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Results: 1-6 |
Results: 6

Authors: GHAHREMANI M CHAN CB BISTRITZER T ALADJEM M TIEDER M PELLETIER J
Citation: M. Ghahremani et al., A NOVEL MUTATION H373Y IN THE WILMS-TUMOR SUPPRESSOR GENE, WT1, ASSOCIATED WITH DENYS-DRASH SYNDROME, Human heredity, 46(6), 1996, pp. 336-338

Authors: POLLAK L KLEIN C TIEDER M ARLAZOROFF A
Citation: L. Pollak et al., THERAPY-RESISTANT SEIZURES IN PSEUDOHYPOPARATHYROIDISM - A CASE-REPORT, Journal of pediatric endocrinology & metabolism, 8(3), 1995, pp. 209-211

Authors: TIEDER M MANOR H PESHIN J ALON US
Citation: M. Tieder et al., THE WEISMANN-NETTER, STUHL SYNDROME - A RARE PEDIATRIC SKELETAL DYSPLASIA, Pediatric radiology, 25(1), 1995, pp. 37-40

Authors: ZISMAN A TIEDER M ALON H EIDELMAN A
Citation: A. Zisman et al., BENIGN FIBROEPITHELIAL POLYPS OF THE URETER AND RENAL PELVIS IN CHILDHOOD - 2 CASE-REPORTS, Scandinavian journal of urology and nephrology, 28(2), 1994, pp. 191-193

Authors: ROBINSON D TIEDER M HALPERIN N BURSHTEIN D NEVO Z
Citation: D. Robinson et al., MAFFUCCIS-SYNDROME - THE RESULT OF NEURAL ABNORMALITIES - EVIDENCE OFMITOGENIC NEUROTRANSMITTERS PRESENT IN ENCHONDROMAS AND SOFT-TISSUE HEMANGIOMAS, Cancer, 74(3), 1994, pp. 949-957

Authors: TIEDER M BLONDER J STRAUSS S SHAKED U MAOR J GABIZON D MANOR H SELA BA
Citation: M. Tieder et al., HYPEROXALURIA IS NOT A CAUSE OF NEPHROCALCINOSIS IN PHOSPHATE-TREATEDPATIENTS WITH HEREDITARY HYPOPHOSPHATEMIC RICKETS, Nephron, 64(4), 1993, pp. 526-531
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