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1.
J Neurosurg ; 122(5): 1042-7, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25748305

RESUMO

Deep brain stimulation (DBS) is approved for several clinical indications; however, the sequencing of DBS surgery and the timeline for implementing stimulation therapy are not standardized. In over 140 cases so far, the authors have reversed the sequencing for staged implantation of DBS systems that was conducive to minimizing patient anxiety and discomfort while providing the opportunity to shorten the time between implantation and programming for therapeutic management of symptoms. Stage I was performed with the patient under general anesthesia and consisted of implantation of the pulse generator and lead extensions and placement of the bur holes. Stage II was completed 1-7 days later, using only local anesthesia, and included stereotactic frame-based microelectrode recordings, semi-microstimulation and macrostimulation, and testing and placement of the stimulating electrodes. Stage I lasted approximately 90 minutes, whereas Stage II lasted approximately 230 minutes. All patients tolerated the procedures and received a complete implanted system. Deep brain stimulation therapy was typically initiated on the same day as lead implantation. When sequencing was reversed and bur holes were placed during the first stage while a patient was under general anesthesia, the patient was able to tolerate the second awake stage and was able to begin stimulation therapy within 48 hours of the second stage.


Assuntos
Estimulação Encefálica Profunda/métodos , Doença de Parkinson/terapia , Adulto , Idoso , Idoso de 80 Anos ou mais , Humanos , Pessoa de Meia-Idade , Adulto Jovem
2.
Hemoglobin ; 27(1): 1-5, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12603087

RESUMO

Thalassemia is a common inherited disease in the Mediterranean region. We here report a mutation new to the Lebanese population: the insertion of a G nucleotide at codons 8/9 [(+G) AAG-TCT (Lys-Ser) --> AAG-G-TCT (beta0)] of the beta-globin gene in a thalassemic patient with a mild phenotype. We discuss the possible factors that play a role in alleviating the severity of the disease in this case.


Assuntos
Códon/genética , Globinas/genética , Talassemia beta/genética , Eletroforese das Proteínas Sanguíneas , Pré-Escolar , Consanguinidade , Hemoglobina Fetal/análise , Hemoglobina Fetal/biossíntese , Genótipo , Hemoglobina A/análise , Hemoglobina A2/análise , Humanos , Líbano/epidemiologia , Masculino , Mutagênese Insercional , Fenótipo , Regiões Promotoras Genéticas/genética , Talassemia alfa/complicações , Talassemia alfa/genética , Talassemia beta/complicações , Talassemia beta/epidemiologia
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