VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q90690258 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241221010739.0
008 241221nneanz||abbn n and d
035 ‎‡a (WKP)Q90690258‏
024 ‎‡a 0000-0002-8970-2740‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q90690258‏
100 0 ‎‡a W Ludo van der Pol‏ ‎‡c researcher (ORCID 0000-0002-8970-2740)‏ ‎‡9 en‏
400 0 ‎‡a W Ludo van der Pol‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's Comparing the NIS vs. MRC and INCAT sensory scale through Rasch analyses‏
670 ‎‡a Author's Correlates of fatigability in patients with spinal muscular atrophy‏
670 ‎‡a Author's Genetic overlap between apparently sporadic motor neuron diseases‏
670 ‎‡a Author's Grip strength comparison in immune-mediated neuropathies: Vigorimeter vs. Jamar‏
670 ‎‡a Author's Impairment measures versus inflammatory RODS in GBS and CIDP: a responsiveness comparison‏
670 ‎‡a Author's Muscle strength and motor function in adolescents and adults with spinal muscular atrophy‏
670 ‎‡a Author's Muscle strength and motor function throughout life in a cross- sectional cohort of 180 patients with SMA types 1c-4.‏
670 ‎‡a Author's Mutations in the TRPV4 gene are not associated with sporadic progressive muscular atrophy‏
670 ‎‡a Author's Natural course of scoliosis and lifetime risk of scoliosis surgery in spinal muscular atrophy‏
670 ‎‡a Author's Outcome measures in MMN revisited: further improvement needed‏
670 ‎‡a Author's Population-based analysis of survival in spinal muscular atrophy‏
670 ‎‡a Author's Rasch-built Overall Disability Scale for Multifocal motor neuropathy (MMN-RODS(©) ).‏
670 ‎‡a Author's T2 relaxation-time mapping in healthy and diseased skeletal muscle using extended phase graph algorithms‏
670 ‎‡a Author's VCP mutations in familial and sporadic amyotrophic lateral sclerosis‏
909 ‎‡a (orcid) 0000000289702740‏ ‎‡9 1‏
919 ‎‡a outcomemeasuresinmmnrevisitedfurtherimprovementneeded‏ ‎‡A Outcome measures in MMN revisited: further improvement needed‏ ‎‡9 1‏
919 ‎‡a t2relaxationtimemappinginhealthyanddiseasedskeletalmuscleusingextendedphasegraphalgorithms‏ ‎‡A T2 relaxation-time mapping in healthy and diseased skeletal muscle using extended phase graph algorithms‏ ‎‡9 1‏
919 ‎‡a vcpmutationsinfamilialandsporadicamyotrophiclateralsclerosis‏ ‎‡A VCP mutations in familial and sporadic amyotrophic lateral sclerosis‏ ‎‡9 1‏
919 ‎‡a naturalcourseofscoliosisandlifetimeriskofscoliosissurgeryinspinalmuscularatrophy‏ ‎‡A Natural course of scoliosis and lifetime risk of scoliosis surgery in spinal muscular atrophy‏ ‎‡9 1‏
919 ‎‡a mutationsinthetrpv4genearenotassociatedwithsporadicprogressivemuscularatrophy‏ ‎‡A Mutations in the TRPV4 gene are not associated with sporadic progressive muscular atrophy‏ ‎‡9 1‏
919 ‎‡a musclestrengthandmotorfunctionthroughoutlifeinacrosssectionalcohortof180patientswithsmatypes1c4‏ ‎‡A Muscle strength and motor function throughout life in a cross- sectional cohort of 180 patients with SMA types 1c-4.‏ ‎‡9 1‏
919 ‎‡a musclestrengthandmotorfunctioninadolescentsandadultswithspinalmuscularatrophy‏ ‎‡A Muscle strength and motor function in adolescents and adults with spinal muscular atrophy‏ ‎‡9 1‏
919 ‎‡a impairmentmeasuresversusinflammatoryrodsingbsandcidparesponsivenesscomparison‏ ‎‡A Impairment measures versus inflammatory RODS in GBS and CIDP: a responsiveness comparison‏ ‎‡9 1‏
919 ‎‡a gripstrengthcomparisoninimmunemediatedneuropathiesvigorimetervsjamar‏ ‎‡A Grip strength comparison in immune-mediated neuropathies: Vigorimeter vs. Jamar‏ ‎‡9 1‏
919 ‎‡a geneticoverlapbetweenapparentlysporadicmotorneurondiseases‏ ‎‡A Genetic overlap between apparently sporadic motor neuron diseases‏ ‎‡9 1‏
919 ‎‡a correlatesoffatigabilityinpatientswithspinalmuscularatrophy‏ ‎‡A Correlates of fatigability in patients with spinal muscular atrophy‏ ‎‡9 1‏
919 ‎‡a comparingthenisvsmrcandincatsensoryscalethroughraschanalyses‏ ‎‡A Comparing the NIS vs. MRC and INCAT sensory scale through Rasch analyses‏ ‎‡9 1‏
919 ‎‡a raschbuiltoveralldisabilityscaleformultifocalmotorneuropathymmnrods‏ ‎‡A Rasch-built Overall Disability Scale for Multifocal motor neuropathy (MMN-RODS(©) ).‏ ‎‡9 1‏
919 ‎‡a populationbasedanalysisofsurvivalinspinalmuscularatrophy‏ ‎‡A Population-based analysis of survival in spinal muscular atrophy‏ ‎‡9 1‏
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996 ‎‡2 NLA|000035774442
996 ‎‡2 NTA|408071281
996 ‎‡2 LIH|LNB:DH0W;=1A
996 ‎‡2 LIH|LNB:V-63282;=BH
996 ‎‡2 DNB|1191380769
996 ‎‡2 NYNYRILM|175532
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏