Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association von Kittleson, Michelle M., Maurer, Mathew S., Ambardekar, Amrut V., Bullock-Palmer, Renee P., Chang, Patricia P., Eisen, Howard J., Nair, Ajith P., Nativi-Nicolau, Jose, Ruberg, Frederick L.

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Expert Consensus Recommendations for the Suspicion and Diagnosis of Transthyretin Cardiac Amyloidosis von Maurer, Mathew S, Bokhari, Sabahat, Damy, Thibaud, Dorbala, Sharmila, Drachman, Brian M, Fontana, Marianna, Grogan, Martha, Kristen, Arnt V, Lousada, Isabelle, Nativi-Nicolau, Jose, Cristina Quarta, Candida, Rapezzi, Claudio, Ruberg, Frederick L, Witteles, Ronald, Merlini, Giampaolo

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2023 ACC Expert Consensus Decision Pathway on Comprehensive Multidisciplinary Care for the Patient With Cardiac Amyloidosis: A Report of the American College of Cardiology Solution... von Kittleson, Michelle M, Ruberg, Frederick L, Ambardekar, Amrut V, Brannagan, Thomas H, Cheng, Richard K, Clarke, John O, Dember, Laura M, Frantz, Janell Grazzini, Hershberger, Ray E, Maurer, Mathew S, Nativi-Nicolau, Jose, Sanchorawala, Vaishali, Sheikh, Farooq H

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Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families von Bouhouche, Ahmed, Birouk, Nazha, Azzedine, Hamid, Benomar, Ali, Durosier, Garry, Ente, Dorothée, Muriel, Marie-Paule, Ruberg, Merle, Slassi, Ilham, Yahyaoui, Mohamed, Dubourg, Odile, Ouazzani, Reda, LeGuern, Eric

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De Novo Expansion of Intermediate Alleles in Spinocerebellar Ataxia 7 von Stevanin, Giovanni, Giunti, Paola, David, Gilles, Belal, Samir, Dürr, Alexandra, Ruberg, Merle, Wood, Nicholas, Brice, Alexis

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Metabolic activity of cerebellar and basal ganglia-thalamic neurons is reduced in parkinsonism von Rolland, Anne-Sophie, Herrero, Maria-Trinidad, Garcia-Martinez, Virginia, Ruberg, Merle, Hirsch, Etienne C., François, Chantal

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Quantification of acetogenins in Annona muricata linked to atypical parkinsonism in guadeloupe von Champy, Pierre, Melot, Alice, Guérineau Eng, Vincent, Gleye, Christophe, Fall, Djibril, Höglinger, Gunter U., Ruberg, Merle, Lannuzel, Annie, Laprévote, Olivier, Laurens, Alain, Hocquemiller, Reynald

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Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia von Depienne, Christel, Fedirko, Estelle, Forlani, Sylvie, Cazeneuve, Cécile, Ribaï, Pascale, Feki, Imed, Tallaksen, Chantal, Nguyen, Karine, Stankoff, Bruno, Ruberg, Merle, Stevanin, Giovanni, Durr, Alexandra, Brice, Alexis

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The mitochondrial complex i inhibitor annonacin is toxic to mesencephalic dopaminergic neurons by impairment of energy metabolism von Lannuzel, A, Michel, P.P, Höglinger, G.U, Champy, P, Jousset, A, Medja, F, Lombès, A, Darios, F, Gleye, C, Laurens, A, Hocquemiller, R, Hirsch, E.C, Ruberg, M

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Atypical parkinsonism in Guadeloupe: a common risk factor for two closely related phenotypes? von Lannuzel, Annie, Höglinger, G. U., Verhaeghe, S., Gire, L., Belson, S., Escobar-Khondiker, M., Poullain, P., Oertel, W. H., Hirsch, E. C., Dubois, B., Ruberg, M.

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years von Namekawa, M, Ribai, P, Nelson, I, Forlani, S, Fellmann, F, Goizet, C, Depienne, C, Stevanin, G, Ruberg, M, Dürr, A, Brice, A

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations von AZZEDINE, H, RAVISE, N, HAMADOUCHE, T, BOUHOUCHE, A, GUILBOT, A, STENDEL, C, RUBERG, M, BRICE, A, BIROUK, N, DUBOURG, O, TAZIR, M, LEGUERN, E, VERNY, C, GABRËELS-FESTEN, A, LAMMENS, M, GRID, D, VALLAT, J. M, DUROSIER, G, SENDEREK, J, NOUIOUA, S

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Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis von Namekawa, M., Muriel, M.-P., Janer, A., Latouche, M., Dauphin, A., Debeir, T., Martin, E., Duyckaerts, C., Prigent, A., Depienne, C., Sittler, A., Brice, A., Ruberg, M.

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Subgroup identification from randomized clinical trial data von Foster, Jared C., Taylor, Jeremy M.G., Ruberg, Stephen J.

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New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p von NABBOUT, R, BAULAC, S, DESGUERRE, I, BAHI-BUISSON, N, CHIRON, C, RUBERG, M, DULAC, O, LEGUERN, E

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Stroke risk interacts with Alzheimer's disease biomarkers on brain aging outcomes von Hohman, Timothy J, Samuels, Lauren R, Liu, Dandan, Gifford, Katherine A, Mukherjee, Shubhabrata, Benson, Elleena M, Abel, Ty, Ruberg, Frederick L, Jefferson, Angela L

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Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease von Dubourg, O, Azzedine, H, Verny, C, Durosier, G, Birouk, N, Gouider, R, Salih, M, Bouhouche, A, Thiam, A, Grid, D, Mayer, M, Ruberg, M, Tazir, M, Brice, A, LeGuern, E

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Cardiac Scintigraphy With Technetium-99m-Labeled Bone-Seeking Tracers for Suspected Amyloidosis von Hanna, Mazen, Ruberg, Frederick L., Maurer, Mathew S., Dispenzieri, Angela, Dorbala, Sharmila, Falk, Rodney H., Hoffman, James, Jaber, Wael, Soman, Prem, Witteles, Ronald M., Grogan, Martha

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The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V von DUBOURG, O, AZZEDINE, H, BEN YAOU, R, POUGET, J, BAROIS, A, MEININGER, V, BOUTEILLER, D, RUBERG, M, BRICE, A, LEGUERN, E

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Re-evaluation of the functional anatomy of the basal ganglia in normal and Parkinsonian states von Levy, R., Hazrati, L.-N., Herrero, M.-T., Vila, M., Hassani, O.-K., Mouroux, M., Ruberg, M., Asensi, H., Agid, Y., Féger, J., Obeso, J.A., Parent, A., Hirsch, E.C.

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