Matches in Nanopublications for { ?s ?p "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- NP1242292.RAsHyAOBVE8qAI5qxtmMOyuYPwhHHeprR9d_egYkzdGnk130_assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242292.RAsHyAOBVE8qAI5qxtmMOyuYPwhHHeprR9d_egYkzdGnk130_provenance.
- NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_provenance.