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Por Deutschman, Alan., Gaines-Ross, Leslie.
Publicado em 1994

Treatment Practices of Mild Cognitive Impairment in California Alzheimer's Disease Centers

Por Weinstein, Andrea M., Barton, Cynthia, Ross, Leslie, Kramer, Joel H., Yaffe, Kristine
Publicado em 2009

The Relationship between Functional Status and Judgment/Problem Solving Among Individuals with Dementia

Por Mayo, Ann M., Wallhagen, Margaret, Cooper, Bruce A., Mehta, Kala, Ross, Leslie, Miller, Bruce
Publicado em 2012

Quality of life (QOL) of older adult community choral singers in Finland

Por Johnson, Julene K, Louhivuori, Jukka, Stewart, Anita L, Tolvanen, Asko, Ross, Leslie, Era, Pertti
Publicado em 2013

Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide p...

Por Wang, Jia-Chi, Mahon, Loretta W., Ross, Leslie P., Anguiano, Arturo, Owen, Renius, Boyar, Fatih Z.
Publicado no Mol Cytogenet (2016)

Inherited and de novo 22q11.2 distal duplications in two patients with autistic features, speech delay and no dysmorphology

Por Hantash, Feras M., Wang, Boris T., Owen, Renius, Ross, Leslie P., Mahon, Loretta W., Boyar, Fatih Z., Anguiano, Arturo, Strom, Charles M.
Publicado no J Pediatr Genet (2012)

Off-Label Medication Use in Frontotemporal Dementia

Por Hu, Bei, Ross, Leslie, Neuhaus, John, Knopman, David, Kramer, Joel, Boeve, Bradley, Caselli, Richard J., Graff-Radford, Neill, Mendez, Mario F., Miller, Bruce L., Boxer, Adam L.
Publicado em 2010

Identification and clinical evaluation of segments of homozygosity, uniparental disomy and complex chromosomal abnormalities revealed by copy-number SNP arrays

Por Wang, Jia-Chi, Ross, Leslie, Mahon, Loretta W, Owen, Renius, Hemmat, Morteza, Wang, Boris T, El Naggar, Mohammed, Kopita, Kimberly A, Haddadin, Mary, Boyar, Fatih Z, Anguiano, Arturo, Strom, Charles M, Sahoo, Trilochan
Publicado em 2014

Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory

Por Wang, Boris T, Chong, Thomas P, Boyar, Fatih Z, Kopita, Kimberly A, Ross, Leslie P, El-Naggar, Mohamed M, Sahoo, Trilochan, Wang, Jia-Chi, Hemmat, Morteza, Haddadin, Mary H, Owen, Renius, Anguiano, Arturo L
Publicado em 2014

Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay

Por Hemmat, Morteza, Yang, Xiaojing, Chan, Patricia, McGough, Robert A, Ross, Leslie, Mahon, Loretta W, Anguiano, Arturo L, Boris, Wang T, Elnaggar, Mohamed M, Wang, Jia-Chi J, Strom, Charles M, Boyar, Fatih Z
Publicado no Mol Cytogenet (2014)

Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements

Por Sahoo, Trilochan, Wang, Jia-Chi, Elnaggar, Mohamed M, Sanchez-Lara, Pedro, Ross, Leslie P, Mahon, Loretta W, Hafezi, Katayoun, Deming, Abigail, Hinman, Lynne, Bruno, Yovana, Bartley, James A, Liehr, Thomas, Anguiano, Arturo, Jones, Marilyn
Publicado no Eur J Hum Genet (2015)

Diagnosing Depression in Alzheimer Disease With the National Institute of Mental Health Provisional Criteria

Por Teng, Edmond, Ringman, John M., Ross, Leslie K., Mulnard, Ruth A., Dick, Malcolm B., Bartzokis, George, Davies, Helen D., Galasko, Douglas, Hewett, Linda, Mungas, Dan, Reed, Bruce R., Schneider, Lon S., Segal-Gidan, Freddi, Yaffe, Kristine, Cummings, Jeffrey L.
Publicado em 2008

Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility

Por Wang, Jia-Chi, Ross, Leslie, Mahon, Loretta W, Owen, Renius, Hemmat, Morteza, Wang, Boris T, El Naggar, Mohammed, Kopita, Kimberly A, Randolph, Linda M, Chase, John M, Matas Aguilera, Maria J, Siles, Juan López, Church, Joseph A, Hauser, Natalie, Shen, Joseph J, Jones, Marilyn C, Wierenga, Klaas J, Jiang, Zhijie, Haddadin, Mary, Boyar, Fatih Z, Anguiano, Arturo, Strom, Charles M, Sahoo, Trilochan
Publicado no Eur J Hum Genet (2015)