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Results: 1-8 |
Results: 8

Authors: Amalfitano, A Bengur, AR Morse, RP Majure, JM Case, LE Veerling, DL Mackey, J Kishnani, P Smith, W McVie-Wylie, A Sullivan, JA Hoganson, GE Phillips, JA Schaefer, GB Charrow, J Ware, RE Bossen, EH Chen, YT
Citation: A. Amalfitano et al., Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial, GENET MED, 3(2), 2001, pp. 132-138

Authors: Cauble, MS Mack-Shipman, L Schaefer, GB Balakrishnan, S Larsen, JL
Citation: Ms. Cauble et al., Idiopathic hypothalamic dysfunction with precocious puberty and adipsic hypernatremia first presenting in adolescence, J PED END M, 14(8), 2001, pp. 1163-1167

Authors: Schaefer, GB
Citation: Gb. Schaefer, Response to the letter to the editor by Gusmao Melo et al. - "Neuroimagingand echocardiographic findings in Sotos syndrome", AM J MED G, 90(5), 2000, pp. 434-434

Authors: Rao, VH Singh, RK Delimont, DC Schaefer, GB Bridge, JA Neff, JR Sanger, WG Sappenfield, JW Buehler, BA Finnell, RH
Citation: Vh. Rao et al., Interleukin-1 beta upregulates MMP-9 expression in stromal cells of human giant cell tumor of bone, J INTERF CY, 19(10), 1999, pp. 1207-1217

Authors: Rao, VH Singh, RK Delimont, DC Finnell, RH Bridge, JA Neff, JR Garvin, BP Pickering, DL Sanger, WG Buehler, BA Schaefer, GB
Citation: Vh. Rao et al., Transcriptional regulation of MMP-9 expression in stromal cells of human giant cell tumor of bone by tumor necrosis factor-alpha, INT J ONCOL, 14(2), 1999, pp. 291-300

Authors: Schaefer, GB Bodensteiner, JB
Citation: Gb. Schaefer et Jb. Bodensteiner, Developmental anomalies of the brain in mental retardation, INT R PSYC, 11(1), 1999, pp. 47-55

Authors: Rao, VH Singh, RK Finnell, RH Dave, BJ Beuhler, BA Sanger, WG Schaefer, GB
Citation: Vh. Rao et al., Matrix metalloproteinases and their inhibitors in tumor invasion and metastasis, P I A S-CH, 111(1), 1999, pp. 239-254

Authors: Cohn, ES Kelley, PM Fowler, TW Gorga, MP Lefkowitz, DM Kuehn, HJ Schaefer, GB Gobar, LS Hahn, FJ Harris, DJ Kimberling, WJ
Citation: Es. Cohn et al., Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1), PEDIATRICS, 103(3), 1999, pp. 546-550
Risultati: 1-8 |