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The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisYI YANG; HENTATI, Afif; COLE, Natalie et al.Nature genetics. 2001, Vol 29, Num 2, pp 160-165, issn 1061-4036Article

Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosisLI, Yi-Ju; PERICAK-VANCE, Margaret A; SAUNDERS, Ann M et al.Neurogenetics (Oxford. Print). 2004, Vol 5, Num 4, pp 209-213, issn 1364-6745, 5 p.Article

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in TunisiaEL EUCH-FAYACHE, Ghada; LALANI, Irfan; AMOURI, Rim et al.Archives of neurology (Chicago). 2003, Vol 60, Num 7, pp 982-988, issn 0003-9942, 7 p.Article

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22HOSLER, Betsy A; SIDDIQUE, Teepu; HUNG, Wu-Yen et al.JAMA, the journal of the American Medical Association. 2000, Vol 284, Num 13, pp 1664-1669, issn 0098-7484Article

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