00115-4

    authors: Newton CR,Marsh K,Peshu N,Kirkham FJ

    更新日期:1996-07-01 00:00:00

  • Benign hereditary chorea improved on stimulant therapy.

    abstract::Stimulant therapy is usually contraindicated in patients with movement disorders such as tics or chorea. A young boy is reported who had benign hereditary chorea and attention deficit disorder, whose chorea, handwriting, and independent ambulation paradoxically improved with methylphenidate treatment. ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(96)00056-2

    authors: Friederich RL

    更新日期:1996-05-01 00:00:00

  • Vision outcome at age 2 years in a low birth weight population.

    abstract::We assess the prevalence of vision problems in a cohort of low birth weight infants at age 2 years and the relationship of these problems to neonatal brain injury. Data on prenatal and neonatal history and brain injury status were prospectively collected on 721 children weighing 500-2,000 gm at birth enrolled in a mul...

    journal_title:Pediatric neurology

    pub_type: 临床试验,杂志文章,多中心研究

    doi:10.1016/0887-8994(96)00051-3

    authors: Pinto-Martin JA,Dobson V,Cnaan A,Zhao H,Paneth NS

    更新日期:1996-05-01 00:00:00

  • Epidemiology of bacterial meningitis in children: Aichi Prefecture, Japan, 1984-1993.

    abstract::The details of 328 patients with bacterial meningitis, admitted from 1984 through 1993, were obtained from 46 departments of pediatrics of large hospitals through questionnaires. The incidence rate per 100,000 child-years was 2.32, being higher in children aged 0-4 years (rate, 7.22) than 5-15 years (rate, 0.49). The ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(96)00024-0

    authors: Ishikawa T,Asano Y,Morishima T,Nagashima M,Sobue G,Watanabe K,Yamaguchi H

    更新日期:1996-04-01 00:00:00

  • Angiodysgenetic necrotizing encephalopathy or diffuse meningocerebral angiomatosis.

    abstract::A patient with angiodysgenetic necrotizing encephalopathy or diffuse meningocerebral angiomatosis complicated by intraventricular hemorrhage, posthemorrhagic hydrocephalus, and signs of heart failure is reported. The hydrocephalus and cardiomegaly were diagnosed by fetal ultrasonography. Based on these pathologic find...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(96)00004-5

    authors: Arvanitis DL,Apostolidou IA,Routsis PV,Biskini EI,Kalpoyannis NS

    更新日期:1996-02-01 00:00:00

  • Immunohistochemical expression of tumor necrosis factor alpha in neonatal leukomalacia.

    abstract::The expression of tumor necrosis factor alpha (TNF alpha) was examined in infants with leukomalacia by means of immunohistochemical methods with an antihuman TNF alpha monoclonal antibody. We studied 23 patients with neonatal leukomalacia, classified as having "focal," "widespread," or "diffuse" disease according to t...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00223-5

    authors: Deguchi K,Mizuguchi M,Takashima S

    更新日期:1996-01-01 00:00:00

  • Availability of frequency-selective fat-saturation pulse (Fat-Sat) MRI in childhood optic neuritis.

    abstract::A 2-year-old boy with acute optic neuritis, confirmed by gadolinium-DTPA enhancement of the optic nerve using frequency-selective fat-saturation pulse magnetic resonance imaging (Fat-Sat MRI), is reported. Because it is difficult in very young children to sufficiently evaluate visual acuity, visual field, and retroocu...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00254-5

    authors: Takanashi J,Sugita K,Matsubayashi J,Sato K,Niimi H

    更新日期:1996-01-01 00:00:00

  • Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophy.

    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

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00187-5

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

    更新日期:1995-11-01 00:00:00

  • Neonatal posthemorrhagic hydrocephalus: neuropathologic and immunohistochemical studies.

    abstract::A neuropathologic study was undertaken to examine associated brain damage in patients with fetal and neonatal posthemorrhagic hydrocephalus (PHH). In PHH the association of periventricular leukomalacia and pontosubicular necrosis was not increased, but that of cerebellar subarachnoid hemorrhage and olivo-cerebellar pa...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00183-g

    authors: Fukumizu M,Takashima S,Becker LE

    更新日期:1995-10-01 00:00:00

  • Prospective follow-up of primitive reflex profiles in high-risk infants: clues to an early diagnosis of cerebral palsy.

    abstract::To clarify reflex profiles in the first year of life in connection with categories of neurologic abnormality, eight primitive reflexes (i.e., the palmar grasp reflex, the plantar grasp reflex, the Galant response, the asymmetric tonic neck reflex, the suprapubic extensor reflex, the crossed extensor reflex, the Rossol...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00143-4

    authors: Zafeiriou DI,Tsikoulas IG,Kremenopoulos GM

    更新日期:1995-09-01 00:00:00

  • Congenital muscular dystrophies: clinical review and proposed classification.

    abstract::The clinical spectrum of the congenital muscular dystrophies is reviewed using as a sample population 10 Sicilian patients with various clinical subtypes. A comprehensive classification scheme for the muscular dystrophies is presented based on recent advances in our understanding of this heterogeneous group of syndrom...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/0887-8994(95)00148-9

    authors: Parano E,Pavone L,Fiumara A,Falsaperla R,Trifiletti RR,Dobyns WB

    更新日期:1995-09-01 00:00:00

  • Renal tubular acidosis complicated with hypokalemic periodic paralysis.

    abstract::Three Chinese girls with hypokalemic periodic paralysis secondary to different types of renal tubular acidosis are presented. One girl has primary distal renal tubular acidosis complicated with nephrocalcinosis. Another has primary Sjögren syndrome with distal renal tubular acidosis, which occurs rarely with hypokalem...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00080-y

    authors: Chang YC,Huang CC,Chiou YY,Yu CY

    更新日期:1995-07-01 00:00:00

  • Transient dystonia of infancy, a result of intrauterine cocaine exposure?

    abstract::Intrauterine cocaine exposure has been associated with multiple transient and permanent neurologic sequelae. Although dystonic reactions have been reported in cocaine users, infantile dystonia following intrauterine exposure has not. We describe 4 infants testing positive for cocaine metabolite at birth with subsequen...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00050-p

    authors: Beltran RS,Coker SB

    更新日期:1995-05-01 00:00:00

  • Cerebrovascular accidents following the Fontan operation.

    abstract::The Fontan operation is one of the most common cardiac operations for children with congenital heart disease beyond the first year of age. Although the surgical mortality of this procedure has improved over the past 2 decades, the neurologic outcome in this population is not well described. We performed a retrospectiv...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00027-d

    authors: du Plessis AJ,Chang AC,Wessel DL,Lock JE,Wernovsky G,Newburger JW,Mayer JE Jr

    更新日期:1995-04-01 00:00:00

  • Changes of P300 latency with age in childhood epilepsy.

    abstract::Auditory event-related potentials (P300 latency; odd-ball paradigm) were examined in 129 patients with childhood epilepsies and 53 controls. The P300 latency in the patients with epilepsies (373 +/- 39.4 ms) was significantly longer than in controls (356 +/- 38.4), and the prolongation was greatest in the patients wit...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00001-v

    authors: Konishi T,Naganuma Y,Hongou K,Murakami M,Yamatani M,Yagi S

    更新日期:1995-02-01 00:00:00

  • Primary malignant melanoma of meninges: atypical presentation of subacute meningitis.

    abstract::Primary malignant melanoma of the meninges is described in a 5-year-old boy who presented with a 3-month history suggestive of subacute meningitis. Clinically the diagnosis of tuberculous meningitis was made and antituberculous treatment was begun. Despite this treatment, the patient's condition continued to deteriora...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)00155-u

    authors: Nicolaides P,Newton RW,Kelsey A

    更新日期:1995-02-01 00:00:00

  • Neurophysiologic studies and MRI in Pelizaeus-Merzbacher disease: comparison of classic and connatal forms.

    abstract::Four patients with the classic form and 1 patient with the connatal form of Pelizaeus-Merzbacher disease were studied with magnetic resonance imaging, electroencephalography, and multimodal evoked potentials, including brainstem auditory evoked potentials, somatosensory evoked potentials, and visual evoked potentials....

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)00124-k

    authors: Wang PJ,Young C,Liu HM,Chang YC,Shen YZ

    更新日期:1995-01-01 00:00:00

  • Clinical manifestations of neurofibromatosis-1 in Chinese children.

    abstract::The complications of 50 Chinese children with neurofibromatosis-1 were found to be different from other ethnic groups. There was a predominance of scoliosis, speech problems, and blood malignancies, but brain tumors were rare. The majority had good prognosis. Clinical manifestations depend on the age of ascertainment ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)90006-x

    authors: Wong VC

    更新日期:1994-11-01 00:00:00

  • West syndrome following deep hypothermic infant cardiac surgery.

    abstract::Postoperative seizures are among the more common complications of cardiac surgery in children. These seizures have traditionally been considered benign, transient phenomena with little, if any, prognostic significance. We report 4 infants with early postoperative seizures following cardiac surgery who later developed ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)90111-2

    authors: du Plessis AJ,Kramer U,Jonas RA,Wessel DL,Riviello JJ

    更新日期:1994-10-01 00:00:00

  • Relationship between the parachute reactions and standing and walking in normal infants.

    abstract::Assumption of the vertical position and independent walking are potentially hazardous motor milestones in the developing infant. It has been presumed that the parachute reactions evolved to protect infants from injury during this developmental stage. To determine the relationship between the appearance of the upper an...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)90087-6

    authors: Jaffe M,Kugelman A,Tirosh E,Cohen A,Tal Y

    更新日期:1994-07-01 00:00:00

  • Infantile progressive spinal muscular atrophy with ophthalmoplegia and pyramidal symptoms.

    abstract::Two siblings presented with identical features of progressive peripheral paralysis of the lower motor neuron type, pyramidal signs, cranial nerve palsy which included external ocular palsy and deafness, and internal ocular palsy; both died before 1 year of age. Pathologic examination of the central nervous system in b...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)90130-9

    authors: Hamano K,Tsukamoto H,Yazawa T,Yoshimura M,Takita H

    更新日期:1994-06-01 00:00:00

  • Rectal temperature changes during sleep state transitions in term and preterm neonates at postconceptional term ages.

    abstract::Mean rectal temperatures in neonates were investigated during sleep state transitions as assessed by visually analyzed electroencephalographic-polygraphic recordings. Continuous 3-hour studies were obtained on 3 term and 5 preterm infants at postconceptional term ages using a 24-channel computerized monitoring system....

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)90022-1

    authors: Scher MS,Dokianakis SG,Sun M,Steppe DA,Guthrie RD,Sclabassi RJ

    更新日期:1994-05-01 00:00:00

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