Masako Taniike, MD, PhD - Publications

Affiliations: 
Pediatrics Osaka University, Toyonaka-shi, Ōsaka-fu, Japan 

115 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Kagitani-Shimono K, Kato H, Kuwayama R, Tominaga K, Nabatame S, Kishima H, Hatazawa J, Taniike M. Clinical evaluation of neuroinflammation in child-onset focal epilepsy: a translocator protein PET study. Journal of Neuroinflammation. 18: 8. PMID 33407581 DOI: 10.1186/s12974-020-02055-1  0.92
2020 Yoshizaki A, Mohri I, Yamamoto T, Shirota A, Okada S, Murata E, Hoshino K, Kato-Nishimura K, Matsuzawa S, Kato T, Taniike M. An Interactive Smartphone App, "Nenne Navi®," to Improve Children's Sleep: A Pilot Study. Jmir Pediatrics and Parenting. PMID 33122163 DOI: 10.2196/22102  0.92
2020 Murata E, Kato-Nishimura K, Taniike M, Mohri I. Evaluation of the validity of psychological preparation for children undergoing polysomnography. Journal of Clinical Sleep Medicine : Jcsm : Official Publication of the American Academy of Sleep Medicine. PMID 31992404 DOI: 10.5664/jcsm.8158  0.92
2019 Yamada T, Miura Y, Oi M, Akatsuka N, Tanaka K, Tsukidate N, Yamamoto T, Okuno H, Nakanishi M, Taniike M, Mohri I, Laugeson EA. Examining the Treatment Efficacy of PEERS in Japan: Improving Social Skills Among Adolescents with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 31823217 DOI: 10.1007/s10803-019-04325-1  0.92
2019 Mizuno Y, Kagitani-Shimono K, Jung M, Makita K, Takiguchi S, Fujisawa TX, Tachibana M, Nakanishi M, Mohri I, Taniike M, Tomoda A. Structural brain abnormalities in children and adolescents with comorbid autism spectrum disorder and attention-deficit/hyperactivity disorder. Translational Psychiatry. 9: 332. PMID 31819038 DOI: 10.1038/s41398-019-0679-z  0.92
2019 Aoki S, Kagitani-Shimono K, Matsuzaki J, Hanaie R, Nakanishi M, Tominaga K, Nagai Y, Mohri I, Taniike M. Lesser suppression of response to bright visual stimuli and visual abnormality in children with autism spectrum disorder: a magnetoencephalographic study. Journal of Neurodevelopmental Disorders. 11: 9. PMID 31200639 DOI: 10.1186/s11689-019-9266-0  0.92
2019 Nochino T, Ohno Y, Kato T, Taniike M, Okada S. Sleep stage estimation method using a camera for home use. Biomedical Engineering Letters. 9: 257-265. PMID 31168430 DOI: 10.1007/s13534-019-00108-w  0.48
2019 Kato Y, Kagitani-Shimono K, Matsuzaki J, Hanaie R, Yamamoto T, Tominaga K, Watanabe Y, Mohri I, Taniike M. White Matter Tract-Cognitive Relationships in Children with High-Functioning Autism Spectrum Disorder. Psychiatry Investigation. 16: 220-233. PMID 30934190 DOI: 10.30773/pi.2019.01.16  0.92
2018 Hanaie R, Mohri I, Kagitani-Shimono K, Tachibana M, Matsuzaki J, Hirata I, Nagatani F, Watanabe Y, Katayama T, Taniike M. Aberrant Cerebellar-Cerebral Functional Connectivity in Children and Adolescents With Autism Spectrum Disorder. Frontiers in Human Neuroscience. 12: 454. PMID 30483084 DOI: 10.3389/fnhum.2018.00454  0.92
2018 Ogawa R, Kagitani-Shimono K, Matsuzaki J, Tanigawa J, Hanaie R, Yamamoto T, Tominaga K, Hirata M, Mohri I, Taniike M. Abnormal cortical activation during silent reading in adolescents with autism spectrum disorder. Brain & Development. PMID 30448302 DOI: 10.1016/j.braindev.2018.10.013  0.92
2018 Kagitani-Shimono K, Kato Y, Hanaie R, Matsuzaki J, Tanigawa J, Iwatani Y, Azuma J, Taniike M. Abnormal cortical activation during an auditory word comprehension task in benign childhood epilepsy with centrotemporal spikes: A magnetoencephalographic study. Epilepsy & Behavior : E&B. PMID 30120072 DOI: 10.1016/j.yebeh.2018.05.035  0.92
2018 Tanigawa J, Kagitani-Shimono K, Matsuzaki J, Ogawa R, Hanaie R, Yamamoto T, Tominaga K, Nabatame S, Mohri I, Taniike M, Ozono K. Atypical auditory language processing in adolescents with autism spectrum disorder. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. PMID 29934264 DOI: 10.1016/j.clinph.2018.05.014  0.92
2018 Honda T, Sofuku K, Matsunaga H, Tachibana M, Mohri I, Taniike M, Tomonaga K. Prevalence of antibodies against Borna disease virus proteins in Japanese children with autism spectrum disorder. Microbiology and Immunology. PMID 29786872 DOI: 10.1111/1348-0421.12603  0.92
2018 Kuwada A, Mohri I, Asano R, Matsuzawa S, Kato-Nishimura K, Hirata I, Mitsuhosi T, Kagitani-Shimono K, Nakanishi M, Tachibana M, Ohno Y, Taniike M. Japanese Sleep Questionnaire for Elementary Schoolers (JSQ-ES): validation and population-based score distribution. Sleep Medicine. 41: 69-77. PMID 29425580 DOI: 10.1016/j.sleep.2017.07.025  0.92
2017 Honda T, Sofuku K, Matsunaga H, Tachibana M, Mohri I, Taniike M, Tomonaga K. Detection of Antibodies against Borna Disease Virus Proteins in an Autistic Child and Her Mother. Japanese Journal of Infectious Diseases. 70: 599. PMID 28943599 DOI: 10.7883/yoken.JJID.2017.E001  0.92
2017 Matsuzaki J, Kagitani-Shimono K, Sugata H, Hanaie R, Nagatani F, Yamamoto T, Tachibana M, Tominaga K, Hirata M, Mohri I, Taniike M. Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic Study. Frontiers in Human Neuroscience. 11: 446. PMID 28932189 DOI: 10.3389/fnhum.2017.00446  0.92
2017 Murata E, Mohri I, Kato-Nishimura K, Iimura J, Ogawa M, Tachibana M, Ohno Y, Taniike M. Evaluation of behavioral change after adenotonsillectomy for obstructive sleep apnea in children with autism spectrum disorder. Research in Developmental Disabilities. 65: 127-139. PMID 28514706 DOI: 10.1016/j.ridd.2017.04.012  0.92
2016 Honda T, Sofuku K, Matsunaga H, Tachibana M, Mohri I, Taniike M, Tomonaga K. Detection of antibodies to Borna disease virus proteins in an autistic child and her mother. Japanese Journal of Infectious Diseases. PMID 27795475 DOI: 10.7883/yoken.JJID.2016.277  0.92
2016 Okuno H, Yamamoto T, Tatsumi A, Mohri I, Taniike M. Simultaneous Training for Children with Autism Spectrum Disorder and Their Parents with a Focus on Social Skills Enhancement. International Journal of Environmental Research and Public Health. 13. PMID 27314372 DOI: 10.3390/ijerph13060590  0.92
2016 Tachibana M, Takafumi K, Kato-Nishimura K, Matsuzawa S, Mohri I, Taniike M. Associations of sleep bruxism with age, sleep apnea and daytime problematic behaviors in children. Oral Diseases. PMID 27087630 DOI: 10.1111/odi.12492  0.92
2016 Hanaie R, Mohri I, Kagitani-Shimono K, Tachibana M, Matsuzaki J, Hirata I, Nagatani F, Watanabe Y, Fujita N, Taniike M. White matter volume in the brainstem and inferior parietal lobule is related to motor performance in children with autism spectrum disorder: A voxel-based morphometry study. Autism Research : Official Journal of the International Society For Autism Research. PMID 26808675 DOI: 10.1002/aur.1605  0.92
2015 Hirata I, Mohri I, Kato-Nishimura K, Tachibana M, Kuwada A, Kagitani-Shimono K, Ohno Y, Ozono K, Taniike M. Sleep problems are more frequent and associated with problematic behaviors in preschoolers with autism spectrum disorder. Research in Developmental Disabilities. 49: 86-99. PMID 26672680 DOI: 10.1016/j.ridd.2015.11.002  0.92
2015 Matsuo Y, Watanabe M, Taniike M, Mohri I, Kobashi S, Tachibana M, Kobayashi Y, Kitamura Y. Gap Effect Abnormalities during a Visually Guided Pro-Saccade Task in Children with Attention Deficit Hyperactivity Disorder. Plos One. 10: e0125573. PMID 26018057 DOI: 10.1371/journal.pone.0125573  0.92
2015 Shibasaki Y, Hayata-Takano A, Hazama K, Nakazawa T, Shintani N, Kasai A, Nagayasu K, Hashimoto R, Tanida M, Katayama T, Matsuzaki S, Yamada K, Taniike M, Onaka Y, Ago Y, et al. Atomoxetine reverses locomotor hyperactivity, impaired novel object recognition, and prepulse inhibition impairment in mice lacking pituitary adenylate cyclase-activating polypeptide. Neuroscience. 297: 95-104. PMID 25841321 DOI: 10.1016/j.neuroscience.2015.03.062  0.92
2015 Tatsumi Y, Mohri I, Shimizu S, Tachibana M, Ohno Y, Taniike M. Daytime physical activity and sleep in pre-schoolers with developmental disorders. Journal of Paediatrics and Child Health. 51: 396-402. PMID 25187236 DOI: 10.1111/jpc.12725  0.92
2014 Azuma H, Mohri I, Tachibana M, Ohno Y, Taniike M. [An analysis of the developmental trajectory of children with autism spectrum disorders]. No to Hattatsu. Brain and Development. 46: 429-37. PMID 25558586  0.92
2014 Yasuda Y, Hashimoto R, Fukai R, Okamoto N, Hiraki Y, Yamamori H, Fujimoto M, Ohi K, Taniike M, Mohri I, Nakashima M, Tsurusaki Y, Saitsu H, Matsumoto N, Miyake N, et al. Duplication of the NPHP1 gene in patients with autism spectrum disorder and normal intellectual ability: a case series. Annals of General Psychiatry. 13: 22. PMID 25126106 DOI: 10.1186/s12991-014-0022-2  0.92
2014 Matsuzaki J, Kagitani-Shimono K, Sugata H, Hirata M, Hanaie R, Nagatani F, Tachibana M, Tominaga K, Mohri I, Taniike M. Progressively increased M50 responses to repeated sounds in autism spectrum disorder with auditory hypersensitivity: a magnetoencephalographic study. Plos One. 9: e102599. PMID 25054201 DOI: 10.1371/journal.pone.0102599  0.92
2014 Hanaie R, Mohri I, Kagitani-Shimono K, Tachibana M, Matsuzaki J, Watanabe Y, Fujita N, Taniike M. Abnormal corpus callosum connectivity, socio-communicative deficits, and motor deficits in children with autism spectrum disorder: a diffusion tensor imaging study. Journal of Autism and Developmental Disorders. 44: 2209-20. PMID 24710811 DOI: 10.1007/s10803-014-2096-8  0.92
2014 Shimizu S, Kato-Nishimura K, Mohri I, Kagitani-Shimono K, Tachibana M, Ohno Y, Taniike M. Psychometric properties and population-based score distributions of the Japanese Sleep Questionnaire for Preschoolers. Sleep Medicine. 15: 451-8. PMID 24636002 DOI: 10.1016/j.sleep.2013.05.020  0.92
2014 Sanefuji W, Wada K, Yamamoto T, Mohri I, Taniike M. Development of preference for conspecific faces in human infants. Developmental Psychology. 50: 979-85. PMID 24294877 DOI: 10.1037/a0035205  0.92
2013 Nakatani M, Okada S, Shimizu S, Mohri I, Ohno Y, Taniike M, Makikawa M. Body movement analysis during sleep for children with ADHD using video image processing. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2013: 6389-92. PMID 24111203 DOI: 10.1109/EMBC.2013.6611016  0.92
2013 Okuno H, Nagai T, Mohri I, Yoshizaki A, Yamamoto T, Sakai S, Iwasaka H, Taniike M. [Effectiveness of a modified parent training of smaller groups and shorter schedules for children with pervasive developmental disorders]. No to Hattatsu. Brain and Development. 45: 26-32. PMID 23593742  0.92
2013 Hanaie R, Mohri I, Kagitani-Shimono K, Tachibana M, Azuma J, Matsuzaki J, Watanabe Y, Fujita N, Taniike M. Altered microstructural connectivity of the superior cerebellar peduncle is related to motor dysfunction in children with autistic spectrum disorders. Cerebellum (London, England). 12: 645-56. PMID 23564050 DOI: 10.1007/s12311-013-0475-x  0.92
2013 Tachibana M, Kagitani-Shimono K, Mohri I, Yamamoto T, Sanefuji W, Nakamura A, Oishi M, Kimura T, Onaka T, Ozono K, Taniike M. Long-term administration of intranasal oxytocin is a safe and promising therapy for early adolescent boys with autism spectrum disorders. Journal of Child and Adolescent Psychopharmacology. 23: 123-7. PMID 23480321 DOI: 10.1089/cap.2012.0048  0.92
2013 Kimura-Ohba S, Kagitani-Shimono K, Hashimoto N, Nabatame S, Okinaga T, Murakami A, Miyake N, Matsumoto N, Osaka H, Hojo K, Tomita R, Taniike M, Ozono K. A case of cerebral hypomyelination with spondylo-epi-metaphyseal dysplasia. American Journal of Medical Genetics. Part A. 161: 203-7. PMID 23239615 DOI: 10.1002/ajmg.a.35686  0.92
2013 Tsuchiya KJ, Matsumoto K, Yagi A, Inada N, Kuroda M, Inokuchi E, Koyama T, Kamio Y, Tsujii M, Sakai S, Mohri I, Taniike M, Iwanaga R, Ogasahara K, Miyachi T, et al. Reliability and validity of autism diagnostic interview-revised, Japanese version. Journal of Autism and Developmental Disorders. 43: 643-62. PMID 22806002 DOI: 10.1007/s10803-012-1606-9  0.92
2012 Hashimoto N, Kagitani-Shimono K, Tominaga K, Kitai Y, Ikeda T, Okinaga T, Taniike M, Ozone K. [Effects of botulinum toxin therapy for respiratory distress in patients with cervical hypertonia]. No to Hattatsu. Brain and Development. 44: 13-8. PMID 22352024  0.92
2012 Mohri I, Kato-Nishimura K, Kagitani-Shimono K, Kimura-Ohba S, Ozono K, Tachibana N, Taniike M. Evaluation of oral iron treatment in pediatric restless legs syndrome (RLS). Sleep Medicine. 13: 429-32. PMID 22341906 DOI: 10.1016/j.sleep.2011.12.009  0.92
2012 Iwatani Y, Kagitani-Shimono K, Tominaga K, Okinaga T, Mohri I, Kishima H, Kato A, Sanefuji W, Yamamoto T, Tatsumi A, Murata E, Taniike M, Nagai T, Ozono K. Long-term developmental outcome in patients with West syndrome after epilepsy surgery. Brain & Development. 34: 731-8. PMID 22336751 DOI: 10.1016/j.braindev.2012.01.008  0.92
2012 Matsuzaki J, Kagitani-Shimono K, Goto T, Sanefuji W, Yamamoto T, Sakai S, Uchida H, Hirata M, Mohri I, Yorifuji S, Taniike M. Differential responses of primary auditory cortex in autistic spectrum disorder with auditory hypersensitivity. Neuroreport. 23: 113-8. PMID 22146579 DOI: 10.1097/WNR.0b013e32834ebf44  0.92
2012 Ikeda T, Nagai T, Kato-Nishimura K, Mohri I, Taniike M. Sleep problems in physically disabled children and burden on caregivers. Brain & Development. 34: 223-9. PMID 21602006 DOI: 10.1016/j.braindev.2011.04.011  0.92
2012 Akagi M, Mohri I, Iwatani Y, Kagitani-Shimono K, Okinaga T, Sakai N, Ozono K, Taniike M. Clinicogenetical features of a Japanese patient with giant axonal neuropathy. Brain & Development. 34: 156-62. PMID 21356581 DOI: 10.1016/j.braindev.2011.02.003  0.92
2011 Kagitani-Shimono K, Kato-Nishimura K, Okinaga T, Mohri I, Tachibana N, Ozono K, Taniike M. Long-term observation of absence of REM sleep caused by pontine cavernous hemangioma. Sleep Medicine. 12: 1045-6. PMID 22024556 DOI: 10.1016/j.sleep.2011.09.002  0.92
2011 Hashimoto N, Kagitani-Shimono K, Sakai N, Otomo T, Tominaga K, Nabatame S, Mogami Y, Takahashi Y, Imai K, Yanagihara K, Okinaga T, Nagai T, Taniike M, Ozono K. SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome. Journal of Human Genetics. 56: 846-51. PMID 22011817 DOI: 10.1038/jhg.2011.115  0.92
2011 Yasuda Y, Hashimoto R, Yamamori H, Ohi K, Fukumoto M, Umeda-Yano S, Mohri I, Ito A, Taniike M, Takeda M. Gene expression analysis in lymphoblasts derived from patients with autism spectrum disorder. Molecular Autism. 2: 9. PMID 21615902 DOI: 10.1186/2040-2392-2-9  0.92
2011 Redensek A, Rathore KI, Berard JL, López-Vales R, Swayne LA, Bennett SA, Mohri I, Taniike M, Urade Y, David S. Expression and detrimental role of hematopoietic prostaglandin D synthase in spinal cord contusion injury. Glia. 59: 603-14. PMID 21294159 DOI: 10.1002/glia.21128  0.92
2011 Okuno H, Nagai T, Sakai S, Mohri I, Yamamoto T, Yoshizaki A, Kato K, Tachibana M, Iwasaka H, Taniike M. Effectiveness of modified parent training for mothers of children with Pervasive Developmental Disorder on parental confidence and children's behavior. Brain & Development. 33: 152-60. PMID 20385459 DOI: 10.1016/j.braindev.2010.03.007  0.92
2010 Munesue T, Yokoyama S, Nakamura K, Anitha A, Yamada K, Hayashi K, Asaka T, Liu HX, Jin D, Koizumi K, Islam MS, Huang JJ, Ma WJ, Kim UH, Kim SJ, ... ... Taniike M, et al. Two genetic variants of CD38 in subjects with autism spectrum disorder and controls. Neuroscience Research. 67: 181-91. PMID 20435366 DOI: 10.1016/j.neures.2010.03.004  0.92
2009 Kagitani-Shimono K, Kato-Nishimura K, Kitai Y, Araya K, Tominaga K, Okinaga T, Mohri I, Taniike M, Ozono K. [Deficiency of REM sleep in a patient with pontine cavernous hemangioma]. No to Hattatsu. Brain and Development. 41: 349-52. PMID 19764454  0.92
2009 Araya K, Sakai N, Mohri I, Kagitani-Shimono K, Okinaga T, Hashii Y, Ohta H, Nakamichi I, Aozasa K, Taniike M, Ozono K. Localized donor cells in brain of a Hunter disease patient after cord blood stem cell transplantation. Molecular Genetics and Metabolism. 98: 255-63. PMID 19556155 DOI: 10.1016/j.ymgme.2009.05.006  0.92
2009 Mohri I, Aritake K, Taniguchi H, Sato Y, Kamauchi S, Nagata N, Maruyama T, Taniike M, Urade Y. Inhibition of prostaglandin D synthase suppresses muscular necrosis. The American Journal of Pathology. 174: 1735-44. PMID 19359520 DOI: 10.2353/ajpath.2009.080709  0.92
2009 Nabatame S, Taniike M, Sakai N, Kato-Nishimura K, Mohri I, Kagitani-Shimono K, Okinaga T, Tachibana N, Ozono K. Sleep disordered breathing in childhood-onset acid maltase deficiency. Brain & Development. 31: 234-9. PMID 18495398 DOI: 10.1016/j.braindev.2008.03.007  0.92
2008 Okada S, Ohno Y, Goyahan, Kato-Nishimura K, Mohri I, Taniike M. Examination of non-restrictive and non-invasive sleep evaluation technique for children using difference images. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2008: 3483-7. PMID 19163459 DOI: 10.1109/IEMBS.2008.4649956  0.92
2008 Mohri I, Kato-Nishimura K, Kagitani-Shimono K, Tachibana N, Ozone K, Taniike M. [Restless-leg syndrome--possible unrecognized cause for insomnia and irritability in children]. No to Hattatsu. Brain and Development. 40: 473-7. PMID 19039990  0.92
2008 Tokimasa S, Ohta H, Takizawa S, Kusuki S, Hashii Y, Sakai N, Taniike M, Ozono K, Hara J. Umbilical cord-blood transplantations from unrelated donors in patients with inherited metabolic diseases: Single-institute experience. Pediatric Transplantation. 12: 672-6. PMID 18798361  0.68
2008 Miyoshi Y, Akagi M, Agarwal AK, Namba N, Kato-Nishimura K, Mohri I, Yamagata M, Nakajima S, Mushiake S, Shima M, Auchus RJ, Taniike M, Garg A, Ozono K. Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings. Clinical Genetics. 73: 535-44. PMID 18435794 DOI: 10.1111/j.1399-0004.2008.00992.x  0.92
2008 Kagitani-Shimono K, Mohri I, Yagi T, Taniike M, Suzuki K. Peripheral neuropathy in the twitcher mouse: accumulation of extracellular matrix in the endoneurium and aberrant expression of ion channels. Acta Neuropathologica. 115: 577-87. PMID 18172657 DOI: 10.1007/s00401-007-0333-3  0.92
2008 Mohri I, Kato-Nishimura K, Tachibana N, Ozono K, Taniike M. Restless legs syndrome (RLS): an unrecognized cause for bedtime problems and insomnia in children. Sleep Medicine. 9: 701-2. PMID 17923435 DOI: 10.1016/j.sleep.2007.08.005  0.92
2008 Namba N, Etani Y, Kitaoka T, Nakamoto Y, Nakacho M, Bessho K, Miyoshi Y, Mushiake S, Mohri I, Arai H, Taniike M, Ozono K. Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter. European Journal of Pediatrics. 167: 785-91. PMID 17899191 DOI: 10.1007/s00431-007-0589-6  0.92
2008 Kato-Nishimura K, Taniike M, Tachibana N. Body weight reduction by CPAP treatment in a bedridden patient. Sleep Medicine. 9: 207-8. PMID 17686655 DOI: 10.1016/j.sleep.2007.01.015  0.76
2007 Mano T, Takizawa S, Mohri I, Okinaga T, Shimono K, Imai K, Taniike M, Ozono K, Fujimura H. Neuronal intranuclear hyaline inclusion disease with rapidly progressive neurological symptoms. Journal of Child Neurology. 22: 60-6. PMID 17608307 DOI: 10.1177/0883073807299952  0.92
2007 Mohri I, Kadoyama K, Kanekiyo T, Sato Y, Kagitani-Shimono K, Saito Y, Suzuki K, Kudo T, Takeda M, Urade Y, Murayama S, Taniike M. Hematopoietic prostaglandin D synthase and DP1 receptor are selectively upregulated in microglia and astrocytes within senile plaques from human patients and in a mouse model of Alzheimer disease. Journal of Neuropathology and Experimental Neurology. 66: 469-80. PMID 17549007 DOI: 10.1097/01.jnen.0000240472.43038.27  0.92
2007 Taniguchi H, Mohri I, Okabe-Arahori H, Kanekiyo T, Kagitani-Shimono K, Wada K, Urade Y, Nakayama M, Ozono K, Taniike M. Early induction of neuronal lipocalin-type prostaglandin D synthase after hypoxic-ischemic injury in developing brains. Neuroscience Letters. 420: 39-44. PMID 17499437 DOI: 10.1016/j.neulet.2007.04.016  0.92
2007 Taniguchi H, Mohri I, Okabe-Arahori H, Aritake K, Wada K, Kanekiyo T, Narumiya S, Nakayama M, Ozono K, Urade Y, Taniike M. Prostaglandin D2 protects neonatal mouse brain from hypoxic ischemic injury. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 4303-12. PMID 17442814 DOI: 10.1523/JNEUROSCI.0321-07.2007  0.92
2007 Kanekiyo T, Ban T, Aritake K, Huang ZL, Qu WM, Okazaki I, Mohri I, Murayama S, Ozono K, Taniike M, Goto Y, Urade Y. Lipocalin-type prostaglandin D synthase/beta-trace is a major amyloid beta-chaperone in human cerebrospinal fluid. Proceedings of the National Academy of Sciences of the United States of America. 104: 6412-7. PMID 17404210 DOI: 10.1073/pnas.0701585104  0.92
2006 Waguri S, Tomiyama Y, Ikeda H, Hida T, Sakai N, Taniike M, Ebisu S, Uchiyama Y. The luminal domain participates in the endosomal trafficking of the cation-independent mannose 6-phosphate receptor. Experimental Cell Research. 312: 4090-107. PMID 17069798 DOI: 10.1016/j.yexcr.2006.09.024  0.92
2006 Mohri I, Taniike M, Taniguchi H, Kanekiyo T, Aritake K, Inui T, Fukumoto N, Eguchi N, Kushi A, Sasai H, Kanaoka Y, Ozono K, Narumiya S, Suzuki K, Urade Y. Prostaglandin D2-mediated microglia/astrocyte interaction enhances astrogliosis and demyelination in twitcher. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 4383-93. PMID 16624958 DOI: 10.1523/JNEUROSCI.4531-05.2006  0.92
2006 Xu C, Sakai N, Taniike M, Inui K, Ozono K. Six novel mutations detected in the GALC gene in 17 Japanese patients with Krabbe disease, and new genotype-phenotype correlation. Journal of Human Genetics. 51: 548-54. PMID 16607461 DOI: 10.1007/s10038-006-0396-3  0.68
2006 Mohri I, Taniike M, Okazaki I, Kagitani-Shimono K, Aritake K, Kanekiyo T, Yagi T, Takikita S, Kim HS, Urade Y, Suzuki K. Lipocalin-type prostaglandin D synthase is up-regulated in oligodendrocytes in lysosomal storage diseases and binds gangliosides. Journal of Neurochemistry. 97: 641-51. PMID 16515539 DOI: 10.1111/j.1471-4159.2006.03753.x  0.92
2006 Kagitani-Shimono K, Mohri I, Oda H, Ozono K, Suzuki K, Urade Y, Taniike M. Lipocalin-type prostaglandin D synthase (beta-trace) is upregulated in the alphaB-crystallin-positive oligodendrocytes and astrocytes in the chronic multiple sclerosis. Neuropathology and Applied Neurobiology. 32: 64-73. PMID 16409554 DOI: 10.1111/j.1365-2990.2005.00690.x  0.92
2006 Kawai M, Sakai N, Miyake S, Tsukamoto H, Akagi M, Inui K, Mushiake S, Taniike M, Ozono K. Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease. Brain & Development. 28: 60-2. PMID 16168595 DOI: 10.1016/j.braindev.2005.03.011  0.68
2005 Tachibana N, Taniike M, Okinaga T, Ripley B, Mignot E, Nishino S. Hypersomnolence and increased REM sleep with low cerebrospinal fluid hypocretin level in a patient after removal of craniopharyngioma. Sleep Medicine. 6: 567-9. PMID 16084764 DOI: 10.1016/j.sleep.2005.04.002  0.68
2005 Takahashi K, Kogaki S, Kurotobi S, Nasuno S, Ohta M, Okabe H, Wada K, Sakai N, Taniike M, Ozono K. A novel mutation in the PTPN11 gene in a patient with Noonan syndrome and rapidly progressive hypertrophic cardiomyopathy. European Journal of Pediatrics. 164: 497-500. PMID 15889278 DOI: 10.1007/s00431-005-1679-y  0.68
2005 Kagitani-Shimono K, Mohri I, Fujitani Y, Suzuki K, Ozono K, Urade Y, Taniike M. Anti-inflammatory therapy by ibudilast, a phosphodiesterase inhibitor, in demyelination of twitcher, a genetic demyelination model. Journal of Neuroinflammation. 2: 10. PMID 15813970 DOI: 10.1186/1742-2094-2-10  0.92
2004 Miyoshi Y, Taniike M, Mohri I, Mushiake S, Nakajima S, Matsumoto N, Ozono K. Hormonal and genetical assessment of a Japanese girl with weaver syndrome. Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society For Pediatric Endocrinology. 13: 17-23. PMID 24790293 DOI: 10.1297/cpe.13.17  0.92
2003 Mohri I, Eguchi N, Suzuki K, Urade Y, Taniike M. Hematopoietic prostaglandin D synthase is expressed in microglia in the developing postnatal mouse brain. Glia. 42: 263-74. PMID 12673832 DOI: 10.1002/glia.10183  0.92
2002 Okinaga T, Mohri I, Fujimura H, Imai K, Ono J, Urade Y, Taniike M. Induction of hematopoietic prostaglandin D synthase in hyalinated necrotic muscle fibers: its implication in grouped necrosis. Acta Neuropathologica. 104: 377-84. PMID 12200624 DOI: 10.1007/s00401-002-0567-z  0.92
2002 Taniike M, Mohri I, Eguchi N, Beuckmann CT, Suzuki K, Urade Y. Perineuronal oligodendrocytes protect against neuronal apoptosis through the production of lipocalin-type prostaglandin D synthase in a genetic demyelinating model. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 4885-96. PMID 12077186  0.92
2000 Mason JL, Jones JJ, Taniike M, Morell P, Suzuki K, Matsushima GK. Mature oligodendrocyte apoptosis precedes IGF-1 production and oligodendrocyte progenitor accumulation and differentiation during demyelination/remyelination. Journal of Neuroscience Research. 61: 251-62. PMID 10900072 DOI: 10.1002/1097-4547(20000801)61:3<251::AID-JNR3>3.0.CO;2-W  0.92
1999 Taniike M, Mohri I, Eguchi N, Irikura D, Urade Y, Okada S, Suzuki K. An apoptotic depletion of oligodendrocytes in the twitcher, a murine model of globoid cell leukodystrophy. Journal of Neuropathology and Experimental Neurology. 58: 644-53. PMID 10374755  0.92
1999 Fujisaki H, Hara J, Takai K, Nakanishi K, Matsuda Y, Ohta H, Osugi Y, Tokimasa S, Taniike M, Hosoi G, Sako M, Okada S. Lineage switch in childhood leukemia with monosomy 7 and reverse of lineage switch in severe combined immunodeficient mice. Experimental Hematology. 27: 826-33. PMID 10340398  0.48
1998 Mohri I, Taniike M, Yoshikawa H, Higashiyama M, Itami S, Okada S. A case of giant axonal neuropathy showing focal aggregation and hypophosphorylation of intermediate filaments. Brain & Development. 20: 594-7. PMID 9865543 DOI: 10.1016/S0387-7604(98)00056-4  0.92
1998 Wada Y, Matsuoka T, Imai K, Taniike M, Mano T, Ono J, Okada S, Kondo I. [A case of juvenile type dentatorubral-pallidoluysian atrophy (DRPLA) with psychomotor retardation since infancy]. No to Hattatsu. Brain and Development. 30: 543-8. PMID 9844421  0.48
1998 Mohri I, Taniike M, Fujimura H, Matsuoka T, Inui K, Nagai T, Okada S. A case of Kearns-Sayre syndrome showing a constant proportion of deleted mitochondrial DNA in blood cells during 6 years of follow-up. Journal of the Neurological Sciences. 158: 106-9. PMID 9667787 DOI: 10.1016/S0022-510X(98)00082-3  0.92
1998 Taniike M, Okada S. [Sandhoff disease (beta-hexosaminidase alpha-chain deficiency)]. RyōIkibetsu ShōKōGun ShirÄ«Zu. 397-9. PMID 9645091  0.48
1998 Okada S, Taniike M. [Tay-Sachs disease (beta-hexosaminidase alpha-chain deficiency)]. RyōIkibetsu ShōKōGun ShirÄ«Zu. 394-6. PMID 9645090  0.48
1998 Taniike M, Marcus JR, Nishigaki T, Fujita N, Popko B, Suzuki K, Suzuki K. Suppressed UDP-galactose: ceramide galactosyltransferase and myelin protein mRNA in twitcher mouse brain. Journal of Neuroscience Research. 51: 536-40. PMID 9514207 DOI: 10.1002/(SICI)1097-4547(19980215)51:4<536::AID-JNR13>3.0.CO;2-1  1
1997 Taniike M, Marcus JR, Popko B, Suzuki K. Expression of major histocompatibility complex class I antigens in the demyelinating twitcher CNS and PNS. Journal of Neuroscience Research. 47: 539-46. PMID 9067863 DOI: 10.1002/(SICI)1097-4547(19970301)47:5<539::AID-JNR9>3.0.CO;2-I  1
1996 Sakai N, Inui K, Tatsumi N, Fukushima H, Nishigaki T, Taniike M, Nishimoto J, Tsukamoto H, Yanagihara I, Ozono K, Okada S. Molecular cloning and expression of cDNA for murine galactocerebrosidase and mutation analysis of the twitcher mouse, a model of Krabbe's disease. Journal of Neurochemistry. 66: 1118-24. PMID 8769874  0.68
1995 Tatsumi N, Inui K, Sakai N, Fukushima H, Nishimoto J, Yanagihara I, Nishigaki T, Tsukamoto H, Fu L, Taniike M. Molecular defects in Krabbe disease. Human Molecular Genetics. 4: 1865-8. PMID 8595408  0.4
1995 Suzuki K, Taniike M. Murine model of genetic demyelinating disease: the twitcher mouse. Microscopy Research and Technique. 32: 204-14. PMID 8527855 DOI: 10.1002/jemt.1070320304  1
1995 Taniike M, Suzuki K. Proliferative capacity of oligodendrocytes in the demyelinating twitcher spinal cord. Journal of Neuroscience Research. 40: 325-32. PMID 7745626 DOI: 10.1002/jnr.490400306  1
1995 Taniike M, Yamanaka S, Proia RL, Langaman C, Bone-Turrentine T, Suzuki K. Neuropathology of mice with targeted disruption of Hexa gene, a model of Tay-Sachs disease. Acta Neuropathologica. 89: 296-304. PMID 7610760 DOI: 10.1007/BF00309622  1
1995 Kaido M, Fujimura H, Taniike M, Yoshikawa H, Toyooka K, Yorifuji S, Inui K, Okada S, Sparaco M, Yanagihara T. Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNA(Ile) 4269 mutation): histochemical, immunohistochemical, and ultrastructural study. Journal of the Neurological Sciences. 131: 170-6. PMID 7595643  0.48
1995 Taniike M, Popko B, Suzuki K. DEVELOPMENTAL EXPRESSION OF GLIAL PROTEINS AND UDP-GALACTOSE Journal of Neuropathology and Experimental Neurology. 54: 470. DOI: 10.1097/00005072-199505000-00253  1
1994 Matsushima GK, Taniike M, Glimcher LH, Grusby MJ, Frelinger JA, Suzuki K, Ting JP. Absence of MHC class II molecules reduces CNS demyelination, microglial/macrophage infiltration, and twitching in murine globoid cell leukodystrophy. Cell. 78: 645-56. PMID 8069913 DOI: 10.1016/0092-8674(94)90529-0  0.92
1994 Yamanaka S, Johnson MD, Grinberg A, Westphal H, Crawley JN, Taniike M, Suzuki K, Proia RL. Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease. Proceedings of the National Academy of Sciences of the United States of America. 91: 9975-9. PMID 7937929 DOI: 10.1073/PNAS.91.21.9975  1
1994 Taniike M, Suzuki K. Spacio-temporal progression of demyelination in twitcher mouse: with clinico-pathological correlation. Acta Neuropathologica. 88: 228-36. PMID 7528964 DOI: 10.1007/BF00293398  1
1993 Tsukamoto H, Sakai N, Taniike M, Nakatsukasa M, Yoshiwara W, Sakamoto H, Fujimura H, Inui K, Okada S. Case of ring chromosome 7: the first report of neuropathological findings. American Journal of Medical Genetics. 46: 632-5. PMID 8362903 DOI: 10.1002/ajmg.1320460606  0.48
1993 Toyooka K, Fujimura H, Yoshikawa H, Taniike M, Inui K, Yorifuji S, Tarui S, Okada S, Yanagihara T. Nephrosialidosis: ultrastructural and lectin histochemical study. Acta Neuropathologica. 86: 198-205. PMID 8213076  0.48
1993 Tsukamoto H, Inui K, Taniike M, Kamiyama K, Hori M, Sumi K, Okada S. Different clinical features in monozygotic twins: a case of 7q--syndrome. Clinical Genetics. 43: 139-42. PMID 7684659  0.48
1992 Taniike M, Fukushima H, Yanagihara I, Tsukamoto H, Tanaka J, Fujimura H, Nagai T, Sano T, Yamaoka K, Inui K. Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy. Biochemical and Biophysical Research Communications. 186: 47-53. PMID 1632786 DOI: 10.1016/S0006-291X(05)80773-9  0.44
1992 Tada K, Taniike M, Ono J, Tsukamoto H, Inui K, Okada S. Serial magnetic resonance imaging studies in a case of late onset globoid cell leukodystrophy. Neuropediatrics. 23: 306-9. PMID 1491749 DOI: 10.1055/s-2008-1071363  0.48
1992 Tsukamoto H, Inui K, Taniike M, Nishimoto J, Midorikawa M, Yoshimine T, Kato A, Ikeda T, Hayakawa T, Okada S. A case of Hallervorden-Spatz disease: progressive and intractable dystonia controlled by bilateral thalamotomy. Brain & Development. 14: 269-72. PMID 1443412 DOI: 10.1016/S0387-7604(12)80246-4  0.92
1992 Inui K, Tsukamoto H, Fukushima H, Taniike M, Tanaka J, Nishigaki T, Okada S. Detection of the A to G(3243) mutation of mitochondrial DNA in Japanese families with mitochondrial encephalomyopathies. Journal of Inherited Metabolic Disease. 15: 311-4. PMID 1405464  0.48
1992 Taniike M, Fujimura H, Kogaki S, Tsukamoto H, Inui K, Midorikawa M, Nishimoto J, Okada S. A case of pigmentary type of orthochromatic leukodystrophy with early onset and globoid cells. Acta Neuropathologica. 83: 427-33. PMID 1374206 DOI: 10.1007/BF00713537  0.92
1992 Inui K, Fukushima H, Tsukamoto H, Taniike M, Midorikawa M, Tanaka J, Nishigaki T, Okada S. Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene. The Journal of Pediatrics. 120: 62-6. PMID 1370535 DOI: 10.1016/S0022-3476(05)80599-2  0.92
1991 Tsukamoto H, Inui K, Fukushima H, Nishigaki T, Taniike M, Tanaka J, Okada S. Molecular study of Duchenne and Becker muscular dystrophies in Japanese. Journal of Inherited Metabolic Disease. 14: 819-24. PMID 1779629  0.48
1991 Tanaka J, Taniike M, Inui K, Nagai T, Okada S. [Peripheral neuropathy in two children with mitochondrial encephalomyopathy]. Rinshō Shinkeigaku = Clinical Neurology. 31: 772-4. PMID 1664789  0.48
1990 Mitsuo K, Nakano T, Kobayashi T, Goto I, Taniike M, Suzuki K. Juvenile Sandhoff disease: a Japanese patient carrying a mutation identical to that found earlier in a Canadian patient. Journal of the Neurological Sciences. 98: 277-86. PMID 2147031  1
1990 Inui K, Nishimoto J, Taniike M, Midorikawa M, Tsukamoto H, Okada S, Yabuuchi H. Study of pathogenesis in twitcher mouse, an enzymatically authentic model of Krabbe's disease. Journal of the Neurological Sciences. 100: 124-30. PMID 2128519 DOI: 10.1016/0022-510X(90)90022-F  0.92
1990 Inui K, Namba R, Ihara Y, Nobukuni K, Taniike M, Midorikawa M, Tsukamoto H, Okada S. A case of chronic GM1 gangliosidosis presenting as dystonia: clinical and biochemical studies. Journal of Neurology. 237: 491-3. PMID 2127425 DOI: 10.1007/BF00314770  0.92
1989 Inui K, Nishimoto J, Taniike M, Midorikawa M, Tsukamoto H, Okada S, Yabuuchi H. Study of pathogenesis in twitcher mouse, an enzymatically authentic model of human Krabbe's disease. Journal of Inherited Metabolic Disease. 12: 383-5. PMID 2512450 DOI: 10.1007/BF03335429  0.92
1989 Taniike M, Inui K, Hirabayashi Y, Tsukamoto H, Nishimoto J, Midorikawa M, Okada S, Yabuuchi H. Immunohistochemical demonstration of GM2-ganglioside in the central nervous system of a 19-week-old fetus of Tay-Sachs disease. Journal of Inherited Metabolic Disease. 12: 372-4. PMID 2512447 DOI: 10.1007/BF03335426  0.92
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