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6 in total

Review 1. Fatty acid oxidation disorders: a new class of metabolic diseases.

Authors: D E Hale; M J Bennett
Journal: J Pediatr Date: 1992-07 Impact factor: 4.406

2. A simple, straightforward assay for long-chain 3-hydroxyacyl-CoA dehydrogenase based on the use of N-ethylmaleimide: potential for pre- and postnatal diagnosis.

Authors: L Ijlst; R J Wanders
Journal: J Inherit Metab Dis Date: 1993 Impact factor: 4.982

3. Pseudo-glutaric aciduria type II in a patient with celiac disease.

Authors: C Largillière; M Fontaine; S Marrakchi; O Voisin-Taboureau
Journal: J Pediatr Date: 1993-03 Impact factor: 4.406

4. 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment.

Authors: M Duran; R J Wanders; J P de Jager; L Dorland; L Bruinvis; D Ketting; L Ijlst; F J van Sprang
Journal: Eur J Pediatr Date: 1991-01 Impact factor: 3.183

5. Urinary 3-hydroxydicarboxylic acids in pathophysiology of metabolic disorders with dicarboxylic aciduria.

Authors: K Y Tserng; S J Jin; D S Kerr; C L Hoppel
Journal: Metabolism Date: 1991-07 Impact factor: 8.694

6. Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Authors: M J Bennett; M J Weinberger; W G Sherwood; A B Burlina
Journal: J Inherit Metab Dis Date: 1994 Impact factor: 4.982

6 in total

1 in total

1. Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease.

Authors: C E Mize; L J Waber; T Anderson; M J Bennett
Journal: J Inherit Metab Dis Date: 1997-07 Impact factor: 4.982

1 in total