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Acta Paediatrica (Oslo, Norway : 1992)|July 1, 1994
Congenital varicella syndrome: studies of the virus-specific humoral and cell-mediated immune responsesV Schuster, G Hofmann, J Pannenbecker, et al.
Infection|July 6, 2000
Limited sequence heterogeneity of Epstein-Barr virus nuclear antigen 1 in benign and malignant EBV-associated disordersV Schuster, G Ott, S Seidenspinner, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1993
[Congenital Epstein-Barr virus infection]V Schuster, W Janssen, S Seidenspinner, et al.
Blood|February 15, 1996
Common Epstein-Barr virus (EBV) type-1 variant strains in both malignant and benign EBV-associated disordersV Schuster, G Ott, S Seidenspinner, et al.
European Journal of Pediatrics|March 1, 1993
Endocrine and molecular biological studies in a German family with Albright hereditary osteodystrophyV Schuster, T Eschenhagen, K Kruse, et al.
American Journal of Diseases of Children (1960)|December 1, 1993
X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysisV Schuster, W Kress, W Friedrich, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|September 1, 1996
An unusual case of refractory Campylobacter jejuni infection in a patient with X-linked agammaglobulinemia: successful combined therapy with maternal plasma and ciprofloxacinI B Autenrieth, V Schuster, J Ewald, et al.
Seminars in Thrombosis and Hemostasis|January 1, 1997
Homozygous type I plasminogen deficiencyA M Mingers, N Heimburger, P Zeitler, et al.
Blood|August 1, 1997
Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitisV Schuster, A M Mingers, S Seidenspinner, et al.
European Journal of Pediatrics|June 1, 1994
Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative diseaseV Schuster, S Seidenspinner, T Grimm, et al.
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