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1.
J Food Sci ; 88(4): 1268-1279, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-36919247

RESUMO

Cahokia Rice, a new biofortified high-protein (10%-12%) variety of rice, was used to develop and analyze a gluten-free pasta. Different pastas were made with high-protein white rice flour (HPWRP), high-protein brown rice flour (HPBRP), commercial white rice flour (CWRP), commercial brown rice flour (CBRP), and wheat flour (WP). Cooking quality of the pasta was evaluated by measuring pasting properties, cooking time, water absorption capacity, and cooking loss. Proximate analysis, color, and texture were done on dry and cooked pasta. Sensory testing was done to determine consumer acceptability and purchase intent of HPWRP and HPBRP in comparison to WP. HPWRP and HPBRP had higher pasting temperatures and lower peak viscosity than commercial rice flour pastas, which was related to the higher protein content. HPWRP and HPBRP had less cooking loss than CWRP and CBRP; all treatments had similar water absorption capacity (∼130%) except for WP that was higher (140%). White rice pastas along with WP took more time to cook than brown rice pastas. HPWRP and HPBRP had higher protein (around 7.5%) and fat content, creating a firmer cooked pasta (138.23 g HPBRP, 179.82 g HPWRP) than commercial rice pastas. Consumers' overall liking of HPBRP (5.37), HPWRP (6.00), and WP (6.81) was acceptable. Color, firmness, and stickiness attributes negatively affected the overall liking of HPWRP and HPBRP. Cooked high-protein rice flour pastas had improved firmness and cooking loss closer to wheat resulting in an acceptable product in overall liking. It is recommended to further improve the color, firmness, and stickiness of the pasta to reach higher sensory acceptability. PRACTICAL APPLICATION: This research provides a possible use for a new high-protein rice flour that can be used in gluten-free products. This will help the rice industry by adding value to the product. Those persons who are Celiac or who desire more nutritional gluten-free products will have a healthier gluten-free pasta option.


Assuntos
Farinha , Oryza , Culinária/métodos , Dieta Livre de Glúten , Farinha/análise , Triticum , Água
2.
Rev Neurol ; 58(12): 529-35, 2014 Jun 16.
Artigo em Espanhol | MEDLINE | ID: mdl-24915028

RESUMO

INTRODUCTION: Tuberous sclerosis complex (TSC) is frequently accompanied by difficult-to-treat epilepsy, which conditions these patients' quality of life and cognitive level. AIM. To describe the epidemiological and clinical characteristics, as well as the treatment of patients affected by TSC with epilepsy. PATIENTS AND METHODS: A retrospective review was carried out of the medical records of 30 patients aged under 18 registered in our database, who had been diagnosed with TSC and epilepsy. RESULTS: The age at onset of epilepsy in the patients with TSC in our series ranged from one month to four years. All of them began with partial crises. Two presented West's syndrome and four others had infantile spasms without hypsarrhythmia. In 19 of the patients, the epilepsy was medication resistant. As regards treatment with antiepileptic drugs, 11 are in monotherapy, 10 in bitherapy, seven in tritherapy and one with four drugs. Two were given ACTH, two carry an implanted vagal nerve stimulator, four receive treatment with everolimus and eight have undergone surgery. CONCLUSIONS: Epilepsy is a very common problem and begins in the early years of life in TSC. There are currently a large number of therapeutic options available, although 63.3% of patients have non-controlled epilepsy and most of them present crises on a daily basis. Poor control of their crises is correlated with mental retardation and autism spectrum disorder. The positive response obtained with other therapeutic possibilities, such as mTOR pathway inhibitors, surgery and vagal nerve stimulator, should be noted.


TITLE: Posibilidades terapeuticas en la epilepsia refractaria en el complejo esclerosis tuberosa.Introduccion. El complejo esclerosis tuberosa (CET) cursa frecuentemente con epilepsia de dificil control, lo que condiciona la calidad de vida y el nivel cognitivo de estos pacientes. Objetivo. Describir las caracteristicas epidemiologicas, clinicas y el tratamiento de los pacientes afectos de CET con epilepsia. Pacientes y metodos. Se han revisado retrospectivamente las historias clinicas de 30 pacientes menores de 18 años, diagnosticados de CET y epilepsia registrados en nuestra base de datos. Resultados. La edad de inicio de la epilepsia en los pacientes con CET en nuestra serie esta comprendida entre el primer mes de vida y los 4 años. Todos comenzaron con crisis parciales. Dos presentaron sindrome de West y cuatro, espasmos infantiles sin hipsarritmia. En 19 de los pacientes, la epilepsia se comporto como farmacorresistente. Respecto al tratamiento con farmacos antiepilepticos, 11 estan en monoterapia, 10 en biterapia, siete en triterapia y uno con cuatro farmacos. Dos recibieron ACTH, dos tienen implantado un estimulador del nervio vago, cuatro reciben tratamiento con everolimus y ocho han sido sometidos a cirugia. Conclusiones. La epilepsia es un problema muy frecuente y de inicio en los primeros años de vida en el CET. Las opciones terapeuticas actuales son muchas, sin embargo el 63,3% de los pacientes tiene una epilepsia no controlada y la mayoria de ellos presenta crisis diarias. El mal control de las crisis se correlaciona con retraso mental y trastorno del espectro autista. Señalar la respuesta positiva obtenida con otras posibilidades terapeuticas: inhibidores de la via mTOR, cirugia y el estimulador del nervio vago.


Assuntos
Epilepsias Parciais/terapia , Esclerose Tuberosa/complicações , Hormônio Adrenocorticotrópico/uso terapêutico , Idade de Início , Anticonvulsivantes/uso terapêutico , Astrocitoma/etiologia , Astrocitoma/fisiopatologia , Astrocitoma/cirurgia , Neoplasias Encefálicas/etiologia , Neoplasias Encefálicas/fisiopatologia , Neoplasias Encefálicas/cirurgia , Criança , Transtornos Globais do Desenvolvimento Infantil/etiologia , Pré-Escolar , Terapia Combinada , Resistência a Medicamentos , Quimioterapia Combinada , Epilepsias Parciais/etiologia , Epilepsias Parciais/cirurgia , Everolimo , Feminino , Humanos , Lactente , Recém-Nascido , Deficiência Intelectual/etiologia , Masculino , Estudos Retrospectivos , Sirolimo/análogos & derivados , Sirolimo/uso terapêutico , Espasmos Infantis/etiologia , Espasmos Infantis/terapia , Serina-Treonina Quinases TOR/antagonistas & inibidores , Esclerose Tuberosa/cirurgia , Estimulação do Nervo Vago
3.
Rev. venez. cir. ortop. traumatol ; 37(1): 7-16, jun. 2005. ilus, tab, graf
Artigo em Espanhol | LILACS | ID: lil-513568

RESUMO

Estudio prospectivo con inyecciones de Toxina Botulínica A en niños con espasticidad por PCI. Se dividió en 2 grupos: 10 casos con marcha patológica establecida (Grup A) y 10 casos sin potencial o inicio de marcha (Grupo B). En el grupo A: se logró mejor patrón, mayor movilidad articular, disminuir temporalmente espasticidad y posponer cirugía ortopédica en el 80 por ciento. En el grupo B: facilitar fisioterapia, uso de férulas, mejor rango articular en igual porcentaje (4/10 casos iniciaron marcha asistida). El Botox representa importante ayuda para niños con PCI espástica durante los primeros años.


Assuntos
Especialidade de Fisioterapia , Espasticidade Muscular/terapia , Paralisia Cerebral/terapia , Toxinas Botulínicas Tipo A/uso terapêutico , Traumatologia , Neurologia , Venezuela
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