Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration von Tsaousidou, Maria K., Ouahchi, Karim, Warner, Tom T., Yang, Yi, Simpson, Michael A., Laing, Nigel G., Wilkinson, Philip A., Madrid, Ricardo E., Patel, Heema, Hentati, Faycal, Patton, Michael A., Hentati, Afif, Lamont, Philippa J., Siddique, Teepu, Crosby, Andrew H.

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Successful utilization of the EMR in a multiple sclerosis clinic to support quality improvement and research initiatives at the point of care von Claire Simon, Kelly, Hentati, Afif, Rubin, Susan, Franada, Tiffani, Maurer, Darryck, Hillman, Laura, Tideman, Samuel, Szela, Monika, Meyers, Steven, Frigerio, Roberta, Maraganore, Demetrius M

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Motor Neuron Degeneration in Mice That Express a Human Cu,Zn Superoxide Dismutase Mutation von Gurney, Mark E., Pu, Haifeng, Chiu, Arlene Y., Mauro C. Dal Canto, Polchow, Cynthia Y., Alexander, Denise D., Caliendo, Jan, Hentati, Afif, Kwon, Young W., Deng, Han-Xiang, Chen, Wenje, Zhai, Ping, Sufit, Robert L., Siddique, Teepu

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VZV encephalitis that developed in an immunized patient during fingolimod therapy von Issa, Naoum P, Hentati, Afif

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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35 von Hentati, Afif, Bejaoui, Khemissa, Pericak-Vance, Margaret A., Hentati, Faycal, Speer, Marcy C., Hung, Wu-Yen, Figlewicz, Denise A., Haines, Jonathan, Rimmler, Jackie, Ben Hamida, Christiane, Ben Hamida, Mongi, Brown, Robert H., Siddique, Teepu

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Correlation Analysis of MRI Lesion Load and Clinical Measures in Multiple Sclerosis Cohort Using Structured Clinical Documentation Support Toolkit (1880) von Hentati, Afif, Franada, Tiffani Stroup, Pula, John, Maurer, Darryck, Hadsell, Bryce, Epshteyn, Alexander, Tideman, Samuel, Pham, Anna, Frigerio, Roberta, Maraganore, Demetrius, Rubin, Susan

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The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis von Yang, Yi, Hentati, Afif, Deng, Han-Xiang, Dabbagh, Omar, Sasaki, Toru, Hirano, Makito, Hung, Wu-Yen, Ouahchi, Karim, Yan, Jianhua, Azim, Anser C., Cole, Natalie, Gascon, Generoso, Yagmour, Ayesha, Ben-Hamida, Mongi, Pericak-Vance, Margaret, Hentati, Fayçal, Siddique, Teepu

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Amyotrophic Lateral Sclerosis and Structural Defects in Cu,Zn Superoxide Dismutase von Deng, Han-Xiang, Hentati, Afif, Tainer, John A., Iqbal, Zafar, Cayabyab, Annarueber, Hung, Wu-Yen, Getzoff, Elizabeth D., Hu, Ping, Herzfeldt, Brian, Roos, Raymond P., Warner, Carolyn, Deng, Gang, Soriano, Edwin, Smyth, Celestine, Parge, Hans E., Ahmed, Aftab, Roses, Allen D., Hallewell, Robert A., Pericak-Vance, Margaret A., Siddique, Teepu

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis von Rosen, Daniel R., Siddique, Teepu, Patterson, David, Figlewicz, Denise A., Sapp, Peter, Hentati, Afif, Donaldson, Deirdre, Goto, Jun, O'Regan, Jeremiah P., Deng, Han-Xiang, Rahmani, Zohra, Krizus, Aldis, McKenna-Yasek, Diane, Cayabyab, Annarueber, Gaston, Sandra M., Berger, Ralph, Tanzi, Rudolph E., Halperin, John J., Herzfeldt, Brian, Van den Bergh, Raymond, Hung, Wu-Yen, Bird, Thomas, Deng, Gang, Mulder, Donald W., Smyth, Celestine, Laing, Nigel G., Soriano, Edwin, Pericak–Vance, Margaret A., Haines, Jonathan, Rouleau, Guy A., Gusella, James S., Horvitz, H. Robert, Brown, Robert H.

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Molecular genetic basis of familial ALS von Siddique, T, Nijhawan, D, Hentati, A

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Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers von Hentati, A, Ouahchi, K, Pericak-Vance, M A, Nijhawan, D, Ahmad, A, Yang, Y, Rimmler, J, Hung, W, Schlotter, B, Ahmed, A, Ben Hamida, M, Hentati, F, Siddique, T

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Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration von Tsaousidou, Maria K, Ouahchi, Karim, Warner, Tom T, Yang, Yi, Simpson, Michael A, Laing, Nigel G, Wilkinson, Philip A, Madrid, Ricardo E, Patel, Heema, Hentati, Faycal, Patton, Michael A, Hentati, Afif, Lamont, Philippa J, Siddique, Teepu, Crosby, Andrew H

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Human α-tocopherol transfer protein: Gene structure and mutations in familial vitamin E deficiency von Hentati, Afif, Deng, Han-Xiang, Hung, Wu-Yen, Nayer, Muhammad, Ahmed, M. Said, He, Xiaoxuan, Tim, Richard, Stumpf, David A., Siddique, Teepu

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Amyotrophic Lateral Ssclerosis and Structural Defects in Cu,Zn Superoxide Dismutase von Deng, Han-Xiang, Hentati, Afif, Tainer, John A., Iqbal, Zafar, Cayabyab, Annarueber, Hung, Wu-Yen, Getzoff, Elizabeth D., Hu, Ping, Herzfeldt, Brian, Roos, Raymond P., Warner, Carolyn, Deng, Gang, Soriano, Edwin, Smyth, Celestine, Parge, Hans E., Ahmed, Aftab, Roses, Allen D., Hallewell, Robert A., Pericak-Vance, Margaret A., Siddique, Teepu

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Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers von Hentati, Afif, Pericak-Vance, Margaret A., Lennon, Felicia, Wasserman, Brad, Hentati, Faycal, Juneja, Tony, Angrist, Misha H., Hung, Wu-Yen, Boustany, Rose-Mary, Bohlega, Saeed, Iqbal, Zafar, Huether, Carl H., Hamida, Mongi Ben, Siddique, Teepu

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Linkage of Scapuloperoneal Spinal Muscular Atrophy to Chromosome 12q24.1-q24.31 von Isozumi, Kazuo, DeLong, Robert, Kaplan, Jocelyn, Deng, Han-Xiang, Iqbal, Zafar, Hung, Wu-Yen, Wilhelmsen, Kirk C., Hentati, Afif, Pericak-Vance, Margaret A., Siddique, Teepu

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Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis von Deng, Han-Xiang, Tainer, John A., Mitsumoto, Hiroshi, Ohnishi, Akio, He, Xiaoxuan, Hung, Wu-Yen, Zhao, Yaliang, Juneja, Tony, Hentati, Afif, Siddique, Teepu

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Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease von Hentati, Afif, Lamy, Catherine, Melki, Judith, Zuber, Mathieu, Munnich, Arnold, Recondo, Jean de

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Amyotropic lateral sclerosis and structural defects in Cu, Zn superoxide dismutase von Hentati, Afif, Tainer, John A, Iqbal, Zafar, Cayabyab, Annarueber, Getzoff, Elizabeth D, Herzfeld, Brian, Roos, Raymond P, Warner, Carolyn, Soriano, Edwin, Smyth, Celestine, Parge, Hans E, Ahmed, Aftab, Roses, Allen D, Hallewell, Robert A, Pericak-Vance, Margaret A, Siddique, Teepu

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alpha-Tocopherol transport protein: compositions and methods von HENTATI AFIF, DENG HAN-XIANG, SIDDIQUE TEEPU

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