Submicroscopic chromosomal imbalances in idiopathic Silver–Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome von Spengler, S, Schönherr, N, Binder, G, Wollmann, H A, Fricke-Otto, S, Mühlenberg, R, Denecke, B, Baudis, M, Eggermann, T

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Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues von Begemann, M, Spengler, S, Kanber, D, Haake, A, Baudis, M, Leisten, I, Binder, G, Markus, S, Rupprecht, T, Segerer, H, Fricke-Otto, S, Mühlenberg, R, Siebert, R, Buiting, K, Eggermann, T

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A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminus von Blankenstein, O, Mühlenberg, R, Kim, C, Wüller, S, Pfäffle, R, Heimann, G

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Growth retardation in Turner syndrome: Aneuploidy, rather than specific gene loss, may explain growth failure von HAVERKAMP, F, WÖLFLE, J, PARTSCH, C. J, SIPPELL, W. G, HOPPE, C, ZERRES, K, BUTENANDT, O, AMENDT, P, HAUFFA, B. P, WEIMANN, E, BETTENDORF, M, KELLER, E, MÜHLENBERG, R

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Growth patterns after for virilising adrenocortical adenoma von Hauffa, B P, Roll, C, Mühlenberg, R, Havers, W

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Growth in children with adrenocortical tumors von Hauffa, B. P., Roll, C., Mühlenberg, R., Havers, W.

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Growth Retardation in Turner Syndrome: Aneuploidy, Rather Than Specific Gene Loss, May Explain Growth Failure von Haverkamp, F, Wölfle, J, Zerres, K, Butenandt, O, Amendt, P, Hauffa, B. P, Weimann, E, Bettendorf, M, Keller, E, Mühlenberg, R, Partsch, C. J, Sippell, W. G, Hoppe, C

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Growth hormone therapy with three dosage regimens in children with idiopathic short stature von Rekers-Mombarg, L.T.M., Massa, G.G., Wit, J.M., Matranga, A.M.C., Buckler, J.M.H., Butenandt, O., Chaussain, J.L., Frisch, H., Leiberman, E., Yturriaga, R.

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Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome von Spengler, S, Schönherr, N, Binder, G, Wollmann, H, Fricke-Otto, S, Mühlenberg, R, Denecke, B, Baudis, Michael, Eggermann, T

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Uterine size in women with Turner syndrome after induction of puberty with estrogens and long-term growth hormone therapy: results of the German IGLU Follow-up Study 2001 von Doerr, Helmuth G., Bettendorf, Markus, Hauffa, Berthold P., Mehls, Otto, Partsch, Carl-Joachim, Said, Elfriede, Sander, Sabine, Schwarz, Hans-Peter, Stahnke, Nikolaus, Steinkamp, Heiner, Ranke, Michael B.

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Adult height after GH therapy in 188 Ullrich-Turner syndrome patients: results of the German IGLU Follow-up Study 2001 von Ranke, MB, Partsch, CJ, Lindberg, A, Dorr, HG, Bettendorf, M, Hauffa, BP, Schwarz, HP, Mehls, O, Sander, S, Stahnke, N, Steinkamp, H, Said, E, Sippell, W

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Central laboratory reassessment of IGF-I, IGF-binding protein-3, and GH serum concentrations measured at local treatment centers in growth-impaired children: implications for the a... von Hauffa, Berthold P, Lehmann, Nils, Bettendorf, Markus, Mehls, Otto, Dörr, Helmuth-Günther, Stahnke, Nikolaus, Steinkamp, Heinz, Said, Elfriede, Ranke, Michael B

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Central reassessment of GH concentrations measured at local treatment centers in children with impaired growth: consequences for patient management von Hauffa, BP, Lehmann, N, Bettendorf, M, Mehls, O, Dorr, HG, Partsch, CJ, Schwarz, HP, Stahnke, N, Steinkamp, H, Said, E, Sander, S, Ranke, MB

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Priapism in childhood (author's transl) von Asbach, H W, Kösters, S, Thomas, P, Mühlenberg, R, Melekos, M

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Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene von SINNECKER, C. H. G, HIORT, O, NITSCHE, E. M, HOLTERHUS, P.-M, KRUSE, K

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A New C-Terminal Located Mutation (V272ter) in the PIT-1 Gene Manifesting with Severe Congenital Hypothyroidism von Blankenstein, O., Mühlenberg, R., Kim, C., Wüller, S., Pfäffle, R., Heimann, G.

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ASYMMETRIC DEVELOPMENT IN PATIENTS WITH GONOSOMAL MOSAICISM von Jung, H, Mühlenberg, R, Willig, R P

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Bedeutung und Charakteristika des LHRH-Testes in der Diagnostik der vorzeitigen Pubertätsentwicklung bei Mädchen: der stimulierte LH/FSH-Quotient differenziert zwischen zentraler P... von PARTSCH, C.-J, HÜMMELINK, R, LORENZEN, F, SIPPELL, W. G

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Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues von Begemann, M, Spengler, S, Kanber, D, Haake, A, Baudis, Michael, Leisten, I, Binder, G, Markus, S, Rupprecht, T, Segerer, H, Fricke-Otto, S, Mühlenberg, R, Siebert, R, Buiting, K, Eggermann, T

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Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome von Spengler, S, Schönherr, N, Binder, G, Wollmann, H A, Fricke-Otto, S, Mühlenberg, R, Denecke, B, Baudis, M, Eggermann, T

Volltext