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Weniger Treffer
Art der Quelle
Thema
- medicine 82 Treffer
- middle aged 77 Treffer
- medicine.disease 75 Treffer
- biology 66 Treffer
- adult 62 Treffer
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45 weitere Werte:
- aged 62 Treffer
- neurology (clinical) 49 Treffer
- genetic predisposition to disease 39 Treffer
- genotype 39 Treffer
- neurology 36 Treffer
- aged, 80 and over 35 Treffer
- allele 26 Treffer
- gene 23 Treffer
- 03 medical and health sciences 22 Treffer
- 0302 clinical medicine 22 Treffer
- 030217 neurology & neurosurgery 22 Treffer
- business 21 Treffer
- business.industry 21 Treffer
- medicine.medical_specialty 21 Treffer
- mutation 21 Treffer
- parkinson disease 21 Treffer
- pedigree 21 Treffer
- polymorphism, single nucleotide 21 Treffer
- age of onset 20 Treffer
- gene frequency 20 Treffer
- genetic linkage 20 Treffer
- adolescent 19 Treffer
- article 19 Treffer
- genetics (clinical) 19 Treffer
- geriatrics and gerontology 19 Treffer
- 0301 basic medicine 18 Treffer
- 030104 developmental biology 18 Treffer
- asian people 17 Treffer
- case-control studies 17 Treffer
- disease 17 Treffer
- dna mutational analysis 15 Treffer
- young adult 15 Treffer
- genetic variation 14 Treffer
- haplotype 14 Treffer
- medicine.disease_cause 14 Treffer
- risk factors 14 Treffer
- genetic analysis 13 Treffer
- haplotypes 13 Treffer
- internal medicine 13 Treffer
- locus (genetics) 13 Treffer
- nerve tissue proteins 13 Treffer
- single-nucleotide polymorphism 13 Treffer
- allele frequency 12 Treffer
- genome-wide association study 12 Treffer
- phenotype 12 Treffer
Verlag
- elsevier bv 15 Treffer
- springer science and business media llc 10 Treffer
- wiley 8 Treffer
- ovid technologies (wolters kluwer health) 6 Treffer
- escholarship, university of california 4 Treffer
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12 weitere Werte:
- public library of science (plos) 4 Treffer
- cold spring harbor laboratory 1 Treffer
- hal ccsd 1 Treffer
- john wiley and sons inc. 1 Treffer
- mary ann liebert inc 1 Treffer
- nature publishing group 1 Treffer
- nature publishing group uk 1 Treffer
- oxford university press 1 Treffer
- oxford university press (oup) 1 Treffer
- proceedings of the national academy of sciences 1 Treffer
- springer-verlag 1 Treffer
- ubiquity press 1 Treffer
Publikation
- parkinsonism & related disorders 8 Treffer
- neurology 6 Treffer
- neuroscience letters 6 Treffer
- movement disorders 5 Treffer
- parkinsonismrelated disorders 4 Treffer
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33 weitere Werte:
- plos one 4 Treffer
- european journal of human genetics 3 Treffer
- movement disorders : official journal of the movement disorder society 3 Treffer
- neurobiology of aging 3 Treffer
- neurogenetics 3 Treffer
- archives of neurology 2 Treffer
- brain 2 Treffer
- european journal of neurology 2 Treffer
- genetics in medicine 2 Treffer
- human genetics 2 Treffer
- pharmacogenetics and genomics 2 Treffer
- scientific reports 2 Treffer
- acta neurologica scandinavica 1 Treffer
- american journal of medical genetics. part a 1 Treffer
- annals of clinical and translational neurology 1 Treffer
- asn neuro 1 Treffer
- bmc neurology 1 Treffer
- clinical genetics 1 Treffer
- clinical neuropharmacology 1 Treffer
- cns neuroscience & therapeutics 1 Treffer
- european journal of clinical investigation 1 Treffer
- genetic testing and molecular biomarkers 1 Treffer
- journal of clinical neuroscience : official journal of the neurosurgical society of australasia 1 Treffer
- journal of human genetics 1 Treffer
- journal of molecular neuroscience : mn 1 Treffer
- journal of neurology 1 Treffer
- medicine 1 Treffer
- nature genetics 1 Treffer
- neurological sciences 1 Treffer
- neuromolecular medicine 1 Treffer
- proceedings of the national academy of sciences 1 Treffer
- proceedings of the national academy of sciences of the united states of america 1 Treffer
- twin research and human genetics : the official journal of the international society for twin studies 1 Treffer
Sprache
Inhaltsanbieter
94 Treffer
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In: Brain, Jg. 129 (2006-09-01), Heft 9Online academicJournal
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In: Genetics in Medicine, Jg. 3 (2001-05-01), Heft 3Online academicJournal
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In: Annals of Clinical and Translational Neurology, Jg. 8 (2020-11-01), Heft 1, S. 119-125Online unknownZugriff:
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In: CNS Neuroscience & Therapeutics, Jg. 26 (2020-03-20), S. 837-841Online unknownZugriff:
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In: Twin research and human genetics : the official journal of the International Society for Twin Studies, Jg. 24 (2021-03-25), Heft 2Online unknownZugriff:
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In: Neuroscience letters, Jg. 740 (2020-05-12)Online unknownZugriff:
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In: Genetic Testing and Molecular Biomarkers, Jg. 22 (2018-06-01), S. 398-402Online unknownZugriff:
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In: Journal of Human Genetics, Jg. 62 (2017-03-16), S. 641-646Online unknownZugriff:
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In: BMC Neurology, Jg. 19 (2019-05-15)Online unknownZugriff:
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In: European Journal of Human Genetics, Jg. 24 (2015-10-28), S. 1009-1015Online unknownZugriff:
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Genetic analysis of ten common degenerative hereditary ataxia loci in patients with essential tremorIn: Parkinsonism & Related Disorders, Jg. 21 (2015-08-01), S. 943-947Online unknownZugriff:
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In: PLOS ONE, Jg. 14 (2019-08-12), S. e0220512Online unknownZugriff:
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In: Parkinsonismrelated disorders, Jg. 53 (2017-11-04)Online unknownZugriff:
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In: Scientific Reports, Jg. 7 (2017-08-01)Online unknownZugriff:
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In: Neuroscience Letters, Jg. 593 (2015-04-01), S. 114-117Online unknownZugriff:
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In: Parkinsonismrelated disorders, Jg. 43 (2017-04-14)Online unknownZugriff:
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In: European journal of clinical investigation, Jg. 47 (2016-09-30), Heft 5Online unknownZugriff: