Zobrazeno 1 - 10 of 209 pro vyhledávání: '"Robert D. Currier"'
1
Akademický článek
Quantifying Karenia brevis bloom severity and respiratory irritation impact along the shoreline of Southwest Florida
Autor: Richard P. Stumpf, Yizhen Li, Barbara Kirkpatrick, R. Wayne Litaker, Katherine A. Hubbard, Robert D. Currier, Katherine Kohler Harrison, Michelle C. Tomlinson
Publikováno v: PLoS ONE, Vol 17, Iss 1 (2022)
Nearly all annual blooms of the toxic dinoflagellate Karenia brevis (K. brevis) pose a serious threat to coastal Southwest Florida. These blooms discolor water, kill fish and marine mammals, contaminate shellfish, cause mild to severe respiratory irr
Externí odkaz: https://doaj.org/article/fa84ef76af36459c93c8a23f14006f17
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3
Akademický článek
HABscope: A tool for use by citizen scientists to facilitate early warning of respiratory irritation caused by toxic blooms of Karenia brevis.
Autor: D Ransom Hardison, William C Holland, Robert D Currier, Barbara Kirkpatrick, Richard Stumpf, Tracy Fanara, Devin Burris, Andrew Reich, Gary J Kirkpatrick, R Wayne Litaker
Publikováno v: PLoS ONE, Vol 14, Iss 6, p e0218489 (2019)
Blooms of the toxic microalga Karenia brevis occur seasonally in Florida, Texas and other portions of the Gulf of Mexico. Brevetoxins produced during Karenia blooms can cause neurotoxic shellfish poisoning in humans, massive fish kills, and the death
Externí odkaz: https://doaj.org/article/f5aa2e9e251e43bc8bc4b93ba4e342ad
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4
Akademický článek
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5
Akademický článek
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6
International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome
Autor: Bala V. Manyam, Paul Trouillas, D. Timann, K. Wessel, Jérôme Honnorat, Robert D. Currier, Alessandro Filla, Alan Bryer, Paula Coutinho, Giuseppe Campanella, Tetsuya Takayanagi, Mark Hallett, Hans-Christoph Diener, S. H. Subramony, Christopher M. Gomez, Norbert Nighoghossian, L. Schut, S. Massaquoi, M. Ben Hamida
Publikováno v: Journal of the Neurological Sciences. 145:205-211
Despite the involvement of cerebellar ataxia in a large variety of conditions and its frequent association with other neurological symptoms, the quantification of the specific core of the cerebellar syndrome is possible and useful in Neurology. Recen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bcb36668b8a66662288b53307f4a10ce
https://doi.org/10.1016/s0022-510x(96)00231-6
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7
Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1
Autor: S. H. Subramony, Robert D. Currier, Durisala Desaiah, Jonathan D. Fratkin, Parminder J. S. Vig
Publikováno v: Neurology. 47:249-253
The distribution of two calcium-binding proteins, calbindin D28k (CaBP) and parvalbumin (PV), was investigated by immunohistochemistry in the brains of three individuals dying of nonneurologic illness and three patients with spinocerebellar ataxia-1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43c9f02fafd6dccdb3ee34dae3bbfb9
https://doi.org/10.1212/wnl.47.1.249
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8
Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, machado-joseph disease, or dentato-rubro-pallido-luysian atrophy locus
Autor: Robert D. Currier, Jonathan D. Fratkin, S. H. Subramony, Bala V. Manyam
Publikováno v: Movement Disorders. 11:174-180
The dominantly inherited ataxias are characterized both by phenotypic variability (phenotypic heterogeneity) within the same genotype and overlapping phenotypes from different genotypes (genotypic heterogeneity). Therefore it is important to characte
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64765f50ddb5b9a5c88daecdad358246
https://doi.org/10.1002/mds.870110210
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9
Decreased insulin-like growth factor I-mediated protein tyrosine phosphorylation in human olivopontocerebellar atrophy and lurcher mutant mouse
Autor: Robert D. Currier, Jonathan D. Fratkin, P. Joshi, Parminder J. S. Vig, Durisala Desaiah, S. H. Subramony
Publikováno v: Journal of the Neurological Sciences. 124:38-44
We examined insulin-like growth factor I (IGF-I)-dependent phosphorylation and protein tyrosine kinase (PTK) activity in cerebellar cortex of normal humans, patients with olivopontocerebellar atrophy (OPCA) ("C" kindred) and in lurcher mutant mouse,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7d8d5ba58024156dfd6aaf5c6af44f1
https://doi.org/10.1016/0022-510x(94)90008-6
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10
Intrafamilial variability in Machado-Joseph disease
Autor: Robert D. Currier, S. H. Subramony
Publikováno v: Movement Disorders. 11:741-743
Dominantly inherited ataxias resulting from different gene mutations are difficult to distinguish based on clinical phenotypes. We believe the phenotypic variability within families can be a clue to clinical diagnosis. We illustrate the range of phen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::005b2f4b8680b26f1c27cd979b6c475b
https://doi.org/10.1002/mds.870110625
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