AAAAAA
Results:
1-7
|
Results: 7
Authors:
VONSCHNAKENBURG C
HULTON SA
MILFORD DV
ROPER HP
RUMSBY G
Citation: C. Vonschnakenburg et al., VARIABLE PRESENTATION OF PRIMARY HYPEROXALURIA TYPE-1 IN 2 PATIENTS HOMOZYGOUS FOR A NOVEL COMBINED DELETION AND INSERTION MUTATION IN EXON-8 OF THE AGXT GENE, Nephron, 78(4), 1998, pp. 485-488
Authors:
SAXTON JM
DONNELLY AE
ROPER HP
BROWN S
CHILD R
DAY S
Citation: Jm. Saxton et al., A NOVEL KNEE EXTENSOR EXERCISE MODEL FOR STUDYING EXPERIMENTAL MUSCLEDAMAGE IN HUMANS, Journal of muscle research and cell motility, 17(1), 1996, pp. 168-168
Authors:
KHAN JY
MOSS C
ROPER HP
Citation: Jy. Khan et al., APLASIA-CUTIS-CONGENITA WITH CHROMOSOME 12Q ABNORMALITY, Archives of Disease in Childhood, 72(3), 1995, pp. 205-206
Authors:
SAXTON JM
DONNELLY AE
ROPER HP
Citation: Jm. Saxton et al., INDEXES OF FREE-RADICAL-MEDIATED DAMAGE FOLLOWING MAXIMUM VOLUNTARY ECCENTRIC AND CONCENTRIC MUSCULAR WORK, European journal of applied physiology and occupational physiology, 68(3), 1994, pp. 189-193
Authors:
PACHUR HJ
AHRENS M
RICKING M
ROPER HP
Citation: Hj. Pachur et al., HEAVY-METAL AND CHLORINATED-HYDROCARBON CONTAMINATION OF SELECTED AQUATIC SEDIMENTS FROM THE BERLIN AREA, Land degradation & rehabilitation, 4(4), 1993, pp. 351-360
Authors:
ROPER HP
Citation: Hp. Roper, MOLECULAR GENET OF MYOTONIC-DYSTROPHY, British Journal of Hospital Medicine, 50(7), 1993, pp. 425-425
Authors:
ROPER HP
Citation: Hp. Roper, NEUROMUSCULAR DISEASES IN CHILDREN, British Journal of Hospital Medicine, 49(8), 1993, pp. 537
Risultati:
1-7
|