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1.
A A Pract ; 11(2): 38-40, 2018 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-29634554

RESUMO

The perioperative implementation of continuous peripheral nerve blocks is poorly described within the literature for replantation surgeries beyond digital replantation. The management of replantation patients presents a challenging balance between pain control and limb perfusion. We report the successful use of a continuous interscalene catheter in a therapeutically anticoagulated patient after midshaft humerus arm replantation. The benefits of the continuous peripheral nerve block for the patient included improved pain control and potentially improved limb perfusion making it a valuable component of this patient's treatment.


Assuntos
Braço/cirurgia , Bloqueio Nervoso , Nervos Periféricos , Reimplante , Adulto , Feminino , Humanos , Adulto Jovem
2.
Oncologist ; 17(3): 384-7, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22334452

RESUMO

Interferon is the only accepted adjuvant treatment for patients with melanoma; hence, oncologists should be aware of the possibility of retinal abnormalities resulting from its use. Interferon-associated retinopathy in patients being treated for resected melanoma is a rare phenomenon with a proposed immunological basis. Patients are usually asymptomatic or have mild visual impairments, with cotton wool infarcts and hemorrhages. These symptoms and signs usually resolve with the discontinuation of interferon, but in a few severe presentations the visual impairments and retinal changes can be irreversible.


Assuntos
Interferon-alfa/efeitos adversos , Melanoma/tratamento farmacológico , Síndromes Paraneoplásicas Oculares/terapia , Adulto , Feminino , Humanos , Interferon-alfa/uso terapêutico , Melanoma/cirurgia , Síndromes Paraneoplásicas Oculares/diagnóstico , Síndromes Paraneoplásicas Oculares/patologia
3.
Hum Mol Genet ; 14(8): 1095-105, 2005 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-15757972

RESUMO

Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disorder caused by the expansion of a glutamine repeat within the SCA1-encoded protein ataxin-1. We have previously shown that serine 776 (S776) of both wild-type and mutant ataxin-1 is phosphorylated in vivo and in vitro. Moreover, preventing phosphorylation of this residue by replacing it with alanine resulted in a mutant protein, which was not pathogenic in spite of its nuclear localization. To further investigate pathways leading to S776 phosphorylation of ataxin-1, we developed a cell-culture based assay to screen for modulators of S776 phosphorylation. In this assay, ataxin-1 expression was monitored by enhanced green fluorescent protein (EGFP) fluorescence in cell lines stably expressing EGFP-ataxin-1 fusion protein. The phospho-S776 ataxin-1 specific antibody (PN1168) was used to assess ataxin-1 S776 phosphorylation. A library of 84 known kinase and phosphatase inhibitors was screened. Analysis of the list of drugs that modified S776 phosphorylation places many of the inhibited kinases into known cell signaling pathways. A pathway associated with calcium signaling resulted in phosphorylation of both wild-type and mutant ataxin-1. Interestingly, inhibitors of the PI3K/Akt pathway predominantly diminished mutant ataxin-1 phosphorylation. These results provide new molecular tools to aid in elucidating the biological role of ataxin-1 phosphorylation and perhaps provide potential leads toward the development of a therapy for SCA1.


Assuntos
Proteínas do Tecido Nervoso/metabolismo , Proteínas Nucleares/metabolismo , Animais , Ataxina-1 , Ataxinas , Bioensaio , Células CHO , Cricetinae , Genes Reporter , Humanos , Fosfoproteínas Fosfatases/antagonistas & inibidores , Fosforilação , Proteínas Tirosina Quinases/antagonistas & inibidores
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