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
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