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Claudius Bartels

Showing results (11-20 of 14) with videos related to

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Journal of Clinical Medicine|May 20, 2020
Clinical, Radiological, and Laboratory Features of Spinal Cord Involvement in Primary Sjögren's SyndromeMichaela Butryn, Jens Neumann, Leoni Rolfes, et al.
Journal of Neuro-Oncology|May 6, 2020
Neurocognitive functioning and health-related quality of life in adult medulloblastoma patients: long-term outcomes of the NOA-07 studyLinda Dirven, Ralf Luerding, Dagmar Beier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 20, 2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2023
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Journal of Clinical Medicine|May 20, 2020
Clinical, Radiological, and Laboratory Features of Spinal Cord Involvement in Primary Sjögren's SyndromeMichaela Butryn, Jens Neumann, Leoni Rolfes, et al.
Journal of Neuro-Oncology|May 6, 2020
Neurocognitive functioning and health-related quality of life in adult medulloblastoma patients: long-term outcomes of the NOA-07 studyLinda Dirven, Ralf Luerding, Dagmar Beier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 20, 2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2023
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
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