J. Toublanc

发表

The pituitary-gonadal axis in cryptorchid infants and children

J. Chaussain, D. Gendrel, M. Roger, 2004, European Journal of Pediatrics.

Four families with loss of function mutations of the thyrotropin receptor.

E. Milgrom, Y. Le Bouc, N. de Roux, 1996, The Journal of clinical endocrinology and metabolism.

Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts in the world.

J. Toublanc, 1992, Hormone research.

Endocrine and immunological findings in cryptorchid infants.

J. Chaussain, D. Gendrel, M. Roger, 1988, Hormone research.

Modifications of Growth Hormone Secretion during Female Puberty

J. Toublanc, 1997, Annals of the New York Academy of Sciences.

Adult Height in Congenital Hypothyroidism: Prognostic Factors and the Importance of Compliance with Treatment

J. Toublanc, P. Bain, 2002, Hormone Research in Paediatrics.

Evaluation of Leydig-cell function in normal prepubertal and pubertal boys.

P. Leymarie, M. Roger, P. Canlorbe, 1975, Journal of steroid biochemistry.

Growth of short normal children in puberty treated for 3 years with growth hormone alone or in association with gonadotropin-releasing hormone agonist.

J. Job, J. Toublanc, F. Landier, 1994, Hormone research.

Treatment of Precocious Puberty with LHRH Agonists

A. Schally, J. Chaussain, M. Roger, 1986 .

Plasma Concentration of Luteinizing Hormone, Testosterone, Dehydroepiandrosterone, Androstenedione Between Brith and One Year in the Male Dog: Longitudinal Study and hCG Stimulation

J. Mialot, R. Scholler, M. Thibier, 2009, Andrologia.

Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome.

J. Weill, J. Lobaccaro, C. Sultan, 1993, The Journal of clinical endocrinology and metabolism.

A possible common origin of “Y-negative” human XX males and XX true hermaphrodites

M. Toublanc, M. Fellous, N. Affara, 1990, Human Genetics.

Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA‐sequences

M. Toublanc, E. Vilain, M. Fellous, 1994, Clinical endocrinology.

Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation

M. Toublanc, E. Vilain, M. Fellous, 2005, European Journal of Pediatrics.

Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome

J. Weill, J. Lobaccaro, C. Sultan, 1992 .

Gonadotropin and alpha-subunit secretion during long term pituitary suppression by D-Trp6-luteinizing hormone-releasing hormone microcapsules as treatment of precocious puberty.

A. Schally, C. Sultan, J. Chaussain, 1987, The Journal of clinical endocrinology and metabolism.

Effects of GnRH Agonists on Pituitary Gonadotropins: Dissociated Secretion of Subunits in Children with Precocious Puberty Treated with [D-Trp6]LHRH Microcapsules

A. Schally, J. Chaussain, N. Lahlou, 1990 .

Effect of synthetic luteinizing hormone-releasing hormone on the release of gonadotropins in hypophysogonadal disorders of children and adolescents. IV. Undescended testes.

J. Chaussain, P. Canlorbe, J. Job, 1974, The Journal of pediatrics.

Hormonal therapy of cryptorchidism with human chorionic gonadotropin(HCG).

J. Garagorri, P. Canlorbe, J. Job, 1982, The Urologic clinics of North America.

The sole presence of the testis-determining region of the Y chromosome (SRY) in 46,XX patients is associated with phenotypic variability.

E. Vilain, M. Fellous, K. McElreavey, 1992, Hormone research.

Etiologies of late puberty.

J. Chaussain, M. Roger, J. Toublanc, 1991, Hormone research.

Adolescent sexuality in europe: A multicentric study

M. Osler, R. Siegberg, J. Orley, 1995 .

Effect of synthetic luteinizing hormone-releasing hormone (LH-RH) on the release of gonadotropins in hypophyso-gonadal disorders of children and adolescents. V. Agonadism.

J. Chaussain, P. Canlorbe, J. Job, 1974, Journal of Clinical Endocrinology and Metabolism.

Effect of synthetic luteinizing hormone-releasing hormone on the release of gonadotropins in hypophysogonadal disorders of children and adolscents. VII. Constitutional delay of puberty in males.

J. Chaussain, J. Job, J. Toublanc, 1976, The Journal of pediatrics.

Earlier Onset of Treatment or Increment in LT4 Dose in Screened Congenital Hypothyroidism: Which Was the More Important Factor for IQ at 7 Years?

P. Boileau, J. Toublanc, P. Bain, 2004, Hormone Research in Paediatrics.

Guidelines for neonatal screening programmes for congenital hypothyroidism

A. Grüters, F. Delange, O. Hníková, 1993, European Journal of Pediatrics.

Hypothyroidism, Congenital, Screening Programs

P. Boileau, J. Toublanc, 2004 .

Townes‐Brocks syndrome: Detection of a SALL1 mutation hot spot and evidence for a position effect in one patient

E. Calzolari, C. Petit, S. Blanchard, 1999, Human mutation.

Three‐year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardation

P. Czernichow, B. Leheup, R. Rappaport, 1998, Acta paediatrica.

Epidemiological inquiry on congenital hypothyroidism in Europe (1985-1988). Working Group on Congenital Hypothyroidism of the Society for Paediatric Endocrinology.

J. Toublanc, 1990, Hormone Research.

[Study of antibody-dependent cell mediated cytotoxicity and thyroid growth blocking antibodies in congenital hypothyroidism].

A. Grüters, U. Bogner, M. Dugué, 1991, Archives francaises de pediatrie.

[Direct assay of free thyroxine in children. Application to the monitoring of the treatment of hypothyroidism].

J. Ingrand, J. Job, Y. Fulla, 1984, Archives francaises de pediatrie.

The effects of treatment combining an agonist of gonadotropin-releasing hormone with growth hormone in pubertal patients with isolated growth hormone deficiency.

J. Job, C. Couprie, J. Toublanc, 1989, Acta endocrinologica.

Treatment of male and female precocious puberty (PP) by monthly injections of a continuous release preparation of D-Trp-6-LH-RH

A. Schally, J. Chaussain, M. Roger, 1984, Pediatric Research.

[Hypopituitarism with diabetes insipidis after tuberculous meningitis. Surgical discovery of 2 tuberculomas].

C. Bach, J. Toublanc, J. Rougerie, 1974, Archives francaises de pediatrie.

Molecular prenatal diagnosis of partial androgen insensitivity syndrome based on the Hind III polymorphism of the androgen receptor gene *

C. Sultan, S. Lumbroso, J. Lobaccaro, 1994, Clinical endocrinology.

A thyroxine dosage of 8 μg/kg per day is appropriate for the initial treatment of the majority of infants with congenital hypothyroidism

P. Czernichow, G. Touati, J. Léger, 1997, European Journal of Pediatrics.

A thyroxine dosage of 8 micrograms/kg per day is appropriate for the initial treatment of the majority of infants with congenital hypothyroidism.

P. Czernichow, G. Touati, J. Léger, 1997, European journal of pediatrics.

Prenatal prediction of androgen insensitivity syndrome using exon 1 polymorphism of the androgen receptor gene

S. Lumbroso, J. Lobaccaro, C. Sultan, 1992, The Journal of Steroid Biochemistry and Molecular Biology.

[Plasma androgens in boys from birth to adolescence].

M. Roger, P. Canlorbe, K. Nahoul, 1979, Annales de pediatrie.

Psychological Indications for Treatment of Tall Stature in Adolescent Girls

J. Toublanc, C. Lecointre, 1997, Journal of pediatric endocrinology & metabolism : JPEM.

[Case of double aneuploidy: trisomy 18 and XXY].

M. Gautier, C. Bach, J. Toublanc, 1973, Annales de genetique.

[Long-term fate of pituitary dwarfs treated with growth hormone].

J. Chaussain, A. Rolland, P. Canlorbe, 1988, Archives francaises de pediatrie.

[Alpha fetoprotein in congenital hypothyroidism before and during treatment].

J. Ingrand, Y. Fulla, J. Toublanc, 1994, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.