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AJR. American Journal of Roentgenology|November 3, 1998
Sonographic guidance when using the right internal jugular vein for central vein accessJ G Caridi, I F Hawkins, B N Wiechmann, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 1, 1996
Effects of peritoneal effluents on mesothelial cells in culture: cell proliferation and extracellular matrix regulationF Perfumo, P Altieri, M L Degl'Innocenti, et al.Journal of Vascular and Interventional Radiology : JVIR|March 31, 2009
False-positive "Cavernous Transformation" secondary to lymphatic filling in parenchymal hepatic CO(2) injection for portal vein visualization in TIPS proceduresIrvin F Hawkins, Kyung J Cho, Frank Fiola, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 18, 1998
Renal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locusG Caridi, L Murer, R Bellantuono, et al.Human Genetics|September 1, 1992
Mapping of the human COL5A1 gene to chromosome 9q34.3G Caridi, A Pezzolo, R Bertelli, et al.Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|July 1, 1988
Prognostic significance of estrogen receptor determination in primary breast cancerS Ciatto, D Palli, A Iossa, et al.The Journal of Pediatrics|October 18, 2000
Resolution of hypoxemia in a liver transplant recipient after ligation of a portosystemic shuntL T Spencer, M R Langham, M H Hoyer, et al.Neoplasma|January 1, 1991
Causes of breast cancer misdiagnosis at physical examinationS Ciatto, M Rosselli del Turco, S Catarzi, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 1, 2000
Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney diseaseS Kroiss, K Huck, S Berthold, et al.European Journal of Human Genetics : EJHG|November 28, 2000
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13R Cusano, S Gangarossa, P Forabosco, et al.Pageof 6