Example of Journal of Child Neurology format
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Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format
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Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format Example of Journal of Child Neurology format
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This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Journal of Child Neurology — Template for authors

Publisher: SAGE
Categories Rank Trend in last 3 yrs
Pediatrics, Perinatology and Child Health #82 of 294 down down by 11 ranks
Neurology (clinical) #179 of 343 down down by 39 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 505 Published Papers | 1668 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 18/07/2020
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Related Journals

open access Open Access

SAGE

Quality:  
High
CiteRatio: 4.3
SJR: 1.395
SNIP: 2.063
open access Open Access
recommended Recommended

Springer

Quality:  
High
CiteRatio: 5.9
SJR: 1.431
SNIP: 1.344
open access Open Access
recommended Recommended

Elsevier

Quality:  
High
CiteRatio: 5.1
SJR: 0.882
SNIP: 1.253
open access Open Access
recommended Recommended

Elsevier

Quality:  
High
CiteRatio: 5.4
SJR: 1.405
SNIP: 1.278

Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

A measure of average citations received per peer-reviewed paper published in the journal.

1.713

18% from 2018

Impact factor for Journal of Child Neurology from 2016 - 2019
Year Value
2019 1.713
2018 2.092
2017 1.665
2016 1.378
graph view Graph view
table view Table view

3.3

21% from 2019

CiteRatio for Journal of Child Neurology from 2016 - 2020
Year Value
2020 3.3
2019 4.2
2018 3.9
2017 3.5
2016 3.1
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 18% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 21% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

0.661

13% from 2019

SJR for Journal of Child Neurology from 2016 - 2020
Year Value
2020 0.661
2019 0.757
2018 0.973
2017 0.799
2016 0.76
graph view Graph view
table view Table view

1.023

10% from 2019

SNIP for Journal of Child Neurology from 2016 - 2020
Year Value
2020 1.023
2019 0.926
2018 0.883
2017 0.832
2016 0.748
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 13% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 10% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Journal of Child Neurology

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SAGE

Journal of Child Neurology

The Journal of Child Neurology (JCN) is an interdisciplinary peer-reviewed biomedical journal publishing articles in the fields of child neurology, pediatric neurosurgery, pediatric neuroradiology, child psychiatry, pediatric neuropsychology, developmental and behavior pediatr...... Read More

Pediatrics, Perinatology, and Child Health

Clinical Neurology

Medicine

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Last updated on
18 Jul 2020
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ISSN
0883-0738
i
Impact Factor
Medium - 0.818
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Acceptance Rate
30%
i
Open Access
Yes
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Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
SageV
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Citation Type
Numbered (Superscripted)
25
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Bibliography Example
Blonder GE, Tinkham M and Klapwijk TM. Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B 1982; 25(7): 4515–4532. URL 10.1103/PhysRevB.25.4515.

Top papers written in this journal

Journal Article DOI: 10.1177/088307389801301206
Tuberous Sclerosis Complex Consensus Conference: Revised Clinical Diagnostic Criteria
E. S. Roach1, Manuel Gómez2, Hope Northrup3

Abstract:

At the recent tuberous sclerosis complex consensus conference, the clinical diagnostic criteria for tuberous sclerosis complex were simplified and revised to reflect both new clinical information about tuberous sclerosis complex and an improved understanding of the disorder derived from molecular genetic studies. Based on thi... At the recent tuberous sclerosis complex consensus conference, the clinical diagnostic criteria for tuberous sclerosis complex were simplified and revised to reflect both new clinical information about tuberous sclerosis complex and an improved understanding of the disorder derived from molecular genetic studies. Based on this new information, some clinical signs once regarded as pathognomonic for tuberous sclerosis complex are now known to be less specific. No single sign is present in all affected patients, and there is no proof that any single clinical or radiographic sign is absolutely specific for tuberous sclerosis complex. Accordingly, the clinical and radiographic features of tuberous sclerosis complex have now been divided into major and minor categories based on the apparent degree of specificity for tuberous sclerosis complex of each feature. A definitive diagnosis of tuberous sclerosis complex now requires two or more distinct types of lesions, rather than multiple lesions of the same type in the same organ system. Although diagnosis on purely clinical grounds can continue to be difficult in a few patients, there should be little doubt about the diagnosis for those individuals who fulfill these strict criteria. Couples with more than one child with tuberous sclerosis complex, no extended family history, and no clinical features of tuberous sclerosis complex are more likely to have germline mosaicism for tuberous sclerosis than nonexpression of the mutation. Germline mosaicism, while fortunately rare, will not be suspected from either diagnostic criteria or molecular testing until a couple has multiple affected children. Genetic counseling for families with one affected child should include a small (1% to 2%) possibility of recurrence, even for parents who have no evidence of tuberous sclerosis complex after a thorough diagnostic evaluation. read more read less

Topics:

Tuberous sclerosis protein (74%)74% related to the paper, TSC1 (65%)65% related to the paper, Subependymal giant cell astrocytoma (57%)57% related to the paper, TSC2 (55%)55% related to the paper, Tuberous sclerosis (55%)55% related to the paper
995 Citations
Journal Article DOI: 10.1177/0883073807305788
Consensus Statement for Standard of Care in Spinal Muscular Atrophy

Abstract:

Spinal muscular atrophy is a neurodegenerative disease that requires multidisciplinary medical care. Recent progress in the understanding of molecular pathogenesis of spinal muscular atrophy and advances in medical technology have not been matched by similar developments in the care for spinal muscular atrophy patients. Varia... Spinal muscular atrophy is a neurodegenerative disease that requires multidisciplinary medical care. Recent progress in the understanding of molecular pathogenesis of spinal muscular atrophy and advances in medical technology have not been matched by similar developments in the care for spinal muscular atrophy patients. Variations in medical practice coupled with differences in family resources and values have resulted in variable clinical outcomes that are likely to compromise valid measure of treatment effects during clinical trials. The International Standard of Care Committee for Spinal Muscular Atrophy was formed in 2005, with a goal of establishing practice guidelines for clinical care of these patients. The 12 core committee members worked with more than 60 spinal muscular atrophy experts in the field through conference calls, e-mail communications, a Delphi survey, and 2 in-person meetings to achieve consensus on 5 care areas: diagnostic/new interventions, pulmonary, gastrointestinal/nutrition, orthopedics/rehabilitation, and palliative care. Consensus was achieved on several topics related to common medical problems in spinal muscular atrophy, diagnostic strategies, recommendations for assessment and monitoring, and therapeutic interventions in each care area. A consensus statement was drafted to address the 5 care areas according to 3 functional levels of the patients: nonsitter, sitter, and walker. The committee also identified several medical practices lacking consensus and warranting further investigation. It is the authors' intention that this document be used as a guideline, not as a practice standard for their care. A practice standard for spinal muscular atrophy is urgently needed to help with the multidisciplinary care of these patients. read more read less

Topics:

Nusinersen (62%)62% related to the paper, Palliative care (62%)62% related to the paper, Spinal muscular atrophy (54%)54% related to the paper
View PDF
738 Citations
Journal Article DOI: 10.1177/088307380201700406
Prevalence Estimation of Williams Syndrome

Abstract:

There are limited population-based data on the occurrence of Williams syndrome. We estimated its prevalence combining data from two investigations. One was an epidemiologic study originally designed to assess the prevalence and etiology of mental retardation among 30,037 Norwegian children born between 1980 and 1985 and livin... There are limited population-based data on the occurrence of Williams syndrome. We estimated its prevalence combining data from two investigations. One was an epidemiologic study originally designed to assess the prevalence and etiology of mental retardation among 30,037 Norwegian children born between 1980 and 1985 and living in Akershus County on January 1, 1993. The other investigation was a national survey of Williams syndrome. In the first study, 213 children were referred for evaluation, whereas the second study comprised 57 cases with Williams syndrome born between 1970 and 1992, who were referred for evaluation from all Norwegian counties. The epidemiologic study revealed three children with Williams syndrome, whereas one additional case complying with our demographic criteria was identified in the national survey, thus giving a prevalence of 1 in 7500. In all cases, a typical chromosome 7q11.23 deletion was detected. We also conclude that Williams syndrome is not an uncommon cause of mental retardation, with a prevalence of approximately 6% of patients with genetic etiology. read more read less

Topics:

Williams syndrome (56%)56% related to the paper, Population (52%)52% related to the paper
680 Citations
Journal Article DOI: 10.1177/088307380001500508
Neurologic Outcome in Survivors of Childhood Arterial Ischemic Stroke and Sinovenous Thrombosis

Abstract:

Ischemic stroke during infancy and childhood has the potential for life-long morbidity. Information on the neurologic outcome of children who survive ischemic stroke is lacking. Children surviving ischemic stroke between January 1, 1995 and July 1, 1999 were prospectively followed. Neurologic deficit severity was based on the... Ischemic stroke during infancy and childhood has the potential for life-long morbidity. Information on the neurologic outcome of children who survive ischemic stroke is lacking. Children surviving ischemic stroke between January 1, 1995 and July 1, 1999 were prospectively followed. Neurologic deficit severity was based on the Pediatric Stroke Outcome Measure (PSOM) developed in this study and parental response to two recovery questions. Predictor variables for poor outcome were tested. One-hundred twenty-three children with arterial ischemic stroke and 38 with sinovenous thrombosis were followed for a mean of 2.1 years (range, 0.8 to 6.6 years). The primary outcome based on PSOM assessment was: normal, 37%; mild deficit, 20%; moderate deficit, 26%; and severe deficit, 16%. The secondary outcome was full recovery in 45% of patients, based on parental response. The primary and secondary outcome measures were moderately correlated (P < .001; K = 0.5). In bivariate analysis, arterial stroke type, male gender,... read more read less

Topics:

Pediatric stroke (64%)64% related to the paper, Stroke (62%)62% related to the paper, Neonatal stroke (58%)58% related to the paper
585 Citations
Journal Article DOI: 10.1177/088307380001500701
Short-term benefit from oral vancomycin treatment of regressive-onset autism.

Abstract:

In most cases symptoms of autism begin in early infancy. However, a subset of children appears to develop normally until a clear deterioration is observed. Many parents of children with "regressive"-onset autism have noted antecedent antibiotic exposure followed by chronic diarrhea. We speculated that, in a subgroup of childr... In most cases symptoms of autism begin in early infancy. However, a subset of children appears to develop normally until a clear deterioration is observed. Many parents of children with "regressive"-onset autism have noted antecedent antibiotic exposure followed by chronic diarrhea. We speculated that, in a subgroup of children, disruption of indigenous gut flora might promote colonization by one or more neurotoxin-producing bacteria, contributing, at least in part, to their autistic symptomatology. To help test this hypothesis, 11 children with regressive-onset autism were recruited for an intervention trial using a minimally absorbed oral antibiotic. Entry criteria included antecedent broad-spectrum antimicrobial exposure followed by chronic persistent diarrhea, deterioration of previously acquired skills, and then autistic features. Short-term improvement was noted using multiple pre- and post-therapy evaluations. These included coded, paired videotapes scored by a clinical psychologist blinded to treatment status; these noted improvement in 8 of 10 children studied. Unfortunately, these gains had largely waned at follow-up. Although the protocol used is not suggested as useful therapy, these results indicate that a possible gut flora-brain connection warrants further investigation, as it might lead to greater pathophysiologic insight and meaningful prevention or treatment in a subset of children with autism. read more read less

Topics:

Regressive autism (68%)68% related to the paper, Autism (61%)61% related to the paper
555 Citations
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Journal of Child Neurology format uses SageV citation style.

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Frequently asked questions

1. Can I write Journal of Child Neurology in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Journal of Child Neurology guidelines and auto format it.

2. Do you follow the Journal of Child Neurology guidelines?

Yes, the template is compliant with the Journal of Child Neurology guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Journal of Child Neurology?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Journal of Child Neurology citation style.

4. Can I use the Journal of Child Neurology templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Journal of Child Neurology.

5. Can I use a manuscript in Journal of Child Neurology that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Journal of Child Neurology that you can download at the end.

6. How long does it usually take you to format my papers in Journal of Child Neurology?

It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Journal of Child Neurology.

7. Where can I find the template for the Journal of Child Neurology?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Journal of Child Neurology's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Journal of Child Neurology's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Journal of Child Neurology an online tool or is there a desktop version?

SciSpace's Journal of Child Neurology is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Journal of Child Neurology?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Journal of Child Neurology?”

11. What is the output that I would get after using Journal of Child Neurology?

After writing your paper autoformatting in Journal of Child Neurology, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Journal of Child Neurology's impact factor high enough that I should try publishing my article there?

To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Journal of Child Neurology?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Journal of Child Neurology. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Journal of Child Neurology?

The 5 most common citation types in order of usage for Journal of Child Neurology are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

15. How do I submit my article to the Journal of Child Neurology?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Journal of Child Neurology's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Journal of Child Neurology in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Journal of Child Neurology Endnote style according to Elsevier guidelines.

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