Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rashika Jain"'
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 9, Iss 11, Pp 5759-5762 (2020)
Hepatic hemangioma is a commonly encountered benign vascular tumour of liver during infancy. Acquired hypothyroidism is one of the rare manifestation of this entity. We report a 4-month-old infant born to a diabetic mother who developed acquired hypo
Externí odkaz:
https://doaj.org/article/20576b8d677f4978a32bd5c5c6590b82
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 9, Iss 8, Pp 4467-4469 (2020)
X-linked lissencephaly, absent corpus callosum, and epilepsy of neonatal onset with ambiguous genitalia are the classical features of XLAG syndrome and as of now very few cases have been reported in the literature. In this study, we present the case
Externí odkaz:
https://doaj.org/article/95c8bf0716d4488b9750f6ffd21e57f0
Publikováno v:
2022 IEEE Aerospace Conference (AERO).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eca4e72bc3a75c7f8cb5116cf267f594
https://doi.org/10.1109/aero53065.2022.9843529
https://doi.org/10.1109/aero53065.2022.9843529
Autor:
Rashika Jain
Publikováno v:
SJCC Management Research Review. :128-146
High level of NPAs leads to loss of income on one hand and on the other hand heavy provisioning requirements on NPAs leads to further erosion of already depleted profits. For any economy which is striving for achieving reasonable growth rate with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c004e8d8dce6469cfa1d975dd8ce3c6b
https://doi.org/10.35737/sjccmrr/v9/i1/2019/145550
https://doi.org/10.35737/sjccmrr/v9/i1/2019/145550
Publikováno v:
Journal of Family Medicine and Primary Care
Journal of Family Medicine and Primary Care, Vol 9, Iss 8, Pp 4467-4469 (2020)
Journal of Family Medicine and Primary Care, Vol 9, Iss 8, Pp 4467-4469 (2020)
X-linked lissencephaly, absent corpus callosum, and epilepsy of neonatal onset with ambiguous genitalia are the classical features of XLAG syndrome and as of now very few cases have been reported in the literature. In this study, we present the case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebb341df09d1a735082528867229f8dd
https://doi.org/10.4103/jfmpc.jfmpc_922_20
https://doi.org/10.4103/jfmpc.jfmpc_922_20