M. de Kerdanet

发表

Growth hormone treatment before the age of 4 years prevents short stature in young girls with Turner syndrome.

J. Carel, J. Chaussain, S. Cabrol, 2011, European journal of endocrinology.

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.

Resistance to leptin-replacement therapy in Berardinelli-Seip congenital lipodystrophy: an immunological origin.

G. Sebag, P. Gressens, M. Polak, 2010, European journal of endocrinology.

Ovarian Hyperandrogenism and Response to Gonadotropin-releasing Hormone Analogues in Primary Severe Insulin Resistance

S. O’Rahilly, M. Jimenez-Linan, Julie Harris, 2021, The Journal of clinical endocrinology and metabolism.

Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy

S. O’Rahilly, M. Lathrop, A. Mégarbané, 2002, Journal of medical genetics.

Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism.

B. Frémont, J. Capeau, M. Bonnaure-Mallet, 2015, Diabetes & metabolism.

Metabolic dysfunction in late-puberty adolescent girls with type 1 diabetes: relationship to physical activity and dietary intakes.

F. Gamelin, P. Delamarche, P. Berthon, 2012, Diabetes & metabolism.

Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)

B. Donadille, C. Vigouroux, B. Eymard, 2022, Orphanet Journal of Rare Diseases.

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.

C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients

L. Pasquier, D. Bonneau, B. Degos, 2010, Clinical genetics.

[Ketoacidosis at time of diagnosis of type 1 diabetes in children and adolescents: effect of a national prevention campaign].

C. Levy-marchal, C. Elie, C. Choleau, 2015, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Ketoacidosis at diagnosis of type 1 diabetes in French children and adolescents.

C. Levy-marchal, C. Elie, C. Choleau, 2014, Diabetes & Metabolism.

Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.

M. Polak, A. Grüters, Z. Hochberg, 2011, The Journal of clinical endocrinology and metabolism.

Impact of OMNIPOD® on the quality of life of adolescents with type 1 diabetes.

E. Nivet, M. de Kerdanet, G. Lo, 2021, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Effect of a gluten-free diet on bone mineral density in children with celiac disease.

P. Guggenbuhl, M. de Kerdanet, A. Dabadie, 2009, Gastroenterologie clinique et biologique.

Markers of recurrence and long-term morbidity in craniopharyngioma: a systematic analysis of 171 patients.

L. Riffaud, C. Sainte-Rose, P. Touraine, 2012, 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.

Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature.

J. Pantel, S. Amselem, Y. Le Bouc, 2006, The Journal of clinical investigation.

GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.

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

Heterozygous Missense Mutations in the Insulin Gene Are Linked to Permanent Diabetes Appearing in the Neonatal Period or in Early Infancy

R. Scharfmann, P. Froguel, M. Polak, 2008, Diabetes.

Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study [corrected].

R. Scharfmann, P. Froguel, M. Phillip, 2013, The lancet. Diabetes & endocrinology.

Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous families.

J. Weissenbach, J. Weissenbach, C. Vigouroux, 1997, The Journal of clinical endocrinology and metabolism.

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

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

Metabolic Correction Induced by Leptin Replacement Treatment in Young Children With Berardinelli-Seip Congenital Lipoatrophy

G. Sebag, M. Polak, C. Levy-marchal, 2007, Pediatrics.

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.

Association between quality of life of adolescents with type 1 diabetes and parents’ illness perception as evaluated by adolescents

M. de Kerdanet, A. Somat, Johanna Terrasson, 2018, Psychology, health & medicine.

Dental and craniofacial features associated with GNAS loss of function mutations.

C. Chaussain, A. Rothenbuhler, A. Linglart, 2019, European journal of orthodontics.

[Mycoplasma pneumoniae pneumopathies in children: clinical, biological and radiological study].

M. de Kerdanet, E. Werner, C. Gambert, 1993, Pediatrie.

GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.

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

[Growth retardation of psychosocial origin. Clinical and biological aspects in four cases].

M. de Kerdanet, M. Lecornu, T. Séveno, 1993, Pediatrie.