S. Baron

发表

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.

Effects of advanced carbohydrate counting on glucose control and quality of life in children with type 1 diabetes

E. Bismuth, P. Barat, N. Bendelac, 2020, Pediatric diabetes.

Sex chromosome aneuploidies and copy-number variants: a further explanation for neurodevelopmental prognosis variability?

B. Gilbert-Dussardier, C. Rooryck, C. Bénéteau, 2017, European Journal of Human Genetics.

Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boys.

C. Bouvattier, S. Cabrol, Y. Morel, 2012, European journal of endocrinology.

Deletion of the CUL4B gene in a boy with mental retardation, minor facial anomalies, short stature, hypogonadism, and ataxia

C. Le Caignec, B. Isidor, O. Pichon, 2010, American journal of medical genetics. Part A.

Axial spondylometaphyseal dysplasia: Confirmation and further delineation of a new SMD with retinal dystrophy

B. Isidor, A. David, M. le Merrer, 2010, American journal of medical genetics. Part A.

46,XY gonadal dysgenesis: Evidence for autosomal dominant transmission in a large kindred

K. McElreavey, C. Le Caignec, A. David, 2003, American journal of medical genetics. Part A.

Growth patterns of patients with Noonan syndrome: correlation with age and genotype.

H. Cavé, A. Verloes, D. Lacombe, 2016, European journal of endocrinology.

Constitutional telomeric association (Y;7) in a patient with a female phenotype

C. Bénéteau, C. Le Caignec, A. David, 2013, American journal of medical genetics. Part A.

Cone‐rod dystrophy, growth hormone deficiency and spondyloepiphyseal dysplasia: Report of a new case without nephronophtisis

B. Isidor, A. David, M. le Merrer, 2009, American journal of medical genetics. Part A.

46,XY pure gonadal dysgenesis: clinical presentations and management of the tumor risk.

A. David, M. Leclair, Y. Heloury, 2011, Journal of pediatric urology.

Familial frameshift SRY mutation inherited from a mosaic father with testicular dysgenesis syndrome.

C. Le Caignec, B. Isidor, C. Sultan, 2009, The Journal of clinical endocrinology and metabolism.

Should 45,X/46,XY boys with no or mild anomaly of external genitalia be investigated and followed up?

B. Donadille, C. Bouvattier, S. Christin‐Maitre, 2018, European journal of endocrinology.

Adrenal rest tissue in gonads of patients with classical congenital adrenal hyperplasia: multicenter study of 45 French male patients.

P. Lecomte, V. Tardy, Y. Morel, 2012, Annales d'endocrinologie.

Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature review

B. Isidor, A. Dieux, V. Cormier-Daire, 2019, Clinical genetics.

GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.

Juan Pedro López, F. Cerutti, O. Kordonouri, 2012, The New England journal of medicine.

Clinical utility gene card for: Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD)

S. Bézieau, J. Albuisson, S. Schmitt, 2012, European Journal of Human Genetics.

Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric population.

K. Busiah, J. Salles, J. Bacchetta, 2020, European journal of endocrinology.

High Diagnostic Yield of Targeted Next-Generation Sequencing in a Cohort of Patients With Congenital Hypothyroidism Due to Dyshormonogenesis

M. Polak, S. Hanein, G. Pinto, 2021, Frontiers in Endocrinology.

Hyperglycaemic hyperosmolar state and cerebral thrombophlebitis in paediatrics: A case report

S. Baron, B. Lauzier, M. Denis, 2023, Endocrinology, diabetes & metabolism.

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.

Estradiol Testing in the Exploration of Early Onset Puberty: Comparison of RIA and Chemiluminescence Immunoassay

D. Masson, S. Baron, N. Graveline, 2023, Annals of laboratory medicine.

Growth patterns of patients with Noonan syndrome: correlation with age and genotype.

H. Cavé, A. Verloes, D. Lacombe, 2016, European journal of endocrinology.

Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern

M. Polak, S. Amselem, P. Crock, 2016 .

GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.

Juan Pedro López, F. Cerutti, O. Kordonouri, 2012, The New England journal of medicine.

[Endocrine side effects of radiation therapy: Diagnosis, prevention, and treatment].

S. Supiot, S. Supiot, S. Baron, 2022, Cancer radiotherapie : journal de la Societe francaise de radiotherapie oncologique.

46,XY pure gonadal dysgenesis: clinical presentations and management of the tumor risk.

A. David, M. Leclair, Y. Heloury, 2011, Journal of pediatric urology.