Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Robert D Currier"'
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, p e0260755 (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/e5f42a51b60d46b8923a47a1e4411189
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
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
https://doi.org/10.1016/s0022-510x(96)00231-6
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
https://doi.org/10.1212/wnl.47.1.249
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
https://doi.org/10.1002/mds.870110210
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
https://doi.org/10.1016/0022-510x(94)90008-6
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
https://doi.org/10.1002/mds.870110625
Publikováno v:
Journal of Urology. 146:1305-1307
Epidemiological data have not yet enabled physicians to look beyond age and race to identify men at increased risk for prostate cancer. We conducted a hospital-based case-control study of familial patterns of prostate cancer with self-reported data f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5fd06fee5705b4d11d2d94be5b0af28
https://doi.org/10.1016/s0022-5347(17)38074-6
https://doi.org/10.1016/s0022-5347(17)38074-6
Autor:
Robert D. Currier, S. H. Subramony
Publikováno v:
Neurology. 47(2)
To the Editor: The editorial by Rosenberg [1] is a superb analysis of the current genotype situation in the field of the hereditary ataxias. Rosenberg is quite right in his comments that the genotype has great importance in clarifying the issue of co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26f76ffcc93ac1b5bc00ae42a35f1cd7
https://pubmed.ncbi.nlm.nih.gov/8757064
https://pubmed.ncbi.nlm.nih.gov/8757064
Publikováno v:
Neurology. 45(12)
We describe a progressive neurologic disorder in three sisters characterized clinically by palatal myoclonus, spastic weakness, hyperreflexia, mild cerebellar dysfunction, and ocular motor abnormalities.Postmortem examination of one patient demonstra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42f6374ef1b097209e59af435931a4a
https://pubmed.ncbi.nlm.nih.gov/9040773
https://pubmed.ncbi.nlm.nih.gov/9040773