听力与言语-语言病理学

行为科学

医学伦理学

你正在浏览JOURNAL OF CHILD NEUROLOGY期刊下所有文献
  • Multicenter prospective study of children with sickle cell disease: radiographic and psychometric correlation.

    abstract::After obtaining familial informed consent, between January 1996 and July 1997, 173 children (5 to 15 years old) with sickle cell disease were enrolled in a prospective multicenter study using blood screening, transcranial Doppler ultrasonography (n = 143), cerebral magnetic resonance imaging (n = 144), and neuropsycho...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/088307380001500510

    authors: Bernaudin F,Verlhac S,Fréard F,Roudot-Thoraval F,Benkerrou M,Thuret I,Mardini R,Vannier JP,Ploix E,Romero M,Cassé-Perrot C,Helly M,Gillard E,Sebag G,Kchouk H,Pracros JP,Finck B,Dacher JN,Ickowicz V,Raybaud C,Ponce

    更新日期:2000-05-01 00:00:00

  • Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus.

    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

    pub_type: 杂志文章

    doi:10.1177/088307380001500407

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

    更新日期:2000-04-01 00:00:00

  • Relationship of cognitive functioning, whole brain volumes, and T2-weighted hyperintensities in neurofibromatosis-1.

    abstract::Using quantitative magnetic resonance imaging morphometry, we report that the whole brain volumes of patients with neurofibromatosis-1 are significantly larger than normal, confirm the prevalence of macrocephaly as about 50%, and report that macrocephaly in patients with neurofibromatosis-1 does not appear to be relat...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500303

    authors: Cutting LE,Koth CW,Burnette CP,Abrams MT,Kaufmann WE,Denckla MB

    更新日期:2000-03-01 00:00:00

  • Venlafaxine in children, adolescents, and young adults with autism spectrum disorders: an open retrospective clinical report.

    abstract::Autism is characterized by social deficits, communication and language impairments, narrow restricted interests, repetitive behaviors, inattention, and hyperactivity. While selective serotonin reuptake inhibitors have demonstrated efficacy in treating core symptoms of autism, norepinephrine reuptake inhibitors have de...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500214

    authors: Hollander E,Kaplan A,Cartwright C,Reichman D

    更新日期:2000-02-01 00:00:00

  • Tuberous sclerosis complex and epilepsy: prognostic significance of electroencephalography and magnetic resonance imaging.

    abstract::Tuberous sclerosis complex is a disease that affects many organs, including the central nervous system. Nervous system involvement in the form of hamartomas often results in seizures. In this study we wanted to determine the outcome of epilepsy in tuberous sclerosis complex and determine whether interictal electroence...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500203

    authors: Husain AM,Foley CM,Legido A,Chandler DA,Miles DK,Grover WD

    更新日期:2000-02-01 00:00:00

  • Neurologic presentations of mitochondrial disorders.

    abstract::This article describes the neurologic presentations of children with mitochondrial disorders. The charts of 42 children with highly suspect mitochondrial disorders were reviewed. Thirty-seven children were diagnosed as having definite mitochondrial disorders based on a suggestive clinical presentation and at least one...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500110

    authors: Nissenkorn A,Zeharia A,Lev D,Watemberg N,Fattal-Valevski A,Barash V,Gutman A,Harel S,Lerman-Sagie T

    更新日期:2000-01-01 00:00:00

  • Postictal psychosis in a child.

    abstract::Postictal psychoses are brief psychotic episodes that usually occur after poorly controlled partial complex seizure clusters. The psychosis commonly appears following a lucid interval, ranging from a few hours to days after seizure termination. An underlying structural brain abnormality is common and usually involves ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901401209

    authors: Nissenkorn A,Moldavsky M,Lorberboym M,Raucher A,Bujanover Y,Lerman-Sagie T

    更新日期:1999-12-01 00:00:00

  • Automated tandem mass spectrometry for mass newborn screening for disorders in fatty acid, organic acid, and amino acid metabolism.

    abstract::Development of acylcarnitine and amino acid profiling using tandem mass spectrometry, and its application for use with dried blood specimens collected on filter-paper cards, has introduced an innovative new technology for detecting inborn errors of fatty acid, organic acid, and amino acid metabolism. From November 1, ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073899014001021

    authors: Naylor EW,Chace DH

    更新日期:1999-11-01 00:00:00

  • Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter.

    abstract::Recently, a new disease entity has been defined: the disease of vanishing white matter. This leukoencephalopathy has an autosomal-recessive mode of inheritance. No cause or biochemical marker is known. We studied cerebrospinal fluid amino acids in five patients with the disease and found a consistent, moderate elevati...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901401108

    authors: van der Knaap MS,Wevers RA,Kure S,Gabreëls FJ,Verhoeven NM,van Raaij-Selten B,Jaeken J

    更新日期:1999-11-01 00:00:00

  • History of Joubert syndrome and a 30-year follow-up of the original proband.

    abstract::The 1960s were a period of great flowering in the recognition of neurologic disorders in children. The so-called ataxic cerebral palsies were an especially fertile field waiting for clarification. Congenital ataxia coupled with hyperpnea-apnea, abnormal eye movements, and retardation was identified as an autosomal-rec...

    journal_title:Journal of child neurology

    pub_type: 历史文章,杂志文章

    doi:10.1177/088307389901400903

    authors: Andermann F,Andermann E,Ptito A,Fontaine S,Joubert M

    更新日期:1999-09-01 00:00:00

  • Rett syndrome: photographic evidence of rapid regression.

    abstract::Rett Syndrome is known to occur in females, around the second year, with loss of hand use, onset of stereotypes and acquired microcephaly. Such regression is often very rapid, but this has never been documented. In one of our patients, photographs taken at different times clearly demonstrate the rapid progression of f...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400815

    authors: Fiumara A,Barone R,D'Asero G,Marzullo E,Pavone L

    更新日期:1999-08-01 00:00:00

  • Restricted unilateral Sydenham's chorea: reversible contralateral striatal hypermetabolism demonstrated on single photon emission computed tomographic scanning.

    abstract::Sydenham's chorea results from group A streptococcus infection and subsequent generation of antineuronal antibodies directed at the caudate nucleus and putamen. Predominantly bilateral, in up to 30% of cases the chorea can be unilaterally restricted. Imaging studies, both structural (magnetic resonance imaging) and fu...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400805

    authors: Dilenge ME,Shevell MI,Dinh L

    更新日期:1999-08-01 00:00:00

  • Congenital intramedullary tumor with neonatal manifestations.

    abstract::The authors report on a 45-day-old boy with a congenital intramedullary tumor with clinical manifestations since birth. Neurologic examination disclosed severe bilateral lower-limb hypotonia and diplegia, with exacerbated deep tendon reflexes and clonus associated with severe pain at manipulation. Further evaluation o...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400711

    authors: Nunes ML,Coutinho LM,Janisch C,Ehlers JA

    更新日期:1999-07-01 00:00:00

  • Plasma baclofen levels in children receiving continuous intrathecal baclofen infusion.

    abstract::To determine the plasma baclofen concentrations of children undergoing continuous intrathecal baclofen infusion for treatment of cerebral spasticity, we assayed plasma samples from six children, 8 to 18 years of age, who were receiving intrathecal baclofen at constant rates of 77 to 400 micrograms/day. Plasma levels w...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/088307389901400611

    authors: Albright AL,Shultz BL

    更新日期:1999-06-01 00:00:00

  • Behavioral and electrophysiologic predictors of treatment response to stimulants in children with attention disorders.

    abstract::Behavioral and quantitative electroencephalography (EEG) techniques were used to evaluate treatment response to stimulant therapy in children with attention disorders. A sample of 130 children with attention disorders were evaluated with Conners and Diagnostic and Statistical Manual of Mental Disorders--III rating sca...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/088307389901400601

    authors: Chabot RJ,Orgill AA,Crawford G,Harris MJ,Serfontein G

    更新日期:1999-06-01 00:00:00

  • Alexander's disease: unique presentation.

    abstract::Subacute necrotizing encephalomyelopathy (Leigh syndrome) refers to a nebulous disease entity characterized by lactic acidosis, a wide variety a clinical manifestations, and a consistent conglomeration of pathologic findings. Several abnormalities in metabolism have been delineated in association with Leigh syndrome, ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400510

    authors: Gingold MK,Bodensteiner JB,Schochet SS,Jaynes M

    更新日期:1999-05-01 00:00:00

  • Clinical diversity in acute necrotizing encephalopathy.

    abstract::Acute necrotizing encephalopathy is a novel disease entity, proposed by Mizuguchi et al in 1995, that shows a characteristic selective and symmetric involvement of the thalamus, brain stem, and cerebellum. It usually leaves sequelae. The etiology of acute necrotizing encephalopathy is unknown. We describe here six pat...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400407

    authors: Yoshikawa H,Watanabe T,Abe T,Oda Y

    更新日期:1999-04-01 00:00:00

  • Genetic susceptibility to neurodevelopmental disorders.

    abstract::A large body of evidence suggests that genetic factors influence liability to many common neurodevelopmental disorders. Examples include Tourette syndrome, attention-deficit hyperactivity disorder, autism, and dyslexia. Characterization of the genetic component of susceptibility to these conditions at a molecular leve...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307389901400310

    authors: Ryan SG

    更新日期:1999-03-01 00:00:00

  • Asymmetries in brain maturation and behavioral disturbances: multivariate electroencephalogram and P300 studies.

    abstract::If behavior results from brain function, some evidence of dysfunction could be expected in children with major behavioral problems. Yet, neurophysiologic studies in these children are frequently normal. We hypothesized a relationship between maturational asymmetry and behavior, given the role of hemispheric imbalance ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400206

    authors: Gerez M,Tello A,Serrano C,Ibarra R,Mallet A

    更新日期:1999-02-01 00:00:00

  • High prevalence of bihemispheric structural and functional defects in Sturge-Weber syndrome.

    abstract::Abnormal cerebral venous drainage is associated with hypoxia and glucose deprivation, which can account for progressive neurologic deterioration in Sturge-Weber syndrome. Although developmental delay is common in Sturge-Weber syndrome, bihemispheric calcification is uncommon. Computed tomography (CT) and magnetic reso...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389801301203

    authors: Maria BL,Neufeld JA,Rosainz LC,Ben-David K,Drane WE,Quisling RG,Hamed LM

    更新日期:1998-12-01 00:00:00

  • Pharmacoeconomic considerations in treatment options for acute seizures.

    abstract::Two pharmacoeconomic studies on the treatment of acute seizures have been conducted. In 1991, Kriel and colleagues surveyed parents of children with a history of cluster seizures, prolonged seizures, or status epilepticus who had been instructed in the use of rectal diazepam. A comparison of data before instruction wi...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073898013001081

    authors: Graves N

    更新日期:1998-10-01 00:00:00

  • Respiratory sinus arrhythmia in children with severe cyanotic and pallid breath-holding spells.

    abstract::In this study we investigated centrally mediated parasympathetic regulation of modulated cardiac vagal tone among children with severe cyanotic and pallid breath-holding spells by examining respiratory sinus arrhythmia. Respiratory sinus arrhythmia was evaluated in 41 children; 17 subjects with cyanotic breath-holding...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389801300905

    authors: DiMario FJ Jr,Bauer L,Baxter D

    更新日期:1998-09-01 00:00:00

  • Pathologic basis of the symptomatic epilepsies in childhood.

    abstract::The epilepsies in childhood are classified as primary (or idiopathic) and secondary (or symptomatic). The primary epilepsies account for two thirds of all childhood epilepsies and are presumed to be genetically determined. In the remaining one third of cases, a neuropathologic lesion can be identified. This paper summ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307389801300801

    authors: Armstrong DD,Mizrahi EM

    更新日期:1998-08-01 00:00:00

  • Event-related potentials (P300) in primary headache in childhood and adolescence.

    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

    pub_type: 杂志文章

    doi:10.1177/088307389801300703

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

    更新日期:1998-07-01 00:00:00

  • Learning disabilities with and without attention-deficit hyperactivity disorder: parents' and teachers' perspectives.

    abstract::Our objective was to delineate the educational and behavioral differences between learning disabled children with and without attention-deficit hyperactivity disorder (ADHD). A restrospective (TROHOC) multimeasure comparative design was employed. Parents' and teachers' questionnaires (ANSER system) pertaining to atten...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389801300606

    authors: Tirosh E,Berger J,Cohen-Ophir M,Davidovitch M,Cohen A

    更新日期:1998-06-01 00:00:00

  • Clinical experience on headache in children: analysis of 92 cases.

    abstract::We analyzed, retrospectively, 92 patients with headache to determine the changes in the order of frequency of causes with the development of neuroimaging studies and its efficacy in the investigation of patients with headache. The type of headache was redefined according to the International Headache Society (IHS) dia...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389801300502

    authors: Aysun S,Yetük M

    更新日期:1998-05-01 00:00:00

  • Children who can't smell the coffee: isolated congenital anosmia.

    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

    pub_type: 杂志文章

    doi:10.1177/088307389801300404

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

    更新日期:1998-04-01 00:00:00

  • Behavioral and cognitive effects of lamotrigine.

    abstract::Lamotrigine is a new antiepileptic drug that may possess unique cognitive and behavioral characteristics. Although lamotrigine can produce neurobehavioral toxicity, it is generally well tolerated. In one study directly comparing lamotrigine to placebo as add-on therapy in patients with intractable epilepsy, no objecti...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073897012001101

    authors: Meador KJ,Baker GA

    更新日期:1997-11-01 00:00:00

  • Neuromotor functioning in children with Tourette syndrome with and without attention deficit hyperactivity disorder.

    abstract::Neuromotor function was assessed in 94 children of normal intelligence with Tourette syndrome, Tourette syndrome and attention-deficit hyperactivity disorder (ADHD), or ADHD only, using the Physical and Neurological Examination of Subtle Signs (PANESS). Time to complete six motor movements was analyzed separately by s...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200705

    authors: Schuerholz LJ,Cutting L,Mazzocco MM,Singer HS,Denckla MB

    更新日期:1997-10-01 00:00:00

  • Aspartylglucosaminuria: radiologic course of the disease with histopathologic correlation.

    abstract::Twelve living patients (aged 19 months to 32 years) with aspartylglucosaminuria were examined by magnetic resonance imaging (MRI), and the magnetic resonance (MR) images of 16 health volunteers (aged 4 to 32 years) were used as controls. One patient was examined twice. Postmortem MRI and histopathologic analysis were ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200606

    authors: Autti T,Raininko R,Haltia M,Lauronen L,Vanhanen SL,Salonen O,Aronen HJ,Wirtavuori K,Santavuori P

    更新日期:1997-09-01 00:00:00

  • Muscle fatigue in spinal muscular atrophy.

    abstract::We previously reported that patients with spinal muscular atrophy do not lose muscle strength over time as measured quantitatively. However, we noted that many patients with spinal muscular atrophy suffer from what they call fatigue. We wondered if we could measure fatigue during a single maximal voluntary contraction...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200507

    authors: Iannaccone ST,White M,Browne R,Russman B,Buncher R,Samaha FJ

    更新日期:1997-08-01 00:00:00

  • Vigabatrin in partial seizures in children.

    abstract::Patients with partial seizures aged 1 week to 19 years (n = 175) were included in several prospective vigabatrin studies at the hospital Saint Vincent de Paul. A decrease in seizure frequency of over 50% was achieved in 70% of patients, with 30% becoming seizure free, and only 6% experiencing an increase. Tuberous scl...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/088307389701200304

    authors: Nabbout RC,Chiron C,Mumford J,Dumas C,Dulac O

    更新日期:1997-04-01 00:00:00

  • Right hemisphere dysfunction in subjects with attention-deficit disorder with and without hyperactivity.

    abstract::The attention-deficit disorder, with and without hyperactivity, is associated with defective attention, response inhibition and, in attention-deficit disorder with hyperactivity, with motor restlessness. In adults, inattention, defective response inhibition, and impersistence are more commonly seen in right hemisphere...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200207

    authors: García-Sánchez C,Estévez-González A,Suárez-Romero E,Junqué C

    更新日期:1997-02-01 00:00:00

  • Study of nerve conduction and late responses in normal Chinese infants, children, and adults.

    abstract::Healthy Chinese individuals (n = 168), aged from 24 hours to 30 years, were studied to establish the following normal values: (1) motor conduction velocity, distal latency, amplitude, and F-wave velocity in the median, ulnar, tibial, and peroneal nerves; (2) H-reflex velocity and latency in the tibial nerve for all su...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200102

    authors: Cai F,Zhang J

    更新日期:1997-01-01 00:00:00

  • Leukoencephalopathy, megalencephaly, and mild clinical course. A recently individualized familial leukodystrophy. Report on five new cases.

    abstract::Five children presented in the first months of life with progressive megalencephaly and leukodystrophy characterized by diffuse swelling of the white matter, cystic cavitations in frontal and temporal lobes, and a slow progressive course contrasting with the intensity of the leukodystrophic process. Four had epilepsy....

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389601100604

    authors: Goutières F,Boulloche J,Bourgeois M,Aicardi J

    更新日期:1996-11-01 00:00:00

  • Sensory rhizotomy for the treatment of childhood spasticity.

    abstract::Sensory rhizotomy in the treatment of spasticity has been evolving over the past century since its first use in 1888. This paper reviews its historical evolution, current physiologic basis, range in current surgical technique, and the outcome, along with complications seen over the past decade since its repopularizati...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073896011001S06

    authors: Abbott R

    更新日期:1996-11-01 00:00:00

  • Electron microscopic examination of skin biopsy as a cost-effective tool in the diagnosis of lysosomal storage diseases.

    abstract::In this report, we have summarized our 9-year experience of over 100 proven cases of lysosomal storage disease using electron microscopic evaluation of skin biopsies as a screening tool. The skin biopsy was very specific in establishing the diagnosis in only two disorders, namely neuronal ceroid lipofuscinosis and muc...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389601100408

    authors: Prasad A,Kaye EM,Alroy J

    更新日期:1996-07-01 00:00:00

  • Hypertensive encephalopathy in childhood.

    abstract::Hypertensive encephalopathy is an uncommon but recognized complication of malignant hypertension in children. We reviewed the clinical course, laboratory studies, and outcomes of 12 patients with hypertensive encephalopathy seen at the University of Iowa Hospitals and Clinics between 1979 and 1994. The most common pre...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389601100305

    authors: Wright RR,Mathews KD

    更新日期:1996-05-01 00:00:00

  • Amylaceous (polyglucosan) bodies in familial cerebral atrophy of early onset.

    abstract::An 8-year-old girl and her 4-year-old sister presented with psychomotor retardation during the 1st year of life. This was followed by spasticity, seizures, and in the older patient, progressive loss of faculties and death. Computed tomographic and magnetic resonance imaging scans demonstrated progressive cerebral atro...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389601100115

    authors: de León GA,Crawford SE,Stack C,Darling CF,Johnson GS

    更新日期:1996-01-01 00:00:00

  • Myalgia and cramps: dystrophinopathy with wide-ranging laboratory findings.

    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

    pub_type: 杂志文章

    doi:10.1177/088307389601100105

    authors: Samaha FJ,Quinlan JG

    更新日期:1996-01-01 00:00:00

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