The Gravity Field of the Saturnian System from Satellite Observations and Spacecraft Tracking Data von Jacobson, R. A, Antreasian, P. G, Bordi, J. J, Criddle, K. E, Ionasescu, R, Jones, J. B, Mackenzie, R. A, Meek, M. C, Parcher, D, Pelletier, F. J, Owen, Jr., W. M, Roth, D. C, Roundhill, I. M, Stauch, J. R

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Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy von IONASESCU, V. V, SEARBY, C, IONASESCU, R, NEUHAUS, I. M, WERNER, R

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Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene von IONASESCU, V. V, IONASESCU, R, SEARBY, C, NEAHRING, R

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New point mutations and deletions of the connexin 32 gene in x-linked charcot-marie-tooth neuropathy von Ionasescu, V., Searby, Ch, Ionasescu, R., Meschino, W.

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Autosomal Dominant Charcot-Marie-Tooth Axonal Neuropathy Mapped on Chromosome 7p (CMT2D) von Ionasescu, Victor, Searby, Charles, Sheffield, Val C., Roklina, Tatiana, Nishimura, Darrell, Ionasescu, Rebecca

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Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot — Marie — Tooth neuropathy von Ionasescu, Victor, Searby, Charles, Ionasescu, Rebecca

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Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-tooth neuropathy von Ionasescu, Victor, Ionasescu, Rebecca, Searby, Charles

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Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene von Ionasescu, Victor V., Searby, Charles C., Ionasescu, Rebecca, Chatkupt, Sansnee, Patel, Nitin, Koenigsberger, Richard

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Increased collagen synthesis by Duchenne myogenic clones von Ionasescu, V., Ionasescu, R.

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Screening of dominantly inherited Charcot-Marie-Tooth neuropathies von Ionasescu, Victor V., Ionasescu, Rebecca, Searby, Charles

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Evidence for linkage of Charcot-Marie-Tooth neuropathy (CMT1) to apolipoprotein A2 (Apo-A2) von IONASESCU, V, ANDERSON, R, BURNS, T. L, SEARBY, C, IONASESCU, R, FERRELL, R

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RECOMBINATION WITH PERT87 (DXS164) IN FAMILIES WITH X-LINKED MUSCULAR DYSTROPHY von Fischbeck, K.H, Ritter, A.W, Tirschwell, D.L, Kunkel, L.M, Bertelson, C.J, Monaco, A.P, Hejtmancik, J.F, Boehm, C, Ionasescu, V, Ionasescu, R, Pericak-Vance, M, Kandt, R, Roses, A.D

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Charcot-marie-tooth neuropathy related to chromosome 1 von Ionasescu, Victor V., Trofatter, James, Haines, Jonathan L., Ionasescu, Rebecca, Searby, Charles

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Consortium Fine Localization of X-Linked Charcot-Marie-Tooth Disease (CMTX1): Additional Support that Connexin32 Is the Defect in CMTX1 von Pericak-Vance, Margaret A., Barker, David F., Bergoffen, JoAnn, Chance, Phillip, Cochrane, Susan, Dahl, Niklas, Exler, Mareike-Christine, Fain, Pamela R., Fairweather, Nicholas D., Fischbeck, Kenneth, Gal, Andreas, Haites, Neva, Ionasescu, R., Ionasescu, Victor V., Kennerson, Marina L., Monaco, Anthony P., Mostaccuiolo, M., Nicholson, Garth A., Sillén, Anna, Haines, Jonathan L.

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Severe Charcot-Marie-Tooth neuropathy type 1A with 1-base pair deletion and frameshift mutation in the peripheral myelin protein 22 gene von Ionasescu, Victor V., Searby, Charles C., Ionasescu, Rebecca, Reisin, Ricardo, Ruggieri, Victor, Arberas, Claudia

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Inherited ophthalmoplegia with intestinal pseudo-obstruction von Ionasescu, V., Thompson, S.H., Ionasescu, R., Searby, Ch, Anuras, S., Christensen, J., Mitros, F., Hart, M., Bosch, P.

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Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy von IONASESCU, V. V, TROFATTER, J, HAINES, J. L, SUMMERS, A. M, IONASESCU, R, SEARBY, C

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X-linked recessive Charcot-Marie-Tooth neuropathy: Clinical and genetic study von Ionasescu, Victor V., Trofatter, James, Haines, Jonathan L., Summers, Anne M., Ionasescu, Rebecca, Searby, Charles

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Charcot — Marie — Tooth neuropathy type 1A with both duplication and non-duplication von lonasescu, Victor V., lonasescu, Rebecca, Searby, Charles, Barker, David F.

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Stimulatory effects of drugs for protein synthesis on muscle cell cultures in duchenne dystrophy von Ionasescu, Victor, Stern, Lawrence Z., Ionasescu, Rebeca, Rubenstein, Peter

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