Growth hormone in Turner syndrome

le PRICE, D, RANKE, M
Foilsithe 2001

Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status

le MERGENTHALER, S., EGGERMANN, K., TOMIUK, J., RANKE, M., WOLLMANN, H., EGGERMANN, T.
Foilsithe 2000

Sex differences in binding of human growth hormone to isolated rat hepatocytes.

le Ranke, M B, Stanley, C A, Rodbard, D, Baker, L, Bongiovanni, A, Parks, J S
Foilsithe 1976

Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome.

le Eggermann, T, Eggermann, K, Mergenthaler, S, Kuner, R, Kaiser, P, Ranke, M B, Wollmann, H A
Foilsithe 1998

Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients

le Eggermann, T., Mergenthaler, S., Eggermann, K., Albers, A., Linnemann, K., Fusch, C., Ranke, M., Wollmann, H.
Foilsithe 2001

Is maternal duplication of 11p15 associated with Silver-Russell syndrome?

le Eggermann, T, Meyer, E, Obermann, C, Heil, I, Schuler, H, Ranke, M, Eggermann, K, Wollmann, H
Foilsithe 2005

Staphylococcus aureus capsular types and antibody response to lung infection in patients with cystic fibrosis.

le Albus, A, Fournier, J M, Wolz, C, Boutonnier, A, Ranke, M, Høiby, N, Hochkeppel, H, Döring, G
Foilsithe 1988

Epigenetic mutations in 11p15 in Silver‐Russell syndrome are restricted to the telomeric imprinting domain

le Eggermann, T, Schönherr, N, Meyer, E, Obermann, C, Mavany, M, Eggermann, K, Ranke, M B, Wollmann, H A
Foilsithe 2006

Activation-dependent expression of the insulin-like growth factor binding protein-2 in human lymphocytes.

le Föll, J L, Dannecker, L, Zehrer, C, Hettmer, S, Berger, J, Elmlinger, M, Niethammer, D, Ranke, M B, Dannecker, G E
Foilsithe 1998

Spontaneous growth in idiopathic short stature. European Study Group.

le Rekers-Mombarg, L T, Wit, J M, Massa, G G, Ranke, M B, Buckler, J M, Butenandt, O, Chaussain, J L, Frisch, H, Leiberman, E
Foilsithe 1996

GH responsiveness in a large multinational cohort of SGA children with short stature (NESTEGG) is related to the exon 3 GHR polymorphism

le Tauber, M, Ester, W, Auriol, F, Molinas, C, Fauvel, J, Caliebe, J, Nugent, T, Fryklund, L, Ranke, M B, Savage, M O, Clark, A J L, Johnston, L B, Hokken-Koelega, A C S
Foilsithe 2007

A role for helix 3 of the TRbeta ligand-binding domain in coactivator recruitment identified by characterization of a third cluster of mutations in resistance to thyroid hormone.

le Collingwood, T N, Wagner, R, Matthews, C H, Clifton-Bligh, R J, Gurnell, M, Rajanayagam, O, Agostini, M, Fletterick, R J, Beck-Peccoz, P, Reinhardt, W, Binder, G, Ranke, M B, Hermus, A, Hesch, R D, Lazarus, J, Newrick, P, Parfitt, V, Raggatt, P, de Zegher, F, Chatterjee, V K
Foilsithe 1998