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Texas Heart Institute Journal
|
August 23, 2016
Serum versus Imaging Biomarkers in Friedreich Ataxia to Indicate Left Ventricular Remodeling and Outcomes
Nishaki Mehta, Paul Chacko, James Jin, et al.
Clinical Chemistry
|
April 12, 2012
Newborn screening for spinal muscular atrophy by calibrated short-amplicon melt profiling
Steven F Dobrowolski, Ha T Pham, Frances Pouch Downes, et al.
Human Mutation
|
April 14, 2025
Clinical <i>SMN1</i> and <i>SMN2</i> Gene-Specific Sequencing to Enhance the Clinical Sensitivity of Spinal Muscular Atrophy Diagnostic Testing
Cecelia R Miller, Jin Fang, Pamela Snyder, et al.
American Journal of Medical Genetics
|
January 25, 2002
Parents of children with spinal muscular atrophy are not obligate carriers: carrier testing is important for reproductive decision-making
Susan Zeesman, Donald T Whelan, Nancy Carson, et al.
Journal of Neuropathology and Experimental Neurology
|
August 18, 2005
Sphingosine kinase-1 expression correlates with poor survival of patients with glioblastoma multiforme: roles of sphingosine kinase isoforms in growth of glioblastoma cell lines
James R Van Brocklyn, Catherine A Jackson, Dennis K Pearl, et al.
Journal of Child Neurology
|
March 29, 2003
Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review
Chang-Yong Tsao, Gail Herman, Daniel R Boué, et al.
Molecular and Cellular Biology
|
June 15, 2011
Cdc25A regulates matrix metalloprotease 1 through Foxo1 and mediates metastasis of breast cancer cells
Xiaoling Feng, Zhaojia Wu, Yongsheng Wu, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
June 10, 2010
Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly
Kim L McBride, Elizabeth A Varga, Matthew T Pastore, et al.
Annals of Neurology
|
April 27, 2005
Natural history of denervation in SMA: relation to age, SMN2 copy number, and function
Kathryn J Swoboda, Thomas W Prior, Charles B Scott, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2013
Duplication of the Xq27.3-q28 region, including the FMR1 gene, in an X-linked hypogonadism, gynecomastia, intellectual disability, short stature, and obesity syndrome
Scott E Hickey, Lauren Walters-Sen, Theresa Mihalic Mosher, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 82) with videos related to
Sort By:
Page
of 9
Texas Heart Institute Journal
|
August 23, 2016
Serum versus Imaging Biomarkers in Friedreich Ataxia to Indicate Left Ventricular Remodeling and Outcomes
Nishaki Mehta, Paul Chacko, James Jin, et al.
Clinical Chemistry
|
April 12, 2012
Newborn screening for spinal muscular atrophy by calibrated short-amplicon melt profiling
Steven F Dobrowolski, Ha T Pham, Frances Pouch Downes, et al.
Human Mutation
|
April 14, 2025
Clinical <i>SMN1</i> and <i>SMN2</i> Gene-Specific Sequencing to Enhance the Clinical Sensitivity of Spinal Muscular Atrophy Diagnostic Testing
Cecelia R Miller, Jin Fang, Pamela Snyder, et al.
American Journal of Medical Genetics
|
January 25, 2002
Parents of children with spinal muscular atrophy are not obligate carriers: carrier testing is important for reproductive decision-making
Susan Zeesman, Donald T Whelan, Nancy Carson, et al.
Journal of Neuropathology and Experimental Neurology
|
August 18, 2005
Sphingosine kinase-1 expression correlates with poor survival of patients with glioblastoma multiforme: roles of sphingosine kinase isoforms in growth of glioblastoma cell lines
James R Van Brocklyn, Catherine A Jackson, Dennis K Pearl, et al.
Journal of Child Neurology
|
March 29, 2003
Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review
Chang-Yong Tsao, Gail Herman, Daniel R Boué, et al.
Molecular and Cellular Biology
|
June 15, 2011
Cdc25A regulates matrix metalloprotease 1 through Foxo1 and mediates metastasis of breast cancer cells
Xiaoling Feng, Zhaojia Wu, Yongsheng Wu, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
June 10, 2010
Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly
Kim L McBride, Elizabeth A Varga, Matthew T Pastore, et al.
Annals of Neurology
|
April 27, 2005
Natural history of denervation in SMA: relation to age, SMN2 copy number, and function
Kathryn J Swoboda, Thomas W Prior, Charles B Scott, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2013
Duplication of the Xq27.3-q28 region, including the FMR1 gene, in an X-linked hypogonadism, gynecomastia, intellectual disability, short stature, and obesity syndrome
Scott E Hickey, Lauren Walters-Sen, Theresa Mihalic Mosher, et al.
Page
of 9