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Author/Creator Jasien, Joan

2. Alternating hemiplegia of childhood: evolution over time and mouse model corroboration. Issue 3 (4th June 2021)

Authors:
Uchitel, Julie; Wallace, Keri; Tran, Linh; Abrahamsen, Tavis; Hunanyan, Arsen; Prange, Lyndsey; Jasien, Joan; Caligiuri, Laura; Pratt, Milton; Rikard, Blaire; Fons, Carmen; De Grandis, Elisa; Vezyroglou, Aikaterini; Heinzen, Erin L; Goldstein, David B; Vavassori, Rosaria; Papadopoulou, Maria T; C...
Journal:
Brain communications
Issue:
Volume 3:Issue 3(2021)
Page Start:
Record Type:
Journal Article
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3. Characterization of sedation and anesthesia complications in patients with alternating hemiplegia of childhood. (May 2022)

Authors:
Parker, Lauren E.; Wallace, Keri; Thevathasan, Arthur; Funk, Emily; Pratt, Milton; Thamby, Julie; Tran, Linh; Prange, Lyndsey; Uchitel, Julie; Boggs, April; Minton, Melissa; Jasien, Joan; Nagao, Kanae Jennifer; Richards, Amanda; Cruse, Belinda; De-Lisle Dear, Guy; Landstrom, Andrew P.; Mikati, Mo...
Journal:
European journal of paediatric neurology
Issue:
Volume 38(2022)
Page Start:
47
Record Type:
Journal Article
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4. Co‐occurring medical conditions in adults with Down syndrome: A systematic review toward the development of health care guidelines. Part II. Issue 7 (27th April 2020)

Authors:
Capone, George; Stephens, Mary; Santoro, Stephanie; Chicoine, Brian; Bulova, Peter; Peterson, Moya; Jasien, Joan; Smith, Anna Jo
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 7(2020)
Page Start:
1832
Record Type:
Journal Article
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5. Epileptic encephalopathy with features of rapid‐onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation. Issue 1 (13th March 2020)

Authors:
Tran, Linh; Richards, Jason; McDonald, Marie; McConkie‐Rosell, Allyn; Stong, Nicholas; Jasien, Joan; Shashi, Vandana; Mikati, Mohamad A.
Journal:
Epileptic disorders
Issue:
Volume 22:Issue 1(2020)
Page Start:
103
Record Type:
Journal Article
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6. Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis. Issue 8 (5th May 2019)

Authors:
Shashi, Vandana; Geist, Janelle; Lee, Youngha; Yoo, Yongjin; Shin, Unbeom; Schoch, Kelly; Sullivan, Jennifer; Stong, Nicholas; Smith, Edward; Jasien, Joan; Kranz, Peter; Lee, Yoonsung; Shin, Yong Beom; Wright, Nathan T.; Choi, Murim; Kontrogianni‐Konstantopoulos, Aikaterini
Other Names:
Acosta Maria T. investigator.; Adams David R. investigator.; Aday Aaron investigator.; Alejandro Mercedes E. investigator.; Allard Patrick investigator.; Ashley Euan A. investigator.; Azamian Mahshid S. investigator.; Bacino Carlos A. investigator.; Bademci Guney investigator.; Baker Eva investig...
Journal:
Human mutation
Issue:
Volume 40:Issue 8(2019)
Page Start:
1115
Record Type:
Journal Article
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10. The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder. Issue 17 (11th April 2022)

Authors:
Barish, Scott; Senturk, Mumine; Schoch, Kelly; Minogue, Amanda L; Lopergolo, Diego; Fallerini, Chiara; Harland, Jake; Seemann, Jacob H; Stong, Nicholas; Kranz, Peter G; Kansagra, Sujay; Mikati, Mohamad A; Jasien, Joan; El-Dairi, Mays; Galluzzi, Paolo; Ariani, Francesca; Renieri, Alessandra; Mari,...
Journal:
Human molecular genetics
Issue:
Volume 31:Issue 17(2022)
Page Start:
2934
Record Type:
Journal Article
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