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Nejvíce citované: 15977647

1 citací v PubMed Filtry

Nejvíce citovaný článek - PubMed ID 15977647

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Článek

Genetic heterogeneity of neuronal intranuclear inclusion disease: What about the infantile variant?

Sikora, Jakub
Autor Sikora, Jakub ORCID Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic Institute of Pathology, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic
Jedlickova, Ivana
Autor Jedlickova, Ivana Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic
Pristoupilova, Anna
Autor Pristoupilova, Anna Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic
Stranecky, Viktor
Autor Stranecky, Viktor Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic
Honzik, Tomas
Autor Honzik, Tomas Research Unit for Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic

Annals of clinical and translational neurology. 2021 Apr ; 8 (4) : 994-1001. [epub] 20210329

Ann Clin Transl Neurol
ISSN 2328-9503
Zdroj

MeSH
genetická heterogenita * MeSH
intranukleární inkluzní tělíska MeSH
lidé MeSH
neurodegenerativní nemoci * genetika MeSH
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lidé MeSH
Publikační typ
dopisy MeSH
komentáře MeSH
práce podpořená grantem MeSH