Skip to main content

Main menu

  • Home
  • Current issue
  • ERJ Early View
  • Past issues
  • Authors/reviewers
    • Instructions for authors
    • Submit a manuscript
    • Open access
    • COVID-19 submission information
    • Peer reviewer login
  • Alerts
  • Podcasts
  • Subscriptions
  • ERS Publications
    • European Respiratory Journal
    • ERJ Open Research
    • European Respiratory Review
    • Breathe
    • ERS Books
    • ERS publications home

User menu

  • Log in
  • Subscribe
  • Contact Us
  • My Cart
  • Log out

Search

  • Advanced search
  • ERS Publications
    • European Respiratory Journal
    • ERJ Open Research
    • European Respiratory Review
    • Breathe
    • ERS Books
    • ERS publications home

Login

European Respiratory Society

Advanced Search

  • Home
  • Current issue
  • ERJ Early View
  • Past issues
  • Authors/reviewers
    • Instructions for authors
    • Submit a manuscript
    • Open access
    • COVID-19 submission information
    • Peer reviewer login
  • Alerts
  • Podcasts
  • Subscriptions

Lung and thorax development during adolescence: relationship with pubertal status

V. Nève, F. Girard, A. Flahault, M. Boulé
European Respiratory Journal 2002 20: 1292-1298; DOI: 10.1183/09031936.02.00208102
V. Nève
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
F. Girard
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
A. Flahault
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
M. Boulé
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Abstract

The aim of the present study was to define reference values for lung volumes and the lung transfer factor for carbon monoxide (TL,CO) for an adolescent population using thoracic volume index (TVI) and an index of pubertal stage in order to account for the variation in growth pattern between adolescents.

TVI, pubertal stage by Tanner scale (PST), time since menarche, functional residual capacity measured using the helium­dilution technique, vital capacity, total lung capacity and TL,CO measured using a steady­state method were determined in 51 males (aged 13–20 yrs; PST T3–T5) and 52 females (aged 13–18 yrs; PST T2–T4; all but three had already undergone menarche).

In male adolescents, height, weight, TVI, lung volumes and TL,CO increased with age. This was not the case in female adolescents. In males, the TVI was the independent variable that best correlated with pulmonary volumes. In females, height was the independent variable that best correlated with pulmonary volumes. In both sexes, the variable that best correlated with TL,CO was PST, associated with height in males.

This cross­sectional study provides prediction equations for lung volumes and the lung transfer factor for carbon monoxide taking into account thoracic volume index and pubertal stage. It shows that, in adolescent males, lung and thoracic development occurs during and until the end of puberty. Conversely, in adolescent females, lung development is almost finished following menarche.

  • adolescence
  • diffusing capacity
  • lung growth
  • reference values
  • thoracic volume index

Many studies have described the increase in forced expiratory flows occurring during adolescence but little is known about the increase in thoracic measurements, lung volumes and lung transfer factor for carbon monoxide (TL,CO).

It is known that lung function increases linearly with age and height until the adolescent growth spurt at ∼10 yrs in females and ∼12 yrs in males 1, 2. At adolescence, lung function no longer increases proportionally to height but rather follows a more complex pattern. Initially, trunk length lags behind leg length temporally; then the lung grows in diameter followed by length 3; and, finally, lung volumes continue to increase after adult height has been reached due to prolonged increase in muscle strength 4–6. Therefore, lung function increases proportionally to trunk and chest dimension rather than to height 7. In addition, the timing of the events of puberty differs dependent on sex, and individual development may deviate considerably from that suggested by the average growth profile 8.

The sudden change in spirometric lung function seen in males and females appears to coincide with the pubertal growth spurt observed in the Tanner chart 9. To account for the variation in growth pattern between adolescents in reference equations, in addition to height, a measure of pubertal status and an estimation of thoracic volume should be incorporated. This would allow for the fact that the growth of the lungs lag behind that of the legs and height 8, 10, 11.

Extrapolation of reference values from children to an adolescent population cannot be used to predict lung volumes and TL,CO. Therefore, summary equations and limits of normal values need to be determined for use in current clinical practice.

Therefore, the aim of the present study was to derive prediction equations for lung volumes and TL,CO for adolescent males and females using refined anthropometric measurements allowing determination of thoracic growth (such as thoracic volume index (TVI)) and an index of growth stage (pubertal stage).

Subjects and methods

Subjects

Having obtained the authorisation of the Department of Education (Versaille, France) to ask all pupils attending two levels of a secondary school (fourth and sixth year) in Paris, France, to participate in the study, 103 pupils (51 males and 52 females) gave their oral consent and were included. Written parental consent was also obtained.

Lung examination and spirometric results were normal on the day of the pulmonary function tests.

Methods

Anthropometric data

Height was determined to the nearest 5 mm and weight to the nearest 500 g. In order to determine TVI (mL), the anteroposterior diameter at the sternal angle (AP2), biacromial diameter (BA), sternal length (SL), anteroposterior diameter at the xiphisternal junction (APx) and transthoracic diameter (TT) were measured during the resting end­tidal phase of respiration using a pelvimetry calliper. The TVI was calculated using the following formula: AP2×TT×SL 10.

Pubertal status

Pubertal status, based on the five­point rating scale (T1–T5) of Tanner 9, was assessed for males and females by an endocrinologist. The qualitative Tanner score was converted into a quantitative variable (pubertal stage by Tanner scale (PST)): T1: 0; T2: 0; T3: 1; T4: 2; and T5: 3. In addition, in females, the time since menarche was evaluated and categorised as follows: 0: menarche had not yet occurred; 1: <2 yrs since menarche; 2: 2–4 yrs since menarche; and 3: >4 yrs since menarche.

Pulmonary function tests

Spirometric measurements included vital capacity (VC), functional residual capacity (FRC), measured using the helium dilution technique, residual volume (RV), obtained by subtracting expiratory reserve from FRC, and total lung capacity (TLC), calculated from VC plus RV. TL,CO was measured using a steady­state method 12. The same person made all the measurements according to the recommendations of the European Respiratory Society 13 with the subject seated in an upright posture and wearing a nose clip.

Statistical analysis

Pulmonary function test results and anthropometric data were analysed separately for males and females. The means of the anthropometric data from males and females were compared by unpaired t‐test. The Pearson correlation coefficient (rP) was used to compare pulmonary function test and anthropometric data. A p‐value of <0.05 was considered significant 14.

In order to determine whether or not logarithmic transformation was required, the variance of the pulmonary function data was determined 15: males and females were divided into groups on the basis of 3‐cm height intervals. The mean and sd of the pulmonary function test results for each group were plotted against each other. Correlation was evaluated using the Spearman correlation coefficient (rS) as only 10 height groups were obtained 14. When sd did not increase with mean (rs>0.05), constant variance was assumed and no transformation was performed before multiple regression. When sd increased with mean, increased scatter with height was assumed and logarithmic transformation of the data was performed. After having checked that this transformation had stabilised the variance, multiple regression of the log­transformed pulmonary function test data was performed.

Multiple regression of pulmonary function parameters or log­transformed pulmonary function parameters on anthropometric data was then performed. Height was chosen in the first step 16, except in the female group when TL,CO was the dependent variable as no correlation between height and TL,CO was found. Other independent variables were included by decreasing partial rP until no further increase in R2 adjusted for the increase in the number of independent variables included in the equation (Embedded Image) was obtained 14.

Results

Anthropometric data

Mean male age (16 yrs, range 13–20 yrs) was not significantly different from mean female age (16 yrs, range 13–18 yrs, p=0.22). Males were taller (172 cm, range 150–184 cm versus 163 cm, range 147–176 cm, p<0.0001) and heavier (61 kg, range 42–84 kg versus 53 kg, range 39–68 kg, p<0.0001) than females.

In males, height and weight increased with age (rP=0.45, p<0.01 and rP=0.42, p<0.01, respectively); the height increase reached a plateau at 16–17 yrs.

Conversely, in females, neither height nor weight increased with age (rP=0.025, ns and rP=0.05, ns, respectively).

Thoracic measurements (mean±sd and range) in males and females are reported in table 1⇓. The mean thoracic measurements of males were greater than those of females, except SL, which was significantly longer in females.

View this table:
  • View inline
  • View popup
Table 1—

Thoracic measurements in adolescent males and females

The correlation of thoracic measurements with anthropometric data is reported in table 2⇓. In males, TVI, BA and AP2 increased with age and continued to increase when height had reached a plateau. APx and SL did not increase with age. In females, neither TVI nor thoracic measurement increased with age.

View this table:
  • View inline
  • View popup
Table 2—

Partial Pearson correlation coefficients for thoracic measurements and anthropometric data in adolescent males and females

Pubertal status

No males were prepubescent (T1), 11 were in early puberty (all T3) and most in late puberty (15 in T4 and 24 in T5). No females were prepubescent, most were in early puberty (two in T2 and 20 in T3) and nine in late puberty (all T4). These Tanner scores were converted into PST as described in the Methods section. Nine of the females were in menarcheal category 1, 14 in category 2 and 12 in category 3.

Pulmonary function tests

Partial Pearson correlation coefficients (rP) between pulmonary function test parameters and anthropometric data are reported in tables 3 and 4⇓⇓. In females, height (H) was the independent variable that best correlated with pulmonary volumes: TLC=0.08H−7.78, rp=0.69, R2=0.48, p=3×10−7; VC=0.06H−5.41, rp=0.71, R2=0.50, p=1×10−7; and FRC=0.04H−5, rp=0.57, R2=0.32, p=4×10−5.

View this table:
  • View inline
  • View popup
Table 3—

Partial Pearson correlation coefficients (rP) and regression equations for pulmonary function parameters with anthropometric data in adolescent females

View this table:
  • View inline
  • View popup
Table 4—

Partial Pearson correlation coefficients (rP) and regression equations for pulmonary function parameters with anthropometric data in adolescent males

In males, TVI was the independent variable that best correlated with pulmonary volumes: TLC=0.0006TVI+1.2, rp=0.77, R2=0.59, p=1×10−7; VC=0.0006TVI+1.16, rp=0.75, R2=0.56, p=2×10−7; and FRC=0.0004TVI+0.36, rp=0.66, R2=0.44, p=2×10−5.

In both sexes, the variable that best correlated with TL,CO was PST, associated to height in males. In females, TL,CO=3.643PST+11.587, rp=0.50, R2=0.25, p=0.015. In males, TL,CO=4.59PST+14.96, rp=0.61, R2=0.37, p=3×10−5; and TL,CO=0.45H−52.68, rp=0.58, R2=0.34, p=1×10−4.

Variance of pulmonary function test data

In males, the sd of FRC, VC and TLC within a 3‐cm height group did not increase with mean (rS=−0.018, 0.57 and 0.24, respectively, all p>0.05). In females, the sd of TL,CO, VC and TLC within a 3‐cm height group did not increase with mean (rS=−0.066, p>0.05 for TL,CO; rS=0.40, p>0.05 for VC; and rS=0.62, p>0.05 for TLC). Therefore constant variance could be assumed and FRC, VC and TLC in males and TL,CO, VC and TLC in females were regressed with anthropometric data.

Conversely, in males, the sd of TL,CO within a 3‐cm height group increased with mean (rS=0.72, p<0.05) and the intercept did not differ from zero (p=0.28). Natural log transformation stabilised variance (rS=0.224, p>0.05). In females, the sd of FRC within a 3‐cm height group increased with mean (rS=0.81, p<0.05) and could be assumed to be proportional to the mean as the intercept of the regression line did not differ significantly from zero (p=0.06). Natural log transformation stabilised variance (rS=0.51, p>0.05). For FRC in females and TL,CO in males, a similar R2 was obtained by fitting by a power or exponential function to the data. Therefore, it was decided to perform simple log transformation and regress natural log­transformed TL,CO on height in males and natural log FRC on height in females.

Multiple regression equation

The rank order in which independent variables were included in the equation and their contribution to the explained variance (Embedded Image) are listed in tables 5 and 6⇓⇓. In males, height and then TVI were included in the multiple regression equation for lung volumes (FRC, TLC and VC). PST was also included in the multiple regression equation for VC and TLC. Height and then PST were included in the regression equation for TL,CO. In females, height and then time since menarche were included in the multiple regression equation for FRC, and height and then TVI in the regression equation for TLC and VC. PST was the only independent variable included in the regression equation for TL,CO as it was the only one that correlated to TL,CO, with height in males. As a general rule, Embedded Image were higher in males than in females.

View this table:
  • View inline
  • View popup
Table 5—

Multiple regression equations for adolescent males

View this table:
  • View inline
  • View popup
Table 6—

Multiple regression equations for adolescent females

Limits of normal

The mean and sd of the residuals (differences between actual and predicted value) for each adolescent are presented in tables 5 and 6⇑⇑. They are expressed as a ratio of lung function to predicted lung function. They range 9–17% pred in males and 10–17% pred in females.

Discussion

The present study provides reference values for TVI, lung volumes and TL,CO for adolescent males and females. No other reports on normal values of TVI and thoracic measurements in an adolescent population could be located. Besides its importance in providing normal values for thoracic mensurations in adolescents for height and age, these reference values could be of help in quantifying the chest wall sequelae of treatments, such as radiotherapy, and the decrease in chest wall volume due to decrease in muscle strength in neuromuscular disease. In addition, this study has the advantage of providing reference values for lung volumes and TL,CO using equations that take height as well as TVI and pubertal stage into consideration, an approach allowing variation in growth pattern between adolescents to be taken into account 8, 11.

Data were obtained from a group of males aged 13–20 yrs whose PST ranged T3–T5 and a group of females aged 13–18 yrs whose PST ranged T2–T4. All but three of the females had undergone menarche. Analysis of the distribution of the subjects within the Tanner rating scales shows that males and females in prepubertal or early pubertal stage (T1 and T2 in males and T1 in females) were lacking, and most females were investigated following menarche. Although the mean ages of the males and females were comparable and the group of males slightly more mature, height, weight, TVI and pulmonary function test measurements in the males continued to increase with age, whereas those in the females did not. These data, although cross­sectional, suggest that, in the present group of males, lung and thoracic development was still occurring, whereas it was almost complete in the females. This is in agreement with the data of Lebowitz and Sherrill 3 showing that, in males, lung and thoracic development is observed during and until the end of puberty. Conversely, in females, lung development occurs over a shorter period of time and earlier in the pubertal process. In addition, the present data show that, in females, lung development is almost complete after menarche.

Analysis of the variance of the pulmonary function test data showed that the variance of TL,CO in males and FRC in females increased with the mean, i.e. the scatter increased in proportion to the predicted value. This heteroscedasticity is frequently observed in the paediatric age range 16. Logarithmic transformations stabilised the variance as anticipated. Conversely, the variance of all other pulmonary function test data did not increase with the mean. This can be explained by the fact that the present sample included a limited range of ages and heights.

In females, the anthropometric parameter best correlated with pulmonary volumes was height. In males, this was the TVI. In both sexes, PST was the anthropometric parameter that best correlated with TL,CO, followed by height in males. Multiple regression equations were therefore determined, entering as independent variable height, TVI, pubertal stage for lung volumes, and height and PST for TL,CO.

Compared with the data of Cook and Hamann 17, suggested for use in the age range 5–18 yrs for gas dilution methods 16, the present equation predicts comparable values for TLC in males and females but slightly lower FRC and RV.

Compared with the equations of regression of FRC, VC and TL,CO with height that have been defined previously in the present authors' laboratory in younger children using the same techniques 12, 18–20, a smooth transition from the equation of younger children to that of adolescents is observed for all lung volumes (FRC, VC and TLC) as a function of height in females and only for FRC in males. In males, the transition is less perfect for VC, TLC and TL,CO as a function of height as the slope increases during adolescence. This marked acceleration in the development of lung volumes, such as VC and TLC, during puberty in males compared to their linear increase from childhood to puberty in females can be related to differences in the development of muscle strength between the sexes. Indeed, muscle strength increases linearly with chronological age from early childhood to ∼13–14 yrs in males, when there is a marked acceleration in strength development until age 20 yrs. In females, muscular strength improves linearly with age until 15 yrs, which is then followed by a tendency to level off 21. Concerning TL,CO, a marked acceleration in the development of TL,CO during puberty is observed more strongly in males than in females and could be related to the adolescence growth spurt of the heart and lung, which become bigger not only in absolute terms but also in relation to body size, whereas a considerable increase in blood haemoglobin concentration provides greater capacity for carrying oxygen 22. In females, as no correlation was observed between TL,CO and height, the prediction equations for the TL,CO of adolescents could not be compared to the children's one.

TVI and pubertal stage were included in the prediction equations in order to maximise the variance explained by the model (Embedded Image). As a general rule, Embedded Image were higher in males than in females. The efficiency of TVI and pubertal stage in increasing Embedded Image depends on sex and the dependent variable studied (lung volumes or TL,CO).

Considering the effect of sex on the prediction equations for lung volumes, as the females in the present study had probably completed most of their lung growth, factors supposed to explain lung growth and increase Embedded Image, such as pubertal stage or TVI, were less efficient 2 in that group. Conversely, Embedded Image were higher in males even though early pubertal stages were not represented due to the fact that lung growth occurs later in puberty in males and the time lag between height and lung growth was still present.

In both sexes, the variable that best predicted TL,CO was PST, associated with height in males. The importance of using an index of maturity when describing the increase in TL,CO in males and females may, in part, be ascribed to the delayed development of cardiac function during the pubertal process compared to the development of lung volumes. Indeed, Seely et al. 6 showed that sex difference in cardiac output develops late in the pubertal process, i.e. age 14 yrs in females and age 16 yrs in males.

In conclusion, the present study provides reference values for thoracic measurements, thoracic volume index, lung volumes (such as vital capacity, functional residual capacity and total lung capacity) and pulmonary diffusing capacity in a group of males aged 13–20 yrs and a group of females aged 13–18 yrs. To date, no reference values of thoracic mensurations in adolescents have been published. The present data provide normal values for thoracic mensurations in adolescents for height and age that could be of help in quantifying the chest wall sequelae of treatments and the decrease in chest wall volume due to decrease in muscle strength in neuromuscular disease. In addition, this study has the advantage of providing reference values for lung volumes and diffusing capacity using equations which take into consideration, height, thoracic volume index and pubertal stage, an approach allowing for the variation in growth pattern between adolescents to be taken into account. Finally, the present data, although cross­sectional, confirm that, in males, lung and thoracic development is observed during and until the end of puberty. They also confirm that, in females, lung growth is of short duration and occurs early in the pubertal process and show that lung development is almost finished after menarche.

  • Received January 29, 2001.
  • Accepted June 9, 2002.
  • © ERS Journals Ltd

References

  1. ↵
    Wang X, Dockery DW, Wypij D, Fay ME, Ferris BG. Pulmonary function between 6 and 18 years of age. Pediatr Pulmonol 1993;15:75–88.
    OpenUrlCrossRefPubMedWeb of Science
  2. ↵
    Sherrill DL, Camilli A, Lebowitz MD. On the temporal relationships between lung function and somatic growth. Am Rev Respir Dis 1989;140:638–644.
    OpenUrlCrossRefPubMedWeb of Science
  3. ↵
    Lebowitz MD, Sherrill DL. The assessment and interpretation of spirometry during the transition from childhood to adulthood. Pediatr Pulmonol 1995;19:143–149.
    OpenUrlPubMedWeb of Science
  4. ↵
    Underwood LE, Van Wyk JJ. Normal and aberrant growth In: Wilson JD, Foster DW, editors. Williams Textbook of Endocrinology. 8th EdnPhiladelphia, PA, WB Saunders Company, 1992; pp. 1079–1138.
  5. Shrader PC, Quanjer PhH, Olievier ICW. Respiratory muscle force and ventilatory function in adolescents. Eur Respir J 1988;1:368–375.
    OpenUrlAbstract/FREE Full Text
  6. ↵
    Seely JE, Guzman CA, Becklake MR. Heart and lung function at rest and during exercise in adolescence. J Appl Physiol 1974;36:34–40.
    OpenUrlFREE Full Text
  7. ↵
    Dockery DW, Speizer FE, Ware JH, Ferris BG. Growth of pulmonary function between 6 and 18 years of age. Am Rev Respir Dis 1987;187:135.
    OpenUrl
  8. ↵
    Borsboom GJJM, van Pelt W, Quanjer PH. Interindividual variation in pubertal growth patterns of ventilatory function, standing height, and weight. Am J Respir Crit Care Med 1996;153:1182–1186.
    OpenUrlPubMedWeb of Science
  9. ↵
    Tanner JM. Growth at Adolescence. 2nd ednOxford, Blackwell Scientific, 1962.
  10. ↵
    Howatt WF, DeMuth GR. Configuration of the chest. Paediatrics 1965;35:177–184.
    OpenUrlAbstract/FREE Full Text
  11. ↵
    Rosenthal M, Bain SH, Cramer D, et al. Lung function in white children aged 4 to 19 years: I – Spirometry. Thorax 1993;48:794–802.
    OpenUrlAbstract/FREE Full Text
  12. ↵
    Chaussain M, Denjean A, Lebeau C, De Lattre J, Badoual J. Lung transfer factor for CO at rest in normal children by a steady state method. Bull Eur Physiopathol Respir 1982;18:411–417.
    OpenUrlPubMedWeb of Science
  13. ↵
    Quanjer PhH, Tammeling GJ, Cotes JE, Pederson OF, Peslin R, Yernault JC. Lung volumes and forced ventilatory flows. Report Working Party “Standardization of Lung Function Tests”, European Community for Steel and Coal. Official Statement of the European Respiratory Society. Eur Respir J 1993;6:Suppl. 16, 5–40.
    OpenUrlFREE Full Text
  14. ↵
    Armitage P, Berry G. Statistical Methods in Medical Research. 3rd ednOxford, Blackwell Science, 1994.
  15. ↵
    Chinn S, Rona RJ. Height and age adjustment for cross sectional studies of lung function in children aged 6–11 years. Thorax 1992;47:707–714.
    OpenUrlAbstract/FREE Full Text
  16. ↵
    Stocks J, Quanjer PhH. Reference values for residual volume, functional residual capacity and total lung capacity. ATS Workshop on Lung Volume Measurements. Official Statement of the European Respiratory Society. Eur Respir J 1995;8:492–506.
    OpenUrlCrossRefPubMedWeb of Science
  17. ↵
    Cook CD, Hamann JF. Relation of lung volumes to height in healthy persons between the ages of 5 and 38 years. J Pediatr 1961;59:710–714.
    OpenUrlCrossRefPubMedWeb of Science
  18. ↵
    Gaultier C, Boulé M, Allaire Y, Clément A, Girard F. Growth of lung volumes during the first three years of life. Bull Eur Physiopathol Respir 1979;15:1103–1116.
    OpenUrlPubMedWeb of Science
  19. Taussig LM, Harris TR, Lebowitz MD. Lung function in infants and young children. Am Rev Respir Dis 1977;116:233–239.
    OpenUrlPubMedWeb of Science
  20. ↵
    Boulé M, Gaultier C, Girard F. Lung transfer for carbon monoxide during the first three years of life. Bull Eur Physiopathol Respir 1986;22:467–471.
    OpenUrlPubMedWeb of Science
  21. ↵
    Malina RM. Growth of muscle tissue and muscle mass In: Falkner F, Tanner JM, editors. Human Growth. Volume 2. Postnatal GrowthLondon, Baillière Tindall, 1978; pp. 273–294.
  22. ↵
    Marshall WA. Puberty In: Falkner F, Tanner JM, editors. Human Growth. Volume 2. Postnatal GrowthLondon, Baillière Tindall, 1978; pp. 141–181.
View Abstract
PreviousNext
Back to top
View this article with LENS
Vol 20 Issue 5 Table of Contents
  • Table of Contents
  • Index by author
Email

Thank you for your interest in spreading the word on European Respiratory Society .

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Lung and thorax development during adolescence: relationship with pubertal status
(Your Name) has sent you a message from European Respiratory Society
(Your Name) thought you would like to see the European Respiratory Society web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
Citation Tools
Lung and thorax development during adolescence: relationship with pubertal status
V. Nève, F. Girard, A. Flahault, M. Boulé
European Respiratory Journal Nov 2002, 20 (5) 1292-1298; DOI: 10.1183/09031936.02.00208102

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero

Share
Lung and thorax development during adolescence: relationship with pubertal status
V. Nève, F. Girard, A. Flahault, M. Boulé
European Respiratory Journal Nov 2002, 20 (5) 1292-1298; DOI: 10.1183/09031936.02.00208102
del.icio.us logo Digg logo Reddit logo Technorati logo Twitter logo CiteULike logo Connotea logo Facebook logo Google logo Mendeley logo
Full Text (PDF)

Jump To

  • Article
    • Abstract
    • Subjects and methods
    • Results
    • Discussion
    • References
  • Figures & Data
  • Info & Metrics
  • PDF
  • Tweet Widget
  • Facebook Like
  • Google Plus One

More in this TOC Section

  • Sequential genotyping of Pseudomonas aeruginosa from upper and lower airways of cystic fibrosis patients
  • RSV bronchiolitis and risk of wheeze and allergic sensitisation in the first year of life
  • Surfactant in children with malignancies, immunosuppression, fever and pulmonary infiltrates
Show more Original Articles: Paediatrics

Related Articles

Navigate

  • Home
  • Current issue
  • Archive

About the ERJ

  • Journal information
  • Editorial board
  • Reviewers
  • Press
  • Permissions and reprints
  • Advertising

The European Respiratory Society

  • Society home
  • myERS
  • Privacy policy
  • Accessibility

ERS publications

  • European Respiratory Journal
  • ERJ Open Research
  • European Respiratory Review
  • Breathe
  • ERS books online
  • ERS Bookshop

Help

  • Feedback

For authors

  • Instructions for authors
  • Publication ethics and malpractice
  • Submit a manuscript

For readers

  • Alerts
  • Subjects
  • Podcasts
  • RSS

Subscriptions

  • Accessing the ERS publications

Contact us

European Respiratory Society
442 Glossop Road
Sheffield S10 2PX
United Kingdom
Tel: +44 114 2672860
Email: journals@ersnet.org

ISSN

Print ISSN:  0903-1936
Online ISSN: 1399-3003

Copyright © 2023 by the European Respiratory Society