Authors:
Bruhl, K
Stoeter, P
Wietek, B
Schwarz, M
Humpl, T
Schumacher, R
Spranger, J
Citation: K. Bruhl et al., Cerebral spinal fluid flow, venous drainage and spinal cord compression inachondroplastic children: impact of magnetic resonance findings for decompressive surgery at the cranio-cervical junction, EUR J PED, 160(1), 2001, pp. 10-20
Authors:
Horn, LC
Faber, R
Meiner, A
Piskazeck, U
Spranger, J
Citation: Lc. Horn et al., Greenberg dysplasia: first reported case with additional non-skeletal malformations and without consanguinity (vol 20, pg 1008, 2000), PRENAT DIAG, 21(5), 2001, pp. 425-425
Citation: J. Spranger, Changes in clinical practice with the unravelling of diseases: Connective-tissue disorders, J INH MET D, 24(2), 2001, pp. 117-126
Authors:
Spranger, J
Mohlig, M
Osterhoff, M
Buhnen, J
Blum, WF
Pfeiffer, AFH
Citation: J. Spranger et al., Retinal photocoagulation does not influence intraocular levels of IGF-I, IGF-II and IGF-BP3 in proliferative diabetic retinopathy - Evidence for combined treatment of PDR with somatostatin analogues and retinal photocoagulation?, HORMONE MET, 33(5), 2001, pp. 312-316
Authors:
Winterpacht, A
Hilbert, K
Stelzer, C
Schweikardt, T
Decker, H
Segerer, H
Spranger, J
Zabel, B
Citation: A. Winterpacht et al., A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasia, PHYSIOL GEN, 2(1), 2000, pp. 9-12
Authors:
Boerkoel, CF
O'Neill, S
Andre, JL
Benke, PJ
Bogdanovic, R
Bulla, M
Burguet, A
Cockfield, S
Cordeiro, I
Ehrich, JHH
Frund, S
Geary, DF
Ieshima, A
Illies, F
Joseph, MW
Kaitila, I
Lama, G
Leheup, B
Ludman, MD
McLeod, DR
Medeira, A
Milford, DV
Ormala, T
Rener-Primec, Z
Santava, A
Santos, HG
Schmidt, B
Smith, GC
Spranger, J
Zupancic, N
Weksberg, R
Citation: Cf. Boerkoel et al., Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature, EUR J PED, 159(1-2), 2000, pp. 1-7
Authors:
Horn, LC
Faber, R
Meiner, A
Piskazeck, U
Spranger, J
Citation: Lc. Horn et al., Greenberg dysplasia: first reported case with additional non-skeletal malformations and without consanguinity, PRENAT DIAG, 20(12), 2000, pp. 1008-1011
Authors:
Spranger, J
Hall, BD
Hane, B
Srivastava, A
Stevenson, RE
Citation: J. Spranger et al., Spectrum of Schwartz-Jampel syndrome includes micromelic chondrodysplasia,kyphomelic dysplasia, and Burton disease, AM J MED G, 94(4), 2000, pp. 287-295
Authors:
Spranger, J
Buhnen, J
Jansen, V
Krieg, M
Meyer-Schwickerath, R
Blum, WF
Schatz, H
Pfeiffer, AFH
Citation: J. Spranger et al., Systemic levels contribute significantly to increased intraocular IGF-I, IGF-II and IGF-BP3 in proliferative diabetic retinopathy, HORMONE MET, 32(5), 2000, pp. 196-200
Authors:
Spranger, J
Hammes, HP
Preissner, KT
Schatz, H
Pfeiffer, AFH
Citation: J. Spranger et al., Release of the angiogenesis inhibitor angiostatin in patients with proliferative diabetic retinopathy: association with retinal photocoagolation, DIABETOLOG, 43(11), 2000, pp. 1404-1407
Authors:
Spranger, J
Meyer-Schwickerath, R
Klein, M
Schatz, H
Pfeiffer, A
Citation: J. Spranger et al., Deficient activation and different expression of transforming growth factor-beta isoforms in active proliferative diabetic retinopathy and neovascular eye disease, EXP CL E D, 107(1), 1999, pp. 21-28
Citation: R. Boor et al., Abnormal subcortical somatosensory evoked potentials indicate high cervical myelopathy in achondroplasia, EUR J PED, 158(8), 1999, pp. 662-667
Citation: M. Heiner et al., A case study in design and verification of manufacturing system control software with hierarchical Petri nets, INT J ADV M, 15(2), 1999, pp. 139-152
Authors:
Superti-Furga, A
Neumann, L
Riebel, T
Eich, G
Steinmann, B
Spranger, J
Kunze, J
Citation: A. Superti-furga et al., Recessively inherited multiple epiphyseal dysplasia with normal stature, club foot, and double layered patella caused by a DTDST mutation, J MED GENET, 36(8), 1999, pp. 621-624
Authors:
Holden, P
Canty, EG
Mortier, GR
Zabel, B
Spranger, J
Carr, A
Grant, ME
Loughlin, JA
Briggs, MD
Citation: P. Holden et al., Identification of novel pro-alpha 2(IX) collagen gene mutations in two families with distinctive olgo-epiphyseal forms of multiple epiphyseal dysplasia, AM J HU GEN, 65(1), 1999, pp. 31-38
Authors:
Fritz, B
Kuster, W
Orstavik, KH
Naumova, A
Spranger, J
Rehder, H
Citation: B. Fritz et al., Pigmentary mosaicism in hypomelanosis of Ito - Further evidence for functional disomy of Xp, HUM GENET, 103(4), 1998, pp. 441-449