V. Madike

发表

Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease

E. Sidransky, D. Stone, N. Tayebi, 2000, Human mutation.

Coding region of NKX3.1, a prostate-specific homeobox gene on 8p21, is not mutated in human prostate cancers.

M. Augustus, E. Gelmann, G. Bova, 1997, Cancer research.

Gaucher disease and parkinsonism: a phenotypic and genotypic characterization.

D. Krasnewich, E. Sidransky, M. Callahan, 2001, Molecular genetics and metabolism.

Glucocerebrosidase gene mutations in patients with type 2 Gaucher diseaseThis article is a US Government work and, as such, is in the public domain in the United States of America.

E. Sidransky, D. Stone, N. Tayebi, 2000 .

Clinico-pathogenetic findings and management of chondrodystrophic myotonia (Schwartz-Jampel syndrome): a case report

M. Dalakas, C. Francomano, V. Madike, 2003, BMC neurology.

Cloning of a putative human neurotransmitter receptor expressed in skeletal muscle and brain.

K. Carter, K. Su, V. Madike, 1998, Biochemical and Biophysical Research Communications - BBRC.

Gene rearrangement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion gene

E. Sidransky, N. Tayebi, Joseph K Park, 2000, Human Genetics.

Glucocerebrosidase mutations among African-American patients with type 1 Gaucher disease.

J. K. Park, E. Sidransky, V. Koprivica, 2001, American journal of medical genetics.

Clinico-pathogenetic findings and management of chondrodystrophic myotonia ( Schwartz-Jampel syndrome )

M. Dalakas, C. Francomano, V. Madike, 2003 .