YANO Tamami

写真a

Affiliation

Graduate School of Medicine  Doctorial Course in Medicine  Organ Function-Oriented Medicine  Department of Pediatrics

Research Fields, Keywords

pediatric neurology

Graduating School 【 display / non-display

  •  
    -
    1992.03

    Akita University   Faculty of Medicine   Graduated

Graduate School 【 display / non-display

  •  
    -
    1997.03

    Akita University  Graduate School,Division of Medicine  Doctor's Course  Completed

Campus Career 【 display / non-display

  • 2009.04
    -
    Now

    Akita University   Graduate School of Medicine   Doctorial Course in Medicine   Organ Function-Oriented Medicine   Lecturer  

Research Field (grants-in-aid-for-scientific-research classification) 【 display / non-display

  • Pediatrics

 

Thesis for a degree 【 display / non-display

  • Accumulation of GM2 Ganglioside in Niemann-Pick Disease Type C Fibroblasts

    Tamami YANO, Miyako TANIGUCHI, Shinjiro AKABOSHI, Marie T. VANIER, Tadashi TAI, Hitoshi SAKURABA, Kousaku OHNO 

    Proceedings of the Japan Academy Series B: Physical and Biological Sciences  72 ( 10 ) 214 - 219   1995.11

    Single author

Published Papers 【 display / non-display

  • A Multi-center Questionnaire Survey on the Management and Treatment of Epilepsy in Akita

    Ken-ichi Shibata, Tamami Yano, Satoshi Okawa, Masahiro Takeshima, Hiroaki Shimizu.

    J. Jpn. Epil. Spc.   37 ( 3 ) 779 - 787   2020.01  [Refereed]

    Domestic Co-author

  • A Multi-center Questionnaire Survey on the Management and Treatment of Epilepsy in Akita

    Shibata Ken-ichi, Yano Tamami, Okawa Satoshi, Takeshima Masahiro, Shimizu Hiroaki

    Journal of the Japan Epilepsy Society ( JAPAN EPILEPSY SOCIETY )  37 ( 3 ) 779 - 787   2020.01

    <p>There are few epilepsy specialists in Akita, and non-specialists manage and treat most of the epilepsy patients. This study surveyed the actual state of the management and treatment for epilepsy in Akita. We conducted a questionnaire survey of 97 medical doctors in four different departments at 35 institutions. The questionnaire contained 24 items regarding the number of patients, type of the tests and treatments conducted, and issues regarding the management and treatment for epilepsy. Completed surveys were obtained from 47 medical doctors. Symptomatic localization-related epilepsy was common. Cerebrovascular disease was the most frequent cause. Evaluation of electroencephalography and magnetic resonance imaging performed in more than 90% of patients contributed to diagnosis of epilepsy. Seizures were well controlled by antiepileptic drugs in 90% of patients. Levetiracetam was selected most often for localization-related epilepsy, followed by carbamazepine and lamotrigine. Valproic acid was selected most often for generalized epilepsy, followed by levetiracetam and lamotrigine. Issues in the management and treatment for epilepsy included difficulties in the interpretation of electroencephalography and the lack of local epilepsy specialists.</p>

    DOI CiNii

  • A novel ZC4H2 gene mutation, K209N, in Japanese siblings with arthrogryposis multiplex congenita and intellectual disability: characterization of the K209N mutation and clinical findings.

    Kondo D, Noguchi A, Takahashi I, Kubota H, Yano T, Sato Y, Toyono M, Sawaishi Y, Takahashi T.

    Brain Dev.   40 ( 9 ) 760 - 767   2018.10  [Refereed]

    Domestic Co-author

  • Elevated Urinary Levels of 8-Hydroxy-2'-deoxyguanosine in a Japanese Child of Xeroderma Pigmentosum/Cockayne Syndrome Complex with Infantile Onset of Nephrotic Syndrome.

    Kondo D, Noguchi A, Tamura H, Tsuchida S, Takahashi I, Kubota H, Yano T, Oyama C, Sawaishi Y, Moriwaki S, Takahashi T.

    Tohoku J Exp Med.   239 ( 3 ) 280 - 284   2016.07  [Refereed]

    Domestic Co-author

  • Loss-of-function mutations of STXBP1 in patients with epileptic encephalopathy.

    Yamamoto T, Shimojima K, Yano T, Ueda Y, Takayama R, Ikeda H, Imai K.

    Brain Dev.   38 ( 3 ) 280 - 284   2016.05  [Refereed]

    Domestic Co-author

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Review Papers 【 display / non-display

  • Lafora disease

        2014.12

    Introduction and explanation (commerce magazine)   Single author

  • Lysosomal menbrane transport disorders -Cystinosis and sialic acid storage disorders(Salla disease, ISSD)-

    Japanese Journal of Dlinical Medicine   53 ( 12 ) 3068 - 3071   1995.12

    Introduction and explanation (commerce magazine)   Single author

Presentations 【 display / non-display

  • A Dravet syndrome girl revealed acute encephalopathy with biphasic seizures and latereduced diffusion

    The 53rd Annual Congress of the Japan Epilepsy Society  2019.10  -  2019.11 

  • A Down syndrome boy of West syndrome with some complications

    2018.10  -  2018.10 

  • A case of rachitis caused by Fanconi syndrome due to valproate

    2017.11  -  2017.11 

  • A Girl with Infantile Epileptic Encephalopathy in whom Weekly Adrenocorticotropic Hormone Therapy was Successful

    Tamami YANO, Hiroki KUBOTA, Toshiyuki YAMAMOTO, Tsutomu TAKAHASHI

    The 14th Asian and Oceanian Congress of Child Neurology  (Fukuoka City)  2017.05  -  2017.05  Asian and Oceanian Congress of Child Neurology