T Kawarai
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Explore the profile of T Kawarai including associated specialties, affiliations and a list of published articles.
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Articles
40
Citations
1012
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Recent Articles
1.
Konno T, Yoshida K, Mizuta I, Mizuno T, Kawarai T, Tada M, et al.
Eur J Neurol
. 2017 Sep;
25(1):142-147.
PMID: 28921817
Background And Purpose: To establish and validate diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) due to colony-stimulating factor 1 receptor (CSF1R) mutation. Methods: We developed...
2.
Konno T, Yoshida K, Mizuno T, Kawarai T, Tada M, Nozaki H, et al.
Eur J Neurol
. 2016 Sep;
24(1):37-45.
PMID: 27680516
Background And Purpose: The clinical characteristics of colony stimulating factor 1 receptor (CSF1R) related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) have been only partially elucidated. Methods: Clinical...
3.
Yoneda S, Kawarai T, Narisawa N, Tuna E, Sato N, Tsugane T, et al.
Mol Oral Microbiol
. 2013 Jun;
28(5):354-65.
PMID: 23731652
Actinomyces naeslundii is an early colonizer and has important roles in the development of the oral biofilm. Short-chain fatty acids (SCFA) are secreted extracellularly as a product of metabolism by...
4.
Pippucci T, Panza E, Pompilii E, Donadio V, Borreca A, Babalini C, et al.
Eur J Neurol
. 2008 Dec;
16(1):121-6.
PMID: 19087158
Background And Purpose: Autosomal Recessive Hereditary Spastic Paraplegia with Thin Corpus Callosum (AR-HSPTCC) is a clinically and genetically heterogeneous complicated form of spastic paraplegia. Two AR-HSPTCC loci have been assigned...
5.
Orlacchio A, Patrono C, Gaudiello F, Rocchi C, Moschella V, Floris R, et al.
Neurology
. 2008 Apr;
70(21):1959-66.
PMID: 18401025
Objective: To perform a clinical and genetic study of two large Italian families (RM-36 and RM-51) showing the cardinal clinical features of Silver syndrome (SS), a rare dominantly inherited form...
6.
Orlacchio A, Patrono C, Borreca A, Babalini C, Bernardi G, Kawarai T
J Neurol Neurosurg Psychiatry
. 2007 Nov;
79(5):606-7.
PMID: 17971434
No abstract available.
7.
Bruni A, Momeni P, Bernardi L, Tomaino C, Frangipane F, Elder J, et al.
Neurology
. 2007 Jul;
69(2):140-7.
PMID: 17620546
Background: Frontotemporal dementia (FTD) in several 17q21-linked families was recently explained by truncating mutations in the progranulin gene (GRN). Objective: To determine the frequency of GRN mutations in a cohort...
8.
Paisan-Ruiz C, Lang A, Kawarai T, Sato C, Salehi-Rad S, Fisman G, et al.
Neurology
. 2005 Sep;
65(5):696-700.
PMID: 16157901
Background: In addition to the four well-confirmed genes linked to early-onset Parkinson disease (PD) (SNCA, PARKIN, DJ-1, and PINK1), mutations in the leucine-rich repeat kinase 2 gene (LRRK2) have recently...
9.
Moonis M, Swearer J, Dayaw M, St George-Hyslop P, Rogaeva E, Kawarai T, et al.
Neurology
. 2005 Jul;
65(2):323-5.
PMID: 16043812
CSF amyloid beta-peptide 42 (Abeta42) levels in presymptomatic subjects with pathogenic mutations in the PS1 gene are significantly lower than in an age-matched control group. Consequently, in these subjects, there...
10.
Bernardi L, Maletta R, Tomaino C, Smirne N, Di Natale M, Perri M, et al.
Neurobiol Aging
. 2005 May;
27(5):702-9.
PMID: 15904995
Frontotemporal dementia (FTD) is a complex dementing syndrome whose genetic/non genetic risk factors are mostly unknown. Aim of the present work was to investigate whether APOE and/or tau gene variability...