• A mouse model of renal tubular injury of tyrosinemia type 1: development of de Toni Fanconi syndrome and apoptosis of renal tubular cells in Fah/Hpd double mutant mice
• A probable case of Toni-Fanconi-Debre syndrome
• Aminoaciduria, glycosuria, and hypophosphatemic rickets (de Toni-Fanconi syndrome)
• Comments on anesthesia procedures in mitochondrial encephalomyopathy
• Contribution to Lignac-Fanconi disease or Debre-de Toni-Fanconi syndrome
• Cystinosis with the De Toni-Fanconi syndrome in a 6 and one-half-year-old boy
• Cystinosis with Toni-Fanconi-Debre syndrome
• De Toni-Fanconi-Debre syndrome in adults
• de Toni-Fanconi-Debre syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency
• DEBR'E-DE TONI-FANCONI SYNDROME
• Debre-de Toni-Fanconi syndrome under the light of various biochemical tests
• Debre-De Toni-Fanconi syndrome with glycogenosis of the liver
• Determination of metabolites of vitamin D in a case of Debre-De Toni-Fanconi syndrome secondary to cystinosis
• Diagnostic significance of calcitonin analysis in children with rickets and rickets-like diseases administered calcium test
• Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient
• Gas chromatographic-mass spectrometric metabolic profiling of patients with fatal infantile mitochondrial myopathy with de Toni-Fanconi-Debre syndrome
• Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debre syndrome, and a defective respiratory chain in voluntary striated muscles
• Hyperaminoaciduria identifies patients at risk of developing renal tubular toxicity associated with ifosfamide and platinate containing regimens
• Hyperaminoaciduria: Toni-Fanconi and Lowe- syndrome
• Multiple myelomas & the De Toni-Fanconi syndrome
• Multiple myelomas & the De Toni-Fanconi syndrome
• Renal and skin involvement in a patient with complete Kearns-Sayre syndrome
• Renal diabetes with incurable osteomalacic rachitism (Toni-Fanconi-Debre syndrome)
• Renal function disorders in congenital metabolic abnormalities. 2. Renal function disorders in Lowe's and de Toni-Fanconi syndrome
• Renal pathology in children with mitochondrial diseases
• Renal rickets, renal diabetes and cystine metabolism; the De Toni-Fanconi-Debre syndrome
• Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome
• Simultaneous metabolic profile studies of three patients with fatal infantile mitochondrial myopathy-de Toni-Fanconi-Debre syndrome by GC/MS
• Suramin-induced weakness from hypophosphatemia and mitochondrial myopathy. Association of suramin with mitochondrial toxicity in humans
• The de Toni-Fanconi syndrome with cystinosis
• The de Toni-Fanconi syndrome with cystinosis; clinical and metabolic study of two cases in a family and a critical review on the nature of the syndrome