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T Kawarai

Showing results (11-20 of 38) with videos related to

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Neurology|May 26, 2004
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cystsA Orlacchio, F Gaudiello, A Totaro, et al.
Neurology|February 26, 2000
Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusionsA Kertesz, T Kawarai, E Rogaeva, et al.
Neurology|November 13, 2002
Clinical and genetic study of a large Italian family linked to SPG12 locusA Orlacchio, T Kawarai, E Rogaeva, et al.
Molecular Oral Microbiology|June 5, 2013
Effects of short-chain fatty acids on Actinomyces naeslundii biofilm formationS Yoneda, T Kawarai, N Narisawa, et al.
Annals of Neurology|April 13, 2000
A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's diseaseH Morino, T Kawarai, Y Izumi, et al.
Neurology|July 27, 2005
Familial Alzheimer disease: decreases in CSF Abeta42 levels precede cognitive declineM Moonis, J M Swearer, M P E Dayaw, et al.
Revue Neurologique|December 17, 2004
[Familial fronto-temporal dementia with brain stem ubiquitin-positive neuronal inclusions]A C Bruni, T Kawarai, M G Spillantini, et al.
European Journal of Neurology|September 19, 2017
Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutationT Konno, K Yoshida, I Mizuta, et al.
European Journal of Neurology|September 30, 2016
Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutationT Konno, K Yoshida, T Mizuno, et al.
Neurology|October 15, 2003
PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifierE Rogaeva, C Bergeron, C Sato, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Neurology|May 26, 2004
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cystsA Orlacchio, F Gaudiello, A Totaro, et al.
Neurology|February 26, 2000
Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusionsA Kertesz, T Kawarai, E Rogaeva, et al.
Neurology|November 13, 2002
Clinical and genetic study of a large Italian family linked to SPG12 locusA Orlacchio, T Kawarai, E Rogaeva, et al.
Molecular Oral Microbiology|June 5, 2013
Effects of short-chain fatty acids on Actinomyces naeslundii biofilm formationS Yoneda, T Kawarai, N Narisawa, et al.
Annals of Neurology|April 13, 2000
A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's diseaseH Morino, T Kawarai, Y Izumi, et al.
Neurology|July 27, 2005
Familial Alzheimer disease: decreases in CSF Abeta42 levels precede cognitive declineM Moonis, J M Swearer, M P E Dayaw, et al.
Revue Neurologique|December 17, 2004
[Familial fronto-temporal dementia with brain stem ubiquitin-positive neuronal inclusions]A C Bruni, T Kawarai, M G Spillantini, et al.
European Journal of Neurology|September 19, 2017
Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutationT Konno, K Yoshida, I Mizuta, et al.
European Journal of Neurology|September 30, 2016
Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutationT Konno, K Yoshida, T Mizuno, et al.
Neurology|October 15, 2003
PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifierE Rogaeva, C Bergeron, C Sato, et al.
Pageof 4