Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Catch-up growth in Fanconi-Bickel syndrome with uncooked cornstarch.

× No keyword cloud information.

9 in total

1. [Chronic aminoaciduria (amino acid diabetes or nephrotic-glucosuric dwarfism) in glycogen storage and cystine disease].

Authors: G FANCONI; H BICKEL
Journal: Helv Paediatr Acta Date: 1949-11

2. Amelioration of proximal renal tubular dysfunction in type I glycogen storage disease with dietary therapy.

Authors: Y T Chen; J I Scheinman; H K Park; R A Coleman; C R Roe
Journal: N Engl J Med Date: 1990-08-30 Impact factor: 91.245

3. Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathy.

Authors: H Hurvitz; O N Elpeleg; V Barash; E Kerem; R M Reifen; W Ruitenbeek; C Mor; D Branski
Journal: Eur J Pediatr Date: 1989-10 Impact factor: 3.183

4. Cornstarch therapy in type I glycogen-storage disease.

Authors: Y T Chen; M Cornblath; J B Sidbury
Journal: N Engl J Med Date: 1984-01-19 Impact factor: 91.245

5. The dietary treatment of children with type I glycogen storage disease with slow release carbohydrate.

Authors: G P Smit; R Berger; R Potasnick; S W Moses; J Fernandes
Journal: Pediatr Res Date: 1984-09 Impact factor: 3.756

6. Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome.

Authors: M Brivet; N Moatti; A Corriat; A Lemonnier; M Odievre
Journal: Pediatr Res Date: 1983-02 Impact factor: 3.756

7. Fanconi's syndrome with hepatorenal glycogenosis associated with phosphorylase b kinase deficiency.

Authors: S A Sanjad; R E Kaddoura; H M Nazer; M Akhtar; N A Sakati
Journal: Am J Dis Child Date: 1993-09

8. Fanconi-Bickel syndrome.

Authors: F Manz; H Bickel; J Brodehl; D Feist; K Gellissen; B Geschöll-Bauer; G Gilli; E Harms; H Helwig; W Nützenadel
Journal: Pediatr Nephrol Date: 1987-07 Impact factor: 3.714

9. Familial Fanconi syndrome with malabsorption and galactose intolerance, normal kinase and transferase activity. A report on two siblings.

Authors: A Aperia; G Bergqvist; T Linné; R Zetterström
Journal: Acta Paediatr Scand Date: 1981-07

9 in total

7 in total

Catch-up growth in Fanconi-Bickel syndrome with uncooked cornstarch.

1. [Chronic aminoaciduria (amino acid diabetes or nephrotic-glucosuric dwarfism) in glycogen storage and cystine disease].

2. Amelioration of proximal renal tubular dysfunction in type I glycogen storage disease with dietary therapy.

3. Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathy.

4. Cornstarch therapy in type I glycogen-storage disease.

5. The dietary treatment of children with type I glycogen storage disease with slow release carbohydrate.

6. Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome.

7. Fanconi's syndrome with hepatorenal glycogenosis associated with phosphorylase b kinase deficiency.

8. Fanconi-Bickel syndrome.

9. Familial Fanconi syndrome with malabsorption and galactose intolerance, normal kinase and transferase activity. A report on two siblings.

1. Fanconi-Bickel syndrome as an example of marked allelic heterogeneity.

2. Phenotypic variability in patients with fanconi-bickel syndrome with identical mutations.

3. Fanconi-Bickel syndrome.

Review 4. Glycogen storage diseases: new perspectives.

5. Fanconi-Bickel syndrome in an infant with cytomegalovirus infection: A case report and review of the literature.

6. Fanconi-Bickel syndrome - mutation in SLC2A2 gene.

Review 7. Fanconi-Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia.