P. Strasberg

发表

FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.

R. Weksberg, D. Chitayat, C. Shuman, 1996, American journal of medical genetics.

I. Rapin, A. Spiro, J. Prineas, 1970, Archives of neurology.

HPLC analysis of urinary sulfatide: an aid in the diagnosis of metachromatic leukodystrophy.

P. Strasberg, J. Lowden, M. Skomorowski, 1985, Clinical biochemistry.

Late-onset Tay-Sachs disease presenting as catatonic schizophrenia: diagnostic and treatment issues.

G. MacQueen, J. Callahan, M. Mazurek, 1995, The Journal of clinical psychiatry.

Lysosphingolipids and mitochondrial function. II. Deleterious effects of sphingosylphosphorylcholine.

J. Callahan, P. Strasberg, Paula M. Strasberg, 1988, Biochemistry and cell biology = Biochimie et biologie cellulaire.

Cytochromes and Oxidative Phosphorylation

C. Moore, P. Strasberg, 1970 .

Cerebrosides and psychosine disrupt mitochondrial functions.

P. Strasberg, 1986, Biochemistry and cell biology = Biochimie et biologie cellulaire.

Genotype‐phenotype pitfalls in Gaucher disease

L. Becker, J. Callahan, J. Clarke, 1994, Journal of clinical laboratory analysis.

X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred.

A. Ballabio, P. Babyn, D. Bulman, 1996, Journal of medical genetics.

Decreased incorporation ofd-glucosamine into glycosphingolipids of intact familial dysautonomia lymphoblasts

A. Novak, P. Strasberg, I. Warren, 2007, Journal of Molecular Neuroscience.

A high recovery method for concentrating microgram quantities of protein from large volumes of solution.

D. Mahuran, P. Clements, P. Strasberg, 1983, Analytical biochemistry.

ENZYMOLOGICAL DIAGNOSIS OF LYSOSOMAL STORAGE DISORDERS

A. Novak, P. Strasberg, J. Lowden, 1982 .

Rapid molecular weight determination for native glucocerebrosidase from human placenta using high-performance liquid chromatography.

P. Strasberg, J. Lowden, 1983, Journal of chromatography.

The assay of glucocerebrosidase activity using the natural substrata.

P. Strasberg, J. Lowden, 1982, Clinica chimica acta; international journal of clinical chemistry.

Simultaneous fractionation of four placental neutral glycosphingolipids with a continuous gradient.

P. Strasberg, M. Skomorowski, A. Grey, 1989, Journal of lipid research.

HPLC analysis of neutral glycolipids: an aid in the diagnosis of lysosomal storage disease.

P. Strasberg, J. Lowden, M. Skomorowski, 1983, Clinica chimica acta; international journal of clinical chemistry.

Further studies on the binding of gamma-aminobutyric acid by brain.

K. Elliott, P. Strasberg, 1967, Canadian Journal of Biochemistry.

3&se Pair Insertional utation in the C horoideremia

I. MacDonald, P. Ray, P. Strasberg, 1998 .

A 3‐base pair insertional mutation in the choroideremia gene

I. MacDonald, P. Ray, P. Strasberg, 1998, Human mutation.

Mitochondrial malic enzyme in mosaic skeletal muscle of mouse chimeras

A. Peterson, P. Strasberg, K. B. Freeman, 1979, Biochemical Genetics.

PENETRATION OF BLOOD‐BRAIN BARRIER BY γ‐AMINOBUTYRIC ACID AT SITES OF FREEZING

K. Elliott, P. Strasberg, S. Schwartz, 1967, Journal of neurochemistry.

Homozygous presence of the crossover (fusion gene) mutation identified in a type II Gaucher disease fetus: is this analogous to the Gaucher knock-out mouse model?

J. Callahan, J. Clarke, P. Strasberg, 1994, Biochemical medicine and metabolic biology.

A novel mutation in the Norrie disease gene predicted to disrupt the cystine knot growth factor motif.

T. Stein, P. Ray, J. Sutherland, 1995, Human molecular genetics.

Regulation of renal sulfoglycolipid biosynthesis.

H. Yeger, C. Lingwood, T. Taylor, 1986, Biochimica et biophysica acta.

Rapid nonradioactive tracer method for detecting carriers of the major Ashkenazi Jewish Tay-Sachs disease mutations.

J. Clarke, P. Strasberg, 1992, Clinical chemistry.

Increased globotriaosylceramide in familial dysautonomia

H. Yeger, P. Strasberg, I. Warren, 1992, Lipids.

Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl.

P. Ray, J. Clarke, W. Greer, 1991, American journal of human genetics.

Mutation analysis in Canadian families with choroideremia.

I. MacDonald, P. Strasberg, N. Nesslinger, 1996, Ophthalmic genetics.

PCR-based test for two cystic fibrosis mutations (A455E, 711 + 1 G-->T) common among French Canadians.

P. Ray, L. McGlynn-Steele, P. Strasberg, 1997, Clinical chemistry.

Heterogeneity of Human Sphingomyelinase: Relatedness of the Major Polypeptides

D. Davidson, J. Callahan, P. Strasberg, 1986 .

On the functional aspects of a preparation of an inner membrane fraction of liver mitochondria. II.

C. Moore, P. Strasberg, 1969, Biochemistry.

Increased globotriaosylceramide on plasma membranes of synchronized familial dysautonomia cells

C. Lingwood, B. Boyd, P. Strasberg, 2007, Journal of Molecular Neuroscience.

Evaluation of the biotinylated (Blugene) vs 32P-labeled cDNA probes of beta-glucocerebrosidase: relative sensitivities in genomic and other systems.

P. Strasberg, 1989, Clinical chemistry.

Homozygosity for the common Ashkenazi Jewish Tay‐Sachs +1 IVS‐12 splice‐junction mutation: First report

A. Feigenbaum, P. Strasberg, M. Skomorowski, 1997, Human mutation.

Psychosine and Sphingosylphosphorylcholine Bind to Mitochondrial Membranes and Disrupt their Function

J. Callahan, P. Strasberg, 1988 .

Charge properties of mitochondrial matrix proteins.

P. Strasberg, K. B. Freeman, 1975, Canadian journal of biochemistry.