Riepe, Felix ; Krone, Nils ; Kruger SN ; Sweep FC ; Lenders JW ; Dotsch J ; Mönig, Heiner ; Sippell, Wolfgang ; Partsch CJ:
Absence of exercise-induced leptin suppression associated with insufficient epinephrine reserve in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency .
In: Exp Clin Endocrinol Diabetes 114 (2006), Nr. 3, S. 105-10

Krone, Nils ; Grischuk Y ; Rubin, Marina ; Rehberg, Volker ; Grotzinger J ; Holterhus, Paul-Martin ; Sippell, Wolfgang ; Riepe, Felix:
Analyzing the functional and structural consequences of two point mutations (P94L, A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia (CAH) due to 11-hydroxylase deficiency. .
In: J Clin Endocrinol Metab 91 (2006), Nr. 7, S. 1268-8

Fölster-Holst, Regina ; Riepe, Felix ; Ahrens W ; Möller, Maike ; Brasch, Jochen ; Partsch, Carl-Joachim ; Hiort O ; Sippell, Wolfgang:
Calcinosis cutis bei hereditärer Albright-Osteodystrophie = [Calcinosis cutis in Albright hereditary osteodystrophy Pseudohypoparathyroidism Type Ia.] .
In: Hautarzt 57 (2006), Nr. 10, S. 893-897

Riepe, Felix ; Finkeldei J ; de Sanctis L ; Einaudi S ; Testa A ; Karges B ; Peter, M ; Viemann, Matthias ; Grötzinger, Joachim ; Sippell, Wolfgang ; Fejes-Toth G ; Krone N:
Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1. .
In: J Clin Endocrinol Metab 91 (2006), Nr. 11, S. 4552-61

Grischuk Y ; Rubtsov P ; Riepe, Felix ; Grotzinger J ; Beljelarskaia S ; Prassolov V ; Kalintchenko N ; Semitcheva T ; Peterkova V ; Tiulpakov A ; Sippell, Wolfgang ; Krone N:
Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia (CAH): identification, functional characterization and structural analysis .
In: J Clin Endocrinol Metab 91 (2006), Nr. 12, S. 4976-80

Partsch, Carl-Joachim ; Riepe, Felix ; Krone N ; Sippell, Wolfgang ; Pohlenz J:
Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literature .
In: Exp Clin Endocrinol Diabetes 114 (2006), Nr. 5, S. 227-34

Heger S ; Rubin, Marina ; Ranke M ; Schwarz HP ; Waldhauser F ; Partsch CJ ; Sippell, Wolfgang:
Long-term GnRH agonist treatment for female central precocious puberty does not impair reproductive function. .
In: Mol Cell Endocrinol 254-255 (2006), S. 217-220

Fernandes-Rosa FL ; de Castro M ; Latronico AC ; Sippell, Wolfgang ; Riepe, Felix ; Antonini SR:
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. .
In: J Clin Endocrinol Metab 91 (2006), Nr. 9, S. 3671-5

Heger S ; Kuester RM ; Volk, Ruth Elisabeth ; Stephani, Ulrich ; Sippell, Wolfgang:
Satoyoshi syndrome: a rare multisystemic disorder requiring systemic and symptomatic treatment .
In: Brain Dev 28 (2006), Nr. 5, S. 300-4

Krone, Nils ; Riepe, Felix ; Partsch CJ ; Vorhoff W ; Bramswig J ; Sippell, Wolfgang:
Three novel point mutations of the CYP21 gene detected in classical forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. .
In: Exp Clin Endocrinol Diabetes 114 (2006), Nr. 3, S. 111-7

Krone, Nils ; Riepe, Felix ; Götze D ; Korsch E ; Rister M ; Commentz J ; Partsch, Carl-Joachim ; Grötzinger, Joachim ; Peter M ; Sippell, Wolfgang:
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 .
In: J Clin Endocrinol Metab 90 (2005), Nr. 6, S. 3724

Mönig, Heiner ; Sippell, Wolfgang:
Congenital adrenal hyperplasia in adulthood: do men need to continue treatment?
In: Hormone Research 64 (2005), Nr. Suppl 2, S. 71-73

Riepe, Felix ; Tatzel S ; Sippell, Wolfgang ; Pleiss J ; Krone, Nils:
Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice .
In: Endocrinology 146 (2005), Nr. 6, S. 2563-2574

Vallette-Kasic S ; Brue T ; Pulichino AM ; Gueydan M ; Barlier A ; David M ; Nicolino M ; Malpuech G ; Dechelotte P ; Deal C ; Van Vliet G ; De Vroede M ; Riepe, Felix ; Partsch, Carl-Joachim ; Sippell, Wolfgang ; Berberoglu M ; Atasay B ; de Zegher F ; Beckers D ; Kyllo J ; Donohoue P ; Fassnacht M ; Allolio B ; Noordam C ; Dunkel L ; Hero M ; Pigeon B ; Pigeon B ; Weill J ; Yigit S ; Brauner R ; Cummings E ; Riddell C ; Enjalbert A ; Drouin J:
CONGENITAL ISOLATED ACTH DEFICIENCY, AN UNDERESTIMATED CAUSE OF NEONATAL DEATH, EXPLAINED BY TPIT MUTATIONS .
In: J Clin Endocrinol Metab. 2004 Dec 21; 90 (2005), Nr. 3, S. 1323-31

Hochberg Z ; Khaesh-Goldberg I ; Partsch CJ ; Zadik Z ; Bistritzer T ; Cohen A ; Doveh E ; Sippell, Wolfgang ; Dunkel L:
Differences in infantile growth patterns in Turner syndrome girls with and without spontaneous puberty. .
In: Horm Metab Res. 37 (2005), Nr. 4, S. 236-41

Riepe, Felix ; Krone, Nils ; Sippell, Wolfgang:
Disproportionate stature but normal height in hypochondroplasia .
In: European Journal of Pediatrics 164 (2005), Nr. 6, S. 397-9
Stichwörter:  Signatur 12/2005

Riepe, Felix ; Ahrens W ; Krone, Nils ; Fölster-Holst, Regina ; Brasch J ; Sippell, Wolfgang ; Hiort O ; Partsch, Carl-Joachim:
Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene .
In: Eur J Endocrinol 152 (2005), Nr. 4, S. 515-519

Krone, Nils ; Riepe, Felix ; Grotzinger J ; Partsch CJ ; Sippell, Wolfgang:
Functional characterization of two novel point mutations in the CYP21 gene causing simple virilizing forms of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. .
In: J Clin Endocrinol Metab. 90 (2005), Nr. 1, S. 445-54

Heger S ; Sippell, Wolfgang ; Partsch CJ:
Gonadotropin-releasing hormone analogue treatment for precocious puberty .
In: Endocr Dev. 8 (2005), S. 94-125

Dotsch J ; Hohenberger I ; Riepe, Felix ; Sippell, Wolfgang ; Dorr HG:
Serum cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy. .
In: J Endocrinol Invest. 28 (2005), Nr. 5, S. 413-6

Krone, Nils ; Riepe, Felix ; Grötzinger, Joachim ; Partsch, Carl-Joachim ; Bramswig J ; Sippell, Wolfgang:
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 .
In: J Mol Med. 83 (2005), Nr. 7, S. 561-568

Krone, Nils ; Riepe, Felix ; Dorr HG ; Morlot M ; Rudorff KH ; Drop SL ; Weigel J ; Pura M ; Kreze A ; Boronat M ; de Luca F ; Tiulpakov A ; Partsch CJ ; Peter M ; Sippell, Wolfgang:
Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita .
In: Hum Mutat. 255 (2005), Nr. 5, S. 502-3

Vallette-Kasic S ; Pulichino AM ; Gueydan M ; Barlier A ; David M ; Malpuech G ; Deal C ; Van Vliet G ; de Vroede M ; Riepe, Felix ; Partsch CJ ; Sippell, Wolfgang ; Berberoglu M ; Atasay B ; de Zegher F ; Kyllo J ; Donohoue P ; Dechelotte P ; Fassnacht M ; Noordam K ; Dunkel L ; Pigeon B ; Weill J ; Yigit S ; Brauner R ; Leger J ; Heinrich JJ ; Enjalbert A ; Brue T ; Drouin J:
A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations. .
In: Endocr Res. 30 (2004), Nr. 4, S. 943-4

Riepe, Felix ; Krone, Nils ; Morlot M ; Peter M ; Sippell, Wolfgang ; Partsch, Carl-Joachim:
Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene. .
In: J Clin Endocrinol Metab. 89 (2004), Nr. 5, S. 2150-2

Kruse, Björn ; Riepe, Felix ; Krone, Nils ; Bosinski HA ; Kloehn, Sievert ; Partsch, Carl-Joachim ; Sippell, Wolfgang ; Mönig, Heiner:
Congenital adrenal hyperplasia - how to improve the transition from adolescence to adult life. .
In: Exp Clin Endocrinol Diabetes 112 (2004), Nr. 7, S. 343-355

Huey CL ; Riepe, Felix ; Sippell, Wolfgang ; Yu AS:
Genetic heterogeneity in autosomal dominant pseudohypoaldosteronism type I: exclusion of claudin-8 as a candidate gene. .
In: Am J Nephrol. 24 (2004), Nr. 5, S. 483-7

Partsch, Carl-Joachim ; Krone, Nils ; Riepe, Felix ; Gromoll J ; Sippell, Wolfgang:
Long-term follow-up of spontaneous development in a boy with familial male precocious puberty. .
In: Horm Res. 62 (2004), Nr. 4, S. 177-81

Riepe, Felix ; Baus, Inka ; Wiest S ; Krone, Nils ; Sippell, Wolfgang ; Partsch, Carl-Joachim:
Treatment of Pubertal Gynecomastia with the Specific Aromatase Inhibitor Anastrozole. .
In: Hormone Research 62 (2004), Nr. 3, S. 113-118

Riepe, Felix ; Krone, Nils ; Peter, M ; Sippell, Wolfgang ; Partsch, Carl-Joachim:
Chromatographic system for the simultaneous measurement of plasma 18-hydroxy-11-deoxycorticosterone and 18-hydroxycorticosterone by radioimmunoassay: reference data for neonates and infants and its application in aldosterone-synthase deficiency. .
In: J Chromatogr B Analyt Technol Biomed Life Sci 5 (2003), Nr. 2, S. 293-301
Stichwörter:  Signatur 3/2003

Pulichino AM ; Vallette-Kasic S ; Couture C ; Gauthier Y ; Brue T ; David M ; Malpuech G ; Deal C ; Van Vliet G ; De Vroede M ; Riepe, Felix ; Partsch, Carl-Joachim ; Sippell, Wolfgang ; Berberoglu M ; Atasay B ; Drouin J:
Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency. .
In: Genes Dev 17 (2003), Nr. 6, S. 711-6

Riepe, Felix ; Krone, Nils ; Morlot M ; Ludwig M ; Sippell, Wolfgang ; Partsch, Carl-Joachim:
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. .
In: J Clin Endocrinol Metab 88 (2003), Nr. 4, S. 1683-6
Stichwörter:  Signatur 8/2003

Sippell, Wolfgang:
Krankheiten der Nebennieren .
In: Lentze, MJ ; Schaub, Jürgen ; Schulte, FJ ; Spranger, J (Hrsg.) : Pädiatrie : Grundlagen und Praxis.
2. Aufl. Berlin : Springer, 2003, S. 535-549. - ISBN 3-540-43628-6
Stichwörter:  Signatur I A 34/2

Chalumeau M ; Hadjiathanasiou CG ; Ng SM ; Cassio A ; Mul D ; Cisternino M ; Partsch, Carl-Joachim ; Theodoridis C ; Didi M ; Cacciari E ; Oostdijk W ; Borghesi A ; Sippell, Wolfgang ; Breart G ; Brauner R:
Selecting girls with precocious puberty for brain imaging: validation of European evidence-based diagnosis rule. .
In: J Pediatr. 143 (2003), Nr. 4, S. 445-50

Partsch, Carl-Joachim ; Japing, I ; Siebert, R ; Gosch, A ; Wessel, A ; Sippell, Wolfgang ; Pankrau, R:
Central precocious puberty in girls with Williams syndrome. .
In: The Journal of pediatrics. 141 (2002), Nr. 3, S. 441-4

Decker, R ; Partsch, Carl-Joachim ; Sippell, Wolfgang:
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?
In: The Journal of clinical endocrinology and metabolism. 87 (2002), Nr. 4, S. 1634-9

Woelfle, J ; Hoepffner, W ; Sippell, Wolfgang ; Bramswig, JH ; Heidemann, P ; Deiss, D:
Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease-related complications. .
In: Clinical endocrinology. 56 (2002), Nr. 2, S. 231-8
Stichwörter:  Signatur 20/2002

Clayton PE ; Miller WL ; Oberfield SE ; Ritzen EM ; Sippell, Wolfgang ; Speiser PW ; ESPE/ LWPES CAH Working Group:
Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society. .
In: Horm Res. 58 (2002), Nr. 4, S. 188-95
Stichwörter:  Signatur 14/2002

Clayton, Peter E. ; Miller, Walter L. ; Oberfield, Sharon E. ; Ritzen, Martin E. ; Sippell, Wolfgang ; Speiser, Phyllis S.:
Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and The European Society for Pediatric Endocrinology .
In: The Journal of Clinical Endocrinology and metabolism 87 (2002), Nr. 9, S. 4048-4053
Stichwörter:  Signatur 13/2002

Schroeter, M ; Baus, Inka ; Sippell, Wolfgang ; Partsch, Carl-Joachim:
Long-term suppression of pituitary-gonadal function with three-month depot of leuprorelin acetate in a girl with central precocious puberty. .
In: Hormone research. 58 (2002), Nr. 6, S. 292-6

Riepe, Felix ; Mahler, P ; Sippell, Wolfgang ; Partsch, Carl-Joachim:
Longitudinal study of plasma pregnenolone and 17-hydroxypregnenolone in full-term and preterm neonates at birth and during the early neonatal period. .
In: The Journal of clinical endocrinology and metabolism. 87 (2002), Nr. 9, S. 4301-6
Stichwörter:  Signatur 17/2002

Partsch, Carl-Joachim ; Heger, Sabine ; Sippell, Wolfgang:
Management and outcome of central precocious puberty. .
In: Clinical endocrinology. 56 (2002), Nr. 2, S. 129-48
Stichwörter:  Signatur 21/2002

Riepe, Felix ; Krone, Nils ; Viemann, Matthias ; Partsch, Carl-Joachim ; Sippell, Wolfgang:
Management of congenital adrenal hyperplasia: results of the ESPE questionnaire. .
In: Hormone research. 58 (2002), Nr. 4, S. 196-205
Stichwörter:  Signatur 18/2002

Brasch J ; Flader S ; Roggentin P ; Wudy S ; Homoki J ; Shackleton CH ; Sippell, Wolfgang:
Metabolismus von Dehydroepiandrosteron durch Epidermophyton floccosum : [Dehydroepiandrosterone metabolism by Epidermophyton floccosum] .
In: Mycoses. 45 (2002), Nr. Suppl 1, S. 37-40
Stichwörter:  Signatur 22/2002

Krone, Nils ; Braun, Andreas ; Weinert, Stefanie ; Peter, Michael ; Roscher, Adelbert A. ; Partsch, Carl-Joachim ; Sippell, Wolfgang:
Multiplex Minisequencing of the 21-Hydroxylase Gene as a Rapid Strategy to Confirm Congenital Adrenal Hyperplasia .
In: Clinical Chemistry 48 (2002), Nr. 6, S. 818-825
Stichwörter:  Signatur 5/2002

Suttorp, M ; Hoffmann, B ; Sippell, Wolfgang:
Prevention of oestradiol-associated toxicosis in a dalmatian by early intervention with granulocyte colony-stimulating factor. .
In: The Veterinary record. 151 (2002), Nr. 8, S. 244-5
Stichwörter:  Signatur 19/2002

Partsch, Carl-Joachim ; Raffenberg ; Sippell, Wolfgang:
Screening for Turner's syndrome by chromosome analysis of all girls with short stature. .
In: The Journal of pediatrics. 140 (2002), Nr. 1, S. 140-1

Partsch, Carl-Joachim ; Sippell, Wolfgang:
Treatment of central precocious puberty. .
In: Best practice & research. Clinical endocrinology & metabolism. 16 (2002), Nr. 1, S. 165-89
Stichwörter:  Signatur 15/2002

Riepe, Felix ; Wonka, S ; Partsch, Carl-Joachim ; Sippell, Wolfgang:
Automated chromatographic system for the simultaneous measurement of plasma pregnenolone and 17-hydroxypregnenolone by radioimmunoassay. .
In: Journal of chromatography. B, Biomedical sciences and applications. 763 (2001), Nr. 1-2, S. 99-106

Dötsch J ; Dörr HG ; Stalla GK ; Sippell, Wolfgang:
Effect of glucocorticoid excess on the cortisol/cortisone ratio. .
In: Steroids 66 (2001), Nr. 11, S. 817-20

Viemann, Matthias ; Peter, Michael ; Lopez-Siguero, Juan Pedro ; Simic-Schleicher, Gunter ; Sippell, Wolfgang:
Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1 : Identification of a Novel Mutation in the Human Mineralocorticoid Receptor in one Sporadic Case and No Mutations in Two Autosomal Dominant Kindreds .
In: The Journal of clinical Endocrinology & Metabolism 86 (2001), Nr. 5, S. 2056-2059
Stichwörter:  Signatur 1/2001

Dötsch, J ; Hohenberger, I ; Sippell, Wolfgang ; Rascher, W ; Dörr, H. G:
Evolution of cortisol/cortisone metabolism in infancy .
In: Nieren- und Hochdruckkrankheiten 30 (2001), Nr. 5, S. 190-191

Riepe, Felix ; Partsch, Carl-Joachim ; Blankenstein, O ; Monig, H ; Pfaffle, R W ; Sippell, Wolfgang:
Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation. .
In: The Journal of clinical endocrinology and metabolism. 86 (2001), Nr. 9, S. 4353-7

Partsch, Carl-Joachim ; Sippell, Wolfgang:
Pathogenesis and epidemiology of precocious puberty. Effects of exogenous oestrogens. .
In: Human reproduction update. 7 (2001), Nr. 3, S. 292-302
Stichwörter:  Signatur 7/2001

Brand, M ; Schoof, E ; Partsch, Carl-Joachim ; Peter, M ; Hoeppfner, W ; Doerr, HG ; Sippell, Wolfgang:
Anorexia nervosa in congenital adrenal hyperplasia: long-term follow-up of 4 cases. .
In: Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association. 108 (2000), S. 430-435
Stichwörter:  Signatur 5/2000

Twesten, W ; Holterhus, P ; Sippell, Wolfgang ; Morlot, M ; Schumacher, H ; Schenk, B ; Hiort, O:
Clinical, endocrine, and molecular genetic findings in patients with 17beta-hydroxysteroid dehydrogenase deficiency. .
In: Horm Res 53 (2000), Nr. 1, S. 26-31
Stichwörter:  Signatur 6/2000

Dötsch, J ; Hohenberger, I ; Peter, M ; Sippell, Wolfgang ; Dörr, H:
Evidence for change of 11beta-hydroxysteroid dehydrogenase activity during infancy and childhood. .
In: Pediatric research. 48 (2000), S. 697-700
Stichwörter:  Signatur 4/2000

Even, L ; Cohen, A ; Marbach, N ; Brand, M ; Kaulli, R ; Sippell, Wolfgang ; Hochberg, Z:
Longitudinal analysis of growth over the first 3 years of life in Turner's syndrome. .
In: The Journal of pediatrics. 137 (2000), S. 460-464

Partsch, Carl-Joachim ; Aukamp ; Sippell, Wolfgang:
Scrotal temperature is increased in disposable plastic lined nappies. .
In: Archives of disease in childhood. 83 (2000), Nr. 4, S. 364-8

Partsch, Carl-Joachim ; Heger, Sabine ; Sippell, Wolfgang:
Treatment of central precocious puberty: lessons from a 15 years prospective trial. German Decapeptyl Study Group. .
In: Journal of pediatric endocrinology & metabolism 13 (2000), Nr. Supp. 1, S. 747-58

Holterhus, P M ; Wiebel, J ; Sinnecker, G H G ; Brüggenwirth, H T ; Sippell, Wolfgang ; Brinkmann, A O ; Kruse, K ; Hiort, O:
Clinical and molecular spectrum of somatic mosaicism in androgen insensitivity syndrome. .
In: Pediatric research. 46 (1999), S. 684-690

Peter, M ; Dubuis, JM ; Sippell, Wolfgang:
Disorders of the aldosterone synthase and steroid 11beta-hydroxylase deficiencies. .
In: Horm Res 51 (1999), Nr. 5, S. 211-22

Korsch, E ; Peter, M ; Hiort, O ; Sippell, Wolfgang ; Ure, B M ; Hauffa, B P ; Bergmann, M:
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. .
In: The Journal of clinical endocrinology and metabolism. 84 (1999), S. 1628-1632

Haverkamp, F ; Wölfle, J ; Zerres, K ; Butenandt ; Weimann, E ; Bettendorf, M ; Keller, E ; Mühlenberg, R ; Partsch, Carl-Joachim ; Sippell, Wolfgang ; Hoppe, C:
Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure. .
In: The Journal of clinical endocrinology and metabolism 84 (1999), S. 4578-4582

Partsch, Carl-Joachim ; Peter, M ; Brand, M ; Sippell, Wolfgang:
Leuprorelindepot zur Behandlung der progressiven Pubertas praecox vera. .
In: Monatsschrift Kinderheilkunde 147 (1999), S. 638-647

Heger, Sabine ; Partsch, Carl-Joachim ; Sippell, Wolfgang:
Long-term outcome after depot gonadotropin-releasing hormone agonist treatment of central precocious puberty: final height, body proportions, body composition, bone mineral density, and reproductive function. .
In: The Journal of clinical endocrinology and metabolism. 84 (1999), Nr. 12, S. 4583-4590
Stichwörter:  Signatur: 1/1999

Partsch, Carl-Joachim ; Aukamp, M ; Sippell, Wolfgang:
Pubertätszeichen beim männlichen Säugling. .
In: Monatschrift Kinderheilkunde 147 (1999), S. 754-755

Heger, Sabine ; Partsch, Carl-Joachim ; Peter, M ; Blum, WF ; Kiess, W ; Sippell, Wolfgang:
Serum leptin levels in patients with progressive central precocious puberty. .
In: Pediatric research. 46 (1999), S. 71-75

Gromoll, J ; Partsch, Carl-Joachim ; Simoni, M ; Nordhoff, V ; Sippell, Wolfgang ; Nieschlag, E ; Saxena, BB:
A mutation in the first transmembrane domain of the lutropin receptor causes male precocious puberty. .
In: Journal of Clinical Endocrinology & Metabolism, The 83 (1998), S. 476-480

De Zegher, F ; Francois, I ; Boehmer, ALM ; Saggese, G ; Müller, J ; Hiort, O ; Sultan, C ; Clayton, P ; Brauner, R ; Cacciari, E ; Ibanez, L ; Van Vliet, G ; Tiulpakov, A ; Saka, N ; Ritzèn, M ; Sippell, Wolfgang:
Androgens and fetal growth. .
In: Hormone Res 50 (1998), S. 243-244

Möning, H ; Peter, M ; Partsch, Carl-Joachim ; Kloehn, Sievert ; Arendt, T ; Sippell, Wolfgang:
Clinical deterioration after cessation of growth hormone replacement therapy in a young adult with severe growth hormone deficiency. .
In: Growth hormone & IGF research 8 (1998), S. 385-387

Peter, M ; Viemann, Matthias ; Partsch, Carl-Joachim ; Sippell, Wolfgang:
Congenital adrenal hypoplasia : clinical spectrum, experience with hormonal diagnosis, and report on new point mutations of the DAX-1 gene. .
In: J Clin Endocrinol Metab 83 (1998), Nr. 8, S. 2666-74

Partsch, Carl-Joachim ; Von Bueren, E ; Brand, M ; Heger, Sabine ; Sippell, Wolfgang:
Efficacy of the subcutaneous reformulated triptorelin depot in children with central precocious puberty. .
In: Acta Paediatr 87 (1998), S. 1240-1244

Peter, M ; Nikischin, Werner ; Heinz-Erian, P ; Fussenegger, W ; Kapelari, K ; Sippell, Wolfgang:
Homozygous deletion of arginine-173 in the CYP11B2 gene in a girl with congenital hypoaldosteronism. Corticosterone methyloxidase deficiency type II. .
In: Hormone research. 50 (1998), S. 222-225

Peter, M ; Bunger, K ; Drop, SL ; Sippell, Wolfgang:
Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies. .
In: Eur J Endocrinol 139 (1998), Nr. 1, S. 96-100

Peter, M ; Bunger, K ; Solyom, J ; Sippell, Wolfgang:
Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II. .
In: Eur J Pediatr 157 (1998), Nr. 5, S. 378-81

Partsch, Carl-Joachim ; Peter, M ; Heger, Sabine ; Sippell, Wolfgang:
Transitorische Pubertas praecox vera. .
In: Monatschrift Kinderheilkunde 146 (1998), S. 678-682

Bosinski, HAG ; Peter, M ; Bonatz, G ; Arndt, R ; Heidenreich, M ; Sippell, Wolfgang ; Wille, R:
A higher rate of hyperandrogenic disorders in female-to-male transsexuals. .
In: Psychoneuroendocrinology 22 (1997), S. 361-380

Bosinki, HAG ; Schröder, I ; Peter, M ; Arndt, R ; Wille, R ; Sippell, Wolfgang:
Anthropometrical measurements and androgen levels in males, females, and hormonally untreated female-to-male transsexuals. .
In: Archives of sexual behavior 26 (1997), S. 143-157

Möning, H ; Sippell, Wolfgang:
Die Betreuung des hypogonadalen männlichen Patienten im Übergang zum Erwachsenalter. .
In: Der Kinderarzt 11 (1997), S. 1221-1227

Peter, M ; Sippell, Wolfgang:
Evidence for endocrinological abnormalities in heterozygotes for adrenal 11 beta-hydroxylase deficiency of a family with the R448H mutation in the CYP11B1 gene. .
In: J Clin Endocrinol Metab 82 (1997), Nr. 10, S. 3506-8

Joss, E E ; Mullis, P ; Werder, E A ; Partsch, Carl-Joachim ; Sippell, Wolfgang:
Growth promotion and Turner-specific bone age after therapy with growth hormone and in combination with oxandrolone: when should therapy be started in Turner syndrome?
In: Hormone research. 47 (1997), S. 102-109

Peter, M ; Fawaz, L ; Drop, SL ; Visser, HK ; Sippell, Wolfgang:
Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997. .
In: Clin Endocrinol Metab 82 (1997), Nr. 11, S. 3525-8

Marx, C ; Bornstein, S R ; Wolkendörfer, G W ; Peter, M ; Sippell, Wolfgang ; Scherbaum, W A:
Relevance of major histocompatibility complex class II expression as a hallmark for the cellular differentiation in the human adrenal cortex. .
In: The Journal of clinical endocrinology and metabolism. 82 (1997), S. 3136-3140

Partsch, Carl-Joachim ; Von Bueren, E ; Kühne, Bianca ; Sippell, Wolfgang ; Brinkmann, G.:
Visualization of injection depot after subcutaneous administration by syringe and needle-free device (Medi-Jector): first results with magnetic resonance imaging. .
In: Eur J Pediatr 156 (1997), S. 893-898

Peter, M ; Sippell, Wolfgang:
Congenital hypoaldosteronism: the Visser-Cost syndrome revisited. .
In: Pediatric research. 39 (1996), S. 554-560

Bosinski, HAG ; Arndt, R ; Sippell, Wolfgang ; Wille, Reinhard:
Geschlechtsidentitaetsstoerungen bei kindern und jugendlichen. .
In: Monatsschrift Kinderheilkunde 144 (1996), S. 1235-1241

Möning, H ; Peter, M ; Sippell, Wolfgang:
Hyporeninaemic hypoaldosteronism after growth hormone treatment. .
In: Lancet 347 (1996), Nr. 8994, S. 119

Peter, M ; Partsch, Carl-Joachim ; Doerr, H G ; Sippell, Wolfgang:
Prenatal diagnosis of congenital adrenal hypoplasia. .
In: Hormone research. 46 (1996), S. 41-45

Partsch, Carl-Joachim ; Hummelink, R ; Sippell, Wolfgang ; Oostdijk, W ; Odink, RJ ; Drop, SL:
[Comparison between complete and incomplete suppression of the hypophyseal-gonadal axis in girls with central precocious puberty: effect on growth and prospective final height] .
In: Monatsschr Kinderheilkd 141 (1993), Nr. 12, S. 935-9

Partsch, Carl-Joachim ; Hummelink, R ; Peter, M ; Sippell, Wolfgang ; Oostdijk, W ; Odink, RJ ; Drop, SL:
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. .
In: Horm Res 39 (1993), Nr. 3-4, S. 111-7

Hummelink, R ; Oostdijk, W ; Partsch, Carl-Joachim ; Odink, RJ ; Drop, SL ; Sippell, Wolfgang:
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. .
In: Horm Metab Res 24 (1992), Nr. 3, S. 122-6

Pankau, R ; Partsch, Carl-Joachim ; Funda, J ; Sippell, Wolfgang:
Hypothalamic-pituitary-gonadal function in two infants with Smith-Lemli-Opitz syndrome. .
In: Am J Med Genet 43 (1992), Nr. 3, S. 513-6

Sippell, Wolfgang ; Partsch, Carl-Joachim ; Hummelink, R ; Lorenzen, F:
[Long-term therapy with delayed-action LHRH-antagonist decapeptyl depot in girls with precocious puberty. Results of an international multicenter study] .
In: Gynakologe 24 (1991), Nr. 2, S. 108-12

Partsch, Carl-Joachim ; Sippell, Wolfgang ; MacKenzie, IZ ; Aynsley-Green, A:
The steroid hormonal milieu of the undisturbed human fetus and mother at 16-20 weeks gestation. .
In: J Clin Endocrinol Metab 73 (1991), Nr. 5, S. 969-74