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American Journal of Ophthalmology|August 2, 2008
Ophthalmological aspects of Pierson syndromeCecilie Bredrup, Verena Matejas, Margaret Barrow, et al.Journal of the American Society of Nephrology : JASN|April 25, 2009
HNF1B mutations associate with hypomagnesemia and renal magnesium wastingShazia Adalat, Adrian S Woolf, Karen A Johnstone, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 4, 2021
Patient and caregiver perspectives on blood pressure in children with chronic kidney diseaseJustin Guang-Ao Wu, Allison Tong, Nicole Evangelidis, et al.Endocrine-Related Cancer|October 31, 2013
Long-term prognosis of patients with pediatric pheochromocytomaBirke Bausch, Ulrich Wellner, Dirk Bausch, et al.Trials|August 14, 2016
Standardised Outcomes in Nephrology-Children and Adolescents (SONG-Kids): a protocol for establishing a core outcome set for children with chronic kidney diseaseAllison Tong, Susan Samuel, Michael Zappitelli, et al.Kidney International Reports|October 27, 2025
Novel RRAGD Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic PerspectivesAnastasia Adella, François Jouret, Leire Madariaga, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 15, 2018
Management of children with congenital nephrotic syndrome: challenging treatment paradigmsStephanie Dufek, Tuula Holtta, Agnes Trautmann, et al.Nature Genetics|September 27, 2016
TSHZ3 deletion causes an autism syndrome and defects in cortical projection neuronsXavier Caubit, Paolo Gubellini, Joris Andrieux, et al.Pediatric Nephrology (Berlin, Germany)|April 26, 2022
Child and caregiver perspectives on access to psychosocial and educational support in pediatric chronic kidney disease: a focus group studyYifan Zhang, Talia Gutman, Allison Tong, et al.The New England Journal of Medicine|May 8, 2009
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutationsDetlef Bockenhauer, Sally Feather, Horia C Stanescu, et al.Pageof 20