<p>Abbreviations: WMH, white matter hyperintensities; NA, not available.</p><p>Characteristics of patients with a <i>NOTCH3</i> mutation.</p
OBJECTIVE: To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 v...
BACKGROUND AND PURPOSE: The most common monogenic cause of cerebral small-vessel disease is cerebral...
Background and Purpose—The most common monogenic cause of cerebral small-vessel disease is cerebral ...
<p>Clinical features of three families carrying pathogenic <i>NOTCH1</i> mutations.</p
<p>Phenotypic characteristics (means and standard deviation) of patients with the p.Gly56Arg mutatio...
<p>Clinical characteristics of <i>EGFR</i> mutation (M) and wildtype (wt) cohorts.</p
Clinicopathological characteristics and associations with somatic mutation status in 313 breast canc...
<p>Clinical and disease characteristics of patients with EGFR gene TKI-sensitive mutations and patie...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy, the most...
<p>The upper panel 1 shows images from patient 1 (R169C), and the lower panel two shows images from ...
Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopat...
Objective To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 v...
To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 variants in ...
<p>Phenotypes of patients homozygous and/or heterozygous for the p. Ala1003Thr missense mutation rep...
To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 variants in ...
OBJECTIVE: To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 v...
BACKGROUND AND PURPOSE: The most common monogenic cause of cerebral small-vessel disease is cerebral...
Background and Purpose—The most common monogenic cause of cerebral small-vessel disease is cerebral ...
<p>Clinical features of three families carrying pathogenic <i>NOTCH1</i> mutations.</p
<p>Phenotypic characteristics (means and standard deviation) of patients with the p.Gly56Arg mutatio...
<p>Clinical characteristics of <i>EGFR</i> mutation (M) and wildtype (wt) cohorts.</p
Clinicopathological characteristics and associations with somatic mutation status in 313 breast canc...
<p>Clinical and disease characteristics of patients with EGFR gene TKI-sensitive mutations and patie...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy, the most...
<p>The upper panel 1 shows images from patient 1 (R169C), and the lower panel two shows images from ...
Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopat...
Objective To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 v...
To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 variants in ...
<p>Phenotypes of patients homozygous and/or heterozygous for the p. Ala1003Thr missense mutation rep...
To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 variants in ...
OBJECTIVE: To determine the small vessel disease spectrum associated with cysteine-altering NOTCH3 v...
BACKGROUND AND PURPOSE: The most common monogenic cause of cerebral small-vessel disease is cerebral...
Background and Purpose—The most common monogenic cause of cerebral small-vessel disease is cerebral ...
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