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You searched for: Author/Creator Rademakers, Rosa

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1. [O2–18–01]: TDP‐43 PATHOLOGY DISRUPTS NUCLEAR PORE COMPLEXES AND NUCLEOCYTOPLASMIC TRANSPORT IN ALS/FTD. (1st July 2017)

2. [P1–254]: CHARACTERISTICS AND PROGRESS ON THE INITIAL 209 SUBJECTS IN THE LONGITUDINAL EVALUATION OF FAMILIAL FRONTOTEMPORAL DEMENTIA SUBJECTS (LEFFTDS) PROTOCOL. (1st July 2017)

4. [P2–303]: ADVANCING RESEARCH AND TREATMENT IN FRONTOTEMPORAL LOBAR DEGENERATION (ARTFL) NORTH AMERICAN RARE DISEASE CLINICAL RESEARCH CONSORTIUM: PROGRESS AND CHARACTERIZATION OF INITIAL PARTICIPANTS. (1st July 2017)

5. [P2–317]: PHENOCONVERSION FROM ASYMPTOMATIC TO MINIMALLY SYMPTOMATIC FTLD: PRELIMINARY DATA IN THE LEFFTDS COHORT. (1st July 2017)

6. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories. Issue 6 (4th April 2014)

7. A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease. Issue 11 (November 2015)

8. Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers. (August 2017)

9. Adult polyglucosan body disease with GBE1 haploinsufficiency and concomitant frontotemporal lobar degeneration. Issue 6 (October 2014)

10. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. Issue 2 (February 2020)