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Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation.

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TAT gene mutation analysis in three Palestinian kindreds with oculocutaneous tyrosinaemia type II; characterization of a silent exonic transversion that causes complete missplicing by exon 11 skipping.

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Evidence for a major gene affecting the transition from normoglycaemia to hyperglycaemia in Psammomys obesus.

Heredity·2005

D-2-hydroxyglutaric aciduria and glutaric aciduria type 1 in siblings: coincidence, or linked disorders?

Neuropediatrics·2004

Antidiabetic effect of novel modulating peptides of G-protein-coupled kinase in experimental models of diabetes.

Diabetologia·2004

Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: possible beneficial effect of vitamin therapy.

Journal of inherited metabolic disease·2004

Electroencephalography in the evaluation of headache patients: a review.

Israel journal of medical sciences·1998

Complementary medicine--a critical review.

Israel journal of medical sciences·1998

The Israel Longitudinal Mortality Study--differential mortality in Israel 1983-1992: objectives, materials, methods and preliminary results.

Israel journal of medical sciences·1998

Detection and typing of human papillomavirus DNAs by restriction endonuclease mapping of the PCR products.

Israel journal of medical sciences·1998

A comparison between arterial- and venous-sampled activated clotting time measurements.

Israel journal of medical sciences·1998

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Israel journal of medical sciences·1998

All-optical multimodal mapping of single-cell-type-specific metabolic activities via REDCAT.

Nature methods·2026

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Journal of inherited metabolic disease·2026

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Molecular biomedicine·2026

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Antioxidants (Basel, Switzerland)·2026

Psoriasis-like skin inflammation drives an elongated mitochondrial network marked by functional failure in keratinocytes.

Journal of dermatological science·2026

Proteomic analysis reveals a metabolic switch and cellular remodeling in pancreatic-like cell spheroids cocultured with hepatocyte-like cells using an interconnected liver-pancreas-on-chip system.

Molecular omics·2026

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Hepatic metabolic pathways and hormonal status in experimental nephrotic syndrome

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Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation.

TAT gene mutation analysis in three Palestinian kindreds with oculocutaneous tyrosinaemia type II; characterization of a silent exonic transversion that causes complete missplicing by exon 11 skipping.

Evidence for a major gene affecting the transition from normoglycaemia to hyperglycaemia in Psammomys obesus.

D-2-hydroxyglutaric aciduria and glutaric aciduria type 1 in siblings: coincidence, or linked disorders?

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Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: possible beneficial effect of vitamin therapy.

Electroencephalography in the evaluation of headache patients: a review.

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A comparison between arterial- and venous-sampled activated clotting time measurements.

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