W. Sippell

发表

New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes.

M. Forest, J. Simard, J. Chaussain, 1999, The Journal of clinical endocrinology and metabolism.

Environmental Factors and Puberty Timing: Expert Panel Research Needs

G. B. Buck Louis, J. Toppari, S. Swan, 2008, Pediatrics.

Prenatal dexamethasone treatment in pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency: effect on midgestational amniotic fluid steroid levels.

H. Dörr, W. Sippell, 1993, The Journal of clinical endocrinology and metabolism.

ACTH and multisteroid responses to corticotropin-releasing factor in depressive illness: Relationship to multisteroid responses after ACTH stimulation and dexamethasone suppression

A. Steiger, F. Holsboer, O. Benkert, 1984, Psychoneuroendocrinology.

Consensus Statement on 21-Hydroxylase Deficiency from The European Society for Paediatric Endocrinology and The Lawson Wilkins Pediatric Endocrine Society

W. Miller, P. Speiser, W. Sippell, 2002, Hormone Research in Paediatrics.

A higher rate of hyperandrogenic disorders in female-to-male transsexuals

W. Sippell, M. Peter, G. Bonatz, 1997, Psychoneuroendocrinology.

Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia: potential relevance of helix C for P450 oxidoreductase-21-hydroxylase interaction.

J. Grötzinger, O. Hiort, W. Sippell, 2008, The Journal of clinical endocrinology and metabolism.

Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia: identification, functional characterization, and structural analysis.

V. Prassolov, J. Grötzinger, W. Sippell, 2006, The Journal of clinical endocrinology and metabolism.

Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination

W. Sippell, M. Peter, E. Westphal, 1990, The Lancet.

Recurrence of the R947X mutation in unrelated families with autosomal dominant pseudohypoaldosteronism type 1: evidence for a mutational hot spot in the mineralocorticoid receptor gene.

M. de Castro, F. Fernandes-Rosa, A. Latronico, 2006, The Journal of clinical endocrinology and metabolism.

Long-term GnRH agonist treatment for female central precocious puberty does not impair reproductive function

F. Waldhauser, M. Ranke, S. Heger, 2006, Molecular and Cellular Endocrinology.

Catch-up growth following transfer from three times weekly im to daily sc administration of hGH in GH deficient patients, monitored by knemometry.

W. Sippell, M. Hermanussen, K. Geiger-Benoit, 1985, Acta endocrinologica.

Awards and Scholarships

W. Sippell, 2011 .

Treatment of children with central precocious puberty by a slow-release gonadotropin-releasing hormone agonist

R. Odink, W. Sippell, S. Drop, 1990, European Journal of Pediatrics.

Gonadotropin-releasing hormone analogue treatment for precocious puberty. Twenty years of experience.

S. Heger, W. Sippell, C. Partsch, 2005, Endocrine development.

Treatment of Pubertal Gynecomastia with the Specific Aromatase Inhibitor Anastrozole

W. Sippell, N. Krone, C. Partsch, 2004, Hormone Research in Paediatrics.

Central precocious puberty in girls with Williams syndrome.

R. Siebert, A. Wessel, W. Sippell, 2002, The Journal of pediatrics.

Treatment of central precocious puberty.

W. Sippell, C. Partsch, 2002, Best practice & research. Clinical endocrinology & metabolism.

Gonadal histology with testicular carcinoma in situ in a 15-year-old 46,XY female patient with a premature termination in the steroidogenic acute regulatory protein causing congenital lipoid adrenal hyperplasia.

B. Ure, M. Bergmann, O. Hiort, 1999, The Journal of clinical endocrinology and metabolism.

Selecting girls with precocious puberty for brain imaging: validation of European evidence-based diagnosis rule.

M. Cisternino, W. Sippell, D. Mul, 2003, The Journal of pediatrics.

Further analysis of the disturbed adrenocortical function in the cerebro-hepato-renal syndrome of zellweger

W. Sippell, L. Monnens, L. Govaerts, 1989, Journal of Inherited Metabolic Disease.

Identification of a novel mutation in the human mineralocorticoid receptor gene in a german family with autosomal-dominant pseudohypoaldosteronism type 1: further evidence for marked interindividual clinical heterogeneity.

M. Ludwig, W. Sippell, N. Krone, 2003, The Journal of clinical endocrinology and metabolism.

Relevance of major histocompatibility complex class II expression as a hallmark for the cellular differentiation in the human adrenal cortex.

W. Scherbaum, S. Bornstein, W. Sippell, 1997, The Journal of clinical endocrinology and metabolism.

Longitudinal analysis of growth over the first 3 years of life in Turner's syndrome.

Z. Hochberg, W. Sippell, L. Even, 2000, The Journal of pediatrics.

Serum Leptin Levels in Patients with Progressive Central Precocious Puberty1

W. Kiess, W. Blum, S. Heger, 1999, Pediatric Research.

Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice.

W. Sippell, N. Krone, J. Pleiss, 2005, Endocrinology.

Disorders of the Aldosterone Synthase and Steroid 11β-Hydroxylase Deficiencies

W. Sippell, M. Peter, J. Dubuis, 1999, Hormone Research in Paediatrics.

Steroid 17alpha-hydroxylase deficiency: functional characterization of four mutations (A174E, V178D, R440C, L465P) in the CYP17A1 gene.

J. Grötzinger, H. Schwarz, W. Sippell, 2009, The Journal of clinical endocrinology and metabolism.

Congenital Adrenal Hyperplasia due to 11-Hydroxylase Deficiency – Insights from Two Novel CYP11B1 Mutations (p.M92X, p.R453Q)

J. Grötzinger, H. Schwarz, W. Sippell, 2009, Hormone Research in Paediatrics.

Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene.

O. Hiort, W. Sippell, N. Krone, 2005, European journal of endocrinology.

Knemometry in childhood: accuracy and standardization of a new technique of lower leg length measurement.

W. Sippell, M. Hermanussen, J. Burmeister, 1988, Annals of human biology.

KNEMOMETRIC MONITORING OF EARLY EFFECTS OF HUMAN GROWTH HORMONE ON LEG LENGTH IN CHILDREN WITH GROWTH HORMONE DEFICIENCY

W. Sippell, M. Hermanussen, IgnazM. Valk, 1985, The Lancet.

Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

A. Ballabio, T. Meitinger, C. Petit, 1990, American journal of human genetics.

Nine Months' Subcutaneous Therapy with Synthetic Growth Hormone Releasing Factor in Children with Short Stature

W. Sippell, W. Sippell, R. Hümmelink, 1987, Acta paediatrica Scandinavica. Supplement.

Clinical and Molecular Spectrum of Somatic Mosaicism in Androgen Insensitivity Syndrome

A. Brinkmann, O. Hiort, G. Sinnecker, 1999, Pediatric Research.

Androgens and Fetal Growth

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

Combined treatment with testosterone (T) and ethinylestradiol (EE2) in constitutionally tall boys: is treatment with T plus EE2 more effective in reducing final height in tall boys than T alone?

W. Sippell, C. Partsch, R. Decker, 2002, The Journal of clinical endocrinology and metabolism.

Heterogeneity of Kallmann's syndrome

W. Sippell, M. Hermanussen, 1985, Clinical genetics.

Diagnosis and treatment of 17-hydroxylase deficiency

W. Sippell, M. Peter, H. Wernze, 1993, The Journal of Steroid Biochemistry and Molecular Biology.

Differentiation of male hypogonadotropic hypogonadism and constitutional delay of puberty by pulsatile administration of gonadotropin-releasing hormone.

W. Sippell, M. Hermanussen, C. Partsch, 1985, The Journal of clinical endocrinology and metabolism.

HLA‐A,B,C,DR typing and 17‐OHP determination for second trimester prenatal diagnosis of 21‐hydroxylase deficient CAH

E. Passarge, W. Sippell, F. Bidlingmaier, 1988, Prenatal diagnosis.

Infusion of low dose etomidate: correction of hypercortisolemia in patients with Cushing's syndrome and dose-response relationship in normal subjects.

B. Allolio, H. Schulte, W. Sippell, 1990, The Journal of clinical endocrinology and metabolism.

Anthropometrical Measurements and Androgen Levels in Males, Females, and Hormonally Untreated Female-To-Male Transsexuals

W. Sippell, M. Peter, R. Arndt, 1997, Archives of sexual behavior.

Increased sensitivity of the dexamethasone suppression test in depressed female patients based on multisteroid analysis

F. Holsboer, W. Sippell, H. Doerr, 1983, Psychiatry Research.

Dexamethasone suppression of 11‐deoxycorticosterone, corticosterone and cortisol in depressed female patients and normal controls

F. Holsboer, W. Sippell, H. Doerr, 1982, Acta psychiatrica Scandinavica.

Functional characterization of three CYP21A2 sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co‐expression system

F. Domínguez, J. Grötzinger, W. Sippell, 2009, Human mutation.

Serum Cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy

J. Dötsch, H. Dörr, W. Sippell, 2005, Journal of endocrinological investigation.

Effect of glucocorticoid excess on the cortisol/cortisone ratio

J. Dötsch, G. Stalla, H. Dörr, 2001, Steroids.

Evidence for Change of 11β-Hydroxysteroid Dehydrogenase Activity during Infancy and Childhood

J. Dötsch, H. Dörr, W. Sippell, 2000, Pediatric Research.

Aldosterone Synthase Deficiency

W. Sippell, M. Peter, 2001 .

Defects in Aldosterone Biosynthesis

W. Sippell, M. Peter, 2000 .

Periodical changes of short term growth velocity ('mini growth spurts') in human growth.

W. Sippell, M. Hermanussen, J. Burmeister, 1988, Annals of human biology.

Longitudinal studies of plasma aldosterone, corticosterone, deoxycorticosterone, progesterone, 17-hydroxyprogesterone, cortisol, and cortisone determined simultaneously in mother and child at birth and during the early neonatal period. I. Spontaneous delivery.

H. Versmold, W. Sippell, F. Bidlingmaier, 1978, The Journal of clinical endocrinology and metabolism.

Can the Knemometer Shorten the Time for Growth Rate Assessment?

W. Sippell, M. Hermanussen, J. Burmeister, 1987, Acta paediatrica Scandinavica. Supplement.

GH Deficient Children Receiving GH Replacement Do not Grow during Intermittent Infectious Illness

W. Sippell, M. Hermanussen, W. Sippell, 1986, Acta paediatrica Scandinavica.

Cystic Fibrosis: Lysosomal and Mitochondrial Enzyme Activities of Lymphoid Cell Lines

H. Shwachman, W. Sippell, I. Antonowicz, 1972, Pediatric Research.

Clinical, Hormonal and Molecular Genetic Characterization of Hungarian Patients with 11β-Hydroxylase Deficiency

K. Rácz, J. Sólyom, W. Sippell, 2001 .

Antenatal betamethasone therapy: effects on maternal, fetal, and neonatal mineralocorticoids, glucocorticoids, and progestins.

H. Versmold, H. Dörr, W. Sippell, 1986, The Journal of pediatrics.

Plasma Mineralocorticoids, Glucocorticoids, and Progestins in Premature Infants: Longitudinal Study during the First Week of Life

H. Versmold, W. Sippell, F. Bidlingmaier, 1988, Pediatric Research.

The Journal of Clinical Endocrinology & Metabolism Printed in U.S.A. Copyright © 2001 by The Endocrine Society Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1: Identification of a Novel Mutation in the Human Mineralocorticoid Receptor

W. Sippell, M. Peter, J. López-Siguero, 2022 .

Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasia.

A. Braun, A. Roscher, W. Sippell, 2002, Clinical chemistry.

The early mineralocorticoid effector mechanism, the sodium—proton exchanger, is sensitized in lymphocytes from patients with Cushing's syndrome

M. Christ, M. Wehling, W. Sippell, 1992, Clinical endocrinology.

Clinical, Endocrine, and Molecular Genetic Findings in Patients with 17β-Hydroxysteroid Dehydrogenase Deficiency

O. Hiort, W. Sippell, P. Holterhus, 2000, Hormone Research in Paediatrics.

“Negative growth” in anorexia nervosa assessed by knemometry

W. Sippell, M. Hermanussen, K. Geiger-Benoit, 1987, European Journal of Pediatrics.

Pseudohypoaldosteronism in a child with Down syndrome. Long-term management of salt loss by ion exchange resin administration

H. Dörr, W. Sippell, H. Saule, 1984, European Journal of Pediatrics.

Development of endogenous glucocorticoids, mineralocorticoids and progestins in the human fetal and perinatal period

W. Sippell, F. Bidlingmaier, D. Knorr, 1980, European Journal of Clinical Pharmacology.

Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene.

W. Sippell, M. Peter, N. Krone, 2004, The Journal of clinical endocrinology and metabolism.

Congenital Hypoaldosteronism: The Visser-Cost Syndrome Revisited

W. Sippell, M. Peter, 1996, Pediatric Research.

Multisteroid analysis in children with terminal aldosterone biosynthesis defects.

W. Sippell, M. Peter, C. Partsch, 1995, The Journal of clinical endocrinology and metabolism.

Plasma Levels of Aldosterone, Corticosterone, 11-Deoxycorticosterone, Progesterone, 17-Hydroxyprogesterone, Cortisol, and Cortisone During Infancy and Childhood

H. Dörr, W. Sippell, F. Bidlingmaier, 1980, Pediatric Research.

Comparison of two tests for heterozygosity in congenital adrenal hyperplasia (CAH).

W. Sippell, F. Bidlingmaier, J. Weil, 1979, Acta endocrinologica.

Prenatal diagnosis of congenital adrenal hypoplasia.

H. Dörr, W. Sippell, M. Peter, 1996, Hormone research.

Simultaneous radioimmunoassay of plasma aldosterone, corticosterone, 11-deoxycorticosterone, progesterone, 17-hydroxyprogesterone, 11-deoxycortisol, cortisol and cortisone.

H. Dörr, W. Sippell, F. Bidlingmaier, 1978, Journal of steroid biochemistry.

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.

Congenital Adrenal Hypoplasia

W. Sippell, M. Peter, 2001 .

Plasma testosterone in male puberty. II. hCG stimulation test in boys with hypospadia.

W. Sippell, F. Bidlingmaier, D. Beckmann, 1979, Acta endocrinologica.

Longitudinal study of progestins, mineralocorticoids, and glucocorticoids throughout human pregnancy.

H. Versmold, H. Dörr, W. Sippell, 1989, The Journal of clinical endocrinology and metabolism.

Lysosomal and mitochondrial enzyme activities in human lymphoid cell lines obtained from children with acute lymphoblastic leukemia and controls.

H. Lazarus, H. Shwachman, W. Sippell, 1975, Experimental cell research.

Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

W. Sippell, F. Riepe, 2007, Reviews in Endocrine and Metabolic Disorders.

Multiplex Ligation-Dependent Probe Amplification Analysis of the NR0B1(DAX1) Locus Enables Explanation of Phenotypic Differences in Patients with X-Linked Congenital Adrenal Hypoplasia

S. Bens, A. Haake, W. Sippell, 2012, Hormone Research in Paediatrics.

Congenital adrenal hypoplasia: clinical spectrum, experience with hormonal diagnosis, and report on new point mutations of the DAX-1 gene.

W. Sippell, M. Peter, C. Partsch, 1998, The Journal of clinical endocrinology and metabolism.

Enhanced at puberty 1 (EAP1) is a new transcriptional regulator of the female neuroendocrine reproductive axis.

S. Ojeda, F. Galimi, C. Roth, 2007, The Journal of clinical investigation.

Management and outcome of central precocious puberty

S. Heger, W. Sippell, C. Partsch, 2002, Clinical endocrinology.

Reference ranges of lutropin and follitropin in the luliberin test in prepubertal and pubertal children using a monoclonal immunoradiometric assay.

W. Sippell, C. Partsch, R. Hümmelink, 1990, Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie.

Simultaneous determination of seven unconjugated steroids in maternal venous and umbilical arterial and venous serum in elective and emergency cesarean section at term.

H. Dörr, W. Sippell, F. Bidlingmaier, 1979, American journal of obstetrics and gynecology.

Functional characterization of two novel point mutations in the CYP21 gene causing simple virilizing forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Nils Krone, J. Grötzinger, W. Sippell, 2005, The Journal of clinical endocrinology and metabolism.

Assessment of the most common CYP21A2 point mutations in a cohort of congenital adrenal hyperplasia patients from Egypt

W. Sippell, M. Peter, M. Essawi, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

Treatment of Silver-Russell type dwarfism with human growth hormone: effects on serum somatomedin-C levels and on longitudinal growth studied by knemometry.

W. Sippell, M. Hermanussen, C. Partsch, 1986, Acta endocrinologica. Supplementum.

Unconjugated cortisol and corticosterone levels in amniotic fluid.

W. Sippell, 1981, American journal of obstetrics and gynecology.

Concentrations of aldosterone, corticosterone, 11-deoxycorticosterone, progesterone, 17-hydroxyprogesterone, 11-deoxycortisol, cortisol, and cortisone determined simultaneously in human amniotic fluid throughout gestation.

H. Dörr, W. Sippell, F. Bidlingmaier, 1981, The Journal of clinical endocrinology and metabolism.

Management of Congenital Adrenal Hyperplasia: Results of the ESPE Questionnaire

W. Sippell, N. Krone, C. Partsch, 2002, Hormone Research in Paediatrics.

Congenital adrenal hyperplasia due to 11-hydroxylase deficiency: functional characterization of two novel point mutations and a three-base pair deletion in the CYP11B1 gene.

Nils Krone, J. Grötzinger, W. Sippell, 2005, The Journal of clinical endocrinology and metabolism.

Long-Term Follow-Up of Spontaneous Development in a Boy with Familial Male Precocious Puberty

W. Sippell, J. Gromoll, N. Krone, 2004, Hormone Research in Paediatrics.

Differential diagnosis of male central hypogonadism by short-term pulsatile LHRH administration.

W. Sippell, M. Hermanussen, J. Partsch, 1984, Upsala journal of medical sciences.

Adrenocortical Steroids in Small-for-Gestational-Age Term Infants during the Early Neonatal Period1,2

H. Versmold, W. Sippell, F. Bidlingmaier, 1989, Pediatric Research.

The development of anorectal continence and its significance in the diagnosiso of Hirschsprung's disease.

W. Sippell, A. Holschneider, E. Kellner, 1976, Journal of pediatric surgery.

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

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

Hyporeninaemic hypoaldosteronism after growth hormone treatment

W. Sippell, M. Peter, H. Mönig, 1996, The Lancet.

Long-Term Suppression of Pituitary-Gonadal Function with Three-Month Depot of Leuprorelin Acetate in a Girl with Central Precocious Puberty

W. Sippell, C. Partsch, Inka Baus, 2002, Hormone Research in Paediatrics.

Hypogonadism in congenital adrenal hypoplasia: evidence for a hypothalamic origin.

W. Sippell, K. Kruse, K. Schnakenburg, 1984, The Journal of clinical endocrinology and metabolism.

Blunted aldosterone response to dexamethasone in female patients with endogenous depression

F. Holsboer, H. Dörr, W. Sippell, 1982, Psychoneuroendocrinology.

Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita

H. Dörr, J. Weigel, W. Sippell, 2005, Human mutation.

CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.

R. Kofler, S. Geley, P. White, 1996, The Journal of clinical endocrinology and metabolism.

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.

Analyzing the functional and structural consequences of two point mutations (P94L and A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia resulting from 11-hydroxylase deficiency.

J. Grötzinger, W. Sippell, N. Krone, 2006, The Journal of clinical endocrinology and metabolism.

Evidence for endocrinological abnormalities in heterozygotes for adrenal 11 beta-hydroxylase deficiency of a family with the R448H mutation in the CYP11B1 gene.

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

[Prenatal diagnosis and therapy of adrenogenital syndrome with 21-hydroxylase deficiency. Position of the Pediatric Endocrinology Study Group of the German Society of Pediatrics and the Section of Pediatric Endocrinology of the German Society of Endocrinology].

H. Dörr, W. Sippell, R. Willig, 1992, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde.

[Prenatal diagnosis and therapy of adrenogenital syndrome with 21-hydroxylase deficiency].

H. Dörr, W. Sippell, R. Willig, 1992, Geburtshilfe und Frauenheilkunde.

Serum Concentrations of Adrenal Steroids and Their Precursors as a Measure of Maturity of Adrenocortical Function in Very Premature Newborns

R. Voutilainen, Päivi Nykänen, W. Sippell, 2010, Hormone Research in Paediatrics.

Aldosterone Synthase Deficiency Type I: Hormonal and Genetic Analyses of Two Cases

W. Sippell, M. Peter, J. López-Siguero, 2000, Hormone Research in Paediatrics.

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.

Amino acid substitution R384P in aldosterone synthase causes corticosterone methyloxidase type I deficiency.

R. Kofler, S. Geley, W. Sippell, 1995, 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.

LONGITUDINAL STUDY OF ADRENOCORTICAL STEROIDS IN LARGE FOR GESTATIONAL AGE (LCA) INFANTS AT BIRTH AND DURING NEONATAL PERIOD

H. Versmold, W. Sippell, F. Bidlingmaier, 1988, Pediatric Research.

Treatment of anorchia with oral testosterone undecanoate: pharmacodynamics and clinical effectiveness.

W. Sippell, F. Bidlingmaier, W. Baumgartner, 1980, Acta endocrinologica.

[Adrenalectomy as therapy in refractory adrenogenital syndrome].

K. E. von Mühlendahl, W. Sippell, 1989, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde.

Congenital Adrenal Hyperplasia in Adulthood: Do Men Need to Continue Treatment?

W. Sippell, H. Mönig, 2005, Hormone Research in Paediatrics.

Congenital Adrenal Hyperplasia in Adult Life

W. Sippell, H. Mönig, 2005 .

Growth Hormone Therapy for Short Children Born Small for Gestational Age

P. Chatelain, A. Carrascosa, W. Sippell, 2007, Hormone Research in Paediatrics.

Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1.

G. Fejes-Tóth, J. Grötzinger, B. Karges, 2006, The Journal of clinical endocrinology and metabolism.

Lactobezoar in an infant: an unusual cause of upper abdominal tumour persisting for several weeks

H. Fendel, W. Sippell, C. Kalb, 1977, European Journal of Pediatrics.

Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice.

W. Sippell, N. Krone, J. Pleiss, 2005, Endocrinology.

Growth and pubertal development during and after treatment with a slow-release gonadotropin-releasing hormone agonist in central precocious puberty.

W. Sippell, S. Drop, C. Partsch, 1991, Hormone research.

Comparison of complete and incomplete suppression of pituitary-gonadal activity in girls with central precocious puberty: influence on growth and predicted final height. The German-Dutch Precocious Puberty Study Group.

R. Odink, W. Sippell, M. Peter, 1993, Hormone research.

Growth, bone maturation and height prediction after three years of therapy with the slow release GnRH-agonist Decapeptyl-Depot in children with central precocious puberty.

R. Odink, W. Sippell, S. Drop, 1992, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Long‐Term Results with a Slow‐Release Gonadotrophin‐Releasing Hormone Agonist in Central Precocious Puberty

R. Odink, W. Sippell, S. Drop, 1991 .

Effects of GnRH Analogues on Growth and Bone Maturation: A Role for Growth Factors and Adrenal Androgens

W. Sippell, S. Drop, C. Partsch, 1990 .

Impairment of 11β-hydroxylase but not 21-hydroxylase in adrenal 'incidentalomas'

B. Allolio, M. Reincke, W. Sippell, 1997 .

Disproportionate stature but normal height in hypochondroplasia

W. Sippell, N. Krone, F. Riepe, 2005, European Journal of Pediatrics.

Dexamethasone suppression test in female patients with endogenous depression: determinations of plasma corticosterone, 11-deoxycorticosterone, 11-deoxycortisol, cortisol and cortisone

F. Holsboer, H. Dörr, W. Sippell, 1982, Psychoneuroendocrinology.

Adrenogenitales Syndrom (AGS) mit 21-Hydroxylase-Defekt

H. Dörr, W. Sippell, 1993 .

Cortisol, 11-deoxycortisol, and ACTH concentrations after dexamethasone in depressed patients and healthy volunteers

F. Holsboer, W. Sippell, H. Doerr, 1984, Psychiatry Research.

Sephadex LH-20 multiple-column chromatography for the simultaneous separation of progesterone, deoxycorticosterone and 17alpha-hydroxyprogesterone from small plasma samples.

W. Sippell, W. Golder, 1976, Journal of chromatography.

Satoyoshi syndrome: A rare multisystemic disorder requiring systemic and symptomatic treatment

U. Stephani, S. Heger, W. Sippell, 2006, Brain and Development.

ESPE - The First 50 Years: A History of the European Society for Paediatric Endocrinology

W. Sippell, 2011 .

Plasma aldosterone and 11-deoxycortisol in term neonates: a reevaluation.

H. Versmold, H. Dörr, W. Sippell, 1987, The Journal of clinical endocrinology and metabolism.

Longitudinal study of plasma pregnenolone and 17-hydroxypregnenolone in full-term and preterm neonates at birth and during the early neonatal period.

W. Sippell, C. Partsch, F. Riepe, 2002, The Journal of clinical endocrinology and metabolism.

Homozygous Deletion of Arginine-173 in the CYP11B2 Gene in a Girl with Congenital Hypoaldosteronism

W. Sippell, M. Peter, K. Kapelari, 1998, Hormone Research in Paediatrics.

Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II

W. Sippell, M. Peter, K. Bünger, 1998, European Journal of Pediatrics.

Evidence of 11 beta‐hydroxylase deficiency in childhood adrenocortical tumors. The plasma corticosterone/11‐deoxycorticosterone ratio as a possible marker for malignancy

W. Sippell, F. Bidlingmaier, S. Drop, 1987, Cancer.

Evidence of I I Beta-Hydroxylase Deficiency in Childhood Adrenocortical Tumors

W. Sippell, F. Bidlingmaier, H. Doerr, 2006 .

Differences in infantile growth patterns in Turner syndrome girls with and without spontaneous puberty.

L. Dunkel, Z. Hochberg, E. Doveh, 2005, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Precocious Puberty as the Presenting Symptom of Adrenal Tumors

H. Dörr, W. Sippell, S. Drop, 1987 .

PITFALLS OF PRENATAL TREATMENT OF CONGENITAL ADRENAL HYPERPLASIA (CAH) DUE TO 21-HYDROXYLASE DEFICIENCY

H. Dörr, D. Haack, W. Sippell, 1986, Pediatric Research.

The steroid hormonal milieu of the undisturbed human fetus and mother at 16-20 weeks gestation.

A. Aynsley-Green, I. Mackenzie, W. Sippell, 1991, The Journal of clinical endocrinology and metabolism.

Long-term results with a slow-release gonadotrophin-releasing hormone agonist in central precocious puberty. Dutch-German Precocious Puberty Study Group.

R. Odink, W. Sippell, S. Drop, 1991, Acta paediatrica Scandinavica. Supplement.

Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1.

F. Baronio, W. Sippell, F. Riepe, 2007, European journal of endocrinology.

Genetic Heterogeneity in Autosomal Dominant Pseudohypoaldosteronism Type I: Exclusion of Claudin-8 as a Candidate Gene

A. Yu, W. Sippell, F. Riepe, 2004, American Journal of Nephrology.

Congenital Adrenal Hyperplasia due to 11-Hydroxylase Deficiency – Insights from Two Novel CYP11B1 Mutations (p.M92X, p.R453Q)

J. Grötzinger, H. Schwarz, W. Sippell, 2009, Hormone Research in Paediatrics.

The residue E351 is essential for the activity of human 21-hydroxylase: evidence from a naturally occurring novel point mutation compared with artificial mutants generated by single amino acid substitutions

J. Grötzinger, W. Sippell, N. Krone, 2005, Journal of Molecular Medicine.

Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure.

K. Zerres, W. Sippell, B. Hauffa, 1999, The Journal of clinical endocrinology and metabolism.

Hypothalamic-pituitary-gonadal function in two infants with Smith-Lemli-Opitz syndrome.

W. Sippell, R. Pankau, C. Partsch, 1992, American journal of medical genetics.

Absence of exercise-induced leptin suppression associated with insufficient epinephrine reserve in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

J. Dötsch, J. Lenders, S. Krüger, 2006, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.