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Matches in Nanopublications for { ?s ?p "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP722527.RAQzO8UNH3rnqH5w-sDvqCL3ISfU868NGKSM3Ejv32AOQ130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722527.RAQzO8UNH3rnqH5w-sDvqCL3ISfU868NGKSM3Ejv32AOQ130_provenance.
• assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP960550.RAU61yWGdpoOLXifBFzCPc0YMpYEpi4SK36c-IVjNkP0U130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960550.RAU61yWGdpoOLXifBFzCPc0YMpYEpi4SK36c-IVjNkP0U130_provenance.
• NP960551.RAaRSVOaSWMuCcbnGiU0EG6eO7q3Vqqdlv2DC_29UNE_c130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960551.RAaRSVOaSWMuCcbnGiU0EG6eO7q3Vqqdlv2DC_29UNE_c130_provenance.
• NP906507.RAuU_K-YxnGfr0nmQOyqoalMMpFDwj-tPcHgItenGfiw8130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906507.RAuU_K-YxnGfr0nmQOyqoalMMpFDwj-tPcHgItenGfiw8130_provenance.
• NP960546.RAulUQPR0IXzTFFTocdT5bVQZSvvoMjHytmx1wdWNl-fY130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960546.RAulUQPR0IXzTFFTocdT5bVQZSvvoMjHytmx1wdWNl-fY130_provenance.
• NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528667.RA02xwb9-wq9icqgnU1JEszllqd8oNCmqmaHBTAvnVOGY130_provenance.
• NP632376.RA-YQulwoSJ-kNklHt6O0bjBvVl300PGn9P1pF9kA8M3Y130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632376.RA-YQulwoSJ-kNklHt6O0bjBvVl300PGn9P1pF9kA8M3Y130_provenance.
• NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632424.RAxf9A0TQOZv-52aHz24D2vaJJCZ1IJ4jmfGFiNtje6to130_provenance.
• NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960547.RANBQunkNvvsWX_OpWg8f0g0bRBDn0jBK7aug7ecr8Ipg130_provenance.
• NP960552.RAPMtGEJlU8Jj-AUXdabocAOfIMMl50bsJFBzdSqJw-T8130_assertion description "[19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 20-item Disability Index (HAQ-DI), the Symptom Check List-90-Revised (SCL-90-R), the Beck Depression Inventory-Short Form (BDI-SF), the Hamilton Depression Rating Scale (HDRS) and the clinical version of the Structured Clinical Interview for the the DSM-IV (SCID-I and SCID-II) As control, 10 patients with hereditary sensorimotor neuropathy (HN), harboring the peripheral myelin protein-22 (PMP22) mutation were examined with the same tools.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960552.RAPMtGEJlU8Jj-AUXdabocAOfIMMl50bsJFBzdSqJw-T8130_provenance.