Befekadu Asfaw

Acid sphingomyelinase deficiency. Phenotype variability with prevalence of intermediate phenotype in a series of twenty‐five Czech and Slovak patients. A multi‐approach study

Hana Pavlú-Pereira, Befekadu Asfaw, H. Poupčtová et al. · Journal of Inherited Metabolic Disease · 2005 · 112 citations

Life Sciences, Biochemistry, Genetics +15

Prosaposin deficiency and saposin B deficiency (activator‐deficient metachromatic leukodystrophy): Report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations

Ladislav Kuchař, J. Ledvinová, Martin Hřebı́ček et al. · American Journal of Medical Genetics Part A · 2009 · 84 citations · Full text

Life Sciences, Biochemistry, Molecular Genetics +17

Quantitation of plasmatic lysosphingomyelin and lysosphingomyelin-509 for differential screening of Niemann-Pick A/B and C diseases

Ladislav Kuchař, Jakub Sikora, Maria Gulinello et al. · Analytical Biochemistry · 2017 · 70 citations

Medicine, Molecular Medicine, Pathology +6

Benzenediazonium Ion Derived from Sudan I Forms an 8-(Phenylazo)guanine Adduct in DNA

Marie Stiborová, Befekadu Asfaw, Eva Frei et al. · Chemical Research in Toxicology · 1995 · 60 citations

Pharmacy, Biochemistry, Toxicology +16

The first identification of the benzenediazonium ion formation from a non-aminoazo dye, 1-phenylazo-2-hydroxynaphthalene (Sudan I) by microsomes of rat livers

Marie Stiborová, Befekadu Asfaw, Pavel Anzenbacher et al. · Cancer Letters · 1988 · 45 citations

Natural Sciences, Chemistry, Toxicology +7