Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 14 de 14
Filtrar
Añadir filtros








Intervalo de año
1.
Indian J Cancer ; 2013 Apr-June; 50(2): 107-111
Artículo en Inglés | IMSEAR | ID: sea-148633

RESUMEN

Background: The Medical Oncology Department at Tata Memorial Hospital, the single largest tertiary cancer care center in Asia, receives in-house registered and referral patient samples from all parts of the country. Our recent studies establish 23% EGFR mutation frequency among Indian population. Here, we extend our study and report further analysis of distribution of different types of EGFR mutations in 1018 non small cell lung cancer patient, and its co-relation with clinical parameters and geographical variations across the country. Material and Methods: This study is a retrospective analysis on all the patients who were referred for EFGR testing as a routine service over a 1.5 year period. This was part of standard care. EGFR kinase domain mutations in exon 18-21 were probed by TaqMan probe-based assays in 1018 NSCLC patients. Results and Discussion: While EGFR exon 19 mutations, the most frequent EGFR mutation, were found be higher among non smokers females, we find surprisingly higher incidence of exon 21 mutations among EGFR mutation positive male smokers of Indian ethnicity. Furthermore, as Indian population is known to be composed of a gradient admixture of Ancestral North Indian (with genetic influence from Middle Easterners, Central Asians, and Europeans harboring variant EGFR mutation frequency) and Ancestral South Indians, as a paradox our study indicates comparable EGFR mutation frequency across different geographical locations within India Conclusion: Geographically there is uniform distribution in the EGFR mutation frequency within India. Further more, while exon 19 mutations are predominant among non smokers, higher incidence of exon 21 mutations exists among EGFR mutation positive male smokers of Indian ethnicity.


Asunto(s)
Pueblo Asiatico/genética , Carcinoma de Pulmón de Células no Pequeñas/genética , Carcinoma de Pulmón de Células no Pequeñas/patología , Genética de Población , Humanos , India , Epidemiología Molecular , Mutación , Receptores ErbB/genética
2.
Neurol India ; 2002 Jun; 50(2): 158-61
Artículo en Inglés | IMSEAR | ID: sea-121630

RESUMEN

An attempt was made to correlate various types of visual field defects on automated perimetry with the findings of computed tomography in 44 patients of supratentorial tumors. All the patients above the age of 10 years were subjected to complete neurological examination including investigations like plain X-rays and CT scan, however, MRI and angiography were performed wherever indicated. Ocular examination particularly pertaining to neuro-ophthalmological profile was carried out with special emphasis on automated perimetry on Humphrey field analyser. The results indicated that automated perimetry was capable of reliably detecting and quantitating the visual field defects and thus established the location of the tumor in 72% patients when compared to CT scan. Hence, any patient with neuro-ophthalmic features should be subjected to automated perimetry for early diagnosis and probable location of intracranial space occupying lesion affecting visual pathways.


Asunto(s)
Adulto , Automatización , Neoplasias Cerebelosas/diagnóstico , Femenino , Humanos , Masculino , Pruebas del Campo Visual , Tomografía Computarizada por Rayos X , Trastornos de la Visión/diagnóstico , Campos Visuales
6.
10.
12.
J Indian Med Assoc ; 1955 Mar; 24(12): 460-1
Artículo en Inglés | IMSEAR | ID: sea-101541
13.
J Indian Med Assoc ; 1954 May; 23(8): 336-8
Artículo en Inglés | IMSEAR | ID: sea-100520
14.
J Indian Med Assoc ; 1951 Jul; 20(10): 365-8
Artículo en Inglés | IMSEAR | ID: sea-103495

Asunto(s)
Otitis Media
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA