C. Sultan

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

Behavioral and Somatic Disorders in Children Exposed in Utero to Synthetic Hormones: A Testimony-Case Study in a French Family Troop

C. Sultan, M. Soyer-Gobillard, 2012 .

Childhood obesity.

A. Eliakim, S. Shalitin, H. Krude, 2005, The Journal of clinical endocrinology and metabolism.

Metformin, oral contraceptives or both to manage oligo-amenorrhea in adolescents with polycystic ovary syndrome? A clinical review

F. Orio, C. Sultan, S. Palomba, 2014, 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.

The quantitative ultrasound method for assessing low bone mass in women with anorexia nervosa

P. Courtet, E. Renard, M. Picot, 2021, Archives of Osteoporosis.

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.

Low Sit-to-Stand Performance is Associated with Low Femoral Neck Bone Mineral Density in Healthy Women

M. Picot, H. Blain, C. Sultan, 2009, Calcified Tissue International.

The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor

M. Fellous, C. Sultan, P. Niaudet, 1999, Human mutation.

Bone remodeling and calcium homeostasis in patients with spinal cord injury: a review.

C. Fattal, C. Sultan, L. Maïmoun, 2011, Metabolism: clinical and experimental.

Effect of Physical Activity on Calcium Homeostasis and Calciotropic Hormones: A Review

C. Sultan, L. Maïmoun, 2009, Calcified Tissue International.

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.

Congenital Nephrotic Syndrome in a Male Pseudohermaphrodite - The Drash Syndrome

G. Landthaler, C. Sultan, S. Marret, 1991 .

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.

Mutational analysis of steroidogenic factor 1 (NR5a1) in 24 boys with bilateral anorchia: a French collaborative study.

P. Philibert, C. Sultan, J. Achermann, 2007, Human reproduction.

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.

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.

Juvenile ovarian granulosa cell tumor: a benign or malignant condition?

N. Kalfa, C. Sultan, 2009, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Management of Peripheral Precocious Puberty in Girls

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

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

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

Competitive season of triathlon does not alter bone metabolism and bone mineral status in male triathletes.

O. Galy, C. Sultan, O. Coste, 2004, International journal of sports medicine.

Isolated 'idiopathic' micropenis: hidden genetic defects?

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

Predominant Sertoli cell deficiency in a 46,XY disorders of sex development patient with a new NR5A1/SF-1 mutation transmitted by his unaffected father.

M. Polak, P. Philibert, C. Sultan, 2011, Fertility and sterility.

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.

Undervirilization in XY newborns may hide a 5α-reductase deficiency: report of three new SRD5A2 gene mutations.

P. Philibert, C. Sultan, C. Pienkowski, 2010, International journal of andrology.

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.

Androgens and Fetal Growth

F. de Zegher, L. Ibáñez, C. Sultan, 1998, Hormone Research in Paediatrics.

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

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

Is Serum Serotonin Involved in the Bone Loss of Young Females with Anorexia Nervosa?

P. Courtet, E. Renard, M. Picot, 2015, Hormone and Metabolic Research.

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.

The IVS1- 2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiency

P. Philibert, C. Sultan, S. Lumbroso, 2010 .

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.

Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.

C. Bouvattier, C. Sultan, J. Carel, 2002, The Journal of clinical endocrinology and metabolism.

Unusual Phenotypical Variations in a Boy with McCune-Albright Syndrome

P. Philibert, C. Sultan, S. Ten, 2010, Hormone Research in Paediatrics.

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.

Searching for somatic mutations in McCune-Albright syndrome: a comparative study of the peptidic nucleic acid versus the nested PCR method based on 148 DNA samples.

N. Kalfa, P. Philibert, C. Sultan, 2006, European journal of endocrinology.

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

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

GH release after GHRH plus arginine administration in obese and overweight women with polycystic ovary syndrome

C. Nappi, F. Orio, A. Colao, 2003, Journal of endocrinological investigation.

Newborn Ambiguous Genitalia Management

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

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.

Salivary adiponectin levels are associated with training intensity but not with bone mass or reproductive function in elite Rhythmic Gymnasts

N. Roupas, N. Georgopoulos, P. Philibert, 2014, Peptides.

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.

Hematopoietic-Prostaglandin D2 synthase through PGD2 production is involved in the adult ovarian physiology

P. Philibert, C. Sultan, B. Boizet-Bonhoure, 2011, Journal of ovarian research.

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.

Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal function.

M. Dattani, N. Sebire, J. Jameson, 2007, The Journal of clinical endocrinology and metabolism.

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

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

Infant cholestasis in McCune‐Albright syndrome

F. Gottrand, J. Weill, C. Sultan, 2004, Acta paediatrica.

Recurrent ovarian cyst and mutation of the Gsα gene in ovarian cyst fluid cells: what is the link with McCune‐Albright syndrome? *

C. Sultan, S. Lumbroso, E. Bieth, 1997, Acta paediatrica.

Androgen Insensitivity Syndrome

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

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.

Consensus statement : Childhood obesity

Henry Anhalt, Cecilia Camacho-Hübner, Robert H. Lustig, 2005 .

Pediatric and adolescent gynecology. Evidence-based clinical practice. Preface.

C. Sultan, 2004, Endocrine development.

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.

Mayer–Rokitansky–Kuster–Hauser syndrome: Recent clinical and genetic findings

P. Philibert, C. Sultan, A. Biason-Lauber, 2009, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

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.

A clinical and molecular project on gonadoblastoma needs international collaboration

N. Kalfa, C. Sultan, O. Maillet, 2009, Rare Tumors.

[Hormonal evaluation in male infertility].

C. Sultan, Y. Iqbal, F. Audran, 1985, Annales de biologie clinique.

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.

Primary amenorrhea in a young Polish woman with complete androgen insensitivity syndrome and Sertoli–Leydig cell tumor: Identification of a new androgen receptor gene mutation and evidence of aromatase hyperactivity and apoptosis dysregulation within the tumor

P. Philibert, C. Sultan, B. Bilińska, 2007, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17βHSD-3 defect confirmed by molecular analysis

P. Philibert, C. Sultan, S. Ten, 2011, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency

C. Sultan, S. Ten, A. Bhangoo, 2010, Hormone Research in Paediatrics.

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.

Hypospadias: etiology and current research.

L. Baskin, N. Kalfa, C. Sultan, 2010, The Urologic clinics of North America.

Mutations of CXorf6 are associated with a range of severities of hypospadias.

O. Klein, L. Baskin, N. Kalfa, 2008, European journal of endocrinology.

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.

SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1‐mutated patient's management

P. Philibert, C. Sultan, C. Lefèvre, 2017, Clinical genetics.

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.

The evolving role of whole-exome sequencing in the management of disorders of sex development

K. McElreavey, C. Sultan, A. Bashamboo, 2021, Endocrine connections.

Ambiguous Genitalia in the Newborn

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

Endocrine disorders in adolescent and young female athletes: impact on growth, menstrual cycles, and bone mass acquisition.

N. Georgopoulos, C. Sultan, L. Maïmoun, 2014, The Journal of clinical endocrinology and metabolism.

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.

Clinical, Biological and Genetic Analysis of Prepubertal Isolated Ovarian Cyst in 11 Girls

K. McElreavey, P. Philibert, C. Sultan, 2010, PloS one.

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.

A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors

R. Veitia, S. Sarnacki, N. Kalfa, 2015, EBioMedicine.

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.

Hypospadias: Interactions between environment and genetics

L. Baskin, N. Kalfa, P. Philibert, 2011, Molecular and Cellular Endocrinology.

The new molecular biology of granulosa cell tumors of the ovary

B. Benayoun, R. Veitia, N. Kalfa, 2009, Genome Medicine.

Unusual Virilization in Girls with Juvenile Granulosa Cell Tumors of the Ovary Is Related to Intratumoral Aromatase Deficiency

C. Patte, N. Kalfa, P. Philibert, 2010, Hormone Research in Paediatrics.

Increased oestradiol level in seminal plasma in infertile men.

C. Sultan, S. Lumbroso, R. Mieusset, 1993, Human reproduction.

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.

Screening of MAMLD1 Mutations in 70 Children with 46,XY DSD: Identification and Functional Analysis of Two New Mutations

M. Polak, G. Pinto, J. Weill, 2012, PloS one.

Polymorphisms of MAMLD1 gene in hypospadias.

J. Valla, C. Béroud, J. Daurès, 2011, Journal of pediatric urology.

The forkhead factor FOXL2: a novel tumor suppressor?

B. Benayoun, R. Veitia, N. Kalfa, 2010, Biochimica et biophysica acta.

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.

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.

Gynecological care in young women: a high-risk period of life

C. Sultan, G. Creatsas, J. Bitzer, 2014, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

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.

Association Between Androgen Receptor Gene CAG Repeat Polymorphism and Plasma Testosterone Levels in Postmenopausal Women

Poli Mara Spritzer, P. Spritzer, I. Brum, 2005, The Journal of the Society for Gynecologic Investigation: JSGI.

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.

Despite a high prevalence of menstrual disorders, bone health is improved at a weight-bearing bone site in world-class female rhythmic gymnasts.

N. Roupas, N. Georgopoulos, P. Philibert, 2013, The Journal of clinical endocrinology and metabolism.

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.

Distinct molecular origins for Denys-Drash and Frasier syndromes

M. Gessler, J. Giltay, C. Sultan, 1993, Human Genetics.

Specific bone mass acquisition in elite female athletes.

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

Low serum IL-6 is associated with high 6-minute walking performance in asymptomatic women aged 20 to 70years

M. Picot, P. Bernard, H. Blain, 2012, Experimental Gerontology.

Appendicular skeletal muscle mass is the strongest independent factor associated with femoral neck bone mineral density in adult and older men

M. Picot, P. Bernard, H. Blain, 2010, Experimental Gerontology.

Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2

B. Benayoun, R. Veitia, M. Fellous, 2009, Journal of Medical Genetics.

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.

Effectiveness of Anastrozole and Cyproterone Acetate in Two Brothers with Familial Male Precocious Puberty

G. Pinto, C. Sultan, M. le Merrer, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

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 IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiency.

P. Philibert, C. Sultan, S. Lumbroso, 2010, Journal of endocrinological investigation.

Effects of physical activity on bone remodeling.

C. Sultan, L. Maïmoun, Laurent Maïmoun, 2011, Metabolism: clinical and experimental.

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.

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.

Effect of antioxidants and exercise on bone metabolism

C. Sultan, C. Caillaud, D. Mariano-Goulart, 2008, Journal of sports sciences.

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.

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.

Oral contraceptives partially protect from bone loss in young women with anorexia nervosa.

P. Courtet, E. Renard, M. Picot, 2019, Fertility and sterility.

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.

Polycystic ovary-like syndrome in adolescent competitive swimmers.

C. Sultan, F. Galtier, O. Coste, 2011, Fertility and sterility.

Circulating leptin concentrations can be used as a surrogate marker of fat mass in acute spinal cord injury patients.

C. Sultan, L. Maïmoun, M. Rossi, 2004, Metabolism: clinical and experimental.

Peripubertal female athletes in high-impact sports show improved bone mass acquisition and bone geometry.

K. Briot, P. Philibert, C. Sultan, 2013, Metabolism: clinical and experimental.

Specific effects of anorexia nervosa and obesity on bone mineral density and bone turnover in young women.

P. Courtet, E. Renard, S. Guillaume, 2019, The Journal of clinical endocrinology and metabolism.

Management of Adolescent Hyperandrogenism: Still a Challenge?

N. Kalfa, C. Sultan, L. Maïmoun, 2019, Menstrual Cycle Related Disorders.

A novel mutation c.118delA in exon 1 of the androgen receptor gene resulting in complete androgen insensitivity syndrome within a large family.

J. Kaufman, K. Decaestecker, P. Philibert, 2008, Fertility and sterility.

A Novel Mutation of the 5α-Reductase Type 2 Gene in Two Unrelated Egyptian Children with Ambiguous Genitalia

C. Sultan, S. Lumbroso, C. Sultan, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

Pediatric and adolescent gynecology. Evidence-based clinical practice. Preface.

C. Sultan, 2004, Endocrine development.

Phenotypic variation in a family with partial androgen insensitivity syndrome.

P. A. Lee, C. Sultan, C. Sultan, 1980, American journal of diseases of children.

Very premature pubarche in girls is not a pubertal variant

N. Kalfa, P. Philibert, C. Sultan, 2012, Hormones.

Macroorchidism due to autonomous hyperfunction of Sertoli cells and G(s)alpha gene mutation: an unusual expression of McCune-Albright syndrome in a prepubertal boy.

R. Rey, C. Sultan, S. Lumbroso, 2001, The Journal of clinical endocrinology and metabolism.

Primary Amenorrhea in Adolescents: Approach to Diagnosis and Management

N. Kalfa, C. Sultan, F. Paris, 2023, Endocrines.

Bone mineral density acquisition in peripubertal female rhythmic gymnasts is directly associated with plasma IGF1/IGF-binding protein 3 ratio.

C. Sultan, F. Galtier, O. Coste, 2010, European journal of endocrinology.

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.

Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.

R. Veitia, S. Caburet, S. Sarnacki, 2015, Human molecular genetics.

Isolated Hypospadias and Exposure to Endocrine Disrupting Chemicals During Pregnancy: a Multi-Institutional Controlled Study in a High Prevalence Area

J. Daurès, N. Kalfa, P. Philibert, 2014 .

Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2

B. Benayoun, R. Veitia, M. Fellous, 2009, Journal of Medical Genetics.

Effects of physical activity on bone remodeling.

C. Sultan, L. Maïmoun, 2011, Metabolism: clinical and experimental.

Endocrine disorders in adolescent and young female athletes: impact on growth, menstrual cycles, and bone mass acquisition.

N. Georgopoulos, C. Sultan, L. Maïmoun, 2014, The Journal of clinical endocrinology and metabolism.

Metformin, oral contraceptives or both to manage oligo-amenorrhea in adolescents with polycystic ovary syndrome? A clinical review

F. Orio, C. Sultan, S. Palomba, 2014, Gynecological Endocrinology.

Management of Adolescent Hyperandrogenism

C. Sultan, F. Paris, L. Gaspari, 2015 .

Oral contraceptives partially protect from bone loss in young women with anorexia nervosa.

P. Courtet, E. Renard, M. Picot, 2019, Fertility and sterility.