S. Drop

发表

Placebo-controlled, double-blind, cross-over trial of growth hormone treatment in prepubertal children with chronic renal failure

T. Stijnen, J. Wit, M. de Jong, 1992, Pediatric Nephrology.

Accuracy of final height prediction and effect of growth-reductive therapy in 362 constitutionally tall children.

T. Stijnen, E. V. van Gurp, S. Drop, 1996, The Journal of clinical endocrinology and metabolism.

FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)

H. Stoop, M. Fellous, L. Looijenga, 2008, The Journal of pathology.

Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity: prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling

H. Stoop, A. Gillis, L. Looijenga, 2017, Human reproduction.

A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty.

J. Martens, H. Brunner, H. Kremer, 1999, The Journal of clinical endocrinology and metabolism.

45,X/46,X,psu dic(Y) Gonadal Dysgenesis: Influence of the Two Cell Lines on the Clinical Phenotype, Including Gonadal Histology

L. Looijenga, M. Šnajderová, J. Lebl, 2013, Sexual Development.

Pubertal androgenization and gonadal histology in two 46,XY adolescents with NR5A1 mutations and predominantly female phenotype at birth.

L. Looijenga, H. Stoop, M. Cools, 2012, European journal of endocrinology.

Partial Deletion of the NR5A1 (SF1) Gene Detected by Synthetic Probe MLPA in a Patient with XY Gonadal Disorder of Sex Development

L. Looijenga, M. Cools, A. Wedell, 2011, Sexual Development.

Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity

R. Siebert, C. Seif, T. Reinehr, 2016, The Journal of clinical endocrinology and metabolism.

Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability.

A. Brinkmann, S. Drop, M. Niermeijer, 2001, The Journal of clinical endocrinology and metabolism.

The Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor Gene

C. Acerini, F. Darendeliler, S. Ahmed, 2016, The Journal of clinical endocrinology and metabolism.

Functional Analysis of Novel Androgen Receptor Mutations in a Unique Cohort of Indonesian Patients with a Disorder of Sex Development

A. Houtsmuller, J. Trapman, M. V. van Royen, 2009, Sexual Development.

Androgen Insensitivity Syndrome (AIS): Emotional Reactions of Parents and Adult Patients to the Clinical Diagnosis of AIS and Its Confirmation by Androgen Receptor Gene Mutation Analysis

F. Slijper, M. Niermeijer, A. Boehmer, 2000, Hormone Research in Paediatrics.

Gonadal Pathology and Tumor Risk in Relation to Clinical Characteristics in Patients with 45,X/46,Xy Mosaicism

L. Looijenga, H. Stoop, L. Looijenga, 2010 .

17 b -Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations*

H. Kayserili, L. Sandkuijl, H. Delemarre-van de Waal, 1999 .

Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious puberty.

H. Kremer, H. Ropers, J. Wit, 1993, Human molecular genetics.

Dose-response study of biosynthetic human growth hormone (GH) in GH-deficient children: effects on auxological and biochemical parameters. Dutch Growth Hormone Working Group.

J. Wit, A. Hokken-Koelega, S. Drop, 1992, The Journal of clinical endocrinology and metabolism.

Twenty-four-hour plasma growth hormone (GH) profiles, urinary GH excretion, and plasma insulin-like growth factor-I and -II levels in prepubertal children with chronic renal insufficiency and severe growth retardation.

T. Stijnen, J. Wit, A. Hokken-Koelega, 1990 .

THE EFFECT OF PUBERTY AND SHORT‐TERM ORAL ADMINISTRATION OF TESTOSTERONE UNDECANOATE ON GH TESTS AND SEX‐STEROID RELATED PLASMA COMPOUNDS IN GH DEFICIENT PATIENTS

S. Drop, H. Visser, L. Sabbe-Claus, 1982, Clinical endocrinology.

High dose testosterone therapy for reduction of final height in constitutionally tall boys: does it influence testicular function in adulthood?

J. Vreeburg, R. Weber, F. H. Jong, 1995, Clinical endocrinology.

A Novel AMH Missense Mutation in a Patient with Persistent Müllerian Duct Syndrome

L. Looijenga, Y. G. van der Zwan, K. Wolffenbuttel, 2012, Sexual Development.

Current Concepts in Tall Stature and Overgrowth Syndromes

M. Cappa, N. Greggio, S. Drop, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Gonadal pathology and tumor risk in relation to clinical characteristics in patients with 45,X/46,XY mosaicism.

L. Looijenga, H. Stoop, M. Cools, 2011, The Journal of clinical endocrinology and metabolism.

Tumor Risk in Disorders of Sex Development

L. Looijenga, J. Oosterhuis, M. Cools, 2010, Sexual Development.

Stem cell factor as a novel diagnostic marker for early malignant germ cells

C. Bokemeyer, H. Stoop, A. McIntyre, 2008, The Journal of pathology.

Gonadal Development and Tumor Formation at the Crossroads of Male and Female Sex Determination

L. Looijenga, M. Cools, K. Wolffenbuttel, 2011, Sexual Development.

Genotype versus phenotype in families with androgen insensitivity syndrome.

W J Kleijer, T. H. van der Kwast, H. Brunner, 2001, The Journal of clinical endocrinology and metabolism.

Etiological studies of severe or familial hypospadias.

M. Mureau, F. de Jong, A. Themmen, 2001, The Journal of urology.

Variable Loss of Functional Activities of Androgen Receptor Mutants in Patients with Androgen Insensitivity Syndrome

A. Houtsmuller, J. Trapman, M. V. van Royen, 2013, Sexual Development.

Final Height after Gonadotrophin Releasing Hormone Agonist Treatment for Central Precocious Puberty: The Dutch Experience

H. Delemarre-van de Waal, B. Otten, D. Mul, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

Psychological assessments before and after treatment of early puberty in adopted children

D. Mul, W. Oostdijk, S. Drop, 2001, Acta paediatrica.

Methionyl human growth hormone in Turner's syndrome.

B. Otten, J. van den Brande, W. Oostdijk, 1988, Archives of disease in childhood.

Linkage and segregation analysis of HLA and congenital hypoaldosteronism due to corticosterone methyl-oxydase deficiency type I and type II.

J. Veldhuis, B. Dupont, B. D. de Jongh, 2008, Tissue antigens.

PROLONGED GALACTORRHOEA IN A 6‐YEAR‐OLD GIRL WITH ISOSEXUAL PRECOCIOUS PUBERTY DUE TO A FEMINIZING ADRENAL TUMOUR

G. Bruining, S. Drop, W. Sippell, 1981, Clinical endocrinology.

Long term sequelae of sex steroid treatment in the management of constitutionally tall stature.

S. Drop, S. de Muinck Keizer-Schrama, M. Torn, 1995, Archives of disease in childhood.

Growth response and levels of growth factors after two years growth hormone treatment are similar for a once and twice daily injection regimen in girls with Turner syndrome

T. Stijnen, H. Delemarre-van de Waal, S. Drop, 1997, Clinical endocrinology.

Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies.

W. Sippell, M. Peter, S. Drop, 1998, European journal of endocrinology.

A Controlled Trial of Methionyl Growth Hormone Therapy in Prepubertal Children with Short Stature, Subnormal Growth Rate and Normal Growth Hormone Response to Secretagogues

J. Wit, B. Otten, W. Oostdijk, 1989, Acta paediatrica Scandinavica.

Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997.

W. Sippell, M. Peter, L. Fawaz, 1997, The Journal of clinical endocrinology and metabolism.

The effect of ACTH stimulation on plasma steroids in two patients with congenital hypoaldosteronism and in their relatives.

H. Dörr, M. Schöneshöfer, W. Sippell, 1982, Acta endocrinologica.

A new model to predict final height in constitutionally tall children

T. Stijnen, S. Drop, S. Keizer‐Schrama, 1996, Acta paediatrica.

Comparative effect of two doses of growth hormone for growth hormone deficiency. The Dutch Growth Hormone Working Group.

J. Wit, A. Hokken-Koelega, S. de Muinck Keizer-Schrama, 1994, Archives of disease in childhood.

Germ-line and somatic mosaicism in the androgen insensitivity syndrome: implications for genetic counseling.

D. Halley, A. Brinkmann, M. Niermeijer, 1997, American journal of human genetics.

A Practical Approach to the Detection of Androgen Receptor Gene Mutations and Pedigree Analysis in Families with X-Linked Androgen Insensitivity

J. Oosterwijk, J. Trapman, D. Halley, 1994, Pediatric Research.

Yearly stepwise increments of the growth hormone dose results in a better growth response after four years in girls with Turner syndrome. Dutch Working Group on Growth Hormone.

T. Stijnen, H. Delemarre-van de Waal, J. Wit, 1996, The Journal of clinical endocrinology and metabolism.

Children Born Small for Gestational Age: Do They Catch Up?

A. Hokken-Koelega, M. D. de Ridder, S. Drop, 1995, Pediatric Research.

Double blind trial comparing the effects of two doses of growth hormone in prepubertal patients with chronic renal insufficiency.

T. Stijnen, W. Blum, M. D. de Jong, 1994, The Journal of clinical endocrinology and metabolism.

The effect of treatment with an LH-RH agonist (Buserelin) on gonadal activity growth and bone maturation in children with central precocious puberty

R. Odink, B. Otten, S. Drop, 1987, European Journal of Pediatrics.