C. Stheneur

发表

[Written asthma action plans: a useful tool for self-management].

R. Gagnayre, C. Feuillet-Dassonval, B. Rossignol, 2005, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case–control study

Pierre Lecomte, A. J. Valleron, Isabelle Guilhem, 2016, BMC Public Health.

Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic FBN1 Mutations

P. Robinson, E. Arbustini, U. Francke, 2009, Pediatrics.

Achondroplasia: from genotype to phenotype.

P. Richette, T. Bardin, C. Stheneur, 2008, Joint, bone, spine : revue du rhumatisme.

Renal injury in pediatric anorexia nervosa: a retrospective study

D. Taddeo, J. Frappier, Anne-Laure Lapeyraque, 2019, Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity.

Renal complications in anorexia nervosa

Anne-Laure Lapeyraque, C. Stheneur, S. Bergeron, 2014, Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity.

Nomograms for aortic root diameters in children using two-dimensional echocardiography.

G. Jondeau, C. Boileau, C. Fermanian, 2010, The American journal of cardiology.

Skeletal evolution in Marfan syndrome: growth curves from a French national cohort

F. Tubach, G. Jondeau, B. Chevallier, 2018, Pediatric Research.

Study of phenotype evolution during childhood in Marfan syndrome to improve clinical recognition

F. Tubach, G. Jondeau, C. Boileau, 2013, Genetics in Medicine.

Congenital heart disease Cardiovascular manifestations in men and women carrying a FBN 1 mutation

P. Robinson, E. Arbustini, U. Francke, 2010 .

A new sporadic case of early-onset Loeys-Dietz syndrome due to the recurrent mutation p.R528C in theTGFBR2 gene substantiates interindividual clinical variability

A. Latos-Bieleńska, A. Paepe, B. Loeys, 2010, Journal of Applied Genetics.

Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype‐phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys‐Dietz syndrome and related disorders

C. Junien, G. Jondeau, M. Claustres, 2008, Human mutation.

Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands

E. Arbustini, U. Francke, D. Halliday, 2008, Journal of Medical Genetics.

A recurrent fibrillin-1 mutation in severe early onset Marfan syndrome

J. Bernstein, G. Arno, S. Odent, 2014, Journal of Pediatric Genetics.

The new Ghent criteria for Marfan syndrome: what do they change?

E. Arbustini, U. Francke, C. Béroud, 2012, Clinical genetics.

Prognosis Factors in Probands With an FBN1 Mutation Diagnosed Before the Age of 1 Year

E. Arbustini, U. Francke, G. Jondeau, 2011, Pediatric Research.

Spinal imaging contributes to the diagnosis of Marfan syndrome.

G. Jondeau, C. Boileau, B. Chevallier, 2010, Joint, bone, spine : revue du rhumatisme.

Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene

G. Jondeau, M. Claustres, G. Collod-Béroud, 2009, European Journal of Human Genetics.

[Marfan syndrome: diagnostic criteria and molecular biology contribution].

B. Chevallier, C. Stheneur, B. Oberkampf, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Medication in AN: A Multidisciplinary Overview of Meta-Analyses and Systematic Reviews

P. Gérardin, S. Guillaume, S. Iceta, 2019, Journal of clinical medicine.

Anorexia nervosa in adolescents: evolution of weight history and impact of excess premorbid weight

D. Taddeo, J. Frappier, C. Stheneur, 2018, European Journal of Pediatrics.

85. Patients with Somatic Symptoms and Related Disorders in a Tertiary Care Pediatric Hospital Center… Clinician’s Experience

D. Taddeo, J. Frappier, P. Jacquin, 2020 .

Hormonal Contraception Effects On Pulmonary Function In Adolescents With Cystic Fibrosis.

D. Taddeo, J. Frappier, C. Stheneur, 2020, Journal of pediatric and adolescent gynecology.

Identification of 23 TGFBR 2 and 6 TGFBR 1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II , Loeys-Dietz syndrome and related disorders

C. Junien, G. Jondeau, M. Claustres, 2019 .

The Bulle: Support and Prevention of Psychological Decompensation of Health Care Workers During the Trauma of the COVID-19 Epidemic

M. Moro, P. Chaste, É. Tordjman, 2020, Journal of Pain and Symptom Management.

Depressive symptoms among teenagers in the emergency department: prevalence estimate and concordance with parental perceptions

I. Ghout, M. Speranza, B. Chevallier, 2013, European Journal of Pediatrics.

Human Papillomavirus vaccination in general practice in France, three years after the implementation of a targeted vaccine recommendation based on age and sexual history

D. Levy-bruhl, S. Kernéis, T. Hanslik, 2016, Human vaccines & immunotherapeutics.

Personality heterogeneity in adolescents with anorexia nervosa: a factor-mixture analysis

D. Taddeo, J. Frappier, C. Bégin, 2023, Current Psychology.

Validation of the “Good2Go”: the first French-language transition readiness questionnaire

P. Jacquin, N. Tubiana-Rufi, N. Trelles, 2019, European Journal of Pediatrics.

[Perception of adolescent medicine among French pediatric residents].

B. Boudailliez, P. Jacquin, C. Stheneur, 2016, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Iron metabolism in patients with anorexia nervosa: elevated serum hepcidin concentrations in the absence of inflammation.

C. Beaumont, H. Puy, B. Chevallier, 2012, The American journal of clinical nutrition.

Somatic outcome among patients hospitalised for anorexia nervosa in adolescence: disorders reported and links with global outcome

N. Godart, C. Stheneur, C. Blanchet, 2013, Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity.

Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.

P. Awadalla, Christoph Preuss, G. Andelfinger, 2016, The Canadian journal of cardiology.

Comparison of Clinical Presentations and Outcomes Between Patients With TGFBR2 and FBN1 Mutations in Marfan Syndrome and Related Disorders

P. Ravaud, C. Béroud, G. Jondeau, 2009, Circulation.

Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: Further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterion

E. Arbustini, U. Francke, C. Béroud, 2009, American journal of medical genetics. Part A.

Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24–32 mutation

E. Arbustini, U. Francke, C. Béroud, 2009, European Journal of Human Genetics.

In malnourished adolescent with anorexia nervosa, Cockroft-Gault formula is the most relevant formula to estimate renal function.

D. Taddeo, J. Frappier, Anne-Laure Lapeyraque, 2020, Clinical nutrition.

[Cannabinoid hyperemesis syndrome: A review of the literature].

C. Stheneur, N. Desjardins, 2016, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

To Improve the Initial Inpatient Management of Adolescents Admitted with Severe Anorexia Nervosa: A Narrative Review and a Convenient Protocol

M. Métras, D. Taddeo, J. Frappier, 2022, Nutrients.

[What Are the Individual, Family, and Social Characteristics Differentiating Prepubertal from Pubertal Anorexia Nervosa?]

G. Bravo, D. Taddeo, J. Frappier, 2017, Canadian journal of psychiatry. Revue canadienne de psychiatrie.

Excessive laboratory monitoring to prevent adolescent’s refeeding syndrome: opportunities for enhancement

D. Taddeo, J. Frappier, C. Stheneur, 2019, Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity.

[Rapid malnutrition in patient with anorexia nervosa: experience of a general pediatric department].

B. Chevallier, M. Sznajder, C. Stheneur, 2010, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 allele.

M. Gross, G. Jondeau, L. Gouya, 2015, Human molecular genetics.

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability

T. Bourgeron, E. Génin, M. Gross, 2018, European Journal of Human Genetics.

Initial inpatient management of adolescents and young adults admitted with severe malnutrition due to anorexia nervosa: protocol for a systematic review

D. Taddeo, J. Frappier, C. Stheneur, 2021, Journal of eating disorders.

Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndrome.

J. Ruidavets, J. Ferrières, G. Jondeau, 2019, Archives of cardiovascular diseases.

[Diagnostic value of the SHAPE questionnaire in recognition of the hyperventilation syndrome in children: a pilot study].

C. Fermanian, B. Chevallier, M. Sznajder, 2009, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Sleep duration, quality of life and depression in adolescents: a school-based survey.

I. Ghout, C. Stheneur, G. Benoist, 2019, Minerva pediatrica.

Faecal calprotectin: Marker of intestinal inflammatory process in anorexia nervosa? A preliminary study.

C. Faure, D. Taddeo, J. Frappier, 2023, European eating disorders review : the journal of the Eating Disorders Association.

Cannabinoid Hyperemesis Syndrome in a 17-Year-Old Adolescent.

D. Taddeo, C. Stheneur, O. Jamoulle, 2015, The Journal of adolescent health : official publication of the Society for Adolescent Medicine.

[Acute gastric dilatation with superior mesenteric artery syndrome in a young girl with anorexia nervosa].

D. Pariente, C. Stheneur, C. Rey, 1995, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Impact of somatic severity on long-term mortality in anorexia nervosa

N. Godart, C. Stheneur, Aminata Ali, 2017, Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity.

Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN 1 mutations

P. Robinson, D. Halliday, C. Béroud, 2019 .

Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case–control study

V. Rigalleau, A. Valleron, Jacques Cohen, 2016, bioRxiv.