Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Surinder Atri"'
Autor:
Rachna Seth, S. K. Kabra, Rajni Sharma, Asis Kumar Karak, Arvind Bagga, Vasantha Thavaraj, Surinder Atri
Publikováno v:
The Indian Journal of Pediatrics. 74:1116-1120
Castleman's disease is an atypical lymphoproliferative disorder having two types of presentation--the localized and the multicentric form. The localized form presents as a slowly growing mass with a relatively benign course. Multicentric Castleman's
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c56e3e0c185c7963062c019816c1f813
https://doi.org/10.1007/s12098-007-0210-z
https://doi.org/10.1007/s12098-007-0210-z
Publikováno v:
NMR in Biomedicine. 16:213-223
The metabolic differences between the muscle biopsies of patients with limb girdle muscular dystrophy (LGMD) and normal controls were characterized using high-resolution 1H and 13C NMR spectroscopy. In all, 44 metabolites were unambiguously assigned
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7891ee2f9550b08d6a04cefe361d4ef0
https://doi.org/10.1002/nbm.832
https://doi.org/10.1002/nbm.832
Autor:
Rajiv Aggarwal, Anup Kumar Das, Nupur Sarkar, Surinder Atri, Ashok K. Deorari, Ramesh Agarwal
Publikováno v:
The Indian Journal of Pediatrics. 69:993-995
Airway malformations such as laryngeal atresia, tracheal agenesis and subglottic stenosis are rare and present at birth with significant respiratory distress with or without stridor. There may be an initial improvement on bag and mask ventilation. Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfcf19912161154a24d4ec915a3c0447
https://doi.org/10.1007/bf02726024
https://doi.org/10.1007/bf02726024
Autor:
Taposh K. Das, Rachna Seth, Veena Kalra, Sheffali Gulati, Surinder Atri, Chitra Sarkar, M. C. Sharma
Publikováno v:
Neurology India. 55(1)
Nemaline rod myopathy (NM) is a rare form of congenital myopathy characterized by slowly progressive or nonprogressive muscle weakness and pathognomonic rod-like structures within the muscle fibers. To the best of our knowledge, this is first documen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d7117137104acd38e63b6e7a0270e69
https://pubmed.ncbi.nlm.nih.gov/17272906
https://pubmed.ncbi.nlm.nih.gov/17272906
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 23(3)
Amongst the mixed glioneuronal tumours, ‘papillary glioneuronal tumour’, a new variant, has been described recently. We report a case of papillary glioneuronal tumour in a 4-year-old boy who presented with fever, weakness of left upper and lower
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80bcf0195b98043344cd95c2f9b2b24e
https://pubmed.ncbi.nlm.nih.gov/17058084
https://pubmed.ncbi.nlm.nih.gov/17058084
Publikováno v:
Magnetic resonance imaging. 21(2)
The metabolic differences in the skeletal muscle of patients with Duchenne muscular dystrophy (DMD) and normal subjects (controls) were investigated using in-vitro high-resolution proton NMR spectroscopy. In all, 56 metabolites were unambiguously ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0344956b80520ddec9696906c7827347
https://pubmed.ncbi.nlm.nih.gov/12670601
https://pubmed.ncbi.nlm.nih.gov/12670601
Publikováno v:
Journal of Neuro-Oncology. 78:103-104
A 55-year old female presented with complaints of progressing weakness of right upper and lower limb for the past 2–3 months and altered sensorium for 5 days. There was no history of vomitings, seizures or any headache. Neurological examination rev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2fe60ac94e94c44ce67ceaae7cead92
https://doi.org/10.1007/s11060-005-9061-5
https://doi.org/10.1007/s11060-005-9061-5
Publikováno v:
Child's Nervous System; Mar2007, Vol. 23 Issue 3, p349-353, 5p
Publikováno v:
NMR in Biomedicine; Jun2003, Vol. 16 Issue 4, p213, 11p
Publikováno v:
Journal of Neuro-Oncology; May2006, Vol. 78 Issue 1, p103-104, 2p