听力与言语-语言病理学

行为科学

医学伦理学

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  • Bilateral demyelinating tumefactive lesions in three children with hemiparesis.

    abstract::We present the results from the evaluations of three children ages of 2, 7, and 11 years with hemiparesis and multiple white-matter lesions on magnetic resonance images (MRIs). The initial symptoms were mainly acute/subacute hemiparesis in all and headache/vomiting in one of them. Before admission, one of them had a h...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700901

    authors: Yapici Z,Eraksoy M

    更新日期:2002-09-01 00:00:00

  • Neurofibromatosis 1: clinical review and exceptions to the rules.

    abstract::Neurofibromatosis 1 is an autosomal dominant, multisystem disorder with myriad clinical manifestations. Between 1991 and 1998, 495 adults and children were diagnosed with neurofibromatosis 1 at a specialized neurogenetics clinic in Sydney, Australia. This review establishes the prevalence of the clinical manifestation...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700812

    authors: Young H,Hyman S,North K

    更新日期:2002-08-01 00:00:00

  • Auditory brainstem evoked potentials in early-treated congenital hypothyroidism.

    abstract::To evaluate the effect of early treatment of congenital hypothyroidism on central nervous system development, auditory brainstem evoked potentials were determined in 32 patients with hyperthyrotropinemia diagnosed during neonatal screening. The patients included 27 with congenital hypothyroidism and 5 with transient h...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700707

    authors: Chou YH,Wang PJ

    更新日期:2002-07-01 00:00:00

  • Cerebral aneurysms in a child with acquired immune deficiency syndrome during rapid immune reconstitution.

    abstract::A 12-year-old boy with perinatally acquired human immunodeficiency virus infection an d Centers for Disease Control and Prevention class C3 disease presented with acute onset of confusion and a right-sided movement disorder 5 months after beginning a new antiretroviral regimen. His CD4 count had been below 50 cells/mi...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307380201700613

    authors: Bonkowsky JL,Christenson JC,Nixon GW,Pavia AT

    更新日期:2002-06-01 00:00:00

  • Levetiracetam in refractory pediatric epilepsy.

    abstract::Levetiracetam, one of the newer-generation antiepilepsy drugs, is not currently approved for use in children. Given its favorable efficacy, pharmacokinetic, and, particularly, safety profile in adults, we felt that it may be a useful antiepilepsy drug for children with refractory epilepsy. We treated 39 patients (mean...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/088307380201700603

    authors: Wheless JW,Ng YT

    更新日期:2002-06-01 00:00:00

  • Primary antiphospholipid syndrome presenting with a branch retinal artery occlusion in a 15-year-old boy.

    abstract::Acute vascular events are rare in the pediatric population, but there is an association with the presence of antiphospholipid antibodies. When there is no other underlying medical disorder, this is referred to as primary antiphospholipid syndrome. We present a case of a 15-year-old boy who developed an acute superior ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700517

    authors: Saxonhouse MA,Bhatti MT,Driebe WT Jr,Freeman BE,Maria BL,Carney PR

    更新日期:2002-05-01 00:00:00

  • Dietary intake and blood folate levels in Honduran women of childbearing age.

    abstract::Neural tube defects are common birth defects, the frequency of which appears to be reduced by maternal supplementation and/or fortification of folic acid. Latin Americans have a high incidence of neural tube defects. We surveyed the dietary intake of Honduran women of childbearing age using a 24-hour dietary recall qu...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700506

    authors: Holden KR,Collins JS,Greene JF,Hinkle S,Nave AF,Portillo JM,Page GP,Stevenson RE,Honduran Neural Tube Defect Project Team.

    更新日期:2002-05-01 00:00:00

  • Unilateral auditory neuropathy: case study.

    abstract::This article reports on an 11-year-old boy who was diagnosed with unilateral auditory neuropathy. After failing his annual medical and school hearing screenings, he was referred for audiologic testing, which identified a profound sensorineural hearing loss in his left ear that has remained stable for the past 3 1/2 ye...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700415

    authors: Podwall A,Podwall D,Gordon TG,Lamendola P,Gold AP

    更新日期:2002-04-01 00:00:00

  • Cerebrospinal fluid neuron-specific enolase following seizures in children: role of etiology.

    abstract::Neuron-specific enolase, a marker for neuronal injury, is elevated following seizures in adults, but relatively few data exist on postictal neuron-specific enolase levels in children. This study measured cerebrospinal fluid (CSF) neuron-specific enolase levels after seizures in 49 consecutive pediatric patients and in...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700404

    authors: Wong M,Ess K,Landt M

    更新日期:2002-04-01 00:00:00

  • Pyridoxine-dependent seizures associated with hypophosphatasia in a newborn.

    abstract::Pyridoxine dependency and congenital hypophosphatasia are unusual metabolic disorders. We report a female infant born from healthy consanguineous parents with shortening of limbs, detected during pregnancy by ultrasonography. Immediately after delivery, the baby was admitted to the neonatal intensive care unit because...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700314

    authors: Nunes ML,Mugnol F,Bica I,Fiori RM

    更新日期:2002-03-01 00:00:00

  • Use of modafinil in spastic cerebral palsy.

    abstract::After an initial patient with cerebral palsy had an apparent dramatic reduction in spasticity when placed on modafinil, a pilot study was undertaken in 10 pediatric patients to confirm or refute the benefit of modafinil in cerebral palsy. Nine of 10 patients completed the 1-month treatment period. The study patients w...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700303

    authors: Hurst DL,Lajara-Nanson W

    更新日期:2002-03-01 00:00:00

  • Gelastic seizure with tectal tumor, lobar holoprosencephaly, and subependymal nodules: clinical report.

    abstract::Gelastic seizures are characterized by inappropriate, stereotyped laughter and are often first recognized when other epileptic manifestations occur. They are frequently associated with hypothalamic hamartomas. Central nervous system developmental abnormalities are rarely reported with gelastic seizures. There is only ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700215

    authors: Akman CI,Schubert R,Duran M,Loh J

    更新日期:2002-02-01 00:00:00

  • Kindergarten readiness skills in children with sickle cell disease: evidence of early neurocognitive damage?

    abstract::Young children with sickle cell disease are at risk of brain damage, including stroke. We tested the hypothesis that such patients are also at risk of cognitive impairment. We characterized the cognitive ability of kindergarten children to minimize the effect of disease-related school absence. The Memphis City Schools...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700204

    authors: Steen RG,Hu XJ,Elliott VE,Miles MA,Jones S,Wang WC

    更新日期:2002-02-01 00:00:00

  • Advancing the medical management of epilepsy: disease modification and pharmacogenetics.

    abstract::Despite the recent development of new antiepilepsy drugs, a significant number of children are still unable to achieve seizure freedom without side effects. Understanding the factors behind individual variability in antiepilepsy drug tolerability and dose response and incorporating these factors into a treatment plan ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738020170011301

    authors: Glauser TA

    更新日期:2002-01-01 00:00:00

  • Diagnostic difficulty in infants and children.

    abstract::Making an accurate diagnosis is the first and most critical step in the treatment of pediatric epilepsy, but it can be a daunting challenge for clinicians. Seizure types and syndromes in infants and very young children do not present with the same clarity and consistency as in adults. Work is currently being done to r...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738020170010401

    authors: Nordli DR Jr

    更新日期:2002-01-01 00:00:00

  • Lumbar spinal stenosis causing congenital clubfoot.

    abstract::Congenital lumbar spinal stenosis is believed to rarely cause neurologic symptoms during childhood. We present a 16-year-old boy with bilateral congenital clubfeet surgically corrected by tendo Achillis releases at 2 years of age who presented with progressive, bilateral footdrop. Magnetic resonance imaging of his lum...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700122

    authors: Ng YT,Mancias P,Butler IJ

    更新日期:2002-01-01 00:00:00

  • Gelastic seizure with hypothalamic hamartoma: proton magnetic resonance spectrometry and ictal electroencephalographic findings in a 4-year-old girl.

    abstract::Gelastic seizure is a rare symptom often associated with hypothalamic hamartoma. We present here a 4-year-old girl with gelastic epilepsy caused by hypothalamic hamartoma and report the magnetic resonance spectrometry and electroencephalographic (EEG) findings. At the age of 2 1/2 years, she developed brief, repetitiv...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700111

    authors: Wakai S,Nikaido K,Nihira H,Kawamoto Y,Hayasaka H

    更新日期:2002-01-01 00:00:00

  • Long-term survival in a child with arthrogryposis multiplex congenita and spinal muscular atrophy.

    abstract::Spinal muscular atrophy type 0 is a severe form of spinal muscular atrophy that is usually fatal in the first months of life. These children present with arthrogryposis multiplex congenita and respiratory compromise. We describe a child with spinal muscular atrophy and arthrogryposis multiplex congenita who has had a ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101601213

    authors: Falsaperla R,Romeo G,Di Giorgio A,Pavone P,Parano E,Connolly AM

    更新日期:2001-12-01 00:00:00

  • Sphenoid sinusitis masquerading as migraine headaches in children.

    abstract::The sphenoid sinus is often referred to as the "neglected sinus." Isolated sphenoid sinusitis is a rare disease with potentially devastating complications. It occurs at an incidence of about 2.7% of all sinus infections. Although headache is the most common presenting symptom, there is no typical headache pattern. Thr...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101601203

    authors: Ng YT,Butler IJ

    更新日期:2001-12-01 00:00:00

  • Prenatal intracranial hemorrhage and neurologic complications in alloimmune thrombocytopenia.

    abstract::Neonatal alloimmune thrombocytopenia results from platelet-antigen incompatibility between mother and fetus, leading to antibody-mediated destruction of fetal platelets. With a prevalence of 1 in 1000 births, approximately 4000 infants born in the United States each year develop neonatal alloimmune thrombocytopenia. T...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738010160111001

    authors: Sharif U,Kuban K

    更新日期:2001-11-01 00:00:00

  • Aicardi-Goutieres syndrome in siblings.

    abstract::Two siblings with familial encephalopathy, calcification of the basal ganglia, and cerebrospinal fluid lymphocytosis, constituting the triad of Aicardi-Goutieres syndrome, are reported. This syndrome resembles congenital intrauterine infections, which must be meticulously excluded. Aicardi-Goutieres syndrome is extrem...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101601009

    authors: Koul R,Chacko A,Joshi S,Sankhla D

    更新日期:2001-10-01 00:00:00

  • Central nervous system Sjögren's syndrome in a child: case report and review of the literature.

    abstract::We describe a case of pediatric Sjögren's syndrome with progressive neurologic involvement. At age 4 years, she had been diagnosed with Melkersson-Rosenthal syndrome. After being stable with facial diplegia and swelling for 5 years, she acutely presented with diplopia, vertigo, and ataxia. Cranial magnetic resonance i...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600911

    authors: Gottfried JA,Finkel TH,Hunter JV,Carpentieri DF,Finkel RS

    更新日期:2001-09-01 00:00:00

  • Neonate with spinal hypoplasia on T12 and a localized vertebral malformation on L4.

    abstract::We report a case of a neonate with sectional narrowing of the spinal cord on the level of T12 to L2 and a deformed vertebral body on a different level, L4. In previously described cases of sectional spinal dysgenesis, the vertebral and spinal cord malformations are usually found on the same level. Our case may represe...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600819

    authors: Weber A,Maier RF,Felderhoff-Mueser U,Lehmann R,Stöver B,Obladen M

    更新日期:2001-08-01 00:00:00

  • Temporal lobectomy in early childhood: the need for long-term follow-up.

    abstract::We retrospectively identified 15 children ages 12 years and under with anticonvulsant resistant epilepsy who underwent a temporal lobectomy at Children's Hospital, Boston, between 1978 and 1993. Our aim was to study the long-term seizure outcome. Data pertaining to preoperative evaluation, electroencephalography (EEG)...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307380101600809

    authors: Sotero de Menezes MA,Connolly M,Bolanos A,Madsen J,Black PM,Riviello JJ Jr

    更新日期:2001-08-01 00:00:00

  • Idiopathic "benign" intracranial hypertension: case series and review.

    abstract::Idiopathic "benign" intracranial hypertension is an uncommon but important cause of headache that can lead to visual loss. This study was undertaken to review our experience in the diagnosis and management of idiopathic intracranial hypertension, giving special attention to treatments used. A retrospective chart revie...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600701

    authors: Salman MS,Kirkham FJ,MacGregor DL

    更新日期:2001-07-01 00:00:00

  • Long-term follow-up of an epidemiologically defined cohort of patients with Tourette syndrome.

    abstract::The goal of this study was to collect prospective longitudinal information on the development of an epidemiologically defined cohort of patients with Tourette syndrome. These data may improve prognostic understanding of the condition. This information will also be important for specification of an adult phenotype for ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600609

    authors: Burd L,Kerbeshian PJ,Barth A,Klug MG,Avery PK,Benz B

    更新日期:2001-06-01 00:00:00

  • Comparative utility of technetium-99m hexamethylpropylenamine oxime single photon emission computed tomography (SPECT) with anatomic neuroimaging and electroencephalography (EEG) in childhood intractable epilepsy.

    abstract::Intractable epilepsies pose a therapeutic challenge. Precise localization of the epileptic focus is imperative before planning surgical intervention. Functional imaging is an important component of presurgical work-up. Positron emission tomography is unavailable in developing countries; hence, the need to evaluate the...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600405

    authors: Kalra V,Gulati S,Rana KS,Bal CS,Bhatia M

    更新日期:2001-04-01 00:00:00

  • Neurodevelopmental delay associated with nonconvulsive status epilepticus in a toddler.

    abstract::Nonconvulsive status epilepticus is a prolonged and continuous state of increased unawareness without overt motor seizures linked with repetitive generalized epileptic discharges. In children, it may occur de novo but more commonly may complicate a preexisting epileptic disorder. We report on a 2-year-old female who p...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600310

    authors: Shinawi M,Shahar E

    更新日期:2001-03-01 00:00:00

  • Incidence of concussion in high school football players of Ohio and Pennsylvania.

    abstract::Football injuries account for more concussions than any other sport in North America. A 1977 survey of high school football players in Minnesota found that 19% of players reported at least one concussion (characterized by loss of awareness) during a season. These results have not been confirmed in subsequent studies. ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600203

    authors: Langburt W,Cohen B,Akhthar N,O'Neill K,Lee JC

    更新日期:2001-02-01 00:00:00

  • Anterior spinal artery syndrome in an adolescent with protein S deficiency.

    abstract::The diagnosis of anterior spinal artery syndrome can be made with high accuracy by thorough clinical examination in combination with typical magnetic resonance imaging findings. Sudden onset of tetra- or paraparesis and dissociated sensory loss with bladder dysfunction are the leading clinical signs. We discuss clinic...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600213

    authors: Ramelli GP,Wyttenbach R,von der Weid N,Ozdoba C

    更新日期:2001-02-01 00:00:00

  • Clinical considerations in cerebral palsy and spasticity.

    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

    pub_type: 杂志文章

    doi:10.1177/088307380101600103

    authors: Brunstrom JE

    更新日期:2001-01-01 00:00:00

  • Evidence for altered basal ganglia and cortical functions in transient idiopathic dystonia.

    abstract::Idiopathic dystonia with onset in the first year of life has been described as a transient movement disorder, in contrast to other forms of idiopathic dystonia We report on a girl who showed, from her 5th month, episodes of dystonic postures of her neck and arm, which lasted for seconds and occurred several times a da...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001501212

    authors: John B,Klemm E,Haverkamp F

    更新日期:2000-12-01 00:00:00

  • Outcome measures in pediatric neurology: why do we need them?

    abstract::Outcome measures should include the patient's values and preferences (from the patient's perspective) in addition to performance ratings and physiologic states. Outcome measures can assess relationships between services and interventions and their end results, can clarify which therapies are worth providing and which ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001501201

    authors: Ronen GM,Rosenbaum MP,Streiner DL

    更新日期:2000-12-01 00:00:00

  • Endocrine disorders in two sisters affected by MELAS syndrome.

    abstract::A variety of endocrine and metabolic defects, including hypothalamopituitary hypofunction and diabetes mellitus, has been reported in association with mitochondrial disorders. We describe two sisters affected by mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome in whom DNA anal...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001501108

    authors: Balestri P,Grosso S

    更新日期:2000-11-01 00:00:00

  • Postinfectious encephalomyelitis: etiologic and diagnostic trends.

    abstract::Fifty cases of postinfectious encephalomyelitis admitted to our Pediatric Department during the period 1980 to 1997 were consecutively collected and reviewed. There were 28 males and 22 females. The age of onset ranged from 9 months to 14 years. The antecedent infections included measles (6 cases), rubella (5 cases), ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001501005

    authors: Hung KL,Liao HT,Tsai ML

    更新日期:2000-10-01 00:00:00

  • Diffusion-weighted imaging in neonatal cerebral infarction: clinical utility and follow-up.

    abstract::We describe the clinical utility of echo-planar diffusion-weighted imaging in neonatal cerebral infarction. Eight full-term neonates aged 1 to 8 days referred for neonatal seizures were studied. Patients were followed for a mean of 17 months with detailed neurologic examinations at regular intervals. Head computed tom...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500905

    authors: Krishnamoorthy KS,Soman TB,Takeoka M,Schaefer PW

    更新日期:2000-09-01 00:00:00

  • Three children with a syndrome of obesity and overgrowth, atypical psychosis, and seizures: a problem in neuropsychopharmacology.

    abstract::Three children presented with a complex syndrome of atypical psychotic and extremely immature behavior, obesity and overgrowth, borderline retardation, and seizures (prominent in two). Weight overgrowth exceeded height overgrowth and was stratospheric (up to 8 SD above mean). Obesity seemed related to lack of satiety....

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500805

    authors: Jobe A,Lewis D,Wainwright M,DeLong GR

    更新日期:2000-08-01 00:00:00

  • Weinberg's syndrome: a disorder of attention and behavior problems needing further research.

    abstract::A subset of inattentive children have an underlying problem in sustaining wakefulness ("vigilance"). This disorder of vigilance, termed Weinberg's syndrome, is characterized by difficulty in maintaining wakefulness and alertness as evidenced by (among other symptoms) motor restlessness (fidgeting and moving about, yaw...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500710

    authors: Brumback RA

    更新日期:2000-07-01 00:00:00

  • Current therapy for West syndrome in Japan.

    abstract::We sent questionnaires concerning the current therapy for West syndrome to 208 institutions at which pediatric care members of the Japan Epilepsy Society were working. Of these, 129 (62%) institutions responded. Vitamin B6 was the preferred first-line drug, followed by the combination of vitamin B6 and valproate or mo...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500615

    authors: Ito M,Seki T,Takuma Y

    更新日期:2000-06-01 00:00:00

  • The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings.

    abstract::The clinical and laboratory data of four pediatric patients and one adult patient with inverted duplication (inv dup) (15) are reported. The most evident findings were dysmorphic features with frontal bossing; genital abnormalities, such as macropenis or hypospadias; mental retardation; autistic behavior; and seizures...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500605

    authors: Buoni S,Sorrentino L,Farnetani MA,Pucci L,Fois A

    更新日期:2000-06-01 00:00:00

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