F. Paris

发表

Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome--a European Collaborative Study.

S. Lumbroso, C. Sultan, F. Paris, 2004, The Journal of clinical endocrinology and metabolism.

Phenylphenols, biphenols, bisphenol-A and 4-tert-octylphenol exhibit alpha and beta estrogen activities and antiandrogen activity in reporter cell lines.

J. Cravedi, J. Nicolas, C. Sultan, 2002, Molecular and cellular endocrinology.

Association between fetal DES-exposure and psychiatric disorders in adolescence/adulthood: evidence from a French cohort of 1002 prenatally exposed children

P. Courtet, C. Sultan, M. Soyer-Gobillard, 2016, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Clinical expression of polycystic ovary syndrome in adolescent girls.

C. Sultan, F. Paris, 2006, Fertility and sterility.

Recombinant cell ultrasensitive bioassay for measurement of estrogens in postmenopausal women.

R. Santen, C. Sultan, L. Demers, 2005, The Journal of clinical endocrinology and metabolism.

Isolated Cushing’s Syndrome: An Unusual Presentation of McCune-Albright Syndrome in the Neonatal Period

N. Kalfa, P. Philibert, C. Sultan, 2009, Hormone Research in Paediatrics.

Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers

M. Picot, C. Sultan, V. Tardy, 2010, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Primary amenorrhea in a 46,XY adolescent girl with partial gonadal dysgenesis: identification of a new SRY gene mutation.

P. Philibert, C. Sultan, S. Lumbroso, 2007, Fertility and sterility.

Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study.

R. Rouzier, P. Philibert, C. Sultan, 2008, The Journal of clinical endocrinology and metabolism.

No negative impact of reduced leptin secretion on bone metabolism in male decathletes

C. Sultan, O. Coste, D. Mariano-Goulart, 2007, European Journal of Applied Physiology.

Endocrine-Disrupting Chemicals and Disorders of Penile Development in Humans

N. Kalfa, C. Sultan, S. Hamamah, 2021, Sexual Development.

Increased serum estrogenic bioactivity in girls with premature thelarche: a marker of environmental pollutant exposure?

P. Philibert, C. Sultan, F. Paris, 2013, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

A new recombinant cell bioassay for ultrasensitive determination of serum estrogenic bioactivity in children.

J. Nicolas, C. Sultan, B. Térouanne, 2002, The Journal of clinical endocrinology and metabolism.

Evaluation of androgenic bioactivity in human serum by recombinant cell line: preliminary results

B. Térouanne, C. Sultan, F. Paris, 2002, Molecular and Cellular Endocrinology.

Evidence that chlormadinone acetate exhibits antiandrogenic activity in androgen-dependent cell line

V. Georget, B. Térouanne, C. Sultan, 2002, Molecular and Cellular Endocrinology.

Experimental Evidence of 2,3,7,8-Tetrachlordibenzo-p-Dioxin (TCDD) Transgenerational Effects on Reproductive Health

N. Kalfa, C. Sultan, M. Soyer-Gobillard, 2021, International journal of molecular sciences.

“Idiopathic” partial androgen insensitivity syndrome in 11 grandsons of women treated by diethylstilbestrol during gestation: a multi-generational impact of endocrine disruptor contamination?

N. Kalfa, C. Sultan, M. Soyer-Gobillard, 2020, Journal of Endocrinological Investigation.

Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations.

P. Philibert, C. Sultan, S. Ten, 2010, Fertility and sterility.

Environmental xenoestrogens, antiandrogens and disorders of male sexual differentiation

J. Nicolas, C. Sultan, S. Lumbroso, 2001, Molecular and Cellular Endocrinology.

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.

Equilibrium Binding Assays Reveal the Elevated Stoichiometry and Salt Dependence of the Interaction between Full-length Human Sex-determining Region on the Y Chromosome (SRY) and DNA*

E. Margeat, C. Royer, S. Lumbroso, 2002, The Journal of Biological Chemistry.

Activating mutations of the stimulatory g protein in juvenile ovarian granulosa cell tumors: a new prognostic factor?

C. Patte, N. Kalfa, S. Lumbroso, 2006, The Journal of clinical endocrinology and metabolism.

Management of Peripheral Precocious Puberty in Girls

N. Kalfa, C. Sultan, F. Paris, 2017 .

Isolated 'idiopathic' micropenis: hidden genetic defects?

P. Philibert, C. Sultan, S. Ten, 2011, International journal of andrology.

Isolated micropenis reveals partial androgen insensitivity syndrome confirmed by molecular analysis.

P. Philibert, C. Sultan, S. Ten, 2010, Asian journal of andrology.

Steroidogenic factor-1 (SF-1) gene mutation as a frequent cause of primary amenorrhea in 46,XY female adolescents with low testosterone concentration

M. Polak, P. Philibert, C. Sultan, 2010, Reproductive biology and endocrinology : RB&E.

Phenotype, hormonal profile and genotype of subjects with partial androgen insensitivity syndrome: report of a family with four adult males and one child with disorder of sexual differentiation

P. Philibert, B. Kulshreshtha, A. Ammini, 2009, Andrologia.

Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine

M. Polak, B. Gilbert-Dussardier, C. Bénéteau, 2022, EBioMedicine.

Disorders of puberty.

N. Kalfa, C. Sultan, L. Maimoun, 2017, Best practice & research. Clinical obstetrics & gynaecology.

Prenatal imaging of genital defects: clinical spectrum and predictive factors for severe forms

N. Kalfa, P. Philibert, C. Sultan, 2019, BJU international.

Endocrine and molecular investigations in a cohort of 25 adolescent males with prominent/persistent pubertal gynecomastia

P. Philibert, C. Sultan, Y. Morel, 2016, Andrology.

Role of sclerostin and dickkopf-1 in the dramatic alteration in bone mass acquisition in adolescents and young women with recent anorexia nervosa.

P. Courtet, E. Renard, J. Bringer, 2014, The Journal of clinical endocrinology and metabolism.

Puberty and pubertal growth dynamics in children with idiopathic short stature

R. Écochard, F. Paris, C. Jeandel, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Molecular diagnosis of 5alpha-reductase-2 gene mutation in two Indian families with male pseudohermaphroditism.

K. Kucheria, P. Philibert, C. Sultan, 2008, Asian journal of andrology.

Primary amenorrhea in four adolescents revealed 5α-reductase deficiency confirmed by molecular analysis.

P. Philibert, C. Sultan, G. Ocal, 2011, Fertility and sterility.

Molecular genetics of hypospadias and cryptorchidism recent developments

N. Kalfa, P. Philibert, C. Sultan, 2018, Clinical genetics.

Maturation of the Hypothalamic-Pituitary-Ovarian Axis and the Onset of Puberty

C. Sultan, F. Paris, L. Gaspari, 2017 .

Testicular function and physical outcome in young adult males diagnosed with idiopathic 46 XY disorders of sex development during childhood.

C. Sultan, Y. Aigrain, J. Carel, 2011, European journal of endocrinology.

Family History is Underestimated in Children with Isolated Hypospadias: A French Multicenter Report of 88 Families

J. Valla, J. Daurès, N. Kalfa, 2018, Journal of Urology.

Prenatal Exposure to Diethylstilbestrol and Multigenerational Psychiatric Disorders: An Informative Family

P. Courtet, N. Kalfa, C. Sultan, 2021, International journal of environmental research and public health.

Fulvestrant treatment of precocious puberty in girls with McCune-Albright syndrome

C. Sultan, Sally Garnett, E. Eugster, 2012, International Journal of Pediatric Endocrinology.

Prevalence of hypospadias in grandsons of women exposed to diethylstilbestrol during pregnancy: a multigenerational national cohort study.

J. Daurès, N. Kalfa, C. Sultan, 2011, Fertility and sterility.

Multigenerational endometriosis : consequence of fetal exposure to diethylstilbestrol ?

N. Kalfa, C. Sultan, M. Soyer-Gobillard, 2021, Environmental Health.

Diethylstilbestrol exposure during pregnancy with primary clear cell carcinoma of the cervix in an 8-year-old granddaughter: a multigenerational effect of endocrine disruptors?

N. Kalfa, C. Sultan, M. Soyer-Gobillard, 2020, Human reproduction.

Molecular diagnosis of 5α-reductase deficiency in 4 elite young female athletes through hormonal screening for hyperandrogenism.

S. Bermon, P. Chevallier, P. Philibert, 2013, The Journal of clinical endocrinology and metabolism.

A Nationwide Study of Granulosa Cell Tumors in Pre- and Postpuberal Girls: Missed Diagnosis of Endocrine Manifestations Worsens Prognosis

D. Orbach, C. Patte, N. Kalfa, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Fetal ovarian cysts: an early manifestation of McCune–Albright syndrome?

N. Kalfa, C. Sultan, C. Pienkowski, 2012, Prenatal diagnosis.

Androgen Insensitivity Syndrome

N. Kalfa, P. Philibert, C. Sultan, 2014 .

Isolated follicle-stimulating hormone (FSH) deficiency in two infertile men without FSH β gene mutation: Case report and literature review.

N. Lahlou, S. Hiéronimus, P. Fénichel, 2019, Annales d'endocrinologie.

Testotoxicosis without Testicular Mass: Revealed by Peripheral Precocious Puberty and Confirmed by Somatic LHCGR Gene Mutation

C. Sultan, P. Barat, M. Yacoub, 2020, Endocrine research.

Testosterone secretion in elite adolescent swimmers does not modify bone mass acquisition: a 1-year follow-up study.

K. Briot, P. Philibert, C. Sultan, 2013, Fertility and sterility.

Adolescent ovarian thecoma presenting as progressive hyperandrogenism: case report and review of the literature

P. Taourel, N. Kalfa, C. Sultan, 2020, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Self- and proxy-reported outcomes after surgery in people with disorders/differences of sex development (DSD) in Europe (dsd-LIFE).

J. Słowikowska-Hilczer, A. Nordenström, B. Kreukels, 2020, Journal of pediatric urology.

Evidence of ERalpha and ERbeta selectivity and partial estrogen agonism in traditional Chinese medicine

Z. Hochberg, C. Sultan, Marina Grimaldi, 2014, Reproductive Biology and Endocrinology.

Management of Disorders of Sex Development

N. Kalfa, C. Sultan, F. Paris, 2017 .

Disorders of sex development: neonatal diagnosis and management.

N. Kalfa, P. Philibert, C. Sultan, 2012, Endocrine development.

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.

Increased serum estrogenic bioactivity in three male newborns with ambiguous genitalia: a potential consequence of prenatal exposure to environmental endocrine disruptors.

C. Sultan, F. Paris, C. Jeandel, 2006, Environmental research.

In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants.

P. Philibert, D. Dewailly, Y. Morel, 2019, Reproductive biomedicine online.

NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiency.

P. Philibert, C. Sultan, S. Christin‐Maitre, 2013, Fertility and sterility.

Functional and Structural Study of the Amino Acid Substitution in a Novel Familial Androgen Receptor Mutation (W752G) Responsible for Complete Androgen Insensitivity Syndrome

N. Kalfa, C. Sultan, W. Bourguet, 2018, Sexual Development.

[Complete androgen insensitivity syndrome: a novel mutation in a Tunisian family].

C. Sultan, M. Sakouhi, S. Mahjoub, 2008, Annales d'endocrinologie.

Participation of adults with disorders/differences of sex development (DSD) in the clinical study dsd-LIFE: design, methodology, recruitment, data quality and study population

J. Słowikowska-Hilczer, A. Nordenström, B. Köhler, 2017, BMC Endocrine Disorders.

Ambiguous Genitalia in the Newborn

C. Sultan, S. Lumbroso, F. Paris, 2002, Seminars in reproductive medicine.

Precocious Puberty and Environmental Endocrine Disruptors

C. Sultan, F. Paris, L. Gaspari, 2016 .

Clinical expression of precocious puberty in girls.

N. Kalfa, C. Sultan, F. Paris, 2012, Endocrine development.

Bone mass acquisition in female rhythmic gymnasts during puberty: no direct role for leptin

C. Sultan, O. Coste, D. Mariano-Goulart, 2010, Clinical endocrinology.

A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations

R. Veitia, S. Caburet, C. Sultan, 2017, Clinical endocrinology.

Is Hypospadias Associated with Prenatal Exposure to Endocrine Disruptors? A French Collaborative Controlled Study of a Cohort of 300 Consecutive Children Without Genetic Defect.

J. Valla, J. Daurès, N. Kalfa, 2015, European urology.

Minor Hypospadias: The “Tip of the Iceberg” of the Partial Androgen Insensitivity Syndrome

J. Valla, J. Daurès, K. McElreavey, 2013, PloS one.

McCune-Albright syndrome: molecular genetics.

S. Lumbroso, C. Sultan, F. Paris, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

[The androgen receptor: molecular pathology].

S. Lumbroso, V. Georget, B. Térouanne, 2002 .

Antiandrogenic activity of norgestimate in a human androgen-dependent stable-transfected cell line

C. Sultan, P. Balaguer, F. Paris, 2007, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants.

P. Philibert, D. Dewailly, Y. Morel, 2019, Reproductive biomedicine online.

Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome).

P. Philibert, C. Sultan, C. Pienkowski, 2011, Fertility and sterility.

Reversible growth failure and complete GH deficiency in a 4-year-old girl with very early Hashimoto’s thyroiditis and subsequent hyperplasia of pituitary thyrotroph cells

A. Bonafe, N. Leboucq, C. Sultan, 2016, European Journal of Pediatrics.

Using Digital Droplet Polymerase Chain Reaction to Detect the Mosaic GNAS Mutations in Whole Blood DNA or Circulating Cell‐Free DNA in Fibrous Dysplasia and McCune‐Albright Syndrome

A. Barlier, L. Ouafik, P. Philibert, 2019, The Journal of pediatrics.

Late surgical correction of hypospadias increases the risk of complications: a series of 501 consecutive patients

J. Daurès, N. Kalfa, P. Philibert, 2017, BJU international.

How Far Should We Explore Hypospadias? Next-generation Sequencing Applied to a Large Cohort of Hypospadiac Patients.

N. Kalfa, P. Philibert, C. Sultan, 2021, European urology.

Prenatal environmental risk factors for genital malformations in a population of 1442 French male newborns: a nested case-control study.

J. Daurès, N. Kalfa, C. Sultan, 2011, Human reproduction.

Apparent Male Gender Identity in a Patient with Complete Androgen Insensitivity Syndrome

P. Philibert, C. Sultan, S. Khandelwal, 2009, Archives of sexual behavior.

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.

Mother-to-Son Transmission of a Luteinizing Hormone Receptor Activating Mutation in a Prepubertal Child with Testotoxicosis

P. Philibert, C. Sultan, B. Kulshreshtha, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

In peripubertal girls, artistic gymnastics improves areal bone mineral density and femoral bone geometry without affecting serum OPG/RANKL levels

K. Briot, P. Philibert, C. Sultan, 2011, Osteoporosis International.

Phenylphenols, biphenols, bisphenol-A and 4-tert-octylphenol exhibit α and β estrogen activities and antiandrogen activity in reporter cell lines

Jean-Pierre Cravedi, J. Cravedi, J. Nicolas, 2002, Molecular and Cellular Endocrinology.

Phenotypic variation of SF1 gene mutations.

M. Polak, G. Pinto, D. Damiani, 2011, Advances in experimental medicine and biology.

Neurodevelopmental disorders in children exposed in utero to synthetic progestins: analysis from the national cohort of the Hhorages Association*

P. Courtet, C. Sultan, M. Soyer-Gobillard, 2019, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

High prevalence of micropenis in 2710 male newborns from an intensive-use pesticide area of Northeastern Brazil.

C. Sultan, F. Paris, L. Gaspari, 2012, International journal of andrology.

Birth Outcomes in DES Children and Grandchildren: A Multigenerational National Cohort Study on Informative Families

N. Kalfa, C. Sultan, M. Soyer-Gobillard, 2023, International journal of environmental research and public health.

Unilateral Cryptorchidism in Mice Mutant for Ptgds

Y. Urade, P. Philibert, C. Sultan, 2013, Human mutation.

Disorders linked to insufficient androgen action in male children

J. Nicolas, C. Sultan, S. Lumbroso, 2001, Human reproduction update.

Specific bone mass acquisition in elite female athletes.

P. Philibert, C. Sultan, F. Galtier, 2013, The Journal of clinical endocrinology and metabolism.

Peripheral precocious puberty in a 4-month-old girl: role of pesticides?

C. Sultan, F. Paris, L. Gaspari, 2011, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

A cover flap reduces the rate of fistula after urethroplasty whatever the severity of hypospadias

N. Kalfa, F. Paris, L. Gaspari, 2020, World Journal of Urology.

Association between androgen receptor gene polymorphism and bone density in older women using hormone replacement therapy.

H. Blain, C. Michelon, F. Retornaz, 2006, Maturitas.

The role of androgens or growth factors in the bone resorption process in recent spinal cord injured patients: a cross-sectional study

C. Sultan, S. Lumbroso, L. Maïmoun, 2006, Spinal Cord.

Testosterone Is Significantly Reduced in Endurance Athletes without Impact on Bone Mineral Density

C. Sultan, S. Lumbroso, L. Maïmoun, 2003, Hormone Research in Paediatrics.

Molecular action of norgestimate: new developments

C. Sultan, P. Balaguer, F. Paris, 2015, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

'Idiopathic' partial androgen insensitivity syndrome in 28 newborn and infant males: impact of prenatal exposure to environmental endocrine disruptor chemicals?

N. Kalfa, P. Philibert, C. Sultan, 2011, European journal of endocrinology.

Effects of the two types of anorexia nervosa (binge eating/purging and restrictive) on bone metabolism in female patients

P. Courtet, E. Renard, M. Picot, 2018, Clinical endocrinology.

Subject Index Vol. 59, 2003

S. Fujimoto, H. Togari, J. Casez, 2003, Hormone Research in Paediatrics.

Evidence of a link between resting energy expenditure and bone remodelling, glucose homeostasis and adipokine variations in adolescent girls with anorexia nervosa

P. Courtet, E. Renard, J. Bringer, 2015, Osteoporosis International.

Disorders of Androgen Action

J. Nicolas, C. Sultan, S. Lumbroso, 2002, Seminars in reproductive medicine.

Ambiguous genitalia in the newborn: diagnosis, etiology and sex assignment.

C. Sultan, S. Lumbroso, J. Picaud, 2004, Endocrine development.