Skip to main content
Sem resultados.
 
Linha de Apoio ao Cliente Unilabs
2ª a 6ª das 8h00 às 20h00
sábado das 8h30 às 13h00
Neurologia

Neurology

WES by CGC Genetics (whole exome sequencing, including CNV analysis)
Movement diseases (WES based NGS panel of 905 genes, including CNV analysis)
Hereditary peripheral neuropathies, including Charcot-Marie-Tooth disease (WES based NGS panel of 178 genes, including CNV analysis)
Generalized epilepsy with febrile seizures plus type 1 (GEFS+, sequence analysis of SCN1B gene)
Parkinson disease and parkinsonism (NGS panel of 56 genes)
Torsion dystonia (DYT1, GAG deletion on TOR1A gene)
Hereditary dementias (NGS panel of 44 genes)
Hereditary spastic paraplegias (deletion/duplication analysis of REEP1 and SPG7 genes)
Hereditary ataxias (WES based NGS panel of 214 genes, including CNV analysis)
Familial hemiplegic migraine type 1 (FHM1, sequence analysis of CACNA1A gene)
Hereditary chorea (WES based NGS panel of 14 genes, including CNV analysis)
Familial cerebral small vessel disease (NGS panel of 15 genes)
Congenital muscular dystrophies (NGS panel for 31 genes)
Limb-girdle muscular dystrophies (NGS panel of 42 genes)
Structural diseases of basal ganglia (WES based NGS panel of 72 genes, including CNV analysis)
Hereditary amyloidosis (NGS panel of 19 genes)
Myopathies, including congenital myopathies (WES based NGS panel of 180 genes, including CNV analysis)
Progressive external ophthalmoplegia (sequence analysis of POLG gene)
x

Bem-vindo ao Unilabs.pt

Visitar unilabs.com

OU ESCOLHA UM PAÍS UNILABS DA LISTA