Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain
Eggermann, T, Schönherr, N, Meyer, E, Obermann, C, Mavany, M, Eggermann, K, Ranke, M B, Wollmann, H A
Published in Journal of medical genetics (01.07.2006)
Published in Journal of medical genetics (01.07.2006)
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Is maternal duplication of 11p15 associated with Silver-Russell syndrome?
Eggermann, T, Meyer, E, Obermann, C, Heil, I, Schüler, H, Ranke, M B, Eggermann, K, Wollmann, H A
Published in Journal of medical genetics (01.05.2005)
Published in Journal of medical genetics (01.05.2005)
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Submicroscopic chromosomal imbalances in idiopathic Silver–Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome
Spengler, S, Schönherr, N, Binder, G, Wollmann, H A, Fricke-Otto, S, Mühlenberg, R, Denecke, B, Baudis, M, Eggermann, T
Published in Journal of medical genetics (01.05.2010)
Published in Journal of medical genetics (01.05.2010)
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Journal Article
Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome
Eggermann, T, Schönherr, N, Eggermann, K, Buiting, K, Ranke, MB, Wollmann, HA, Binder, G
Published in Clinical genetics (01.01.2008)
Published in Clinical genetics (01.01.2008)
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Journal Article
IGF-II Serum Levels Are Normal in Children with Silver-Russell Syndrome Who Frequently Carry Epimutations at the IGF2 Locus
Binder, G, Seidel, A.-K, Weber, K, Haase, M, Wollmann, H. A, Ranke, M. B, Eggermann, T
Published in The journal of clinical endocrinology and metabolism (01.11.2006)
Published in The journal of clinical endocrinology and metabolism (01.11.2006)
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Journal Article
The d3/fl-Growth Hormone (GH) Receptor Polymorphism Does Not Influence the Effect of GH Treatment (66 μg/kg per Day) or the Spontaneous Growth in Short Non-GH-Deficient Small-for-Gestational-Age Children: Results from a Two-Year Controlled Prospective Study in 170 Spanish Patients
Carrascosa, A, Esteban, C, Espadero, R, Fernández-Cancio, M, Andaluz, P, Clemente, M, Audí, L, Wollmann, H, Fryklund, L, Parodi, L
Published in The journal of clinical endocrinology and metabolism (01.09.2006)
Published in The journal of clinical endocrinology and metabolism (01.09.2006)
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Journal Article
Growth hormone treatment of short children born small for gestational age : Growth responses with continuous and discontinuous regimens over 6 years
DE ZEGHER, F, ALBERTSSON-WIKLAND, K, WOLLMANN, H. A, CHATELAIN, P, CHAUSSAIN, J.-L, LÖFSTRÖM, A, JONSSON, B, ROSENFELD, R. G
Published in The journal of clinical endocrinology and metabolism (01.08.2000)
Published in The journal of clinical endocrinology and metabolism (01.08.2000)
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Journal Article
Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion
BLAGITKO, N, MERGENTHALER, S, SCHULZ, U, WOLLMANN, H. A, CRAIGEN, W, EGGERMANN, T, ROPERS, H.-H, KALSCHEUER, V. M
Published in Human molecular genetics (01.07.2000)
Published in Human molecular genetics (01.07.2000)
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Journal Article
Segmental maternal UPD(7q) in Silver-Russell syndrome
Eggermann, T, Schönherr, N, Jäger, S, Spaich, C, Ranke, MB, Wollmann, HA, Binder, G
Published in Clinical genetics (01.11.2008)
Published in Clinical genetics (01.11.2008)
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Journal Article
(Epi)mutations in 11p15 significantly contribute to Silver–Russell syndrome: but are they generally involved in growth retardation?
Schönherr, N., Meyer, E., Eggermann, K., Ranke, M.B., Wollmann, H.A., Eggermann, T.
Published in European journal of medical genetics (01.09.2006)
Published in European journal of medical genetics (01.09.2006)
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Journal Article
Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease-related complications
Woelfle, J., Hoepffner, W., Sippell, W. G., Brämswig, J. H., Heidemann, P., Deiß, D., Bökenkamp, A., Roth, C., Irle, U., Wollmann, H. A., Zachmann, M., Kubini, K., Albers, N.
Published in Clinical endocrinology (Oxford) (01.02.2002)
Published in Clinical endocrinology (Oxford) (01.02.2002)
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Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients
Eggermann, Thomas, Mergenthaler, Susanne, Eggermann, Katja, Albers, Alexandra, Linnemann, Knud, Fusch, Christoph, Ranke, Michael B, Wollmann, Hartmut A
Published in Journal of medical genetics (01.02.2001)
Published in Journal of medical genetics (01.02.2001)
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Journal Article
Association Analysis of Ten Candidate Genes in a Large Multinational Cohort of Small for Gestational Age Children and Children with Idiopathic Short Stature (NESTEGG study)
de Graaff, L.C.G., Clark, A.J.L., Tauber, M., Ranke, M.B., Johnston, L.B., Caliebe, J., Molinas, C., Amin, N., van Duijn, C., Wollmann, H., Wallaschofski, H., Savage, M.O., Hokken-Koelega, A.C.S.
Published in Hormone research in paediatrics (01.01.2013)
Published in Hormone research in paediatrics (01.01.2013)
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Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients
Wollmann, H A, Kirchner, T, Enders, H, Preece, M A, Ranke, M B
Published in European journal of pediatrics (01.12.1995)
Published in European journal of pediatrics (01.12.1995)
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The exon 3-deleted/full-length Growth Hormone Receptor Polymorphism Does Not Influence the Effect of Puberty or Growth Hormone Therapy on Glucose Homeostasis in Short Non-Growth Hormone-Deficient Small-for-Gestational-Age Children: Results from a Two-Year Controlled Prospective Study
Audí, L, Carrascosa, A, Esteban, C, Fernández-Cancio, M, Andaluz, P, Yeste, D, Espadero, R, Granada, M. L, Wollmann, H, Fryklund, L
Published in The journal of clinical endocrinology and metabolism (01.07.2008)
Published in The journal of clinical endocrinology and metabolism (01.07.2008)
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Journal Article
Reference values for height and weight in Prader-Willi syndrome based on 315 patients
WOLLMANN, H. A, SCHULTZ, U, GRAUER, M. L, RANKE, M. B
Published in European journal of pediatrics (01.08.1998)
Published in European journal of pediatrics (01.08.1998)
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Journal Article
CYP11B1 Mutations Causing Non-Classic Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency
Joehrer, Karin, Geley, Stephan, Strasser-Wozak, Elisabeth M.C., Azziz, Ricardo, Wollmann, Hartmut A., Schmitt, Klaus, Kofler, Reinhard, White, Perrin C.
Published in Human molecular genetics (01.10.1997)
Published in Human molecular genetics (01.10.1997)
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