AAAAAA

   
Results: 1-8 |
Results: 8
MOLECULAR HETEROGENEITY OF 2ND AND 4TH COMPONENTS OF COMPLEMENT AND THEIR GENES IN SYSTEMIC-SCLEROSIS AND ASSOCIATION OF HLA ALLELES A1, B8AND DR3 WITH LIMITED AND DR5 WITH DIFFUSE SYSTEMIC-SCLEROSIS
Authors: VENNEKER GT VANDENHOOGEN FHJ VANMEEGEN M DEKOKNAZARUK M HULSMANS RFHJ BOERBOOMS AMT DEWAAL LP BOS JD ASGHAR SS
Citation: Gt. Venneker et al., MOLECULAR HETEROGENEITY OF 2ND AND 4TH COMPONENTS OF COMPLEMENT AND THEIR GENES IN SYSTEMIC-SCLEROSIS AND ASSOCIATION OF HLA ALLELES A1, B8AND DR3 WITH LIMITED AND DR5 WITH DIFFUSE SYSTEMIC-SCLEROSIS, Experimental and clinical immunogenetics, 15(2), 1998, pp. 90-99
RESTRICTIVE DERMOPATHY - REPORT OF 12 CASES
Authors: SMITT JHS VANASPEREN CJ NIESSEN CM BEEMER FA VANESSEN AJ HULSMANS RFHJ ORANJE AP STEIJLEN PM WESBYVANSWAAY E TAMMINGA P BRESLAUSIDERIUS EJ
Citation: Jhs. Smitt et al., RESTRICTIVE DERMOPATHY - REPORT OF 12 CASES, Archives of dermatology, 134(5), 1998, pp. 577-579
MELANOSIS NAEVIFORMIS OF BECKER AND SCOLIOSIS - A COINCIDENCE
Authors: MAESSENVISCH MB HULSMANS RFHJ HULSMANS FJH NEUMANN HAM
Citation: Mb. Maessenvisch et al., MELANOSIS NAEVIFORMIS OF BECKER AND SCOLIOSIS - A COINCIDENCE, Acta dermato-venereologica, 77(2), 1997, pp. 135-136
INCOMPLETE FUNCTIONAL DEFICIENCIES OF THE 4TH (C4) AND 2ND (C2) COMPONENTS OF COMPLEMENT IN A PATIENT WITH LINEAR FRONTOPARIETAL SCLERODERMA AND HIS FAMILY - DEFICIENCIES DETERMINED BY A GENE NOT LINKED TO HUMAN-LEUKOCYTE ANTIGEN SYSTEM
Authors: VENNEKER GT VANMEEGEN M DEKOKNAZARUK M HULSMANS RFHJ DEWAALL LP BOS JD ASGHAR SS
Citation: Gt. Venneker et al., INCOMPLETE FUNCTIONAL DEFICIENCIES OF THE 4TH (C4) AND 2ND (C2) COMPONENTS OF COMPLEMENT IN A PATIENT WITH LINEAR FRONTOPARIETAL SCLERODERMA AND HIS FAMILY - DEFICIENCIES DETERMINED BY A GENE NOT LINKED TO HUMAN-LEUKOCYTE ANTIGEN SYSTEM, Experimental and clinical immunogenetics, 13(2), 1996, pp. 104-111
DEFICIENCIES OF 4TH (C4) AND 2ND (C2) COMPONENTS OF COMPLEMENT AND MOLECULAR HETEROGENEITY OF C4 AND ITS GENE IN SYSTEMIC-SCLEROSIS
Authors: VENNEKER GT VANDENHOOGEN FHJ HULSMANS RFHJ DEWAAL LP ASGHAR SS
Citation: Gt. Venneker et al., DEFICIENCIES OF 4TH (C4) AND 2ND (C2) COMPONENTS OF COMPLEMENT AND MOLECULAR HETEROGENEITY OF C4 AND ITS GENE IN SYSTEMIC-SCLEROSIS, Journal of investigative dermatology, 105(3), 1995, pp. 509-509
MOSAIC EXPRESSION OF HYPOHIDROTIC ECTODERMAL DYSPLASIA IN AN ISOLATEDAFFECTED FEMALE CHILD
Authors: BARTSTRA HLJ HULSMANS RFHJ STEIJLEN PM RUIGE M DEDIESMULDERS CEM CASSIMAN JJ
Citation: Hlj. Bartstra et al., MOSAIC EXPRESSION OF HYPOHIDROTIC ECTODERMAL DYSPLASIA IN AN ISOLATEDAFFECTED FEMALE CHILD, Archives of dermatology, 130(11), 1994, pp. 1421-1424
ADHESION MOLECULE EXPRESSION IN VENOUS LEG ULCERS
Authors: VERAART JCJM VERHAEGH MEJM NEUMANN HAM HULSMANS RFHJ ARENDS JW
Citation: Jcjm. Veraart et al., ADHESION MOLECULE EXPRESSION IN VENOUS LEG ULCERS, VASA, 22(3), 1993, pp. 213-218
AN OPEN PROSPECTIVE CLINICAL-TRIAL WITH SYSTEMIC RANITIDINE IN THE TREATMENT OF PSORIASIS
Authors: WITKAMP L VELTHUIS PJ VERHAEGH MEJM HULSMANS RFHJ BOSSUYT PMM BOS JD MEINARDI MMHM
Citation: L. Witkamp et al., AN OPEN PROSPECTIVE CLINICAL-TRIAL WITH SYSTEMIC RANITIDINE IN THE TREATMENT OF PSORIASIS, Journal of the American Academy of Dermatology, 28(5), 1993, pp. 778-781
Risultati: 1-8 |