Diagnostic criteria for schwannomatosis von MACCOLLIN, M, CHIOCCA, E. A, SANG, C. N, STEMMER-RACHAMIMOV, A, ROACH, E. S, EVANS, D. G, FRIEDMAN, J. M, HORVIT, R, JARAMILLO, D, LEV, M, MAUTNER, V. F, NIIMURA, M, PLOTKIN, S. R

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Tuberous Sclerosis Complex Consensus Conference: Revised Clinical Diagnostic Criteria von Roach, E.S., Gomez, Manuel R., Northrup, Hope

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Prolonged hemiplegic episodes in children due to mutations in ATP1A2 von Jen, J C, Klein, A, Boltshauser, E, Cartwright, M S, Roach, E S, Mamsa, H, Baloh, R W

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A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16 von BENNETT, L. B, ROACH, E. S, BOWCOCK, A. M

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Tuberous Sclerosis Consensus Conference: Recommendations for Diagnostic Evaluation von Roach, E.S., DiMario, Francis J., Kandt, Raymond S., Northrup, Hope

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Cerebral Venous Sinus Thrombosis in Children: A Multicenter Cohort From the United States von Wasay, Mohammad, Dai, Alper I., Ansari, Mohsin, Shaikh, Zubair, Roach, E.S.

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Malignant tumors of the kidney, brain, and soft tissues in children and young adults with the tuberous sclerosis complex von Al‐Saleem, Tahseen, Wessner, Lisa L., Scheithauer, Bernd W., Patterson, Kathleen, Roach, E. Steven, Dreyer, Stephen J., Fujikawa, Keita, Bjornsson, Johannes, Bernstein, Jay, Henske, Elizabeth Petri

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Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease von Kandt, R. S, Haines, J. L, Smith, M, Northrup, H, Gardner, R. J. M, Short, M. P, Dumars, K, Roach, E. S, Steingold, S, Wall, S, Blanton, S. H, Flodman, P, Kwiatkowski, D. J, Jewell, A, Weber, J. L, Roses, A. D, Pericak-Vance, M. A

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Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies von Swoboda, K J, Soong, B, McKenna, C, Brunt, E R, Litt, M, Bale, Jr, J F, Ashizawa, T, Bennett, L B, Bowcock, A M, Roach, E S, Gerson, D, Matsuura, T, Heydemann, P T, Nespeca, M P, Jankovic, J, Leppert, M, Ptácek, L J

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Germ-Line Mosaicism in Tuberous Sclerosis: How Common? von Rose, Verna M., Au, Kit-Sing, Pollom, Gretchen, Roach, E. Steve, Prashner, Heather R., Northrup, Hope

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Complete Inactivation of the TSC2 Gene Leads to Formation of Hamartomas von Au, Kit-Sing, Hebert, Adelaide A., Roach, E. Steve, Northrup, Hope

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Seeing With New Eyes: Using Positron Emission Tomography (PET) to Identify Epileptogenic Tubers von Roach, E.S.

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The tuberous sclerosis complex: a comprehensive review von Weiner, DavidM, Ewalt, DavidH, Roach, E.Steve, Hensle, TerryW

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Germ-Line Mutational Analysis of the TSC2 Gene in 90 Tuberous-Sclerosis Patients von Au, Kit-Sing, Rodriguez, Joseph A., Finch, Jennifer L., Volcik, Kelly A., Roach, E. Steve, Delgado, Mauricio R., Rodriguez, Estanislado, Northrup, Hope

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Tuberous sclerosis complex von Sparagana, S P, Roach, E S

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Report of the Diagnostic Criteria Committee of the National Tuberous Sclerosis Association von Roach, E.S., Smith, Moyra, Huttenlocher, Peter, Bhat, Mohandes, Alcorn, Deborah, Hawley, Louise

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Gabapentin for familial paroxysmal dystonic choreoathetosis von CHUDNOW, R. S, MIMBELA, R. A, OWEN, D. B, ROACH, E. S

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Unexpected Acute Neurologic Toxicity in the Treatment of Children With Acute Lymphoblastic Leukemia von Winick, Naomi J., Bowman, W. Paul, Kamen, Barton A., Roach, E. Steve, Rollins, Nancy, Jacaruso, Diana, Buchanan, George R.

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Von Hippel-Lindau disease: how does one gene cause multiple tumors? von Roach, E S

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Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography von Adams, Robert J, McKie, Virgil C, Hsu, Lewis, Files, Beatrice, Vichinsky, Elliott, Pegelow, Charles, Abboud, Miguel, Gallagher, Dianne, Kutlar, Abdullah, Nichols, Fenwick T, Bonds, Duane R, Brambilla, Donald, Woods, Gerald, Olivieri, Nancy, Driscoll, Catherine, Miller, Scott, Wang, Winfred, Hurlett, Anne, Scher, Charles, Berman, Brian, Carl, Elizabeth, Jones, Anne M, Roach, E. Steve, Wright, Elizabeth, Zimmerman, Robert A, Waclawiw, Myron

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