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Familial primary progressive aphasia.
Alzheimer Dis Assoc Disord. 2003 Apr-Jun;17(2):106-12. doi: 10.1097/00002093-200304000-00009.
Alzheimer Dis Assoc Disord. 2003.
PMID: 12794388
Prominent phenotypic variability associated with mutations in Progranulin.
Kelley BJ, Haidar W, Boeve BF, Baker M, Graff-Radford NR, Krefft T, Frank AR, Jack CR Jr, Shiung M, Knopman DS, Josephs KA, Parashos SA, Rademakers R, Hutton M, Pickering-Brown S, Adamson J, Kuntz KM, Dickson DW, Parisi JE, Smith GE, Ivnik RJ, Petersen RC.
Kelley BJ, et al.
Neurobiol Aging. 2009 May;30(5):739-51. doi: 10.1016/j.neurobiolaging.2007.08.022. Epub 2007 Oct 18.
Neurobiol Aging. 2009.
PMID: 17949857
Free PMC article.
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Normal pressure hydrocephalus and large head size.
Krefft TA, Graff-Radford NR, Lucas JA, Mortimer JA.
Krefft TA, et al.
Alzheimer Dis Assoc Disord. 2004 Jan-Mar;18(1):35-7. doi: 10.1097/00002093-200401000-00007.
Alzheimer Dis Assoc Disord. 2004.
PMID: 15195461
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Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.
Mesulam M, Johnson N, Krefft TA, Gass JM, Cannon AD, Adamson JL, Bigio EH, Weintraub S, Dickson DW, Hutton ML, Graff-Radford NR.
Mesulam M, et al. Among authors: krefft ta.
Arch Neurol. 2007 Jan;64(1):43-7. doi: 10.1001/archneur.64.1.43.
Arch Neurol. 2007.
PMID: 17210807
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An Iranian family with Alzheimer's disease caused by a novel APP mutation (Thr714Ala).
Pasalar P, Najmabadi H, Noorian AR, Moghimi B, Jannati A, Soltanzadeh A, Krefft T, Crook R, Hardy J.
Pasalar P, et al.
Neurology. 2002 May 28;58(10):1574-5. doi: 10.1212/wnl.58.10.1574.
Neurology. 2002.
PMID: 12034808
No abstract available.
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