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diabetes insipidus-diabetes mellitus-optic atrophy-deafness syndrome相关文献:
[Wolfram syndrome or diabetes insipidus-diabetes mellitus-optic atrophy-deafness syndrome].
PMID:
Successful pregnancy in the DIDMOAD syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, deafness).
PMID:
[DIDMOAD syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) with cerebello-pontine atrophy].
PMID:
The syndrome of diabetes insipidus, diabetes mellitus, optic atrophy, deafness, and other abnormalities (DIDMOAD-syndrome). Two affected sibs and a short review of the literature (98 cases).
Dreyer M, Rüdiger HW, Bujara K, Herberhold C, Kühnau J, Maack P, Bartelheimer H.
Klin Wochenschr. 1982 May 3;60(9):471-5. doi: 10.1007/BF01720362.
PMID:7045512
Wolfram Syndrome presenting with optic atrophy and diabetes mellitus: two case reports.
Manaviat MR, Rashidi M, Mohammadi SM.
Cases J. 2009 Dec 19;2:9355. doi: 10.1186/1757-1626-2-9355.
PMID:20062605
Successful pregnancy in the DIDMOAD syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, deafness).
Wilson JD, Moore G.
Aust N Z J Obstet Gynaecol. 1995 Feb;35(1):100-1. doi: 10.1111/j.1479-828x.1995.tb01844.x.
PMID:7771984
Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy.
Scolding NJ, Kellar-Wood HF, Shaw C, Shneerson JM, Antoun N.
Ann Neurol. 1996 Mar;39(3):352-60. doi: 10.1002/ana.410390312.
PMID:8602754
Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease.
Rigoli L, Bramanti P, Di Bella C, De Luca F.
Pediatr Res. 2018 May;83(5):921-929. doi: 10.1038/pr.2018.17. Epub 2018 Feb 28.
PMID:29774890
[DIDMOAD syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) with cerebello-pontine atrophy].
Kehl O, Keller U.
Schweiz Med Wochenschr. 1982 Mar 6;112(10):348-52.
PMID:7079680
The syndrome of diabetes insipidus, diabetes mellitus, optic atrophy, deafness and other abnormalities (DIDMOAD, Wolfram syndrome).
Panamonta O, Vitoonchart C, Chitpimonmas P.
J Med Assoc Thai. 1987 Sep;70(9):531-5.
PMID:3681183
[From gene to disease; mutations in the WFS1-gene as the cause of juvenile type I diabetes mellitus with optic atrophy (Wolfram syndrome)].
Pennings RJ, Dikkeschei LD, Cremers CW, van den Ouweland JM.
Ned Tijdschr Geneeskd. 2002 May 25;146(21):985-7.
PMID:12058630
MRI of Wolfram syndrome (DIDMOAD).
Galluzzi P, Filosomi G, Vallone IM, Bardelli AM, Venturi C.
Neuroradiology. 1999 Oct;41(10):729-31. doi: 10.1007/s002340050832.
PMID:10552021
The subtle signs of Wolfram (DIDMOAD) syndrome: not all juvenile diabetes is type 1 diabetes.
Boettcher C, Brosig B, Zimmer KP, Wudy SA.
J Pediatr Endocrinol Metab. 2011;24(1-2):71-4. doi: 10.1515/jpem.2011.114.
PMID:21528819
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