Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Anita Pikus"'
Autor:
Muriel I. Kaiser-Kupfer, Anita Pikus, Rafael C. Caruso, Fumino Iwata, Joy B. Redman, Benjamin I. Rubin, Ekaterini Tsilou, James F. Hejtmancik, George F. Reed
Publikováno v:
Acta Ophthalmologica Scandinavica. 80:196-201
Purpose: Usher syndrome types I and II are clinical syndromes with substantial genetic and clinical heterogeneity. We undertook the current study in order to identify ocular symptoms and signs that could differentiate between the two types. Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::010677d7ffab2fd02e4649f79dd3c6d1
https://doi.org/10.1034/j.1600-0420.2002.800215.x
https://doi.org/10.1034/j.1600-0420.2002.800215.x
Autor:
Anita Pikus
Publikováno v:
Seminars in Hearing. 23:113-120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::034e31a1ba01ece9b1adcf663280f5fc
https://doi.org/10.1055/s-2002-33004
https://doi.org/10.1055/s-2002-33004
Autor:
David Ishizawar, Monica C. Skarulis, Anita Pikus, Bruce D. Weintraub, Françoise Brucker-Davis, Mary-Ann Mastroianni, Myles Koby
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 81:2768-2772
Hearing impairment was anecdotally reported in resistance to thyroid hormone (RTH), a condition caused by mutations in the beta-thyroid hormone receptor (beta TR) gene. Because of its ontogenic distribution in the cochlea, the beta TR may have a pivo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5367ef93ac12b25aaf396f8d60717e1d
https://doi.org/10.1210/jcem.81.8.8768826
https://doi.org/10.1210/jcem.81.8.8768826
Autor:
Anita Pikus, Alan J. Zametkin, Ashley P. Hanahan, Tracy Aquino, Susan D. Hamburger, Robert M. Cohen, A. Catherine King, Paul J. Andreason, Judith M. Rumsey
Publikováno v:
Biological Psychiatry. 36:171-180
A prior study documented the failure of dyslexic men to activate left temporoparietal cortex during phonologic processing. Because of reports of an anomalous right planum temporale in developmental dyslexia, the functional implications of which are u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03c148231f40fd83518a115a45a4bed6
https://doi.org/10.1016/0006-3223(94)91222-x
https://doi.org/10.1016/0006-3223(94)91222-x
Autor:
Anita Pikus
Publikováno v:
Ear and Hearing. 19:333-335
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d806411c5517b9222804476059fee1a
https://doi.org/10.1097/00003446-199808000-00009
https://doi.org/10.1097/00003446-199808000-00009
Autor:
Janine A. Smith, Anita Pikus, Frank G. Ondrey, Mary Ann Mastroianni, Eric Moldestad, Robert Nusenblatt, Estelle Vernon, Daniel A. Sklare
Publikováno v:
The Laryngoscope. 116(10)
Background: Vogt-Koyanagi-Harada (VKH) syndrome is a systemic condition characterized by ocular inflammatory disease as well as skin, ear, and meningeal manifestations. Patients with VKH often report tinnitus and hearing loss, but these symptoms tend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2541be86fe7f2266ed6bf029235add51
https://pubmed.ncbi.nlm.nih.gov/17003710
https://pubmed.ncbi.nlm.nih.gov/17003710
Autor:
Ekaterini T, Tsilou, Benjamin I, Rubin, Rafael C, Caruso, George F, Reed, Anita, Pikus, James F, Hejtmancik, Fumino, Iwata, Joy B, Redman, Muriel I, Kaiser-Kupfer
Publikováno v:
Acta ophthalmologica Scandinavica. 80(2)
Usher syndrome types I and II are clinical syndromes with substantial genetic and clinical heterogeneity. We undertook the current study in order to identify ocular symptoms and signs that could differentiate between the two types.Sixty-seven patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f53220ea3f19fb1088a0d47045ebd1de
https://pubmed.ncbi.nlm.nih.gov/11952489
https://pubmed.ncbi.nlm.nih.gov/11952489
Neurofibromatosis 2 (Bilateral Acoustic or Central Neurofibromatosis), a Treatable Cause of Deafness
Publikováno v:
Annals of the New York Academy of Sciences. 630:305-307
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3466b869f803c94f8726b232cf2b03d
https://doi.org/10.1111/j.1749-6632.1991.tb19615.x
https://doi.org/10.1111/j.1749-6632.1991.tb19615.x
Autor:
Gerald J. Chader, Susan Gentleman, Rhea A Lloyd-Muhammad, Anita Pikus, Muriel I. Kaiser-Kupfer, W. Gerald Robison, Richard J. Sherins, Rafael C. Caruso, Mary Alice Crawford
Publikováno v:
Human pathology. 27(1)
This study examined the ultrastructural morphology and posttranslationally modified alpha-tubulin isoforms in the sperm flagella of a patient presenting with infertility and retinal degeneration. Clinical evaluation showed impaired motility and gross
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a07a1b744c2709d8221023fde65076ab
https://pubmed.ncbi.nlm.nih.gov/8543316
https://pubmed.ncbi.nlm.nih.gov/8543316
Autor:
M. A. Zasloff, Jerry N. Thompson, J. Danoff, L. Rodén, Anita Pikus, Muriel I. Kaiser-Kupfer, G. Constantopoulos, H. D. McDonald, E. F. Neufeld, Rafael C. Caruso, J. Muenzer, R. R. Berry
Publikováno v:
Journal of inherited metabolic disease. 15(1)
Amnion membrane implantation has been proposed as an approach to enzyme replacement in mucopolysaccharidoses. Human amnion membranes have been subcutaneously implanted in the abdominal wall in 19 patients with mucopolysaccharidoses (MPS I, II and III
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55d158831d603346268fe62e5da17a59
https://pubmed.ncbi.nlm.nih.gov/1533888
https://pubmed.ncbi.nlm.nih.gov/1533888