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Baker, Matthew

https://orcid.org/0000-0002-0002-1907

A5064561010 | I1330342723

Mayo Clinic

Citations 52

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)

Neurology | May 13, 2012 | Volume: 59 | Issue: 11 | Pages: 1791-1793

10.1212/01.wnl.0000038909.49164.4b | PMID 12473774

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers

Neurology | December 22, 2010 | Volume: 76 | Issue: 5 | Pages: 467-474

10.1212/wnl.0b013e31820a0e3b | PMID 21178100

Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?

Neurology | December 14, 2010 | Volume: 75 | Issue: 24 | Pages: 2212-2220

10.1212/wnl.0b013e31820203c2 | PMID 21172844

P2‐379: (18)F‐Fluorodeoxyglucose positron emission tomography in presymptomatic progranulin mutation carriers

Alzheimer's & Dementia | July 11, 2010 | Volume: 6 | Issue: 4S_Part_14 | Pages: No page available

10.1016/j.jalz.2010.05.1431

IC‐O1‐04: Patterns of brain atrophy in frontotemporal dementia with mutations in MAPT or PGRN

Alzheimer's & Dementia | June 25, 2009 | Volume: 5 | Issue: 4S_Part_1 | Pages: No page available

10.1016/j.jalz.2009.05.014

P3‐212: Patterns of brain atrophy in frontotemporal dementia with mutations in MAPT or PGRN

Alzheimer's & Dementia | June 25, 2009 | Volume: 5 | Issue: 4S_Part_13 | Pages: No page available

10.1016/j.jalz.2009.04.985

P1‐059: Hippocampal sclerosis (HpScl) in the elderly with dementia: Clinical, genetic and pathologic findings

Alzheimer's & Dementia | June 25, 2009 | Volume: 5 | Issue: 4S_Part_6 | Pages: No page available

10.1016/j.jalz.2009.04.063

Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN

Neurology | March 2, 2009 | Volume: 72 | Issue: 9 | Pages: 813-820

10.1212/01.wnl.0000343851.46573.67 | PMID 19255408

Plasma amyloid β protein is elevated in late-onset Alzheimer disease families

Neurology | October 3, 2007 | Volume: 70 | Issue: 8 | Pages: 596-606

10.1212/01.wnl.0000278386.00035.21 | PMID 17914065

Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1

Neurology | September 6, 2007 | Volume: 70 | Issue: 16_part_2 | Pages: 1377-1383

10.1212/01.wnl.0000275527.35752.c5 | PMID 17804835