M. Tauber

发表

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.

C. Francks, A. Bailey, G. Baird, 1998, Human molecular genetics.

Cardiovascular abnormalities in Turner's syndrome: what prevention?

P. Acar, M. Tauber, C. Pienkowski, 2008, Archives of cardiovascular diseases.

Medical, psychological and social features in a large cohort of adults with Prader-Willi syndrome: experience from a dedicated centre in France.

J. Jauregi, P. Copet, V. Laurier, 2015, Journal of intellectual disability research : JIDR.

Is glutamate decarboxylase 2 (GAD2) a genetic link between low birth weight and subsequent development of obesity in children?

P. Boutin, B. Heude, D. Meyre, 2005, The Journal of clinical endocrinology and metabolism.

Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature

B. Neel, P. Valet, J. Salles, 2012, Proceedings of the National Academy of Sciences.

How do Shp2 mutations that oppositely influence its biochemical activity result in syndromes with overlapping symptoms?

B. Parfait, J. Salles, M. Dance, 2007, Cellular and Molecular Life Sciences.

Endothelial Function and Mechanical Arterial Properties in Children Born Small for Gestational Age: Comparison with Obese Children

J. Salles, C. Arnaud, M. Tauber, 2011, Hormone Research in Paediatrics.

Economic burden and health-related quality of life associated with Prader-Willi syndrome in France.

C. Poitou, K. Chevreul, M. Tauber, 2016, Journal of intellectual disability research : JIDR.

Prevalence of IGF1 deficiency in prepubertal children with isolated short stature.

J. Salles, M. Tauber, I. Gennero, 2009, European journal of endocrinology.

[Growth follow-up of SGA children after 3 years of GH treatment].

J. Salles, M. Tauber, C. Pienkowski, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[Delayed puberty].

M. Tauber, T. Edouard, 2010, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Intracranial hypotension in a girl with Marfan syndrome: case report and review of the literature

C. Cancés, M. Mejdoubi, M. Tauber, 2008, Child's Nervous System.

[New molecular mechanisms of growth hormone insensitivity].

J. Salles, M. Tauber, F. Conte-Auriol, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

Role of Environmental Factors in Childhood Obesity

M. Tauber, B. Jouret, 2004 .

Associations of glucocorticoid receptor and corticosteroid-binding globulin gene polymorphisms on fat mass and fat mass distribution in prepubertal obese children

M. Moisan, J. Corcuff, P. Barat, 2012, Journal of Physiology and Biochemistry.

Breathing deficits of the Prader-Willi syndrome

S. Zanella, M. Tauber, F. Muscatelli, 2009, Respiratory Physiology & Neurobiology.

Identification of a region critical for proteolysis of the human growth hormone receptor.

J. Salles, E. Bieth, M. Tauber, 2002, Biochemical and biophysical research communications.

Recommendations for the diagnosis and management of Prader-Willi syndrome.

M. Tauber, A. Hokken-Koelega, M. Tauber, 2008, The Journal of clinical endocrinology and metabolism.

Adult height and pubertal growth in Turner syndrome after treatment with recombinant growth hormone.

J. Coste, J. Carel, J. Chaussain, 2005, The Journal of clinical endocrinology and metabolism.

Gonadotropin treatment of hypogonadotropic hypogonadal adolescents.

C. Bouvattier, M. Tauber, J. Chaussain, 1999, Journal of pediatric endocrinology & metabolism : JPEM.

Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity.

D. Meyre, P. Froguel, C. Levy-marchal, 2005, Diabetes.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Joseph T. Glessner, Stephen J. Guter, D. Pinto, 2011, Human Genetics.

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

Stephen J. Guter, A. Bailey, G. Baird, 2001, American journal of human genetics.

Implication of the Pro12Ala polymorphism of the PPAR-gamma 2 gene in type 2 diabetes and obesity in the French population

K. Clément, G. Charpentier, D. Meyre, 2005, BMC Medical Genetics.

Necdin Plays a Role in the Serotonergic Modulation of the Mouse Respiratory Network: Implication for Prader-Willi Syndrome

S. Zanella, F. Watrin, M. Tauber, 2008, The Journal of Neuroscience.

Adult height after long term treatment with recombinant growth hormone for idiopathic isolated growth hormone deficiency: observational follow up study of the French population based registry

J. Coste, J. Carel, J. Chaussain, 2002, BMJ : British Medical Journal.

Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature

H. Cavé, M. Tauber, M. Denuelle, 2017, American journal of medical genetics. Part A.

A common polymorphism of the growth hormone receptor is associated with increased responsiveness to growth hormone

L. Essioux, C. Teinturier, P. Bougnères, 2004, Nature Genetics.

[TSH, FT4 and T3T evaluation in normal and preterm hospitalized newborns].

J. Salles, M. Tauber, C. Cristini, 2007, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

An N-terminal WT1 mutation (P181S) in an XY patient with ambiguous genitalia, normal testosterone production, absence of kidney disease and associated heart defect: enlarging the phenotypic spectrum of WT1 defects.

B. Köhler, C. Sultan, S. Lumbroso, 2004, European journal of endocrinology.

Psychotropic treatments in Prader-Willi syndrome: a critical review of published literature

D. Cohen, D. Thuilleaux, M. Tauber, 2015, European Journal of Pediatrics.

Quality of life determinants in young women with turner's syndrome after growth hormone treatment: results of the StaTur population-based cohort study.

J. Coste, J. Carel, J. Chaussain, 2005, The Journal of clinical endocrinology and metabolism.

Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome.

N. Philip, A. Verloes, C. Lejeune, 2020, European journal of medical genetics.

Treatment for 24 months with recombinant human GH has a beneficial effect on bone mineral density in young adults with childhood-onset GH deficiency.

P. Chanson, G. Conway, M. Zacharin, 2009, European journal of endocrinology.

Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort

M. Polak, A. Barlier, I. Bergadá, 2020, Clinical endocrinology.

Contribution of LHX4 Mutations to Pituitary Deficits in a Cohort of 417 Unrelated Patients

D. Larizza, M. Maghnie, M. Polak, 2016, The Journal of clinical endocrinology and metabolism.

[Nonadherence to GH therapy in children treated with growth hormone].

M. Tauber, 2009, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

The use of the Montreal Cognitive Assessment (MoCA) to assess cognitive impairment in Prader-Willi syndrome

J. Chevalère, V. Laurier, D. Thuilleaux, 2020 .

Genetic study of the melanin-concentrating hormone receptor 2 in childhood and adulthood severe obesity.

B. Heude, D. Meyre, P. Froguel, 2007, The Journal of clinical endocrinology and metabolism.

No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases

E. Petretto, D. Meyre, P. Froguel, 2007, European Journal of Human Genetics.

The cumulative effect of small dietary changes may significantly improve nutritional intakes in free-living children and adults

F. Bornet, P. Valensi, D. Paineau, 2010, European Journal of Clinical Nutrition.

Family dietary coaching to improve nutritional intakes and body weight control: a randomized controlled trial.

Béatrice Jouret, Chantal Simon, Véronique Chapalain, 2008, Archives of pediatrics & adolescent medicine.

Growth hormone in combination with leuprorelin in pubertal children with idiopathic short stature

J. Carel, M. Tauber, M. Rosilio, 2018, Endocrine connections.

[Early education for children with Prader-Willi syndrome].

M. Tauber, G. Diene, P. Fichaux-Bourin, 2009, Revue de laryngologie - otologie - rhinologie.

Impact of transitional care on endocrine and anthropometric parameters in Prader–Willi syndrome

J. Oppert, M. Polak, G. Pinto, 2018, Endocrine connections.

[Translational studies in children].

J. Salles, M. Tauber, F. Conte-Auriol, 2009, Archives de pédiatrie.

[Risks and benefits of oestrogen treatment for tall stature girls].

M. Tauber, C. Pienkowski, T. Edouard, 2009, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Associations of glucocorticoid receptor and corticosteroid-binding globulin gene polymorphisms on fat mass and fat mass distribution in prepubertal obese children

M. Moisan, J. Corcuff, P. Barat, 2012, Journal of Physiology and Biochemistry.

Treatment for 24 months with recombinant human GH has a beneficial effect on bone mineral density in young adults with childhood-onset GH deficiency.

G. Conway, M. Zacharin, M. Tauber, 2009, European journal of endocrinology.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Stephen J. Guter, D. Pinto, S. Scherer, 2011, Human Genetics.

[Growth follow-up of SGA children after 3 years of GH treatment].

M. Tauber, C. Pienkowski, B. Jouret, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.