Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis von Boyd, C, Smith, MJ, Kluwe, L, Balogh, A, MacCollin, M, Plotkin, SR

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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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Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1) von GUTMANN, D. H, RASMUSSEN, S. A, WOLKENSTEIN, P, MACCOLLIN, M. M, GUHA, A, INSKIP, P. D, NORTH, K. N, POYHONEN, M, BIRCH, P. H, FRIEDMAN, J. M

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Germ-line mutations in the neurofibromatosis 2 gene : Correlations with disease severity and retinal abnormalities von PARRY, D. M, MACCOLLIN, M. M, KAISER-KUPFER, M. I, PULASKI, K, NICHOLSON, H. S, BOLESTA, M, ELDRIDGE, R, GUSELLA, J. F

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Familial schwannomatosis: Exclusion of the NF2 locus as the germline event von MACCOLLIN, M, WILLETT, C, HEINRICH, B, JACOBY, L. B, ACIERNO, J. S, PERRY, A, LOUIS, D. N

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Neurofibromatosis 2 in the Pediatric Population von Nunes, Fabio, MacCollin, Mia

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Molecular study of frequency of mosaicism in neurofibromatosis 2 patients with bilateral vestibular schwannomas von Kluwe, L, Mautner, V, Heinrich, B, Dezube, R, Jacoby, L B, Friedrich, R E, MacCollin, M

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Schwannomatosis : A clinical and pathologic study von MACCOLLIN, M, WOODFIN, W, KRONN, D, SHORT, M. P

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Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations von Smith, MJ, Boyd, CD, MacCollin, MM, Plotkin, SR

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Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas von RUBIO, M.-P, CORREA, K. M, RAMESH, V, MACCOLLIN, M. M, JACOBY, L. B, VON DEIMLING, A, GUSELLA, J. F, LOUIS, D. N

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Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease von Ruttledge, M H, Andermann, A A, Phelan, C M, Claudio, J O, Han, F Y, Chretien, N, Rangaratnam, S, MacCollin, M, Short, P, Parry, D, Michels, V, Riccardi, V M, Weksberg, R, Kitamura, K, Bradburn, J M, Hall, B D, Propping, P, Rouleau, G A

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The diagnosis and management of neurofibromatosis 2 in childhood von MacCollin, Mia, Mautner, Victor-Felix

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor von Trofatter, James A., MacCollin, Mia M., Rutter, Joni L., Murrell, Jill R., Duyao, Mabel P., Parry, Dilys M., Eldridge, Roswell, Kley, Nikolai, Menon, Anil G., Pulaski, Karen, Haase, Volker H., Ambrose, Christine M., Munroe, David, Bove, Catherine, Haines, Jonathan L., Martuza, Robert L., MacDonald, Marcy E., Seizinger, Bernd R., Short, M.Priscilla, Buckler, Alan J., Gusella, James F.

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor von Trofatter, J A, MacCollin, M M, Rutter, J L, Murrell, J R, Duyao, M P, Parry, D M, Eldridge, R, Kley, N, Menon, A G, Pulaski, K

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Multiple meningiomas in brain and lung due to acquired mutation of the NF2 gene von ECKSTEIN, O, STEMMER-RACHAMIMOV, A, NUNES, F, HOCH, D, OJEMANN, R, MACCOLLIN, M

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Exon scanning for mutations of the nf2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas von Slavc, Irene, Maccollin, Mia M., Dunn, Michael, Jones, Susan, Sutton, Leslie, Gusella, James F., Biegel, Jaclyn A.

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Random-clone strategy for genomic restriction mapping in yeast von Olson, M.V, Dutchik, J.E, Graham, M.Y, Brodeur, G.M, Helms, C, Frank, M, MacCollin, M, Scheinman, R, Frank, T

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Dopa-responsive hypersomnia and mixed movement disorder due to sepiapterin reductase deficiency von Friedman, Jennifer, Hyland, Keith, Blau, Nenad, MacCollin, Mia

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Glioblastoma multiforme presenting as bilateral internal auditory canal tumors von Lee, J W, Houtchens, M, Hochberg, F, Price, B, M, Lev, Cunnane, M, Pfannl, R, MacCollin, M

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Mutational analysis of patients with neurofibromatosis 2 von MACCOLLIN, M, VIJAYA RAMESH, PARRY, D. M, GUSELLA, J. F, JACOBY, L. B, LOUIS, D. N, RUBIO, M.-P, PULASKI, K, TROFATTER, J. A, SHORT, M. P, BOVE, C, ELDRIDGE, R

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