How to get your paper accepted for publication.

Abstract:

:This paper is an attempt to convey in a lucid way how to go about writing a scientific article for publication in an appropriate journal. Topics covered are: a) reasons to write a paper b) types of papers c) asking a question and formulating an hypothesis d) the complex series of steps necessary before you begin your study e) additional considerations once your study is complete f) the process of writing the paper and g) writing skills. In the concluding remarks I comment on the possibility of rejection of your submission which should not be taken personally. If this does occur it should not deter you from contributing to medical science.

journal_name

Paediatr Respir Rev

authors

Chernick V

doi

10.1016/j.prrv.2011.02.004

subject

Has Abstract

pub_date

2012-06-01 00:00:00

pages

130-2

issue

2

eissn

1526-0542

issn

1526-0550

pii

S1526-0542(11)00018-2

journal_volume

13

pub_type

杂志文章
  • Pediatric asthma: how significant it is for the whole life?

    abstract::Asthma is most frequent chronic disease in childhood. Childhood asthma frequently persists to adulthood and the available evidence suggests that the severity of childhood asthma predicts the severity of asthma in the adulthood. To prevent long term remodeling of the airways and improve prognosis, early diagnosis and t...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2006.04.171

    authors: Pohunek P

    更新日期:2006-01-01 00:00:00

  • Newborn screening for cystic fibrosis offers an advantage over symptomatic diagnosis for the long term benefit of patients: the motion for.

    abstract::Comprehensive newborn screening for cystic fibrosis has occurred for more than 25 years in some regions and the results of randomised controlled trials reporting the outcomes have been published. Testing protocols for CF have recently been reviewed and the sensitivity and specificity of these protocols are high. In sp...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2008.09.004

    authors: McKay K,Wilcken B

    更新日期:2008-12-01 00:00:00

  • Cardiac abnormalities and sudden infant death syndrome.

    abstract::Many factors have been implicated in SIDS cases including environmental influences such as sleeping arrangements and smoking. Most recently, cardiac abnormalities have been hypothesised to play a role in some cases, particularly the primary genetic arrhythmogenic disorders such as familial long QT syndrome (LQTS). Bot...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2014.09.006

    authors: Sweeting J,Semsarian C

    更新日期:2014-12-01 00:00:00

  • The burden of asthma in children: an Australian perspective.

    abstract::The burden of asthma among children is high in Australia compared with many other countries. Recent data show that 14-16% of children report a diagnosis of asthma that remains a problem. Boys, children under the age of 5 years and urban indigenous children experience a greater burden of asthma than other children. Mor...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2004.11.004

    authors: Poulos LM,Toelle BG,Marks GB

    更新日期:2005-03-01 00:00:00

  • Real-world respiratory and bulbar comorbidities of SMA type 1 children treated with nusinersen: 2-Year single centre Australian experience.

    abstract:AIM:To describe the respiratory and nutritional supportive care and hospitalisations required in the real-world scenario in children with SMA type 1 treated with nusinersen. METHODS:Single-centre observational cohort study of children with SMA1 commencing nusinersen from November 2016 to September 2018. Motor, respira...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2020.09.002

    authors: Chen KA,Widger J,Teng A,Fitzgerald DA,D'Silva A,Farrar M

    更新日期:2020-09-22 00:00:00

  • Primary ciliary dyskinesia among Arabs: Where do we go from here?

    abstract::Primary ciliary dyskinesia (PCD), also known as immotile-cilia syndrome, is a rare genetic disease that is inherited in an autosomal recessive manner. Several studies have explored certain aspects of PCD in the Arab world, yet much is still lacking in terms of identifying the different characteristics of this disease....

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2018.09.002

    authors: Hammoudeh S,Gadelhak W,Janahi IA

    更新日期:2019-02-01 00:00:00

  • Small for gestational age birth weight: impact on lung structure and function.

    abstract::Accumulating data suggest that prenatal compromises leading to intrauterine growth restriction (IUGR) increase the risk for respiratory deficiencies after birth. In this respect, a growing body of epidemiological evidence in infants, children and adults indicates that small for gestational (SGA) birth weight can adver...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2012.10.001

    authors: Briana DD,Malamitsi-Puchner A

    更新日期:2013-12-01 00:00:00

  • Community-acquired pneumonia.

    abstract::Pneumonia is highly prevalent in both developed and developing countries. In this review we list the main organisms affecting children with pneumonia and we propose a summary of the best possible diagnostic and therapeutic measures. ...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2006.04.221

    authors: Stein RT,Marostica PJ

    更新日期:2006-01-01 00:00:00

  • Interventions in the paediatric sleep laboratory: the use and titration of respiratory support therapies.

    abstract::During sleep changes in central and peripheral neurological pathways and muscle tone result in unique vulnerabilities in the respiratory system. Abnormalities of the respiratory system that are not apparent in wakefulness can become evident during particular sleep states, making overnight polysomnography (PSG) a valua...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2008.01.003

    authors: Waters K

    更新日期:2008-09-01 00:00:00

  • Chest wall abnormalities and their clinical significance in childhood.

    abstract::The thorax consists of the rib cage and the respiratory muscles. It houses and protects the various intrathoracic organs such as the lungs, heart, vessels, esophagus, nerves etc. It also serves as the so-called "respiratory pump" that generates the movement of air into the lungs while it prevents their total collapse ...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2013.12.003

    authors: Koumbourlis AC

    更新日期:2014-09-01 00:00:00

  • Cystic fibrosis and renal disease.

    abstract::Renal disease is relatively rare in cystic fibrosis even though the cystic fibrosis transmembrane regulator (CFTR) protein is expressed in abundance in the kidney. Aberrant CFTR expression probably explains the subtle abnormalities in renal concentrating and diluting ability described in cystic fibrosis and possibly t...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章

    doi:

    authors: Stephens SE,Rigden SP

    更新日期:2002-06-01 00:00:00

  • Clinical outcomes of congenital lung abnormalities.

    abstract::Individually, congenital abnormalities of the lung are rare but collectively they form an important group of conditions. The range of malformations is broad and the clinical impact is very variable, depending on the degree of malformation. This article groups these conditions under their traditional headings and consi...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1053/prrv.2000.0072

    authors: Wallis C

    更新日期:2000-12-01 00:00:00

  • Tracheostomy care in the home.

    abstract::There are hardly any controlled studies in paediatric tracheostomy care; instead, most established standards, procedures and details have been elaborated at the bedside by trial and error. Once the appropriate tube is chosen, tube care consists of tube change, fixation, management of secretions, humidification of insp...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2006.06.003

    authors: Oberwaldner B,Eber E

    更新日期:2006-09-01 00:00:00

  • Disease-modifying drug therapy in cystic fibrosis.

    abstract::Whilst substantial progress has been made in the treatment of cystic fibrosis, the disease still carries a significant burden in terms of symptoms, requirement for treatment and early mortality. The last decade has witnessed a new era in the development of small molecule drugs targeting the CFTR protein, which for the...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2017.03.008

    authors: Harman K,Dobra R,Davies JC

    更新日期:2018-03-01 00:00:00

  • Respiratory support for infants with bronchiolitis, a narrative review of the literature.

    abstract::Bronchiolitis is a common viral disease that significantly affects infants less than 12 months of age. The purpose of this review is to present a review of the current knowledge of the uses of respiratory support in the management of infants with bronchiolitis presenting to hospital. We electronically searched MEDLINE...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2018.10.001

    authors: Franklin D,Fraser JF,Schibler A

    更新日期:2019-04-01 00:00:00

  • Pulmonary complications of endocrine and metabolic disorders.

    abstract::There are many important respiratory manifestations of endocrine and metabolic diseases in children. Acute and chronic pulmonary infections are the most common respiratory abnormalities in patients with diabetes mellitus, although cardiogenic and non-cardiogenic pulmonary oedema are also possible. Pseudohypoaldosteron...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2011.01.004

    authors: Milla CE,Zirbes J

    更新日期:2012-03-01 00:00:00

  • Investigating sudden unexpected death in infancy and early childhood.

    abstract::Sudden unexpected death is one of the most frequent ways of dying in the first year of life after the neonatal period. It is however, much less frequent after the first birthday. Investigations into the cause of death are very important, for a significant proportion of these sudden deaths can be explained only after a...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2009.12.002

    authors: Côté A

    更新日期:2010-12-01 00:00:00

  • Parental smoking: asthma and wheezing illnesses in infants and children.

    abstract::Parental smoking has an important impact on asthma and wheezing illnesses in infants and children. In utero exposure is associated with impaired lung growth and wheezing illnesses, particularly in preschool children. Exposure to environmental tobacco smoke is associated with increased wheezing illnesses and increased ...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1053/prrv.2001.0141

    authors: Landau LI

    更新日期:2001-09-01 00:00:00

  • Telemedicine is the way forward for the management of cystic fibrosis- the case against.

    abstract::It is reasonable to suggest that Telemedicine could help in the management of chronic diseases by giving patients more flexibility to remain at home with opportunities to forward electronic data to healthcare professionals, reduce hospital emergency attendances and reduce overall costs. The reality, particularly in cy...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2017.03.005

    authors: Lenney W

    更新日期:2018-03-01 00:00:00

  • Congenital cyst adenomatoid malformations: resect some and observe all?

    abstract::With the advent of improved antenatal imaging over the past 10 years, the diagnosis, assessment and management of congenital cystic lung abnormalities have changed. These were once considered the exclusive domain of the surgeon, who had the authority to operate on all congenital cystic lung abnormalities regardless of...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2006.10.001

    authors: Fitzgerald DA

    更新日期:2007-03-01 00:00:00

  • Cystic fibrosis: Priorities and progress for future therapies.

    abstract::Significant improvement in the survival of patients with CF has been achieved in the last decades. The improved clinical status of the patients is mainly the result of a better understanding of the natural course of infection and inflammation in CF that has led to the implementation of strategies that increase the lif...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2017.06.004

    authors: Kerem E

    更新日期:2017-09-01 00:00:00

  • Does newborn screening improve early lung function in cystic fibrosis?

    abstract::Despite evidence showing an improvement in nutritional outcomes following diagnosis by newborn screening (NBS) for cystic fibrosis (CF), the impact on pulmonary outcomes has been less clear. In this review the approaches to measurement of early lung function and knowledge gained from NBS CF cohorts will be described. ...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2020.08.005

    authors: Davies G

    更新日期:2020-08-20 00:00:00

  • Nitric oxide in critical respiratory failure of very low birth weight infants.

    abstract::Inhaled nitric oxide (iNO) is a selective pulmonary vasodilator. In randomised trials, iNO increased gas exchange modestly and had no effect on the outcome (survival, chronic lung disease, CLD) in very low birth-weight (VLBW) infants. NO is an important component of the innate immune system and a lipid- soluble free r...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/s1526-0542(04)90047-4

    authors: Hallman M,Aikio O

    更新日期:2004-01-01 00:00:00

  • CFTR modulator therapy in patients with cystic fibrosis and an organ transplant.

    abstract::CFTR modulators are a class of drugs which directly target the defective CFTR protein in cystic fibrosis (CF), improving its function with resultant clinical improvements. Currently these drugs are confined to people with a limited selection of genetic mutations. New modulators are in development which will lead to th...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2018.04.003

    authors: Mitchell RM,Jones AM,Barry PJ

    更新日期:2018-06-01 00:00:00

  • Thoracic interventional radiology in children.

    abstract::Significant technological advancements have been achieved in radiology with the introduction of a branch speciality known as interventional radiology. Radiology has moved into the therapeutic arena, performing minimally invasive diagnostic and therapeutic procedures. The interventional radiologist can treat certain va...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1053/prrv.2000.0121

    authors: John P

    更新日期:2001-06-01 00:00:00

  • Chronic cough in children.

    abstract::Chronic cough has been variably defined as a cough lasting longer than 3, 4 or 8 weeks. Many post viral or pertussis like illnesses are associated with prolonged coughing that resolves over time. Management involves first trying to make a diagnosis and identify the presence of any underlying condition. Targeted treatm...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2012.05.002

    authors: Shields MD,Doherty GM

    更新日期:2013-06-01 00:00:00

  • Congenital upper airway obstruction.

    abstract::Most causes of upper airway obstruction are rare in the neonatal period and during infancy. They may, however, cause major respiratory problems either initially or during the first few weeks of life. It is important to recognise these problems at an early stage so that appropriate measures to overcome airway obstructi...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2003.10.001

    authors: Dinwiddie R

    更新日期:2004-03-01 00:00:00

  • CFTR2: How will it help care?

    abstract::The Clinical and Functional Translation of CFTR (CFTR2) project presents a novel approach to clinical and functional annotation of mutations identified in disease-causing genes. Phenotype and genotype information on approximately 40,000 cystic fibrosis (CF) patients were collected from registries and large clinics. Th...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章

    doi:10.1016/j.prrv.2013.01.006

    authors: Castellani C,CFTR2 team.

    更新日期:2013-05-01 00:00:00

  • Treatment of interstitial lung disease in children.

    abstract::The treatment of interstitial lung disease in children depends on the nature of the underlying pathology. In approximately 50% of cases a specific aetiology can be found such as: chronic viral infection, an auto-immune process, sarcoidosis or alveolar proteinosis. In the remainder, the process is idiopathic and the pa...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2004.01.004

    authors: Dinwiddie R

    更新日期:2004-06-01 00:00:00

  • Options for assessing and measuring chest wall motion.

    abstract::Assessing chest wall motion is a basic and vital component in managing the child with respiratory problems, whether these are due to pathology in the lungs, airways, chest wall or muscles. Since the 1960s, clinical assessment has been supplemented with an ever-growing range of technological options for measuring chest...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2014.10.006

    authors: Seddon P

    更新日期:2015-01-01 00:00:00