The examination of peer review and publication in neurology.

Abstract:

:Despite remarkable growth in the clinical neurology literature, there is little research on peer review and biomedical publication in neurology. Biomedical publication research encompasses every step of the research process, from the methodology to the publication of research findings. Some general medical journals have served as leaders in improving scientific publication. Many medical fields have taken it upon themselves to characterize journals and peer reviewers within their own fields. Not all of these data can be applied to the clinical neurology literature; research methodologies, article types, and the journals themselves are unique to every medical field. This article reviews current publication research in the neurology literature and concludes that, to sustain and improve upon the integrity of clinical neurology research, further study is needed of the journals and the peer review process in neurology. Otherwise, the value of clinical research findings and patient care guidelines will be diminished.

journal_name

J Child Neurol

authors

Wong VS

doi

10.1177/0883073810374647

subject

Has Abstract

pub_date

2010-10-01 00:00:00

pages

1298-301

issue

10

eissn

0883-0738

issn

1708-8283

pii

0883073810374647

journal_volume

25

pub_type

杂志文章,评审
  • Ambulatory electroencephalography (EEG) in children: diagnostic yield and tolerability.

    abstract::Sixty-four children, aged 0-17 years, undergoing ambulatory electroencephalography (EEG) were prospectively recruited during a 12-month period. The diagnostic yield of ambulatory electroencephalography was determined for each of the following groups: group 1: differentiation of seizures from nonepileptic events; group...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808314158

    authors: Wirrell E,Kozlik S,Tellez J,Wiebe S,Hamiwka L

    更新日期:2008-06-01 00:00:00

  • Acute respiratory failure precipitated by general anesthesia in Leigh's syndrome.

    abstract::Three patients with Leigh's syndrome developed respiratory failure following general anesthesia. Although all three had respiratory symptoms prior to the anesthetic, the diagnosis was not suspected at the time of the procedure in two of the children. We reviewed the case notes of 16 other patients with Leigh's syndrom...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389000500214

    authors: Grattan-Smith PJ,Shield LK,Hopkins IJ,Collins KJ

    更新日期:1990-04-01 00:00:00

  • Prospective preliminary analysis of the development of autism and epilepsy in children with infantile spasms.

    abstract::The objective of this study was to compare the efficacy of corticotropin (ACTH) versus vigabatrin in treating infantile spasms and to determine which medication has a more favorable long-term outcome in terms of cognitive function, evolution of epilepsy, and incidence of autism. Patients with infantile spasms were inc...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/08830738030180030801

    authors: Askalan R,Mackay M,Brian J,Otsubo H,McDermott C,Bryson S,Boyd J,Snead C 3rd,Roberts W,Weiss S

    更新日期:2003-03-01 00:00:00

  • Cardiac and central nervous system vasculitis in a child with dermatomyositis.

    abstract::Cerebral vasculitis and clinically important myocardial inflammation are rare in juvenile dermatomyositis. We report a previously healthy 6-year-old girl with dermatomyositis who died after a fulminating clinical deterioration. Postmortem examination of the heart revealed characteristic endothelial tubuloreticular agg...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389400900315

    authors: Jimenez C,Rowe PC,Keene D

    更新日期:1994-07-01 00:00:00

  • Macrocephaly-capillary malformation syndrome in a newborn with tetralogy of fallot and sagittal sinus thrombosis.

    abstract::Macrocephaly-capillary malformation syndrome is characterized by cutaneous vascular malformations with associated anomalies as macrocephaly, macrosomia, hemihypertrophy, hypotonia, developmental delay, lax joints, loose skin, polysyndactyly, and neuroimaging abnormalities. We present a newborn with a prenatal diagnosi...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073812439346

    authors: Ercan TE,Oztunc F,Celkan T,Bor M,Kizilkilic O,Vural M,Perk Y,Islak C,Tuysuz B

    更新日期:2013-01-01 00:00:00

  • A case of infantile de novo primary antiphospholipid syndrome revealed by a neonatal arterial ischemic stroke.

    abstract::The few cases of antiphospholipid syndrome that have been reported in neonates are believed to have resulted from a transplacental transfer of antiphospholipid antibodies. Here we report on a boy with a neonatal stroke revealing a de novo primary antiphospholipid, the mother being free of antiphospholipid antibodies. ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811435238

    authors: Merlin E,Doré E,Chabrier S,Biard M,Marques-Verdier A,Stéphan JL

    更新日期:2012-10-01 00:00:00

  • Impact of recent seizures on cerebral blood flow in patients with sturge-weber syndrome: study of 2 cases.

    abstract::Patients with refractory seizures, including those with Sturge-Weber syndrome, undergo functional studies in preparation for surgery. Perfusion studies in Sturge-Weber syndrome by single photon emission computed tomography and positron emission tomography generally demonstrate hypoperfusion in the diseased tissue. We ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073807302597

    authors: Oguz KK,Senturk S,Ozturk A,Anlar B,Topcu M,Cila A

    更新日期:2007-05-01 00:00:00

  • Histocompatibility determinants in childhood postinfectious encephalomyelitis.

    abstract::Postinfectious encephalomyelitis and multiple sclerosis have clinical, immunologic, and neuroradiographic similarities. We studied HLA determinants in six white children consecutively diagnosed with postinfectious encephalomyelitis. Each of the children had HLA determinants which have been associated with multiple scl...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388900400311

    authors: Woody RC,Steele RW,Charlton RK,Smith V

    更新日期:1989-07-01 00:00:00

  • The multiple causes of multiple sclerosis: the importance of age of infections in childhood.

    abstract::The geographic distribution of multiple sclerosis (MS) may relate to the age of initial exposure and degree of sensitization to common viruses or bacteria which have proteins with epitopes (antigenic determinants) which are homologous with potentially encephalitogenic peptides in central myelin proteins, such as basic...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388700200418

    authors: Alvord EC Jr,Jahnke U,Fischer EH,Kies MW,Driscoll BF,Compston DA

    更新日期:1987-10-01 00:00:00

  • Gait assessment in children with duchenne muscular dystrophy during long-distance walking.

    abstract::The aim of this study was to investigate the alteration of the gait pattern in 25 children with Duchenne muscular dystrophy, using body-worn inertial sensors during a long walking distance. Normalized spatiotemporal gait parameters and their variability were extracted from the angular velocity of the shanks; the smoot...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811413581

    authors: Ganea R,Jeannet PY,Paraschiv-Ionescu A,Goemans NM,Piot C,Van den Hauwe M,Aminian K

    更新日期:2012-01-01 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

  • Morvan syndrome following B-cell lymphoma.

    abstract::Morvan syndrome is a rare autoimmune disease named after the French physician Augustin Marie Morvan. It is characterized by multiple, irregular contractions of the long muscles, weakness, pruritus, hyperhidrosis, insomnia, and delirium. Here, we describe a 17-year-old young man, previously diagnosed with B-cell lympho...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809356108

    authors: El-Bitar MK,Muwakkit SA,Abboud MR,Sawaya RA,Boustany RM

    更新日期:2010-08-01 00:00:00

  • Psychologic and neurologic function following treatment for childhood temporal lobe astrocytoma.

    abstract::Seven school-aged children treated for temporal lobe astrocytomas with surgical resection and irradiation were prospectively tested to evaluate their intellectual, academic, personality, and neurologic status after therapy. At their most recent follow-up examination, neuropsychologic functioning was adequate in only t...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388800300111

    authors: Mulhern RK,Kovnar EH,Kun LE,Crisco JJ,Williams JM

    更新日期:1988-01-01 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

  • Trihexyphenidyl improves motor function in children with dystonic cerebral palsy: a retrospective analysis.

    abstract::There are conflicting reports regarding the efficacy of trihexyphenidyl, an anticholinergic drug, for treatment of dystonia in cerebral palsy. The author hypothesized that trihexyphenidyl may be more effective in specific subgroups and performed a retrospective analysis of 31 children (8.2 ± 5.8 years) with dystonia f...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810392582

    authors: Ben-Pazi H

    更新日期:2011-07-01 00:00:00

  • Pediatric to Adult Transitions of Ketogenic Dietary Therapy for Epilepsy.

    abstract::Ketogenic therapy is now an accepted treatment for pediatric and adult patients with medically refractory epilepsy.1-3 However, young adults treated with a ketogenic diet face unique challenges when transitioning to adult neurology providers.4 The variable acceptance of dietary therapy, paucity of nutritionists and ad...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820938587

    authors: Seaborg K,Wang X,Olson C,Felton EA

    更新日期:2020-11-01 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

  • Outcomes of preterm neonates with frontal horn cysts: a retrospective study.

    abstract::Isolated paraventricular frontal horn cysts are sometimes encountered on cranial ultrasound examinations of preterm neonates. The etiology and clinical significance of these lesions are unclear. The authors aimed to identify antenatal/intrapartum risk factors associated with the occurrence of these cysts and to assess...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810366600

    authors: Trawber R,Rao S,Srinivasjois R,Thonell S,Nagarajan L,French N,Jacoby P,McMichael J

    更新日期:2010-11-01 00:00:00

  • Tests for juvenile myasthenia gravis: comparative diagnostic yield and prediction of outcome.

    abstract::The clinical picture, family history, laboratory data, treatment modalities, and outcome in 27 juvenile myasthenics seen over a 25-year period are presented. Onset was after 10 years of age in the majority of patients. Half presented with ocular signs, the other half with generalized-onset myasthenia. Half of those wi...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307389300800422

    authors: Afifi AK,Bell WE

    更新日期:1993-10-01 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

  • Joubert syndrome: early diagnosis by recognition of the behavioral phenotype and confirmation by cranial sonography.

    abstract::Our experience with two children with Joubert syndrome demonstrates how the diagnosis, if suspected by recognition of the behavioral phenotype, can rapidly be made by employing cranial sonography. This technique also may afford prenatal diagnosis of the syndrome in future siblings of confirmed cases. We have produced ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388800300403

    authors: Edwards BO Jr,Fischer AQ,Flannery DB

    更新日期:1988-10-01 00:00:00

  • Seizures and epilepsy among children with language regression and autistic spectrum disorders.

    abstract::Clinical and subclinical seizures occur frequently among children with autistic spectrum disorders. Electrographic status epilepticus in sleep, or continuous spike-wave in slow-wave sleep, is a typical feature of acquired epileptic aphasia and Landau-Kleffner syndrome. Seizures and epilepsy are more common among child...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307380401900106

    authors: Trevathan E

    更新日期:2004-08-01 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

  • Meralgia paresthetica in the pediatric population: a propos of 2 cases.

    abstract::Meralgia paresthetica is a mononeuropathy affecting the lateral femoral cutaneous nerve that is extremely rare in children. Two adolescent females, aged 11 and 13 years, presented due to tingling and pain on the side of the thigh of 2 to 3 weeks duration. The general examination revealed mild obesity; the neurological...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809336130

    authors: Fernández-Mayoralas DM,Fernández-Jaén A,Jareño NM,Pérez BC,Fernández PM,Sola AG

    更新日期:2010-01-01 00:00:00

  • Clinical Presentation and Outcome in Autoimmune Encephalitis Associated With N-Type Voltage-Gated Calcium Channels in Children.

    abstract:OBJECTIVE:We present the diagnostic and clinical course of the first multicenter case series of pediatric patients with autoimmune encephalitis associated with N-type voltage-gated calcium channel antibodies. METHODS:Data from 2 university hospitals were retrospectively reviewed and records of 3 patients with autoimmu...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073819840448

    authors: Kornitzer J,Taha F,Segal E

    更新日期:2019-08-01 00:00:00

  • Bilateral basal ganglia lesions after hypoglycemic coma in a 6-year-old child.

    abstract::Imaging findings of brain damage due to neonatal hypoglycemia are known; however, the effect of childhood hypoglycemia on the brain has not been described well. The authors present the case of a 6-year-old girl who had seizures secondary to hypoglycemia followed up for 1 year as epilepsy. The patient had experienced a...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073807300299

    authors: Kara C,Aydin OF,Aslan B,Gürer YK

    更新日期:2007-02-01 00:00:00

  • Neuropsychological findings in childhood narcolepsy.

    abstract::Narcolepsy with cataplexy is a severely disabling disorder very often arising in childhood. Data on neuropsychological impairment in children are scant. We administered standardized neuropsychological tests to 13 children with narcolepsy with cataplexy. Overall, our patients displayed multiple patterns of cognitive an...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813508315

    authors: Posar A,Pizza F,Parmeggiani A,Plazzi G

    更新日期:2014-10-01 00:00:00

  • Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy.

    abstract::A 3 1/2-year-old boy presented with megaloblastic anemia and recurrent episodes of severe lactic acidosis and coma. At age 4 years, he developed sepsis and died; postmortem examination failed to show any gross abnormality in any tissue. Biochemical analysis of muscle showed decreased activities for all respiratory cha...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380401900403

    authors: Akman CI,Sue CM,Shanske S,Tanji K,Bonilla E,Ojaimi J,Krishna S,Schubert R,DiMauro S

    更新日期:2004-04-01 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

  • Longitudinal electroencephalographic (EEG) findings in pediatric anti-N-methyl-D-aspartate (anti-NMDA) receptor encephalitis: the Padua experience.

    abstract::To contribute to characterize electroencephalographic (EEG) activity in pediatric anti-N-methyl-d-aspartate (anti-NMDA) receptor encephalitis, we reviewed electroclinical data of 5 children with anti-NMDA receptor encephalitis diagnosed in our department. We identified 4 longitudinal electroencephalographic phases: in...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813515947

    authors: Nosadini M,Boniver C,Zuliani L,de Palma L,Cainelli E,Battistella PA,Toldo I,Suppiej A,Sartori S

    更新日期:2015-02-01 00:00:00