Zobrazeno 1 - 10
of 114
pro vyhledávání: '"N. Sreedevi"'
Publikováno v:
Global Medical Genetics, Vol 10, Iss 02, Pp 105-108 (2023)
Congenital disorder of glycosylation (CDG) is an autosomal recessively inherited disorder. Hypotonia, stroke-like episodes, and peripheral neuropathy are also associated with the condition that typically develops during infancy. The patient, a 12-yea
Externí odkaz:
https://doaj.org/article/2b66589928614bfc8e5ed01baa054e8d
Publikováno v:
F1000Research, Vol 6 (2017)
Microcephaly is a genetically heterogeneous disorder and is one of the frequently notable conditions in paediatric neuropathology which exists either as a single entity or in association with other co-morbidities. More than a single gene is implicate
Externí odkaz:
https://doaj.org/article/f73cd3a162ea4b8ebe9a52c31c0ec0bc
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue, Pp 82-82 (2017)
DNA sequencing technologies played a critical role in the last two decades in expanding our understanding of genetic spectrum behind neurodevelopmental disorders. Recently, induction MPS in the area of medical genetics provided chance for differentia
Externí odkaz:
https://doaj.org/article/c854bd3b6ae84b9c885ba97028f839c7
Autor:
Lakshmi Deepika Yarlagadda, Rachel Jacob, D Liza Rajasekhar, Krishna Mohan Iyyapu, Sai Baba S S. Kompella, Vijaya Bhaskar Madrol, N N Sreedevi, Siraj Ahmed Khan, Noorjahan Mohammed
Publikováno v:
Indian Journal of Rheumatology, Vol 15, Iss 3, Pp 175-180 (2020)
Context: The lack of sensitivity and specificity of the existing diagnostic markers in Rheumatoid arthritis (RA) stimulates the search for new biomarkers to improve diagnostic sensitivity especially in seronegative cases. Aims: To estimate the levels
Externí odkaz:
https://doaj.org/article/c8ec00ab1d4047629f7e69e90617d5dc
Publikováno v:
Indian Journal of Otolaryngology and Head & Neck Surgery. 75:16-22
Autor:
Nair, M. Krishnan, Nambi, K. S. V., Amma, N. Sreedevi, Gangadharan, P., Jayalekshmi, P., Jayadevan, S., Cherian, Varghese, Reghuram, K. Nair
Publikováno v:
Radiation Research, 1999 Dec 01. 152(6), S145-S148.
Externí odkaz:
https://www.jstor.org/stable/3580134
Autor:
N. Sreedevi, Anusmitha Mathew
Publikováno v:
Journal of Hearing Science. 12:49-59
BackgroundSpeech sound errors are often exhibited by children with hearing impairment. Articulatory error pattern analyses show a tendency towards vowel substitutions and consonant omissions. There is a dearth of literature on the articulatory charac
Association of apolipoprotein ε4 allele with intellectual disability in children with cerebral palsy
Publikováno v:
Archives of Mental Health.
Autor:
S. Savitha, N. Sreedevi
Publikováno v:
Innovations in Computer Science and Engineering ISBN: 9789811974540
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95a0ba0ce3df108b9e20a19785324c07
https://doi.org/10.1007/978-981-19-7455-7_54
https://doi.org/10.1007/978-981-19-7455-7_54
Autor:
V Monish, N Sreedevi
Publikováno v:
IP Journal of Otorhinolaryngology and Allied Science. 4:149-152
Aim of the work was to highlight the speech and swallowing difficulties that are associated with osmotic demyelination syndrome and also the importance of speech and language therapy in patients with osmotic demyelination syndrome. In this case repor