<p>Ages at onset of both diabetes mellitus (A) and optic atrophy (B) in each patient in the three groups are shown graphically with the mean age indicated on the vertical axis. Patients are color-coated according to the mutation categories: group 1 (n = 15) in red, group 2 (n = 9) in blue and group 3 (n = 3) in green. The differences between group 1 and group 2 were statistically significant: diabetes mellitus 4.4±1.9 years vs. 13.4±9.9 years, <i>p</i> = 0.008, and optic atrophy 9.6±6.9 years vs. 22.5±12.4 years, <i>p</i> = 0.014, respectively. Data are expressed as means ± SD.</p
Purpose: Leukoencephalopathy with vanishing white matter (VWM) is an autosomal recessive leukoenceph...
<p>Association analysis of the investigated <i>WFS1</i> SNPs and diabetes mellitus by Cochran–Armita...
<div><p>Background</p><p>Wolfram syndrome (WFS) is a recessive neurologic and endocrinologic degener...
<p>*Data are expressed as means±SD.</p><p>Comparison of ages at onset of diabetes mellitus and optic...
<p>*M, male; F, female; DM, diabetes mellitus; OA, optic atrophy; D, deafness; DI, diabetes insipidu...
Purpose: Wolfram syndrome is a degenerative, recessive rare disease with an onset in childhood. It i...
<p>Genotype-wise association analysis of the investigated <i>WFS1</i> SNPs and diabetes mellitus usi...
<p>Graphic representation of the evolution exponential tendency curves of the functional disability ...
OBJECTIVE: To evaluate the pattern of vision loss and genotype-phenotype correlations in WFS1-associ...
International audiencePURPOSE:To search for WFS1 mutations in patients with optic atrophy (OA) and a...
OBJECTIVE — Wolfram syndrome is an extremely rare autosomal-recessive disorder that predisposes the ...
Objective: Wolfram syndrome is an extremely rare autosomal-recessive disorder that predisposes the d...
<p>Allele-wise association analysis of the investigated <i>WFS1</i> SNPs and diabetes mellitus.</p
Objective: Vanishing white matter (VWM) is an autosomal recessive leukoencephalopathy characterized ...
center dot OBJECTIVE: To evaluate the pattern of vision loss and genotype-phenotype correlations in ...
Purpose: Leukoencephalopathy with vanishing white matter (VWM) is an autosomal recessive leukoenceph...
<p>Association analysis of the investigated <i>WFS1</i> SNPs and diabetes mellitus by Cochran–Armita...
<div><p>Background</p><p>Wolfram syndrome (WFS) is a recessive neurologic and endocrinologic degener...
<p>*Data are expressed as means±SD.</p><p>Comparison of ages at onset of diabetes mellitus and optic...
<p>*M, male; F, female; DM, diabetes mellitus; OA, optic atrophy; D, deafness; DI, diabetes insipidu...
Purpose: Wolfram syndrome is a degenerative, recessive rare disease with an onset in childhood. It i...
<p>Genotype-wise association analysis of the investigated <i>WFS1</i> SNPs and diabetes mellitus usi...
<p>Graphic representation of the evolution exponential tendency curves of the functional disability ...
OBJECTIVE: To evaluate the pattern of vision loss and genotype-phenotype correlations in WFS1-associ...
International audiencePURPOSE:To search for WFS1 mutations in patients with optic atrophy (OA) and a...
OBJECTIVE — Wolfram syndrome is an extremely rare autosomal-recessive disorder that predisposes the ...
Objective: Wolfram syndrome is an extremely rare autosomal-recessive disorder that predisposes the d...
<p>Allele-wise association analysis of the investigated <i>WFS1</i> SNPs and diabetes mellitus.</p
Objective: Vanishing white matter (VWM) is an autosomal recessive leukoencephalopathy characterized ...
center dot OBJECTIVE: To evaluate the pattern of vision loss and genotype-phenotype correlations in ...
Purpose: Leukoencephalopathy with vanishing white matter (VWM) is an autosomal recessive leukoenceph...
<p>Association analysis of the investigated <i>WFS1</i> SNPs and diabetes mellitus by Cochran–Armita...
<div><p>Background</p><p>Wolfram syndrome (WFS) is a recessive neurologic and endocrinologic degener...