Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Peter R. Kollros"'
Autor:
Elaine H. Zackai, Ralph J. DeBerardinis, Beverly S. Emanuel, Jennifer H. Kaplan, Danielle Conforto, Peter R. Kollros, Karen L. Russell
Publikováno v:
American Journal of Medical Genetics. :31-36
Autosomal dominant myoclonus-dystonia syndrome (MDS) is characterized by myoclonic and/or dystonic movements with onset as early as infancy. In most families, MDS is caused by mutations in the gene SGCE, which encodes epsilon -sarcoglycan and is loca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6018cf3294f5de095270617d513e3fc6
https://doi.org/10.1002/ajmg.a.20162
https://doi.org/10.1002/ajmg.a.20162
Autor:
James A. Cullen, Peter R. Kollros, Leonard J. Graziani, Michael Goodman, Stephen Baumgart, Christian Stanley, Leopold J. Streletz, Shobhana A. Desai
Publikováno v:
The Journal of Pediatrics. 131:233-239
Objective: We determined the sensitivity and specificity of neonatal brain-stem auditory evoked potentials (BAEP) as markers for subsequent hearing impairment and for developmental problems found later in infancy and childhood. Methods: BAEP studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18e0ad86d8cc5f54560177c237221a09
https://doi.org/10.1016/s0022-3476(97)70159-8
https://doi.org/10.1016/s0022-3476(97)70159-8
Autor:
Peter R. Kollros, Barbara A. Konkle
Publikováno v:
European Journal of Cardiovascular Prevention & Rehabilitation. 4:70-75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4f2c250d4ac175827fa9141136518c3
https://doi.org/10.1177/174182679700400202
https://doi.org/10.1177/174182679700400202
Publikováno v:
Muscle & Nerve. 19:88-91
Mononeuropathies are unusual at birth, and electromyographic (EMG) definition the first day of life has not been reported previously. Although neonatal mononeuropathies may be related to obstetric complications, prenatal mechanisms also merit conside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::609d972c104fb5480e5635266bcb6df2
https://doi.org/10.1002/(sici)1097-4598(199601)19:1<88::aid-mus12>3.0.co
https://doi.org/10.1002/(sici)1097-4598(199601)19:1<88::aid-mus12>3.0.co
Publikováno v:
Journal of Biological Chemistry. 265:21867-21873
Plasminogen activator inhibitor-1 (PAI-1) inhibits the tissue plasminogen activator (tPA) and urokinase activation of plasminogen to plasmin, a protease of trypsin-like specificity which is involved in a number of processes, including fibrinolysis, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9ba5955858a31e249da4d25cfd6d067
https://doi.org/10.1016/s0021-9258(18)45819-x
https://doi.org/10.1016/s0021-9258(18)45819-x
Publikováno v:
Journal of neurochemistry. 63(3)
Patients with diabetes are predisposed to microvascular disease. In the retina and brain, this is characterized by neovascularization and new capillary formation. Because of the potential importance of plasmin generation in these processes, we evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18ae7273ef051352641f3d2ec9385570
https://pubmed.ncbi.nlm.nih.gov/7519664
https://pubmed.ncbi.nlm.nih.gov/7519664
Publikováno v:
Pediatric neurology. 7(4)
A patient with Menkes Kinky Hair disease was treated with infusions of copper-histidine which resulted in normal copper values in the cerebrospinal fluid. This tends to confirm the in vitro data that copper is transported into the central nervous sys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d962b5c124d6a38b53c02ff60c0533c9
https://pubmed.ncbi.nlm.nih.gov/1930426
https://pubmed.ncbi.nlm.nih.gov/1930426