Authors:
Ozcelik, U
Akcoren, Z
Anadol, D
Kiper, N
Orhon, M
Gocmen, A
Irkec, M
Schuster, V
Citation: U. Ozcelik et al., Pulmonary involvement in a child with ligneous conjunctivitis and homozygous type I plasminogen deficiency, PEDIAT PULM, 32(2), 2001, pp. 179-183
Authors:
Schuster, V
Zeitler, P
Seregard, S
Ozcelik, U
Anadol, D
Luchtman-Jones, L
Meire, F
Mingers, AM
Schambeck, C
Kreth, HW
Citation: V. Schuster et al., Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis, THROMB HAEM, 85(6), 2001, pp. 1004-1010
Citation: V. Schuster et al., Manifestations of X-linked lymphoproliferative disease without prior Epstein-Barr virus exposure, BLOOD, 98(6), 2001, pp. 1986-1986
Authors:
Kern, M
Lagomarcino, ND
Misell, LM
Schuster, V
Citation: M. Kern et al., The effect of medium-chain triacylglycerols on the blood lipid profile of male endurance runners, J NUTR BIOC, 11(5), 2000, pp. 288-292
Authors:
Schuster, V
Ott, G
Seidenspinner, S
Kreth, H
Citation: V. Schuster et al., Limited sequence heterogeneity of Epstein-Barr virus nuclear antigen 1 in benign and malignant EBV-Associated disorders, INFECTION, 28(3), 2000, pp. 137-142
Citation: V. Schuster et Hw. Kreth, X-linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain-containing signal transduction adaptor protein, IMMUNOL REV, 178, 2000, pp. 21-28
Authors:
Brandau, O
Schuster, V
Weiss, M
Hellebrand, H
Fink, FM
Kreczy, A
Friedrich, W
Strahm, B
Niemeyer, C
Belohradsky, BH
Meindl, A
Citation: O. Brandau et al., Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP), HUM MOL GEN, 8(13), 1999, pp. 2407-2413
Authors:
Amram, P
Anvar, S
Aslanides, E
Aubert, JJ
Azoulay, R
Basa, S
Benhammou, Y
Bernard, F
Berthier, R
Bertin, V
Billault, M
Biller, S
Blanc, F
Blanc, PE
Bland, RW
Blondeau, F
de Botton, N
Bottu, N
Boulesteix, J
Brooks, B
Brunner, J
Calzas, A
Carloganu, C
Carr, J
Carton, PH
Cartwright, S
Cases, R
Cassol, F
Charles, F
Charles, J
Desages, F
Destelle, JJ
Dispau, G
Duval, PY
Engelen, J
Feinstein, F
Flores, EC
Fopma, J
Fuda, JL
Goret, P
Gosset, L
Gournay, JF
Hernandez, JJ
Hubaut, F
Hubbard, R
Huss, D
Jaquet, M
Jelley, N
Kajfasz, E
Kouchner, A
Kudryavtsev, V
Lachartre, D
Lafoux, H
Lamare, P
Languillat, JC
Laugier, JP
Le Provost, H
Loiseau, D
Loucatos, S
Magnier, P
Marc, K
Marcelin, M
Martin, L
Mazeau, B
Mazure, A
McMillan, J
Meessen, C
Millot, C
Mols, P
Montanet, F
Moorhead, M
Moscoso, L
Navas, S
Nooren, V
Olivetto, C
Palanque-Delabrouille, N
Pallares, A
Payre, P
Perrin, P
Poinsignon, J
Potheau, R
Qian, Z
Raymond, M
Roberts, J
Sacquin, Y
Schuller, JP
Schuster, V
Spooner, N
Stolarczyk, T
Tabary, A
Talby, M
Tao, C
Thompson, L
Triay, R
Valdy, M
Velasco, J
Vigeolas, E
Vignaud, D
Vilanova, D
Wark, D
Zuniga, J
Citation: P. Amram et al., The ANTARES project, NUCL PH B-P, 75A, 1999, pp. 415-417
Authors:
Schuster, V
Seidenspinner, S
Muller, C
Rempen, A
Citation: V. Schuster et al., Prenatal diagnosis in a family with severe type I plasminogen deficiency, ligneous conjunctivitis and congenital hydrocephalus, PRENAT DIAG, 19(5), 1999, pp. 483-487
Authors:
Rutkowski, S
Scheurlen, W
Girschick, H
Schuster, V
Citation: S. Rutkowski et al., Agranulocytosis in a 15-months old girl: congenital neutropenia or cyclic neutropenia, MONATS KIND, 147(11), 1999, pp. 1018-1022
Authors:
Yu, DW
Yu, SH
Schuster, V
Kruse, K
Clericuzio, CL
Weinstein, LS
Citation: Dw. Yu et al., Identification of two novel deletion mutations within the G(s)alpha gene (GNAS1) in albright hereditary osteodystrophy, J CLIN END, 84(9), 1999, pp. 3254-3259
Authors:
Schuster, V
Seidenspinner, S
Zeitler, P
Escher, C
Pleyer, U
Bernauer, W
Stiehm, ER
Isenberg, S
Seregard, S
Olsson, T
Mingers, AM
Schambeck, C
Kreth, HW
Citation: V. Schuster et al., Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis, BLOOD, 93(10), 1999, pp. 3457-3466
Authors:
Schott, D
Dempfle, CE
Beck, P
Liermann, A
Mohr-Pennert, A
Goldner, M
Mehlem, P
Azuma, H
Schuster, V
Mingers, AM
Schwarz, HP
Kramer, MD
Citation: D. Schott et al., Therapy with a purified plasminogen concentrate in an infant with ligneousconjunctivitis and homozygous plasminogen deficiency, N ENG J MED, 339(23), 1998, pp. 1679-1686