Neuropsychological status at seizure onset in children: Risk factors for early cognitive deficits von FASTENAU, P. S, JOHNSON, C. S, PERKINS, S. M, BYARS, A. W, DEGRAUW, T. J, AUSTIN, J. K, DUNN, D. W

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Behavior problems in children at time of first recognized seizure and changes over the following 3 years von Austin, J.K, Perkins, S.M, Johnson, C.S, Fastenau, P.S, Byars, A.W, deGrauw, T.J, Dunn, D.W

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Multimodality imaging in the surgical treatment of children with nonlesional epilepsy von SEO, J. H, HOLLAND, K, MILES, L, MANGANO, F. T, HORN, P, LEE, K. H, ROSE, D, ROZHKOV, L, FUJIWARA, H, BYARS, A, ARTHUR, T, DEGRAUW, T, LEACH, J. L, GELFAND, M. J

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Academic problems in children with seizures: Relationships with neuropsychological functioning and family variables during the 3 years after onset von Dunn, David W, Johnson, C.S, Perkins, S.M, Fastenau, P.S, Byars, A.W, deGrauw, T.J, Austin, J.K

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High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation von Rosenberg, Efraim H., Almeida, Ligia S., Kleefstra, Tjitske, deGrauw, Rose S., Yntema, Helger G., Bahi, Nadia, Moraine, Claude, Ropers, Hans-Hilger, Fryns, Jean-Pierre, deGrauw, Ton J., Jakobs, Cornelis, Salomons, Gajja S.

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X‐linked creatine transporter defect: An overview von Salomons, G. S., Van Dooren, S. J. M., Verhoeven, N. M., Marsden, D., Schwartz, C., Cecil, K. M., DeGrauw, T. J., Jakobs, C.

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Effectiveness of Amitriptyline in the Prophylactic Management of Childhood Headaches von Hershey, Andrew D., Powers, Scott W., Bentti, Anna-Liisa, DeGrauw, Ton J.

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Characterization of chronic daily headaches in children in a multidisciplinary headache center von HERSHEY, A. D, POWERS, S. W, BENTTI, A.-L, LECATES, S, DEGRAUW, T. J

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X-Linked Creatine-Transporter Gene ( SLC6A8) Defect: A New Creatine-Deficiency Syndrome von Salomons, Gajja S., van Dooren, Silvy J.M., Verhoeven, Nanda M., Cecil, Kim M., Ball, William S., Degrauw, Ton J., Jakobs, Cornelis

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Congenital Creatine Transporter Deficiency von deGrauw, T. J., Salomons, G. S., Cecil, K. M., Chuck, G., Newmeyer, A., Schapiro, M. B., Jakobs, C.

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Glycine decarboxylase mutations : A distinctive phenotype of nonketotic hyperglycinemia in adults von DINOPOULOS, A, KURE, S, CHUCK, G, SATO, K, GILBERT, D. L, MATSUBARA, Y, DEGRAUW, T

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Irreversible brain creatine deficiency with elevated serum and urine creatine: A creatine transporter defect? von Cecil, Kim M., Salomons, Gajja S., Ball Jr, William S., Wong, Brenda, Chuck, Gail, Verhoeven, Nanda M., Jakobs, Cornelis, DeGrauw, Ton J.

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Screening of Male Patients with Autism Spectrum Disorder for Creatine Transporter Deficiency von Newmeyer, A., deGrauw, T., Clark, J., Chuck, G., Salomons, G.

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Brain MRI and Proton MRS Findings in Infants and Children with Respiratory Chain Defects von Dinopoulos, A., Cecil, K. M., Schapiro, M. B., Papadimitriou, A., Hadjigeorgiou, G. M., Wong, B., deGrauw, T., Egelhoff, J. C.

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Discrepancy Between Neuroimaging Findings and Clinical Phenotype in Alexander Disease von Dinopoulos, A, Gorospe, J.R, Egelhoff, J.C, Cecil, K.M, Nicolaidou, P, Morehart, P, DeGrauw, T

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Seizure frequency and characteristics in children with Down syndrome von Goldberg-Stern, Hadassa, Strawsburg, Richard H., Patterson, Bonnie, Hickey, Fran, Bare, Mary, Gadoth, Natan, Degrauw, Ton J.

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First Case of 2019 Novel Coronavirus in the United States von Holshue, Michelle L, DeBolt, Chas, Lindquist, Scott, Lofy, Kathy H, Wiesman, John, Bruce, Hollianne, Spitters, Christopher, Ericson, Keith, Wilkerson, Sara, Tural, Ahmet, Diaz, George, Cohn, Amanda, Fox, LeAnne, Patel, Anita, Gerber, Susan I, Kim, Lindsay, Tong, Suxiang, Lu, Xiaoyan, Lindstrom, Steve, Pallansch, Mark A, Weldon, William C, Biggs, Holly M, Uyeki, Timothy M, Pillai, Satish K

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Two Phase 3 Trials of Inclisiran in Patients with Elevated LDL Cholesterol von Ray, Kausik K, Wright, R. Scott, Kallend, David, Koenig, Wolfgang, Leiter, Lawrence A, Raal, Frederick J, Bisch, Jenna A, Richardson, Tara, Jaros, Mark, Wijngaard, Peter L.J, Kastelein, John J.P

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Diagnosis of Migraine in Children Attending a Pediatric Headache Clinic von de Grauw, Ton J., Hershey, Andrew D., Powers, Scott W., Bentti, Anna-Liisa

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Presence of normal creatine in the muscle of a patient with a mutation in the creatine transporter: a case study von Pyne-Geithman, Gail J, deGrauw, Ton J, Cecil, Kim M, Chuck, Gail, Lyons, Melissa A, Ishida, Yukisato, Clark, Joseph F

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