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Author/Creator Synofzik, Matthis

1. [P4–189]: SYMPTOM ONSET IN GENETIC FRONTOTEMPORAL DEMENTIA. (1st July 2017)

Authors:
Dick, Katrina M.; van Swieten, John C.; Gerhard, Alexander; Le Ber, Isabelle; Frisoni, Giovanni B.; Dickerson, Bradford C.; Graff, Caroline; Ghoshal, Nupur; Borroni, Barbara; Galimberti, Daniela; Mackenzie, Ian R.; Synofzik, Matthis; Sanchez‐Valle, Raquel; Santana, Isabel; Moreno, Fermin; Levin, ...
Journal:
Alzheimer's & dementia
Issue:
Volume 13:Supplement 7S(2017)Part 28
Page Start:
P1337
Record Type:
Journal Article
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2. A cognitive composite for genetic frontotemporal dementia: GENFI‐cog. (31st December 2021)

Authors:
Poos, Jackie M.; Nicholas, Jennifer M; Moore, Katrina M; Russell, Lucy L; Peakman, Georgia; Jiskoot, Lize C.; van den Berg, Esther; Papma, Janne M.; Seelaar, Harro; Pijnenburg, Yolande A.L.; Moreno, Fermin; Sanchez‐Valle, Raquel; Borroni, Barbara; Laforce, Robert; Masellis, Mario; Tartaglia, Mari...
Journal:
Alzheimer's & dementia
Issue:
Volume 17(2021)Supplement 6
Page Start:
n/a
Record Type:
Journal Article
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3. A data‐driven disease progression model of fluid biomarkers in genetic FTD. (31st December 2021)

Authors:
van der Ende, Emma; Bron, Esther E.; Poos, Jackie M.; Jiskoot, Lize C.; Panman, Jessica L.; Papma, Janne M.; Wilke, Carlo; Synofzik, Matthis; Heller, Carolin; Swift, Imogen J.; Esteve, Aitana Sogorb; Bouzigues, Arabella; Borroni, Barbara; Sanchez‐Valle, Raquel; Moreno, Fermin; Graff, Caroline; La...
Journal:
Alzheimer's & dementia
Issue:
Volume 17(2021)Supplement 5
Page Start:
n/a
Record Type:
Journal Article
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4. A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort. Issue 1 (2nd January 2022)

Authors:
Moore, Katrina; Convery, Rhian; Bocchetta, Martina; Neason, Mollie; Cash, David M.; Greaves, Caroline; Russell, Lucy L.; Clarke, Mica T. M.; Peakman, Georgia; van Swieten, John; Jiskoot, Lize; Moreno, Fermin; Barandiaran, Myriam; Sanchez-Valle, Raquel; Borroni, Barbara; Laforce, Robert; Doré, Mar...
Journal:
Applied neuropsychology
Issue:
Volume 29:Issue 1(2022)
Page Start:
112
Record Type:
Journal Article
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5. A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats. Issue 2 (4th January 2013)

Authors:
van der Zee, Julie; Gijselinck, Ilse; Dillen, Lubina; Van Langenhove, Tim; Theuns, Jessie; Engelborghs, Sebastiaan; Philtjens, Stéphanie; Vandenbulcke, Mathieu; Sleegers, Kristel; Sieben, Anne; Bäumer, Veerle; Maes, Githa; Corsmit, Ellen; Borroni, Barbara; Padovani, Alessandro; Archetti, Silvana;...
Journal:
Human mutation
Issue:
Volume 34:Issue 2(2013:Feb.)
Page Start:
363
Record Type:
Journal Article
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6. A recessive ataxia diagnosis algorithm for the next generation sequencing era. Issue 6 (21st November 2017)

Authors:
Renaud, Mathilde; Tranchant, Christine; Martin, Juan Vicente Torres; Mochel, Fanny; Synofzik, Matthis; van de Warrenburg, Bart; Pandolfo, Massimo; Koenig, Michel; Kolb, Stefan A.; Anheim, Mathieu
Other Names:
Alonso Isabel investigator.; Azzedine Hamid investigator.; Barbot Clara investigator.; Bereau Matthieu investigator.; Berkovic Sam investigator.; Bernard Geneviéve investigator.; Bindoff Laurence A. investigator.; Bompaire Flavie investigator.; Bonneau Dominique investigator.; Bonneau Patrizia in...
Journal:
Annals of neurology
Issue:
Volume 82:Issue 6(2017)
Page Start:
892
Record Type:
Journal Article
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7. A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. Issue 4 (9th September 2016)

Authors:
Helbig, Katherine L.; Hedrich, Ulrike B.S.; Shinde, Deepali N.; Krey, Ilona; Teichmann, Anne‐Christin; Hentschel, Julia; Schubert, Julian; Chamberlin, Adam C.; Huether, Robert; Lu, Hsiao‐Mei; Alcaraz, Wendy A.; Tang, Sha; Jungbluth, Chelsy; Dugan, Sarah L.; Vainionpää, Leena; Karle, Kathrin N.; S...
Journal:
Annals of neurology
Issue:
Volume 80:Issue 4(2016:Oct.)
Page Start:
n/a
Record Type:
Journal Article
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8. Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort. Issue 12 (5th August 2020)

Authors:
Convery, Rhian S; Bocchetta, Martina; Greaves, Caroline V; Moore, Katrina M; Cash, David M; Van Swieten, John; Moreno, Fermin; Sánchez-Valle, Raquel; Borroni, Barbara; Laforce Jr, Robert; Masellis, Mario; Tartaglia, Maria Carmela; Graff, Caroline; Galimberti, Daniela; Rowe, James B; Finger, Eliza...
Other Names:
author non-byline.; Rossor M N author non-byline.; Fox N C author non-byline.; Woollacott I O C author non-byline.; Shafei R author non-byline.; Heller C author non-byline.; Peakman G author non-byline.; Swift I author non-byline.; Todd E author non-byline.; Guerreiro R author non-byline.; Bras ...
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 91:Issue 12(2020)
Page Start:
1325
Record Type:
Journal Article
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10. Adult‐Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERDND): Time to Move Beyond the Skin. Issue 8 (14th June 2022)

Authors:
Cordts, Isabell; Önder, Demet; Traschütz, Andreas; Kobeleva, Xenia; Karin, Ivan; Minnerop, Martina; Koertvelyessy, Peter; Biskup, Saskia; Forchhammer, Stephan; Binder, Johannes; Tzschach, Andreas; Meiss, Frank; Schmidt, Axel; Kreiß, Martina; Cremer, Kirsten; Mensah, Martin A.; Park, Joohyun; Raut...
Journal:
Movement disorders
Issue:
Volume 37:Issue 8(2022)
Page Start:
1707
Record Type:
Journal Article
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