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Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|January 1, 1996
Complications linked to chronic peritoneal dialysis in children after kidney transplantation: experience of the Italian Registry of Pediatric Chronic Peritoneal DialysisB Andreetta, E Verrina, P Sorino, et al.
American Journal of Human Genetics|April 25, 2000
COL5A1 haploinsufficiency is a common molecular mechanism underlying the classical form of EDSR J Wenstrup, J B Florer, M C Willing, et al.
The Journal of Clinical Investigation|January 1, 1997
In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemiaM Bai, S H Pearce, O Kifor, et al.
Journal of the Neurological Sciences|August 1, 1990
Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case reportR J Wanders, E Boltshauser, B Steinmann, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 3, 2007
Prospective monitoring of polyomavirus BK replication and impact of pre-emptive intervention in pediatric kidney recipientsF Ginevri, A Azzi, H H Hirsch, et al.
Transplantation Proceedings|April 26, 2005
Mycophenolate mofetil pharmacokinetic monitoring in pediatric kidney transplant recipientsL Ghio, M Ferraresso, S M Viganò, et al.
Nature Genetics|October 1, 1993
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2M R Pollak, Y H Chou, J J Cerda, et al.
Pediatric Research|April 1, 1985
Prenatal diagnosis of hereditary tyrosinemia by determination of fumarylacetoacetase in cultured amniotic fluid cellsE A Kvittingen, B Steinmann, R Gitzelmann, et al.
Schweizer Archiv Fur Tierheilkunde|April 3, 2010
[Swiss warmblood horse with symptoms of hereditary equine regional dermal asthenia without mutation in the cyclophylin B gene (PPIB)]S Rüfenacht, R Straub, B Steinmann, et al.
Transplantation|April 30, 2003
Polyomavirus BK infection in pediatric kidney-allograft recipients: a single-center analysis of incidence, risk factors, and novel therapeutic approachesF Ginevri, R De Santis, P Comoli, et al.
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