Zobrazeno 1 - 6
of 6
pro vyhledávání: '"SANDEEPAN HALDER"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 7, Pp XD12-XD13 (2017)
Polyneuropathy, Organomegaly, Endocrinopathy, M protein and Skin changes (POEMS) syndrome is rare plasma cell dyscrasia with multisystem involvement. The name comes from the five characteristic features: Polyneuropathy, organomegaly, endocrinopathy,
Externí odkaz:
https://doaj.org/article/8e046ca45e454aedadbababff342250d
Autor:
Sunil Vitthalrao Jagtap, Sushama Desai, Sandeepan Halder, Swati S. Jagtap, Anuya Shrikant Badwe
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 3, Pp 117-118 (2014)
Adrenocortical carcinoma (ACC) is an extremely rare tumour. We are reporting a 45-year-male patient who had a history of sudden severe worsening epigastric pain and fullness in abdomen, with giddiness. The radiological investigations showed a large
Externí odkaz:
https://doaj.org/article/806a036c9dab4556b5c507c807cc94ae
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 7, Pp XD12-XD13 (2017)
Polyneuropathy, Organomegaly, Endocrinopathy, M protein and Skin changes (POEMS) syndrome is rare plasma cell dyscrasia with multisystem involvement. The name comes from the five characteristic features: Polyneuropathy, organomegaly, endocrinopathy,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::affc7d4ddfeb8a4fafed47affe653d90
https://jcdr.net/articles/PDF/10265/24800_CR_PF1(RB_SS)_PFA(RB_SS).pdf
https://jcdr.net/articles/PDF/10265/24800_CR_PF1(RB_SS)_PFA(RB_SS).pdf
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 34(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d33a40b5a999f8ef2743d17dade0f5e0
https://pubmed.ncbi.nlm.nih.gov/29398832
https://pubmed.ncbi.nlm.nih.gov/29398832
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 17:e148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6925a2f0619d963e00372d51a9a5d4e
https://doi.org/10.1016/j.clml.2017.03.266
https://doi.org/10.1016/j.clml.2017.03.266
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 3, Pp 117-118 (2014)
Adrenocortical carcinoma (ACC) is an extremely rare tumour. We are reporting a 45-year-male patient who had a history of sudden severe worsening epigastric pain and fullness in abdomen, with giddiness. The radiological investigations showed a large r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8fb93c02e6340627a83592c9e9e5210