Zobrazeno 11 - 20
of 134
pro vyhledávání: '"W, Serrano"'
Autor:
Cynthia M. Hartung, Elizabeth K. Lefler, Loren M Ranson, Judah W. Serrano, Anne E. Stevens, Patrick A. LaCount, Erik G. Willcutt, Will H. Canu
Publikováno v:
Journal of Learning Disabilities. 54:403-411
Attention-deficit/hyperactivity disorder (ADHD) is characterized by inattentive, hyperactive, and impulsive behaviors. Impairment in individuals diagnosed with ADHD is significant; one such domain of impairment is achieving a college education. Colle
Autor:
Tomas S, Aleman, Rachel M, Huckfeldt, Leona W, Serrano, Denise J, Pearson, Grace K, Vergilio, Sarah, McCague, Kathleen A, Marshall, Manzar, Ashtari, Tu M, Doan, Carol A, Weigel-DiFranco, Bethany S, Biron, Xiao-Hong, Wen, Daniel C, Chung, Emily, Liu, Kevin, Ferenchak, Jessica I W, Morgan, Eric A, Pierce, Dean, Eliott, Jean, Bennett, Jason, Comander, Albert M, Maguire
Publikováno v:
Ophthalmology. 129(10)
To assess the safety of the subretinal delivery of a recombinant adeno-associated virus serotype 2 (AAV2) vector carrying a human choroideremia (CHM)-encoding cDNA in CHM.Prospective, open-label, nonrandomized, dose-escalation, phase I/II clinical tr
Autor:
Will H. Canu, Cynthia M. Hartung, Judah W. Serrano, Anne E. Stevens, Anna M. Garner, Elizabeth K. Lefler
Publikováno v:
Journal of Psychopathology and Behavioral Assessment. 42:488-499
Changes were made in DSM-5 to address the criticism that ADHD symptoms in DSM-IV were not developmentally appropriate for adults. Specifically, parenthetical examples were added to symptoms, and the symptom threshold was lowered. ADHD diagnosis in co
Publikováno v:
RETINAL Cases & Brief Reports. 16:385-392
PURPOSE To describe in detail the phenotype of two siblings with biallelic NMNAT1 mutations. METHODS A 4-year-old male patient (P1) and his 7-year-old sister (P2), product of a nonconsanguineous union of Egyptian ancestry, underwent a comprehensive o
Autor:
Zhangyong Wei, Michael J. Ammar, Vivian S. Lee, Tomas S. Aleman, Shangzhen Zhou, Lindsey Weed, Junwei Sun, Albert M. Maguire, Jean Bennett, Leona W. Serrano
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 133-148 (2019)
We have demonstrated safe and effective subretinal readministration of recombinant adeno-associated virus serotype (rAAV) to the contralateral eye in large animals and humans even in the setting of preexisting neutralizing antibodies (NAbs). Readmini
Autor:
Tomas S. Aleman, Jessica I. W. Morgan, Denise J. Pearson, Grace Vergilio, Albert M. Maguire, Yu You Jiang, Leona W. Serrano, Jean Bennett
Subretinal injection for gene augmentation in retinal degenerations forcefully detaches the neural retina from the retinal pigment epithelium (RPE), potentially damaging photoreceptors and/or RPE cells. Here, we use adaptive optics scanning light oph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ae24a1c12ce096e422fcdb842b41ba8
https://doi.org/10.1101/2021.09.17.459817
https://doi.org/10.1101/2021.09.17.459817
Autor:
Jean Bennett, Leona W. Serrano, Drew Scoles, Grace K. Han, Kayla E Cunningham, Tomas S. Aleman, Erin C O'Neil, John Chiang
Publikováno v:
Ophthalmic Genetics. 40:267-275
Purpose: To confirm the pathogenic role of a novel mutation in PNPLA6 and detail the phenotype of a patient presenting with choroideremia-like chorioretinal degeneration. Methods: A 40-year-old man with presumed choroideremia underwent a complete oph
Autor:
Patrick A, LaCount, Cynthia M, Hartung, John M, Vasko, Judah W, Serrano, Halle A, Wright, Derek T, Smith
Publikováno v:
Ment Health Phys Act
We sought to elucidate the acute effects of high-intensity interval training (HIIT) among college students with and without attention-deficit/hyperactivity disorder (ADHD). Participants were age- and sex-matched across ADHD (n = 18) and non-ADHD grou
Autor:
Ivan Shpylchak, Vidyullatha Vasireddy, Katherine E. Uyhazi, Denise J. Pearson, Zhangyong Wei, Jean Bennett, Lanfranco Leo, Leona W. Serrano, Puya Aravand, Tomas S. Aleman, Brent A. Bell, Jennifer Pham
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose To determine the therapeutic window for gene augmentation for Leber congenital amaurosis (LCA) associated with mutations in LCA5. Methods Five patients (ages 6-31) with LCA and biallelic LCA5 mutations underwent an ophthalmic examination incl
Publikováno v:
Retinal casesbrief reportsReferences. 16(3)
To describe in detail the phenotype of two siblings with biallelic NMNAT1 mutations.A 4-year-old male patient (P1) and his 7-year-old sister (P2), product of a nonconsanguineous union of Egyptian ancestry, underwent a comprehensive ophthalmic examina