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Clinical evidence-based cutoff limits for GH stimulation tests in children with a backup of results with reference to mass spectrometry
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Published in European journal of endocrinology (01.09.2014)
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Reference intervals for TSH and thyroid hormones are mainly affected by age, body mass index and number of blood leucocytes, but hardly by gender and thyroid autoantibodies during the first decades of life
Kratzsch, J., Schubert, G., Pulzer, F., Pfaeffle, R., Koerner, A., Dietz, A., Rauh, M., Kiess, W., Thiery, J.
Published in Clinical biochemistry (01.09.2008)
Published in Clinical biochemistry (01.09.2008)
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Effects of Dehydroepiandrosterone Therapy on Pubic Hair Growth and Psychological Well-Being in Adolescent Girls and Young Women with Central Adrenal Insufficiency: A Double-Blind, Randomized, Placebo-Controlled Phase III Trial
Binder, G, Weber, S, Ehrismann, M, Zaiser, N, Meisner, C, Ranke, M. B, Maier, L, Wudy, S. A, Hartmann, M. F, Heinrich, U, Bettendorf, M, Doerr, H. G, Pfaeffle, R. W, Keller, E
Published in The journal of clinical endocrinology and metabolism (01.04.2009)
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An Insulin-Like Growth Factor-I Receptor Defect Associated with Short Stature and Impaired Carbohydrate Homeostasis in an Italian Pedigree
Mohn, A., Marcovecchio, M.L., de Giorgis, T., Pfaeffle, R., Chiarelli, F., Kiess, W.
Published in Hormone research in paediatrics (01.01.2011)
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Kiess, W., Kratzsch, J., Sergeyev, E., Neef, M., Adler, M., Pfaeffle, R., Hiemisch, A., Körner, A.
Published in Clinical biochemistry (01.06.2014)
Published in Clinical biochemistry (01.06.2014)
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Clinical and Functional Characteristics of the Human Arg59Ter Insulin-Like Growth Factor I Receptor (IGF1R) Mutation: Implications for a Gene Dosage Effect of the Human IGF1R
Raile, K, Klammt, J, Schneider, A, Keller, A, Laue, S, Smith, R, Pfäffle, R, Kratzsch, J, Keller, E, Kiess, W
Published in The journal of clinical endocrinology and metabolism (01.06.2006)
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Papillary thyroid carcinoma in an adolescent girl with graves' disease
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Published in Klinische Padiatrie (01.11.2014)
Published in Klinische Padiatrie (01.11.2014)
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A novel GNAS1 mutation in a German family with Albright's hereditary osteodystrophy
Klagge, A, Jessnitzer, B, Pfaeffle, R, Stumvoll, M, Fuhrer, D
Published in Experimental and clinical endocrinology & diabetes (01.10.2010)
Published in Experimental and clinical endocrinology & diabetes (01.10.2010)
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Effects of Dehydroepiandrosterone Therapy on Pubic Hair Growth and Psychological Well-Being in Adolescent Girls and Young Women with Central Adrenal Insufficiency: A Double-Blind, Randomised, Placebo-Controlled Phase III Trial
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Published in Endocrinology (Philadelphia) (01.02.2009)
Published in Endocrinology (Philadelphia) (01.02.2009)
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Administration of Arginine plus Growth Hormone Releasing Hormone to Evaluate Growth Hormone (GH) Secretory Status in Children with GH Deficiency
Keller, A., Donaubauer, J., Kratzsch, J., Pfaeffle, R., Hirsch, W., Kiess, W., Keller, E.
Published in Journal of Pediatric Endocrinology and Metabolism (01.12.2007)
Published in Journal of Pediatric Endocrinology and Metabolism (01.12.2007)
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IGF1R mutations as cause of SGA
Klammt, J., PhD, Kiess, W., MD, Pfäffle, R., MD
Published in Baillière's best practice & research. Clinical endocrinology & metabolism (01.02.2011)
Published in Baillière's best practice & research. Clinical endocrinology & metabolism (01.02.2011)
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IGF-I Receptor Mutations Resulting in Intrauterine and Postnatal Growth Retardation
Abuzzahab, M. Jennifer, Schneider, Anke, Goddard, Audrey, Grigorescu, Florin, Lautier, Corinne, Keller, Eberhard, Kiess, Wieland, Klammt, Jürgen, Kratzsch, Jürgen, Osgood, Doreen, Pfäffle, Roland, Raile, Klemens, Seidel, Berthold, Smith, Robert J, Chernausek, Steven D
Published in The New England journal of medicine (04.12.2003)
Published in The New England journal of medicine (04.12.2003)
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Functional Characterization of a Heterozygous GLI2 Missense Mutation in Patients With Multiple Pituitary Hormone Deficiency
Flemming, G. M. C, Klammt, J, Ambler, G, Bao, Y, Blum, W. F, Cowell, C, Donaghue, K, Howard, N, Kumar, A, Sanchez, J, Stobbe, H, Pfäffle, R. W
Published in The journal of clinical endocrinology and metabolism (01.03.2013)
Published in The journal of clinical endocrinology and metabolism (01.03.2013)
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Mutations in PROP1 cause familial combined pituitary hormone deficiency
WEI WU, COGAN, J. D, PHILLIPS, J. A, ROSENFELD, M. G, PFÄFFLE, R. W, DASEN, J. S, FRISCH, H, O'CONNELL, S. M, FLYNN, S. E, BROWN, M. R, MULLIS, P. E, PARKS, J. S
Published in Nature genetics (01.02.1998)
Published in Nature genetics (01.02.1998)
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Genetic Analysis of GHR Should Contain Sequencing of All Coding Exons and Specific Intron Sequences, and Screening for Exon Deletions
Walenkamp, M.J.E., Klammt, J., Feigerlova, E., Losekoot, M., van Duyvenvoorde, H.A., Hwa, V., Pfäffle, R., Wit, J.M.
Published in Hormone research in paediatrics (01.01.2013)
Published in Hormone research in paediatrics (01.01.2013)
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