Matches in Nanopublications for { ?s ?p "[Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn alpha-motoneurons and manifesting in the first 6months of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP856998.RADYWPVPxGoOv4F18fnVyzNguiSQWKn5NElIG_Eaw9zaw130_assertion description "[Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn alpha-motoneurons and manifesting in the first 6months of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856998.RADYWPVPxGoOv4F18fnVyzNguiSQWKn5NElIG_Eaw9zaw130_provenance.
- NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_assertion description "[Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn alpha-motoneurons and manifesting in the first 6months of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_provenance.
- NP483588.RAyOsXe8qMPSsMIHX7buOPT6LQ3OUkq82UqoLD7jmgRXs130_assertion description "[Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn alpha-motoneurons and manifesting in the first 6months of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483588.RAyOsXe8qMPSsMIHX7buOPT6LQ3OUkq82UqoLD7jmgRXs130_provenance.
- NP557206.RAsWy6EIhJDTmJY0UMKsX_31k-Pa77XlF9NRqkD_sii_Y130_assertion description "[Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn alpha-motoneurons and manifesting in the first 6months of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557206.RAsWy6EIhJDTmJY0UMKsX_31k-Pa77XlF9NRqkD_sii_Y130_provenance.