Gaucher type 2 disease: identification of a novel transversion mutation in a French-Irish patient
Choy, F Y, Humphries, M L, Ben-Yoseph, Y
Published in American journal of medical genetics (16.06.1998)
Published in American journal of medical genetics (16.06.1998)
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Maternal serum hexosaminidase A in pregnancy: effects of gestational age and fetal genotype
Ben-Yoseph, Y, Pack, B A, Thomas, P M, Nadler, H L, Kaback, M M
Published in American journal of medical genetics (01.04.1988)
Published in American journal of medical genetics (01.04.1988)
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Intrauterine fetal death due to Farber disease: case report
van Lijnschoten, G, Groener, J E, Maas, S M, Ben-Yoseph, Y, Dingemans, K P, Offerhaus, G J
Published in Pediatric and developmental pathology (01.11.2000)
Published in Pediatric and developmental pathology (01.11.2000)
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A CASE OF LATE-ONSET ACID MALTASE DEFICIENCY (AMD)
Wolfe, David, Ben-Yoseph, Yoav
Published in Journal of neuropathology and experimental neurology (01.05.1985)
Published in Journal of neuropathology and experimental neurology (01.05.1985)
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Abnormal breakdown of α2-macroglobulin-trypsin complex in cystic fibrosis
Shapira, Emmanuel, Ben-Yoseph, Yoav, Nadler, Henry L.
Published in Clinica chimica acta (01.08.1977)
Published in Clinica chimica acta (01.08.1977)
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Leukocyte and plasma N-laurylsphingosine deacylase (ceramidase) in Farber disease
Ben-Yoseph, Y, Gagné, R, Parvathy, M R, Mitchell, D A, Momoi, T
Published in Clinical genetics (01.07.1989)
Published in Clinical genetics (01.07.1989)
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Lactosyl ceramidosis: Deficient activity of neutral β-Galactsidase in liver and cultivated fibroblasts?
Burton, Barbara K., Ben-Yoseph, Yoav, Nadler, Henry L.
Published in Clinica chimica acta (15.09.1978)
Published in Clinica chimica acta (15.09.1978)
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