Výsledky vyhledávání - "A L, Taratuto"

Publikováno v: Brain Pathol

Trichinosis is a worldwide zoonotic disease closely related to cultural and dietary habits caused by a nematode Trichinella spp. Human infection is acquired through ingestion of undercooked meat containing infective encysted larvae. There are two cyc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6a013177201ca92b201f7a5388ee707
https://doi.org/10.1111/j.1750-3639.1997.tb01081.x

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Familial bulbospinal neuronopathy with optic atrophy: a distinct entity

Autor: Guillermo Paradiso, A L Taratuto, Federico Micheli, I C Parera

Publikováno v: Journal of Neurology, Neurosurgery & Psychiatry. 61:196-199

A 61 year old woman and her 58 year old brother presented with the clinical picture of late onset progressive bulbar and spinal muscular atrophy with family history of involvement in successive generations. The sister also had optic neuropathy and th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5db376fcfb28b6f822a03165effec4e
https://doi.org/10.1136/jnnp.61.2.196

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Chagasic Granulomatous Encephalitis in Immunosuppressed Patients; Computed Tomography and Magnetic Resonance Imaging Findings

Autor: Francisco J Meli, Guillermo A. Di Lorenzo, Ana L Taratuto, Miguel A. Pagano, Marcelo D Pomsztein, María Laura Garau

Publikováno v: Journal of Neuroimaging. 6:94-97

American trypanosomiasis (Chagas' disease), a zoonosis caused by Trypanosoma cruzi with a high incidence in Latin America, may induce an uncommon form of localized encephalitis termed "chagoma", found in few immunocompromised patients. The computed t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beb5d1af5f85f5527762a0808aeb8aba
https://doi.org/10.1111/jon19966294

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Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

Autor: J A, Bevilacqua, N, Monnier, M, Bitoun, B, Eymard, A, Ferreiro, S, Monges, F, Lubieniecki, A L, Taratuto, A, Laquerrière, K G, Claeys, I, Marty, M, Fardeau, P, Guicheney, J, Lunardi, N B, Romero

Publikováno v: Neuropathology and Applied Neurobiology
Neuropathology and Applied Neurobiology, Wiley, 2011, 37 (3), pp.271-84. ⟨10.1111/j.1365-2990.2010.01149.x⟩
Neuropathology and Applied Neurobiology, 2011, 37 (3), pp.271-84. ⟨10.1111/j.1365-2990.2010.01149.x⟩

International audience; AIMS: To report the clinical, pathological and genetic findings in a group of patients with a previously not described phenotype of congenital myopathy due to recessive mutations in the gene encoding the type 1 muscle ryanodin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1b12c36ecadc22190a7ef1cdfc235886
https://www.hal.inserm.fr/inserm-00639292

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Abstracts for the Tenth International Conference on Brain Tumour Research and Therapy

Autor: Tore G. Abrahamsen, Finn Wesenberg, Sverre Mørk, Jeffrey Allen, Roberta Hayes, Robert DaRosso, Anita Nirenberg, Francis Ali-Osman, Nike Akande, V. Amberger, H. Seulberger, P. A. Paganetti, M. E. Schwab, N. Arita, T. Ohnishi, S. Hiraga, H. Yamamoto, T. Taki, S. Izumoto, M. Higuchi, T. Hayakawa, M. Kusakabe, T. Sakakura, N. G. Baldwin, C. D. Rice, R. E. Merchant, Sally M. Ashmore, J. L. Darling, C. C. Bailey, C. Balmaceda, B. Diez, J. Villablanca, R. Walker, J. Finlay, A. Tommy Bergenheim, Magdalena Hartman, Jonas Bergh, PerÅke Ridderheim, Roger Henriksson, Michael E. Berens, Monique D. Rief, Alf Giese, Björn Zackrisson, Jörgen Elfversson, Mark Bernstein, Alberto Cabantog, Jennifer Glen, David Mikulis, Rolf Bjerkvig, Paal-Henning Pedersen, Berit Mathisen, Rupavathana Mahesparan, Hans Kristian Haugland, Normand Laperriere, Cindy Thomason, Phil Leung, M. S. Bobola, M. S. Berger, J. R. Silber, Erik Bongcam-Rudloff, Jia-Lun Wang, Monica Nistér, Bengt Westermark, Steven Brem, Gary Breslow, Jason Ho, Stephen Gately, Shingo Takano, William Ward, M. Brada, R. Laing, J. Warrington, Herbert Engelhard, Barry Landau, Hau Kwaan, Elaine Verrusio, J. C. Buckner, T. L. Cascino, P. S. Schomberg, J. R. O'Fallon, R. P. Dinapoli, P. A. Burch, E. G. Shaw, William C. Broaddus, Kathryn Hager-Loudon, Randall E. Merchant, William Loudon, William T. Couldwell, Jack B. Jiang, David Burns, Martin H. Weiss, Michael L. J. Apuzzo, I. Desbaillets, M. Tada, N. de Tribolet, E. Van Meir, R. L. Davis, K. Onda, M. D. Prados, M. Eileen Dolan, Matthew J. Fleig, Henry S. Friedman, A. Jonas Ekstrand, Nicola Longo, C. David James, D. Chou, B. Wijnhoven, M. Bellinzona, M. Nakagawa, B. G. Feuerstein, H. S. Basu, M. E. Dolan, C. Bergeron, M. Pellarm, D. F. Deen, L. J. Marton, Jonathan Finlay, D. S. Fulton, R. C. Urtasun, Adrienne C. Scheck, J. Geddes, G. M. Vowles, S. M. Ashmore, G. Y. Gillespie, C. K. Goldman, M. T. Tucker, E. Lyon, J. -C. Tsai, G. T. Gobbel, P. H. Chan, Hairy S. Greenberg, W. F. Chandler, W. D. Ensminger, L. Junck, H. Sandler, J. Bromberg, P. McKeever, G. G. Gonzalez, A. Sarkar, H. Basu, Kr. Haugland, Ole-Bjørn Tysnes, Shoju Hiraga, Norio Arita, Takanori Ohnishi, Takuyu Taki, Hiroshi Yamamoto, Masahide Higuchi, Toru Hayakawa, Erik Isern, Geirmund Unsgaard, Anne Beate Langeland Marthinsen, Trond Strickert, Eirik Helseth, F. Hochberg, R. Cosgrove, R. Valenzuela, F. Pardo, N. Zervas, Robert B. Jenkins, Steven R. Ritland, Kevin C. Hailing, Stephen N. Thibodeau, L. Juillerat, P. Darekar, R. C. Janzer, M. F. Hamou, Tsutomu Kato, Yutaka Sawamura, Mitsuhiro Tada, Shirou Sakuma, Masako Sudo, Hiroshi Abe, M. Kallio, J. Leppää, T. Nikula, P. Nikkinen, H. Gylling, M. Färkkilä, J. Hiltunen, J. Jääskeläinen, K. Liewendahl, G. Evren Keles, Mitchel S. Berger, Anna Deliganis, S. J. Kellie, S. S. N. De Graaf, H. Bloemhof, I. Johnston, D. D. R. Uges, M. Besser, R. W. Chaseling, R. A. Ouvrier, N. D. Kitchen, S. Hughes, R. Beaney, D. G. T. Thomas, D. H. Kim, T. Maeda, G. Mohapatra, S. Park, F. W. Waldman, J. W. Gray, D. Koala, J. Silber, M. Berger, P. Krauseneck, B. Müller, H. Strik, M. Warmuth-Metz, Jun-ichi Kuratsu, Hideo Takeshima, Yukitaka Ushio, C. Kretschmar, H. Grodman, R. Linggood, A. P. Kyritsis, M. Bondy, J. Cunningham, M. Xiao, V. Levin, N. Leeds, J. Bruner, W. K. A. Yung, H. Saya, L. A. Lampson, M. R. Nichols, M. A. Lampson, A. D. Dunne, Hong Li, Marie-France Hamou, Rehana Jaufeerally, Annie-Claire Diserens, Erwin Van Meir, Nicolas de Tribolet, V. A. Levin, M. Maor, R. Sawaya, M. Leavens, S. Woo, P. Thall, M. J. Gleason, Bertrand C. Liang, D. A. Ross, P. S. Meltzer, J. M. Trent, H. S. Greenberg, K. O. Lillehei, Q. Kong, B. K. DeMasters, S. J. Withrow, D. R. Macdonald, J. G. Cairncross, S. Ludwin, D. Lee, T. Cascino, J. Buckner, E. Dropcho, D. Fulton, D. Stewart, C. Schold, N. Wainman, E. Eisenhauer, S. Kirby, B. J. Fisher, L. Magrassi, G. Butti, S. Pezzotta, G. Milanesi∘, Masao Matsutani, Kirsten Marienhagen, Ole Didrik Laerum, Abderrahim Merzak, Shahriar Koocheckpour, Yannis Roxanis, Geoffrey J. Pilktngton, Masakatsu Nagai, Kunihiko Watanabe, Jun-ichi Narita, Hideaki Hagiwara, Mark Noble, K. Nomura, H. Oyama, M. Motoo, S. Shibui, K. Tokuue, Y. Akine, Svein J. Tjoflaat Nygaard, F. S. Pardo, D. W. Hsu, E. T. Hedley-Whyte, J. Efird, E. V. Schmidt, Paal-Henning Pedersenl Kirsten Marienhagen, Geoffrey J. Pilkington, Tracey M. Clarke, Hui Tian Yu, Joan P. Rogers, Robert Stern, Surasak Phuphanich, Harvey Greenberg, R. Murtagh, Jesus Viloria, Joseph Ransohoff, Kimberly Martin, V. Erika Hatva, Jasti S. Rao, S. Mohanam, Sandra A. Rempel, Karl Schwechheimer, Richard L. Davis, Webster K. Cavenee, Mark L. Rosenblum, Guido Reifenberger, Lu Liu, Koichi Ichimura, Esther E. Schmidt, V. Peter Collins, T. Revesz, F. Scaravilli, H. Cockburn, R. T. Biron, James McKerrow, Bonnie Sloane, Tom Mikkelsen, Norbert Roosen, Peter Coopersmith, Robert Smith, Harcharan Kaur Rooprai, Steven Maidment, Garry Rucklidge, Anton Volovsek, J. T. Rutka, S. L. Smith, K. Matsuzawa, A. A. Sankar, S. R. Williams, K. Fukuyama, Jun Ikeda, R. G. Selker, F. T. Vertosick, M. T. Goldenberg, R. Bindal, A. Taratuto, P. Picco, J. Monges, M. Martinez, G. Pacheco, M. Gamboni, M. Schultz, B. A. Mueller, T. G. Ewers, T. Shiraishi, K. Tabuchi, S. Nakagawa, S. Kihara, D. J. Stewart, L. Eapen, O. Agboola, P. Popovic, R. Goel, P. Raaphorst, P. T. T. Wong, S. Shimokawa, M. Oh-uchida, K. Hori, C. Markert, K. -W. Pflughaupt, A. -C. Diserens, R. Jauferrally, M. -F. Hamou, H. Takeshima, H. Mochizuki, J. L. Clifford, T. Nishi, R. Lotan, A. J. A. Terzis, H. Arnold, O. D. Laerum, R. Bjerkvig, A. L. Taratuto, G. Sevlever, D. Diaz, M. Di Tella, V. Cuccia, H. Pomata, G. Gallo, A. Dietze, U. Knopp, R. Thomas, P. Carnochan, G. Flux, N. Kitchen, D. Thomas, M. Zalutsky, D. Bigner, Philip Tofilon, Paul Borchardt, Sverre H. Torp, Are Dalen, Takashi Tohyama, Osami Kubo, Kintomo Takakura, Virginia M. -Y. Lee, John Q. Trojanowski, Svein Nygaard, M. B. Parliament, A. J. McEwan, R. H. Mannan, L. I. Weibe, G. Unsgårp, U. Sonnewald, I. Gribbestad, E. Isern, S. B. Petersen, J. Wang, D. A. Delgado, Tracy J. Warr, Denise Sheer, Pat Gorman, F. Yamaguchi, M. Westphal, L. Anker, W. Hamel, M. Lücke, M. Shepard, P. Kleihues, H. D. Herrmann, W. K. Alfred Yung, Scott Taylor, Peter A. Steck

Publikováno v: Journal of Neuro-Oncology. 15:S1-S30

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a141616716109a67579948bafa65b590
https://doi.org/10.1007/bf02041900

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Alpha vs. gamma sarcoglycanopathy: DNA tests solve a case from Argentina

Autor: S, Avila De Salman, A L, Taratuto, G, Dekomien, R, Carrero-Valenzuela

Publikováno v: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology. 26(2)

Immunohistochemical and DNA results are described in a patient with sarcoglycanopathy. Immunostaining was comparatively normal for alpha-, attenuated for beta- and delta-, and markedly attenuated for gamma-sarcoglycan, thus sarcoglycanopathy was diag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::533d33e0664c6ce9e8643191d44b86fd
https://pubmed.ncbi.nlm.nih.gov/18421900

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Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus

Autor: N B, Romero, M, Herasse, N, Monnier, J P, Leroy, D, Fischer, A, Ferreiro, L, Viollet, B, Eymard, P, Laforêt, S, Monges, F, Lubieniecki, A L, Taratuto, P, Guicheney, J, Lunardi, M, Fardeau

Publikováno v: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology. 24(2)

We analysed the clinical, histochemical, ultrastructural and genetic data of patients affected by central core disease (CCD) studied during the last 20 years. From a total series of 86 CCD-families, we have identified 46 CCD families with RYR1 mutati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d548babf8c34dff045fe315d51c05333
https://pubmed.ncbi.nlm.nih.gov/16550918

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