Post-Traumatic Headache in Children and Genetic Risk of Migraine An Observational Cohort Study
Orr, Serena L.; Hershey, Andrew D.; Kurowski, Brad G.; Langevin, Lisa Marie; Martin, Lisa J.; Pilipenko, Valentina; Tang, Ken; Beauchamp, Miriam H.; Craig, William R.; Zemek, Roger; Doan, Quynh; Yeates, Keith O.
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Save Precision Diagnosis of Wilson Disease Using a MultiGene Panel
Lin, Jie; Wang, You-Liang; Qu, Yongqiang; Dong, Senwei; Fang, Yaofeng; Chen, Rukai; Ding, Ying; Lin, Weihong; Chen, Jian; Cai, Naiqing; Wang, Ning; Chen, Wan-Jin; Lin, Yi; Wang, Zhiqiang
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Save Clinical Heterogeneity and Candidate Biomarkers in POLG-Related Mitochondrial Disease
Bermejo-Guerrero, Laura; Restrepo-Vera, Juan Luis; Martin-Jimenez, Paloma; Navarro-Riquelme, Maria; Garrido-Moraga, Rocio; Ochoa, Luz Edith; Gonzalez-Quintana, Adrian; Hernandez-Lain, Aurelio; Castillo-Villalba, Jessica; Moris, German; Muelas, Nuria; Garcia-Arumi, Elena; Gonzalez, Victoria; Martinez-Saez, Elena; Vesperinas, Ana; Llanso, Laura; Juntas-Morales, Raul; Paradas, Carmen; Kapetanovic, Solange; Blazquez, Alberto; Marti, Ramon; Arenas, Joaquin; Martin, Miguel A.; Dominguez-Gonzalez, Cristina
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Save Genetic Landscape and Diagnostic Outcomes of UK Patients With Congenital Myopathies and Muscular Dystrophies Over a 10-Year Period
Cicala, Gianpaolo; Mccauley, Jo; Phadke, Rahul; Mueller, Juliane; Robb, Stephanie Ann; Manzur, Adnan Y.; Munot, Pinki; Baranello, Giovanni; Scoto, Mariacristina; Tedesco, Francesco Saverio; Mein, Rachael A.; Walsh, Cheryl; Muntoni, Francesco; Sarkozy, Anna
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Save Toward Trial Readiness in Congenital Myotonic Dystrophy
Kiefer, Michael; Hartman, Julia M.; Berggren, Kiera N.; Butler, Amanda; Jones, Aileen S.; McIntyre, Melissa; Hung, Man; Carrell, Samuel; Hale, Melissa A.; Campbell, Craig; Sansone, Valeria Ada; Johnson, Nicholas E.
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Save Quantitative Measurement of Glycosylated α-Dystroglycan as a Biomarker for Disease Severity in Limb-Girdle Muscular Dystrophy Type 2I/R9
Vissing, John; Mozaffar, Tahseen; Johnson, Nicholas E.; Mathews, Katherine D.; Wicklund, Matthew P.; Weihl, Conrad; Leung, Doris G.; Statland, Jeffrey M.; Kang, Peter B.; Zingariello, Carla D.; Lowes, Linda Pax; Desai, Urvi; Bates, Kameron; Alfano, Lindsay N.; Xie, Han; St Romain, Jessica; Blankenbiller, Tricia; McLendon, George; Rajasingham, Thulashitha; Heitzer, Marjet; Wu-Zhang, Alyssa X.; Tripp, Kenneth; Rodriguez, Hector M.; Sproule, Douglas
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Save Expanding the Clinicoradiologic Phenotype of the CTSA-Associated Small Vessel Disease CARASAL: A Comparison With CADASIL
Cerfontaine, Minne N.; Gravesteijn, Gido; Hack, Remco J.; Gesierich, Benno; Kruit, Mark C.; Van Den Wijngaard, Ido R.; Notting, Irene C.; Nibbeling, Esther A. R.; Bugiani, Marianna; Van Der Knaap, Marjo S.; Boon, Camiel J. F.; Duering, Marco; Rutten, Julie W.; Oberstein, Saskia A. J. Lesnik
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Save The Genetics of TDP-43 Type C Neurodegeneration A Whole-Genome Sequencing Study and Literature Review
Nassan, Malik; Ayala, Ivan; Sloan, Jennifer; Bonfitto, Anna; Stark, Bobbi; Song, Serena; Naymik, Marcus; Geula, Changiz; Gefen, Tamar; Barbieri, Elena; Piras, Ignazio; Mesulam, M. -Marsel; Huentelman, Matthew
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