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Matches in Nanopublications for { ?s ?p "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP923733.RAsr5fdVix5VszcqIRdXUvCKLDzucLKOMt1GnDoXC3TGs130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923733.RAsr5fdVix5VszcqIRdXUvCKLDzucLKOMt1GnDoXC3TGs130_provenance.
• NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718211.RAps6oCy3c4D8a7lxJBijXdGV25BCsEP9Z6rv6mA1qZHc130_provenance.
• NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908690.RAcbtEZ0_9t6KWrs_rxV1ulu9MJXRKrfQ4hKV3ArCwQ8Q130_provenance.
• NP913072.RAdMAULvK3PCLHKDjK0hjwCr4dHVAl5XsBEjrgu1pA37Q130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913072.RAdMAULvK3PCLHKDjK0hjwCr4dHVAl5XsBEjrgu1pA37Q130_provenance.
• NP580712.RAjUKwP2TZeQchcYvmtW9bOyTIDoEjv-U3_-_nsX3hJsM130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580712.RAjUKwP2TZeQchcYvmtW9bOyTIDoEjv-U3_-_nsX3hJsM130_provenance.
• NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596324.RAYehc4N2lcOAwIgjCsO5Q1QSE56haRbAMfXwzTxERsAg130_provenance.
• NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596502.RAV_f7SBOcEryXAZMmbB4-rschir0hY8S7ekmdlKJgyWw130_provenance.
• NP768803.RA7mvMibt_DZ_0YbjUEg32dwbjMEXeBV_jAgfpoll6sv0130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768803.RA7mvMibt_DZ_0YbjUEg32dwbjMEXeBV_jAgfpoll6sv0130_provenance.
• assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
• NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491457.RAar7AFbFOiVe97Mgg0Xq3u3dvP2OL8eF_rs8wpLH5ngk130_provenance.
• NP491456.RAPfQgUjgjhciXcgTWuiKo3os8JZ63AnkOIYdQyxAqb3w130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491456.RAPfQgUjgjhciXcgTWuiKo3os8JZ63AnkOIYdQyxAqb3w130_provenance.
• NP491458.RALlhiJ6pOF_UdQUJOBBjhfNdM-kXNaOrgmQ9zYmp9F04130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491458.RALlhiJ6pOF_UdQUJOBBjhfNdM-kXNaOrgmQ9zYmp9F04130_provenance.
• NP491459.RA6apZFObXCx72jBpaIeudL_lmsir1dSTbenAZDwWpGBs130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491459.RA6apZFObXCx72jBpaIeudL_lmsir1dSTbenAZDwWpGBs130_provenance.