Vitamin D status of elderly outpatients in Saudi Arabia King Faisal specialist Hospital and research von Halabi A., Bissar L.

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Effect of Experimental Azotemia on Intestinal Transport of Butyric Acid von Vaziri, N. D., Barbari, A., Hollander, D., Vincent, T., Tran, L., Oveisi, F., Pahl, M. V., Bissar, L.

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Vance, Jeffery M, Züchner, Stephan, Mersiyanova, Irina V, Muglia, Maria, Bissar-Tadmouri, Nisrine, Rochelle, Julie, Dadali, Elena L, Zappia, Mario, Nelis, Eva, Patitucci, Alessandra, Senderek, Jan, Parman, Yesim, Evgrafov, Oleg, Jonghe, Peter De, Takahashi, Yuji, Tsuji, Shoij, Pericak-Vance, Margaret A, Quattrone, Aldo, Battologlu, Esra, Polyakov, Alexander V, Timmerman, Vincent, Schröder, J Michael

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X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblings von Bissar-Tadmouri, Nesrine, Donahue, Whithey L., Al-Gazali, Lihadh, Nelson, Stanley F., Bayrak-Toydemir, Pinar, Kantarci, Sibel

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X chromosome exome sequencing reveals a novel ALG 13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblings von Bissar‐Tadmouri, Nesrine, Donahue, Whithey L., Al‐Gazali, Lihadh, Nelson, Stanley F., Bayrak‐Toydemir, Pinar, Kantarci, Sibel

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Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients von Bissar-Tadmouri, N, Parman, Y, Boutrand, L, Deymeer, F, Serdaroglu, P, Vandenberghe, A, Battaloglu, E

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Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Züchner, S, Mersiyanova, I V, Muglia, M, Bissar-Tadmouri, N, Rochelle, J, Dadali, E L, Zappia, M, Nelis, E, Patitucci, A, Senderek, J, Parman, Y, Evgrafov, O, Jonghe, P De, Takahashi, Y, Tsuji, S, Pericak-Vance, M A, Quattrone, A, Battologlu, E, Polyakov, A V, Timmerman, V, Schröder, J M, Vance, J M

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Correction: Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Züchner, S, Mersiyanova, I V, Muglia, M, Bissar-Tadmouri, N, Rochelle, J, Dadali, E L, Zappia, M, Nelis, E, Patitucci, A, Senderek, J, Parman, Y, Evgrafov, O, Jonghe, P De, Takahashi, Y, Tsuji, S, Pericak-Vance, M A, Quattrone, A, Battologlu, E, Polyakov, A V, Timmerman, V, Schröder, J M, Vance, J M

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Erratum: Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Züchner, S, Mersiyanova, I V, Muglia, M, Bissar-Tadmouri, N, Rochelle, J, Dadali, E L, Zappia, M, Nelis, E, Patitucci, A, Senderek, J, Parman, Y, Evgrafov, O, Jonghe, P De, Takahashi, Y, Tsuji, S, Pericak-Vance, M A, Quattrone, A, Battologlu, E, Polyakov, A V, Timmerman, V, Schröder, J M, Vance, J M

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von ZÜCHNER, Stephan, MERSIYANOVA, Irina V, PARMAN, Yesim, EVGRAFOV, Oleg, DE JONGHE, Peter, TAKAHASHI, Yuji, TSUJI, Shoij, PERICAK-VANCE, Margaret A, QUATTRONE, Aldo, BATTOLOGLU, Esra, POLYAKOV, Alexander V, TIMMERMAN, Vincent, MUGLIA, Maria, SCHRÖDER, J. Michael, VANCE, Jeffery M, BISSAR-TADMOURI, Nisrine, ROCHELLE, Julie, DADALI, Elena L, ZAPPIA, Mario, NELIS, Eva, PATITUCCI, Alessandra, SENDEREK, Jan

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