Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Deependra mandal"'
Autor:
Parash Rayamajhi, Janak Khadka, Pravesh Bhattarai, Anjana Bohaju, Apsara Adhikari, Deependra Mandal
Publikováno v:
Journal of Nepal Medical Association, Vol 62, Iss 269 (2024)
Introduction: Diabetes mellitus is a major public health concern and a continuously growing chronic disease worldwide. Diabetes mellitus is one of the modifiable, independent, and major risk factors of ischemic stroke. This study aimed to find the pr
Externí odkaz:
https://doaj.org/article/53eb651f850b43a1b9fc534c336bbb2d
Publikováno v:
Journal of Nepal Medical Association, Vol 61, Iss 257 (2023)
Congenital Adrenal Hyperplasia is a group of autosomal recessive diseases due to deficiencies of enzymes involved in steroidogenesis. If not diagnosed and treated adequately, Congenital Adrenal Hyperplasia can lead to an acute adrenal crisis with hem
Externí odkaz:
https://doaj.org/article/63c25c7763154b3184805b7ca5ddbc6a
Autor:
Tunam Khadka, Ganesh Kumar Giri, Deependra Mandal, Ashmita Shrestha, Alok Dhungel, Abhinav Vaidya
Publikováno v:
Journal of Nepal Medical Association, Vol 61, Iss 257 (2023)
Introduction: Multimorbidity is defined as the co-occurrence of two or more chronic conditions in the same individual. Type 2 Diabetes Mellitus rarely occurs without coexisting diseases. With an increasing elder population and longevity, elder adults
Externí odkaz:
https://doaj.org/article/193b7bc475204e16b047e823451cf5c8
Publikováno v:
Journal of Nepal Medical Association, Vol 58, Iss 232 (2020)
Posterior reversible encephalopathy syndrome is a clinical-radiological syndrome neurological disorder with varied symptoms which include headache, visual field defects, seizures, altered consciousness. It is a rare complication of post-streptococcal
Externí odkaz:
https://doaj.org/article/247cbf789a594a329b9733070525fbd1
Publikováno v:
Journal of Nepal Medical Association, Vol 58, Iss 225 (2020)
Though squamous cell carcinoma is the commonest tumor, it rarely presents in the middle ear and follows a history of chronic ear discharge. Postauricular mastoid fistula is also a rare complication of chronic otitis media. These two pathological chan
Externí odkaz:
https://doaj.org/article/436e7d48b42c48f5a7f3aba5a1d6bff7
Publikováno v:
Journal of Nepal Medical Association, Vol 58, Iss 224 (2020)
Fecalith is a concretion of dry compact feces or hard stony mass of faeces in the intestinal tract. Though appendicular fecoliths are commonly encountered, caecal fecoliths are rare entities. Fecoliths are amenable to conservative management with lax
Externí odkaz:
https://doaj.org/article/c49d07bcc6a04c0d95b5f787b3192719
Autor:
Mandeeep Guragai, Deependra Mandal
Publikováno v:
Journal of Nepal Medical Association, Vol 58, Iss 224 (2020)
NA
Externí odkaz:
https://doaj.org/article/ec8a4f6cedca40d4a164eb207450cfeb
Publikováno v:
Journal of Nepal Medical Association, Vol 58, Iss 221 (2020)
Congenital Adrenal Hyperplasia is a group of autosomal recessive disorders due to deficiencies of enzymes involved in steroidogenesis. The most common form is a 21-hydroxylase deficiency which can be classical or non-classical. The severe form also c
Externí odkaz:
https://doaj.org/article/02b0c711fc1048ab8f33da8d25ff4546
Publikováno v:
JNMA: Journal of the Nepal Medical Association
Journal of Nepal Medical Association, Vol 58, Iss 224 (2020)
Journal of Nepal Medical Association, Vol 58, Iss 224 (2020)
Fecalith is a concretion of dry compact feces or hard stony mass of faeces in the intestinal tract. Thoughappendicular fecoliths are commonly encountered, caecal fecoliths are rare entities. Fecoliths areamenable to conservative management with laxat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e979ee53fdce0fd8a7f249826221fb8a
http://europepmc.org/articles/PMC7580469
http://europepmc.org/articles/PMC7580469
Publikováno v:
JNMA: Journal of the Nepal Medical Association
Journal of Nepal Medical Association, Vol 58, Iss 221 (2020)
Journal of Nepal Medical Association, Vol 58, Iss 221 (2020)
Congenital Adrenal Hyperplasia is a group of autosomal recessive disorders due to deficiencies of enzymes involved in steroidogenesis. The most common form is a 21-hydroxylase deficiency which can be classical or non-classical. The severe form also c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f0e9ef485538e87079fa8f02f01500a
http://europepmc.org/articles/PMC7580480
http://europepmc.org/articles/PMC7580480