Results 51 to 60 of about 794 (114)

GT-WGS: an efficient and economic tool for large-scale WGS analyses based on the AWS cloud service. [PDF]

BMC Genomics, 2018
Wang Y, Li G, Ma M, He F, Song Z, Zhang W, Wu C.   +6 more
europepmc   +1 more source

Globus Nexus: A Platform-as-a-Service Provider of Research Identity, Profile, and Group Management. [PDF]

Future Gener Comput Syst, 2016
Chard K, Lidman M, McCollam B, Bryan J, Ananthakrishnan R, Tuecke S, Foster I.   +6 more
europepmc   +1 more source

Beyond <i>SGCE</i>: expanding the clinical and molecular spectrum of <i>KCTD17</i>- and <i>KCNN2</i>-related myoclonus-dystonia. [PDF]

Front Neurol
Krygier M, Sitek EJ, Chylińska M, Ziętkiewicz S, Zawadzka M, Dulski J, Schinwelski M, Kostrzewa G, Wierzba J, Płoski R, Zech M, Mazurkiewicz-Bełdzińska M.   +11 more
europepmc   +1 more source

The evolution of IT standards in academic and commercial communities:Grid standardization [PDF]

, 2008
Bunduchi, R., Graham, Ian, Williams, Robin   +2 more
core  

Achieving cell-type specific transduction with adeno-associated viral vectors in pigeons. [PDF]

Curr Res Neurobiol
Tuff JM, Haselhuhn K, Surdin T, Herlitze S, Ziegler M, Güntürkün O, Rook N.   +6 more
europepmc   +1 more source

<i>VPS16</i>-Associated Dystonia: A Cohort-Based Clinical, Imaging and Genetic Profile. [PDF]

Tremor Other Hyperkinet Mov (N Y)
Mahale RR, Padmanabha H.
europepmc   +1 more source

Rare <i>PANK2</i> variants and pantothenate-kinase-associated neurodegeneration in the Dominican Republic. [PDF]

Brain Commun
Vardarajan BN, Roa PS, Kim CY, Stoeter P, Rivera Mejia D, Houck A, Chan A, Reyes-Dumeyer D, Piriz A, Fee R, Blanco-Abinader F, Roedan FA, Rice E, Christenson S, Chiu R, Gunasekaran TI, Lantigua RA, Dalgard C, Przedborski S, Mayeux R.   +19 more
europepmc   +1 more source

¹⁸F- FDG PET Reveals a Nucleus Accumbens-Centered Metabolic Network Correlating With Clinical Severity in Anti-LGI1 Encephalitis. [PDF]

MedComm (2020)
Nie B, Xu X, Dong W, Yuan L, Cong H, Ma Y, Wang H, Tian DC, Yin L, Song T, Zhao Y, Chang G, Lyu T, Liu Y, Ma W, Shi FD, Ai L, Xu W.   +17 more
europepmc   +1 more source

<i>GNAO1</i> encephalopathy: Broadening the phenotype and evaluating treatment and outcome. [PDF]

Neurol Genet, 2017
Danti FR, Galosi S, Romani M, Montomoli M, Carss KJ, Raymond FL, Parrini E, Bianchini C, McShane T, Dale RC, Mohammad SS, Shah U, Mahant N, Ng J, McTague A, Samanta R, Vadlamani G, Valente EM, Leuzzi V, Kurian MA, Guerrini R.   +20 more
europepmc   +1 more source

Molecular characterization, clinical phenotype, and neurological outcome of twelve Palestinian children with beta-ketothiolase deficiency: report of two novel variants in the ACAT1 gene. [PDF]

BMC Med Genomics
Dweikat IM, Abdul-Hafez HA, Zayed A, Kanaan M, Kasem H, Bzour R.   +5 more
europepmc   +1 more source