Published Data Registry

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TitleAuthorsJournalPublication year
DOI
PMID
A TRAPPC6B splicing variant associates to restless legs syndrome.Aridon P, De Fusco M, (...), Casari GParkinsonism & related disorders2016
Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy.(Open Access) Kremer LS, Distelmaier F, (...), Haack TBAmerican journal of human genetics2016
Occurrence of Anti-Drug Antibodies against Interferon-Beta and Natalizumab in Multiple Sclerosis: A Collaborative Cohort Analysis.(Open Access) Bachelet D, Hässler S, (...), Broët PPloS one2016
A restricted period for formation of outer subventricular zone defined by Cdh1 and Trnp1 levels.(Open Access) Martínez-Martínez MÁ, De Juan Romero C, Fernández V, Cárdenas A, Götz M, Borrell VNature communications2016
NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood.(Open Access) Kremer LS, Danhauser K, (...), Prokisch HAmerican journal of human genetics2016
BACE1 Physiological Functions May Limit Its Use as Therapeutic Target for Alzheimer's Disease.Barão S, Moechars D, Lichtenthaler SF, De Strooper BTrends in neurosciences2016
Single-cell in vivo imaging of adult neural stem cells in the zebrafish telencephalon.(Open Access) Barbosa JS, Di Giaimo R, Götz M, Ninkovic JNature protocols2016
Adult neural stem cell behavior underlying constitutive and restorative neurogenesis in zebrafish.(Open Access) Barbosa JS, Ninkovic JNeurogenesis (Austin, Tex.)2016
Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9.(Open Access) Danhauser K, Herebian D, (...), Distelmaier FEuropean journal of human genetics : EJHG2016
A Novel Imaging Marker for Small Vessel Disease Based on Skeletonization of White Matter Tracts and Diffusion Histograms.Baykara E, Gesierich B, (...), Duering MAnnals of neurology2016