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pigmentation,edema,polyneuropathy syndrome相关文献:
Syndrome of plasma cell dyscrasia, polyneuropathy, and endocrine disturbances. Report of a case.
Imawari M, Akatsuka N, Ishibashi M, Beppu H, Suzuki H.
Ann Intern Med. 1974 Oct;81(4):490-3. doi: 10.7326/0003-4819-81-4-490.
PMID:4416017
Kennedy Disease Misdiagnosed as Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes (POEMS) Syndrome: A Case Report.
Yuan M, Chen W, Zhou H, Xiao Z, Wang W, Wang W, Yin X, Xu L.
Med Princ Pract. 2016;25(3):286-9. doi: 10.1159/000442822. Epub 2015 Nov 30.
PMID:26618536
Syndrome of polyneuropathy, skin hyperpigmentation, oedema and hepatosplenomegaly.
Tang LM, Hsi MS, Ryu SJ, Minauchi Y.
J Neurol Neurosurg Psychiatry. 1983 Dec;46(12):1108-14. doi: 10.1136/jnnp.46.12.1108.
PMID:6663309
Polyneuropathy, skin hyperpigmentation, edema, and hypertrichosis in localized osteosclerotic myeloma.
Iwashita H, Ohnishi A, Asada M, Kanazawa Y, Kuroiwa Y.
Neurology. 1977 Jul;27(7):675-81. doi: 10.1212/wnl.27.7.675.
PMID:559975
Plasma cell dyscrasia with polyneuropathy and endocrine disorder: clinical and laboratory features of 109 reported cases.
Takatsuki K, Sanada I.
Jpn J Clin Oncol. 1983 Sep;13(3):543-55.
PMID:6315993
Accelerated conversion of androgen to estrogen in plasma-cell dyscrasia associated with polyneuropathy, anasarca, and skin pigmentation.
Matsumine H.
N Engl J Med. 1985 Oct 17;313(16):1025-6. doi: 10.1056/NEJM198510173131616.
PMID:2995806
[POEMS syndrome: report of a case and review of the literature].
Castro Ríos MA, Kniznik DO.
Medicina (B Aires). 1990;50(2):149-52.
PMID:2101848
[Marked endocrine abnormalities in polyneuritis with skin hyperpigmentation, hypertrichosis, edema and increased lambda type immunoglobulin A: a case report].
Yoshida T, Kumakura H, Asato H, Sugano J, Yanagisawa H.
Nihon Naibunpi Gakkai Zasshi. 1983 Sep 20;59(9):1237-43. doi: 10.1507/endocrine1927.59.9_1237.
PMID:6416899
[A case of anaphylactoid shock occurring immediately after the initiation of second intravenous administration of high-dose immunoglobulin (IVIg) in a patient with Crow-Fukase syndrome].
Takahashi T, Ono S, Ogawa K, Tamura M, Mizutani T.
Rinsho Shinkeigaku. 2003 Jun;43(6):350-5.
PMID:14503355
[A case of Crow-Fukase syndrome which developed seven years following myelopathy of unknown origin].
Furuzono H, Moritoyo T, Yamada H, Sugihara R, Nagamatsu K.
Rinsho Shinkeigaku. 1993 Jan;33(1):56-60.
PMID:8334776
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