M. David

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Prenatal Treatment of Congenital Adrenal Hyperplasia

M. Forest, Y. Morel, M. David, 1998, Trends in Endocrinology & Metabolism.

Clinical and Radiological Characteristics of 22 Children with SHOX Anomalies and Familial Short Stature Suggestive of Léri-Weill Dyschondrosteosis

V. Cormier-Daire, M. Nicolino, C. Huber, 2011, Hormone Research in Paediatrics.

Endocrine involvement in pediatric-onset Langerhans' cell histiocytosis: a population-based study.

K. Hoang-Xuan, D. Frappaz, M. Polak, 2004, The Journal of pediatrics.

Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.

M. Forest, J. Bertrand, W. Miller, 1989, The Journal of clinical investigation.

21-Hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease.

M. Forest, M. Nicolino, V. Tardy, 2005, Annales d'endocrinologie.

Study of final height in Turner's syndrome: ethnic and genetic influences.

C. Sultan, J. Limal, G. Simonin, 1994, Acta paediatrica.

Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo.

J. Bertrand, A. Morera, J. Saez, 1971, The Journal of clinical endocrinology and metabolism.

Clinical and biological assessments of the undervirilized male

M. Forest, N. Bendelac, M. Nicolino, 2004, BJU international.

Evaluation of gonadal function in 107 intersex patients by means of serum antimüllerian hormone measurement.

M. Forest, P. Czernichow, F. Baş, 1999, The Journal of clinical endocrinology and metabolism.

New management strategy of pregnancies at risk of congenital adrenal hyperplasia using fetal sex determination in maternal serum: French cohort of 258 cases (2002-2011).

N. Philip, C. Baumann, S. Odent, 2014, The Journal of clinical endocrinology and metabolism.

Prenatal treatment in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: up-date 88 of the French multicentric study.

M. Forest, H. Bétuel, M. David, 1989, Endocrine research.

Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency.

M. Forest, M. David, 1984, The Journal of pediatrics.

Effects of Human Chorionic Gonadotropin, Androgens, Adrenocorticotropin Hormone, Dexamethasone and Hyperprolactinemia on Plasma Sex Steroid‐Binding Protein a

M. Forest, M. Pugeat, A. Lecoq, 1988, Annals of the New York Academy of Sciences.

LINEAR GROWTH AND PUBERTAL DEVELOPMENT IN TREATED CONGENITAL ADRENAL HYPERPLASIA DUE TO 21‐HYDROXYLASE DEFICIENCY

I. Ghali, M. David, L. David, 1977 .

Usefulness of plasma pregnenolone sulfate in testing pituitary-adrenal function in children.

M. Forest, J. Bertrand, Y. Morel, 1986, Acta endocrinologica. Supplementum.

Adrenarche does not occur in treated patients with congenital adrenal hyperplasia resulting from 21‐hydroxylase deficiency

M. Forest, M. David, V. Brunelli, 1995, Clinical endocrinology.

[Pseudo-hypoaldosteronism in infants. Apropos of 4 cases, 2 concerning brothers].

F. Freycon, B. Lauras, M. David, 1978, Pediatrie.

Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.

P. Donohoue, M. Fassnacht, L. Dunkel, 2005, The Journal of clinical endocrinology and metabolism.

Effect of Sodium Restriction and Angiotensin II Infusion in Bartter's Syndrome

L. Sann, J. Sassard, D. Floret, 1976, Pediatric Research.

Aetiological diagnosis of male sex ambiguity: a collaborative study

M. Forest, C. Teinturier, M. Fellous, 2001, European Journal of Pediatrics.

Endocrine screening in 32 consecutive patients with hypospadias.

M. Forest, P. Chatelain, P. Mouriquand, 2002, The Journal of urology.

[2 cases of trisomy 11q(q23.2-- qter) with the same abnormality of external genitalia].

M. Bethenod, C. Laurent, L. Cret, 1975, Annales de genetique.

Gonadal dysgenesis without adrenal insufficiency in a 46, XY patient heterozygous for the nonsense C16X mutation: a case of SF1 haploinsufficiency.

Y. Morel, F. Dijoud, D. Mallet, 2004, The Journal of clinical endocrinology and metabolism.

Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development

A. Munnich, A. Molven, O. Bruland, 2011, Journal of Medical Genetics.

Late prenatal dexamethasone and phenotype variations in 46,XX CAH: concerns about current protocols and benefits for surgical procedures.

P. Chatelain, A. Brac de la Perrière, P. Mouriquand, 2014, Journal of pediatric urology.

Nonsalt-losing male pseudohermaphroditism due to the novel homozygous N100S mutation in the type II 3 beta-hydroxysteroid dehydrogenase gene.

M. Forest, J. Simard, É. Rhéaume, 1995, The Journal of clinical endocrinology and metabolism.

Undescended testis: comparison of two protocols of treatment with human chorionic gonadotropin. Effect on testicular descent and hormonal response.

M. Forest, J. Bertrand, P. Chatelain, 1988, Hormone research.

Kinetics of the HCG-induced Steroidogenic Response of the Human Testis. III. Studies in Children of the Plasma Levels of Testosterone and HCG: Rationale for Testicular Stimulation Test

M. Forest, A. Lecoq, M. David, 1980, Pediatric Research.

[Adrenal hypoplasia congenita: four new cases in children].

M. Forest, M. Nicolino, F. Prieur, 2005, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Prenatal diagnosis and treatment of 21-hydroxylase deficiency

M. Forest, Y. Morel, M. David, 1993, The Journal of Steroid Biochemistry and Molecular Biology.

Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1)

N. Roux, D. Zénaty, J. Léger, 2006, Molecular and Cellular Endocrinology.

Prenatal treatment of congenital adrenal hyperplasia: Report of a new case

M. Forest, G. Loeuille, M. David, 2005, European Journal of Pediatrics.

PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY

M. Forest, H. Dörr, Y. Morel, 1993, Pediatric Research.

Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21‐hydroxylase deficiency by steroid analysis in the amniotic fluid of mid‐pregnancy: Comparison with HLA typing in 17 pregnancies at risk for CAH

M. Forest, H. Plauchu, H. Bétuel, 1981, Prenatal diagnosis.

Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.

V. Sulmont, V. Tardy, Y. Morel, 2010, The Journal of clinical endocrinology and metabolism.

123 LATE ONSET 21-OH-DEFICIENCY (21-OHD) CAN BE MISDIAGNOSED AS “TYPICAL PREMATURE PUBARCHE” (PP) IN CHILDHOOD

M. Forest, M. David, E. Peretti, 1985, Pediatric Research.

Incidence of growth hormone deficiency in pediatric-onset Langerhans cell histiocytosis: efficacy and safety of growth hormone treatment.

C. Garel, M. Polak, F. Doz, 2004, The Journal of clinical endocrinology and metabolism.

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency.

J. Drouin, C. Deal, A. Pulichino, 2003, Genes & development.

[Prolactin adenoma in a 14-year-old boy].

Y. Morel, F. Grisoli, P. Jaquet, 1985, Pediatrie.

[2 infants born of a mother with phenylketonuria. Failure of a low phenylalanine diet during the 2d pregnancy].

F. Freycon, C. Dorche, M. David, 1974, Pediatrie.

The virilized female: endocrine background

M. Forest, M. Nicolino, Y. Morel, 2004, BJU international.

Juvenile granulosa cell tumor of the ovary in infants: a clinicopathologic study of three cases and review of the literature.

E. Bouffet, P. Mollard, F. Dijoud, 1997, Journal of pediatric surgery.

Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A 10 year experience

M. Forest, M. David, 1992, Indian journal of pediatrics.

Growth curves for congenital adrenal hyperplasia from a national retrospective cohort

P. Chatelain, M. Nicolino, B. Riche, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

[21 hydroxylase deficiency: new strategies emerging from molecular studies].

M. Forest, V. Tardy, Y. Morel, 2003, Annales d'endocrinologie.

[Final height in 69 patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].

M. Forest, M. Nicolino, Y. Morel, 1994, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[Retropharyngeal abscess].

B. Contamin, M. David, 1991, Pediatrie.

Urinary melatonin, LH, oestradiol, progesterone excretion during the menstrual cycle or in women taking oral contraceptives.

B. Claustrat, J. Brun, M. David, 1987, Acta endocrinologica.

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.

Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness: report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectively.

M. Forest, M. Nicolino, C. Godinot, 1997, The Journal of clinical endocrinology and metabolism.

[Trial classification of D group chromosome long arm deletions. Apropos of a 15q- case].

B. Noel, C. Laurent, M. David, 1971, Annales de genetique.

Linear growth and pubertal development in treated congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

I. Ghali, M. David, L. David, 1978, Clinical endocrinology.

[Familial congenital adrenal hyperplasia caused by 11 beta-hydroxylase. Failure of prevention of sexual ambiguity and prenatal diagnosis].

M. Forest, H. Déchaud, M. David, 1989, Pediatrie.

Comparative study of persistant mullerian structures in 5 boys with ambiguous genitalia and in 2 true hermaphrodites (TH): implication for sex orientation

M. Forest, P. Mollard, M. David, 1981, Pediatric Research.

Studies of a cohort of 46,XY with DSD including steroid biosynthesis deficiencies.

P. Chatelain, M. Nicolino, Y. Morel, 2011, Advances in experimental medicine and biology.