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Scholar Results 1 - 10 of about 101 related to Cano: Microvascular Diabetes Complications in Wolfram Syndrome (Diabetes Insipidus, Diabetes.... (0.11 sec) 

Microvascular Diabetes Complications in Wolfram Syndrome (Diabetes Insipidus, Diabetes …


A Cano, L Molines, R Valéro, G Simonin, V … - Diabetes Care, 2007 - Am Diabetes Assoc
OBJECTIVE—Some previous studies suggested that patients suffering from Wolfram
syndrome or DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and
deafness) might be relatively preserved from diabetic retinopathy and ...
Related articles - BL Direct - All 4 versions

Microvascular diabetic complications in Wolfram Syndrome (DIDMOAD): an age-and …


A CanoMD, L Molines, MD René Valéro, G … - Am Diabetes Assoc
Page 1. Microvascular diabetic complications in Wolfram Syndrome (DIDMOAD): an age-
and duration-matched comparison with common Type 1 diabetes. ...
Related articles

Microvascular diabetic complications in Wolfram Syndrome (DIDMOAD): an age-and …

- diabetesjournals.org [PDF] 
A Cano, L Molines, R Valéro, G Simonin, V … - Diabetes Care, 2007 - Am Diabetes Assoc
Page 1. Microvascular diabetic complications in Wolfram Syndrome (DIDMOAD): an age-
and duration-matched comparison with common Type 1 diabetes. ...
Related articles - All 2 versions

Renal failure in two patients with Wolfram syndrome.


… A Vongjirad, V Suntornpoch, K Angsusingha … - Journal of pediatric endocrinology & metabolism: JPEM - ncbi.nlm.nih.gov
We describe a Thai family with three children, two of whom presented with
Wolfram syndrome, which is a rare syndrome characterised by diabetes insipidus,
diabetes mellitus, optic atrophy, deafness and urinary tract dilatation. A ...
Cited by 6 - Related articles - BL Direct - All 2 versions

A Chinese family with Wolfram syndrome presenting with rapidly progressing diabetic …


MC Lim, AC Thai - Annals of the Academy of Medicine, Singapore, 1990 - ncbi.nlm.nih.gov
We describe a Chinese family with three siblings, all females, presenting with
the Wolfram Syndrome. All three cases had almost similar clinical presentation
of insulin-dependent diabetes mellitus, with rapid development of severe ...
Cited by 6 - Related articles - All 2 versions

[CITATION] Detection, monitoring and treatment of diabetic retinopathy. Recommendations of ALFEDIAM …


P Massin, K Angioi-Duprez, F Bacin, B … - Diabetes & metabolism, 1996 - ncbi.nlm.nih.gov
1: Diabetes Metab. 1996 Jun;22(3):203-9. [Detection, monitoring and treatment
of diabetic retinopathy. Recommendations of ALFEDIAM. ...
Cited by 7 - Related articles

Contrasting features of insulin dependent diabetes mellitus associated with neuroectodermal …


PP Garcia-Luna, E Villechenous, A Leal- … - Acta Pædiatrica - interscience.wiley.com
ABSTRACT. The Wolfram, or DIDMOAD, syndrome is a rare congenital disease that is
associated with diabetes insipidus, insulin dependent diabetes mellitus of an
early onset, bilateral optic atrophy and deafness. Urological disorders are ...
Cited by 8 - Related articles - All 4 versions

Four cases of Wolfram syndrome: ophthalmologic findings and complications.


H Seynaeve, A Vermeiren, A Leys, L Dralands - Bulletin de la Société belge d'ophtalmologie, 1994 - ncbi.nlm.nih.gov
The association of diabetes insipidus, diabetes mellitus, optic atrophy and
deafness (DIDMOAD) is known as Wolfram syndrome. The ophthalmic signs are
progressive decrease in visual acuity, constriction of the peripheral ...
Cited by 8 - Related articles - BL Direct - All 3 versions

Unabhängigkeit von Retinopathie und Optikusatrophie beim DIDMOAD-Syndrom …


R Hennekes, S Koletzko, H Hockauf - Klin Monatsbl Augenheilkd, 1984 - thieme-connect.com
Ein Geschwisterpaar mit DIDMOAD-Syndrom (Diabetes insipidus, Diabetes mellitus,
Optikusatrophie, perzeptiver Schwerhörigkeit - deafness -, Atonie der
ableitenden Harnwege und anderen - fakultativen - Symptomen) wurde ...
Cited by 4 - Related articles - All 2 versions

Wolfram syndrome in French population: characterization of novel mutations and …


F Giuliano, S Bannwarth, S Monnot, A Cano, B … - Human Mutation, 2005 - interscience.wiley.com
Wolfram syndrome (WS), a rare autosomal recessive neurodegenerative disorder,
results in most cases from mutations in the WFS1 gene. In this study, a total of
19 patients with Wolfram syndrome and 36 relatives from 17 families were ...
Cited by 13 - Related articles - All 2 versions


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