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1.
Phys Rev Lett ; 130(4): 046202, 2023 Jan 27.
Artículo en Inglés | MEDLINE | ID: mdl-36763432

RESUMEN

Using time- and angle-resolved photoemission, we present momentum- and energy-resolved measurements of exciton coupling in monolayer WS_{2}. We observe strong intravalley coupling between the B_{1s} exciton and A_{n>1} states. Our measurements indicate that the dominant valley depolarization mechanism conserves the exciton binding energy and momentum. While this conservation is consistent with Coulomb exchange-driven valley depolarization, we do not observe a momentum or energy dependence to the depolarization rate as would be expected for the exchange-based mechanism.

2.
Oper Neurosurg (Hagerstown) ; 19(5): 502-509, 2020 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-32542367

RESUMEN

BACKGROUND: Facial nerve paralysis (FP) is a possible complication of cerebellopontine angle tumor surgery. Several donor nerves have been used in the past for facial reanimation. We report the results of 30 cases of masseter-to-facial anastomosis. OBJECTIVE: To prospectively evaluate the efficacy of V to VII anastomosis after FP. METHODS: In a prospective study, we included 30 consecutive patients with FP (20 women and 10 men) whose mean age was 48.8 yr (32-76 yr). In almost all cases, FP developed after cerebellopontine angle tumor surgery (29 patients), whereas in one case, FP occurred after skull base trauma. Pre- and postoperative evaluation of facial nerve function was performed using the House-Brackmann (HB) scale and the Sokolovsky scale, as well as by electromyography. Follow-up ranged from 11 to 51 mo and averaged 22 mo. RESULTS: All patients achieved functional recovery of the facial nerve from VI to either III or IV HB degree. Patients with short time FP showed significantly better postoperative recovery. CONCLUSION: The results of the V to VII anastomosis demonstrate a significant improvement of facial nerve function and virtually no complications.


Asunto(s)
Parálisis Facial , Nervio Hipogloso , Adulto , Anciano , Anastomosis Quirúrgica , Nervio Facial/cirugía , Parálisis Facial/etiología , Parálisis Facial/cirugía , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos
3.
J Interferon Cytokine Res ; 38(7): 298-310, 2018 07.
Artículo en Inglés | MEDLINE | ID: mdl-29932796

RESUMEN

Besides initiation of tumor-specific T cell immunity, dendritic cells (DCs) are endowed with tumoricidal activity. Previously, we showed that monocyte-derived DCs of high-grade glioma patients generated in the presence of interferon alpha (IFNα) (IFN-DCs) have impaired cytotoxic activity against tumor necrosis factor alpha (TNFα)-sensitive HEp-2 tumor cells. Herein, we demonstrate that decreased transmembrane TNFα (tmTNFα) expression, but not soluble TNFα (sTNFα) production by high-grade glioma patient IFN-DCs, determines the defective tumoricidal activity against TNFα-sensitive HEp-2 cells. Blocking TNFα-converting enzyme or stimulation of patient IFN-DCs with rIL-2 or dsDNA enhances tmTNFα expression on IFN-DCs and significantly increases their cytotoxicity. Decreased tmTNFα expression on patient IFN-DCs is not caused by downregulation of pNFκB. Neither rIL-2 nor dsDNA upregulates tmTNFα expression on patient IFN-DCs via an increase of pNFκB. The current study shows an important role of tmTNFα as mediator of IFN-DC tumoricidal activity and as molecular target for the restoration of defective DC killer activity in high-grade glioma patients.


Asunto(s)
ADN/inmunología , Células Dendríticas/inmunología , Glioma/inmunología , Glioma/patología , Interleucina-2/inmunología , Factor de Necrosis Tumoral alfa/metabolismo , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Proliferación Celular/efectos de los fármacos , Niño , Células Dendríticas/metabolismo , Ensayos de Selección de Medicamentos Antitumorales , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proteínas Recombinantes/inmunología , Células Tumorales Cultivadas , Factor de Necrosis Tumoral alfa/biosíntesis , Adulto Joven
4.
World Neurosurg ; 116: 337-342, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29715570

RESUMEN

BACKGROUND: Neoplasms located in the Meckel cave account for 0.2%-0.5% of all intracranial tumors. This area is the site of many types of pathologic lesions, most often trigeminal nerve schwannomas and meningiomas. Melanin-containing tumors are rare in this area. These tumor types can be suspected if the magnetic resonance characteristics of a tumor has some differences in comparison with other types of central nervous system neoplasms. In fact, differential diagnosis of melanotic tumors is based mainly on the histopathologic criteria and immunohistochemical profile. This article presents a case report of melanotic schwannoma of the Meckel cave and a literature review of the problem. CASE DESCRIPTION: A 23-year-old man underwent a 2-stage surgery for a dumbbell pigmented mass lesion located in the Meckel cave. No signs of recurrence were seen on follow-up magnetic resonance imaging (MRI) 3.5 years after the operation. CONCLUSIONS: Melanin-containing tumor can be suspected in the presence of radiologic characteristics, such as a hyperintense MRI signal on T1-weighted images and a hypointense signal on T2-weighted images. If a black extracerebral tumor is detected, the main course of surgical treatment is maximal excision despite it possibly being a malignant melanoma and the temptation to perform partial resection because of an unfavorable prognosis. Chemotherapy can be justified in the presence of an aggressive melanotic schwannoma.


Asunto(s)
Neoplasias Encefálicas/cirugía , Melanoma/cirugía , Neurilemoma/cirugía , Procedimientos Neuroquirúrgicos/métodos , Neoplasias Encefálicas/diagnóstico por imagen , Humanos , Antígeno Ki-67/metabolismo , Imagen por Resonancia Magnética , Masculino , Melanoma/complicaciones , Melanoma/diagnóstico por imagen , Antígenos Específicos del Melanoma/metabolismo , Neurilemoma/complicaciones , Neurilemoma/diagnóstico por imagen , Proteínas S100/metabolismo , Tomógrafos Computarizados por Rayos X , Adulto Joven , Antígeno gp100 del Melanoma
5.
Inorg Chem ; 51(2): 1094-103, 2012 Jan 16.
Artículo en Inglés | MEDLINE | ID: mdl-22191576

RESUMEN

Three different perovskite-related phases were isolated in the SrGa(1-x)Sc(x)O(2.5) system: Sr(2)GaScO(5), Sr(10)Ga(6)Sc(4)O(25), and SrGa(0.75)Sc(0.25)O(2.5). Sr(2)GaScO(5) (x = 0.5) crystallizes in a brownmillerite-type structure [space group (S.G.) Icmm, a = 5.91048(5) Å, b = 15.1594(1) Å, and c = 5.70926(4) Å] with complete ordering of Sc(3+) and Ga(3+) over octahedral and tetrahedral positions, respectively. The crystal structure of Sr(10)Ga(6)Sc(4)O(25) (x = 0.4) was determined by the Monte Carlo method and refined using a combination of X-ray, neutron, and electron diffraction data [S.G. I4(1)/a, a = 17.517(1) Å, c = 32.830(3) Å]. It represents a novel type of ordering of the B cations and oxygen vacancies in perovskites. The crystal structure of Sr(10)Ga(6)Sc(4)O(25) can be described as a stacking of eight perovskite layers along the c axis ...[-(Sc/Ga)O(1.6)-SrO(0.8)-(Sc/Ga)O(1.8)-SrO(0.8)-](2).... Similar to Sr(2)GaScO(5), this structure features a complete ordering of the Sc(3+) and Ga(3+) cations over octahedral and tetrahedral positions, respectively, within each layer. A specific feature of the crystal structure of Sr(10)Ga(6)Sc(4)O(25) is that one-third of the tetrahedra have one vertex not connected with other Sc/Ga cations. Further partial replacement of Sc(3+) by Ga(3+) leads to the formation of the cubic perovskite phase SrGa(0.75)Sc(0.25)O(2.5) (x = 0.25) with a = 3.9817(4) Å. This compound incorporates water molecules in the structure forming SrGa(0.75)Sc(0.25)O(2.5)·xH(2)O hydrate, which exhibits a proton conductivity of ∼2.0 × 10(-6) S/cm at 673 K.

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