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abdominal aortic aneurysm
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1. Autor: Suchopár, Josef
MeSH:
Isodesmosine-analogs & derivatives
MeSH:
Thrombocytopenia-ethnology
MeSH:
Trigeminal Nerve Diseases-classification
MeSH:
MutS Proteins-toxicity
MeSH:
Lactates-biosynthesis
MeSH:
Furcation Defects-prevention & control
MeSH:
Syndecans-urine
MeSH:
Secologanin Tryptamine Alkaloids-standards
MeSH:
Xanthomonas-ultrastructure
MeSH:
Auricularia-ultrastructure
MeSH:
Nucleosides-ultrastructure
Autor:
Velková, Alice
Pracoviště:
Sanofi Research and Development Vitry Sur Seine
MeSH:
Calcium Signaling-immunology
MeSH:
Mycosphaerella-isolation & purification
Autor:
Phdungsilp, Aumnad
MeSH:
Ligases-poisoning
MeSH:
Erythema Induratum-diagnostic imaging
MeSH:
plyometrická cvičení
MeSH:
percepce tíhy
MeSH:
Receptors, Cytoplasmic and Nuclear-classification
Nejvíce citované:
23883322
Nejvíce citovaný článek - PubMed ID 23883322
Homozygous EXOSC3 mutation c.92G→C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma
Journal of neurogenetics.
2013 Dec ;
27 (4) :
163-9.
[epub] 20130725