Long-term study of family with Fanconi syndrome without cystinosis (Detoni-Debré-Fanconi syndrome)

Author:

Hunt David D.,Stearns Genevieve,McKinley J.B.,Froning Edward,Hicks Patricia,Bonfiglio Michael

Publisher

Elsevier BV

Subject

General Medicine

Reference67 articles.

1. The Fanconi syndrome;Harrison;J. Chron. Dis.,1958

2. Der renale Gluko-Amino-Phosphat-Diabetes (DeToni — Debré — Fanconi syndrome);Prader von;Schweiz. med. Wchnschr.,1959

3. Cystine storage disease with aminoaciduria and dwarfism (Lignac-Fanconi disease);Bickel;Acta Paediat.,1952

4. Die chronische Aminoaciduria (Aminosäurediabetes oder nephrotisch-glukosurischer Zwergwuchs) bei der Glycogenose und der Cystinkrankheit;Fanconi von;Helvet. paediat. acta,1949

5. The defective absorption of phosphorus and calcium and the effect of vitamin D in the Fanconi syndrome;Davies;Guy's Hosp. Reports,1958

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1. Novel Fanconi renotubular syndromes provide insights in proximal tubule pathophysiology;American Journal of Physiology-Renal Physiology;2021-02-01

2. TheHNF4AR76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype;Journal of Medical Genetics;2013-11-27

3. Renal Tubular Disorders;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

4. Hyperreninemia, Lysozymuria, and Erythrocytosis in Fanconi Syndrome with Medullary Cystic Kidney;Acta Medica Scandinavica;2009-04-24

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