Zobrazeno 1 - 10
of 142
pro vyhledávání: '"M. Rohatgi"'
Autor:
Christy Lyona, Satishkumar S. Chavan, Mayura Gavhane, Joyce Menezes, Ragini M. Rohatgi, Tushar Shinde
Publikováno v:
2020 2nd International Conference on Advances in Computing, Communication Control and Networking (ICACCCN).
Diabetic retinopathy (DR) is an advanced stage of retinal disease with increasing prevalence and the major cause of blindness. In DR, blood vessels get damaged over time at the back of the retina. Large numbers of retinal images are generated as diab
Akademický článek
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Akademický článek
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Publikováno v:
Developmental Medicine & Child Neurology. 16:144-151
SUMMARY The results are presented of intraventricular and intrathecal risa studies in 25 children with myelomeningocele. Scans of the head and neck were done in all cases, and in five patients composite scans were done to cover the head, neck and tru
Publikováno v:
Documenta Ophthalmologica. 83:271-278
Optic nerve (ON) damage especially from papilloedema can be prevented with timely detection. The detailed ocular and radiographic status of 33 unoperated craniosynostosis (CS) was documented prospectively; the ON was also assessed by flash VER and A-
Autor:
Amanpreet Sethi, P. S. N. Menon, A. K. Gupta, Anju Virmani, I. C. Verma, Dikshi Gupta, M. Rohatgi
Publikováno v:
The Indian Journal of Pediatrics. 59:531-535
During 1981-88, 63 cases of female pseudohermaphroditism (FPH) were seen at the Intersex clinic at AIIMS, of whom 34 (54%) were diagnosed as due to congenital adrenal hyperplasia (CAH). Though ambiguity was present at birth in most cases, only one ch
Autor:
M. Rohatgi
Publikováno v:
Acta Neurochirurgica. 108:45-52
This is a study of 6 patients of cloverleaf skull (CLS) who were treated between 1980 and 1988. All of them had mild to severe degree of craniofacial dysostosis of Crouzon type with variable degrees of exorbitism (pseudoexophthalmus), raised intracra
Kniha
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Publikováno v:
Annals of Saudi medicine. 14(2)
Publikováno v:
Journal of pediatric surgery. 27(9)
A rare case of single system cecoureterocele associated with ipsilateral dysplastic kidney in a 4-year-old girl is reported. The preoperative radiological and endoscopic investigations identified ureterocele but not its cecal extension. The latter wa