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Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes
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Scopri
Tipologia
- 1 Contributo su Rivista22627
- 2 Contributo in Volume2
Data di pubblicazione
- In corso di stampa18
- 2020 - 20267683
- 2010 - 20198635
- 2000 - 20093794
- 1990 - 19991811
- 1980 - 1989642
- 1973 - 197945
Editore
- Academic Press, Elsevier2
- Elsevier2
- Wiley-Blackwell2
- Betham Science Publishers Ltd1
- EDIZIONI MINERVA MEDICA1
- Elsevier Ltd1
- Frontiers Media S.A.1
- Harold H. Trimm, Willam Hunter1
- ieee1
- Morgan Kaufmann1
Rivista
- JOURNAL OF CLINICAL MEDICINE216
- PLOS ONE178
- INTERNATIONAL JOURNAL OF MOLECULA...163
- EPILEPSIA123
- NUTRIENTS119
- SCIENTIFIC REPORTS110
- THE JOURNAL OF CLINICAL ENDOCRINO...103
- CANCERS101
- NEUROLOGICAL SCIENCES88
- NEUROLOGY88
Keyword
- Humans1111
- Female551
- Male482
- COVID-19334
- Aged329
- Middle Aged314
- Adult282
- Italy184
- SARS-CoV-2172
- Treatment Outcome153
Lingua
- eng17064
- ita2504
- spa46
- fre28
- ger20
- und11
- por2
- rus2
- aze1
- bos1
Accesso al fulltext
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