舘延忠 (Tachi Nobutada) - マイポータル

基本情報

所属: 元北海道千歳リハビリテーション大学健康科学部リハビリテーション学科客員教授

学位: 医学博士

研究者番号: 80136944
J-GLOBAL ID: 200901014873146680
researchmap会員ID: 1000053090

研究キーワード

研究分野

ライフサイエンス / 胎児医学、小児成育学 /

学歴

- 1973年

札幌医科大学
- 1973年

札幌医科大学

論文

脊髄性筋萎縮症の診断と治療の進歩

舘延忠, 須鎌康介, 仙石泰仁

北海道作業療法 35(4) 190-200 2018年12月査読有り招待有り
小児期発症の遺伝性ジストニア Dopa-responsive Dystonia

舘延忠, 高橋悟

北海道千歳リハビリテーション大学研究紀要 2 9-15 2018年10月
A myotonic dystrophy 1 patient complicated with placental adherence after miscarriage of one dichorionic diamniotic twin following her tenth in vitro fertilization and embryo transfer

Toshiaki Endo, Tsuyoshi Baba, Asuka Sugio, Miyuki Morishita, Madoka Takahashi, Yushi Akashi, Shinichi Ishioka, Nobutada Tachi, Tomihiro Imai, Mitsuharu Tamakawa …

ARCHIVES OF GYNECOLOGY AND OBSTETRICS 286(6) 1605-1608 2012年12月査読有り
A new mutation of GCH1 in triplets family with dopa-responsive dystonia

N. Tachi, S. Takahashi, M. Jo, M. Shinoda

EUROPEAN JOURNAL OF NEUROLOGY 18(9) 1191-1193 2011年9月査読有り
New mutation of CACNA1A gene in episodic ataxia type 2

Koki Nikaido, Nobutada Tachi, Kazuhiro Ohya, Takahito Wada, Hiroyuki Tsutsumi

PEDIATRICS INTERNATIONAL 53(3) 415-416 2011年6月査読有り
The acid-sensing ion channel 2 (ASIC2) of ciliated cells in the developing rat nasal septum

Shin Kikuchi, Takafumi Ninomiya, Tomoyuki Kawamata, Noriko Ogasawara, Takashi Kojima, Nobutada Tachi, Haruyuki Tatsumi

ARCHIVES OF HISTOLOGY AND CYTOLOGY 73(2) 81-89 2010年査読有り
[Case of Pitt-Hopkins syndrome].

Fukumura S, Tachi N

No to hattatsu = Brain and development 41(5) 365-367 2009年9月査読有り
The Change of Grip Strength in a Patient with Congenital Myotonic Dystrophy Over a 4-year Period.

Kikuchi S, Kozuka N, Uchida E, Ninomiya T, Tatsumi H, Takeda H, Tachi N

Journal of the Japanese Physical Therapy Association = Rigaku ryoho 11(1) 23-27 2008年査読有り
Carbamazepine-induced hemolytic and aplastic crises associated with reduced glutathione peroxidase activity of erythrocytes

Masaki Yamamoto, Nobuhiro Suzuki, Naoki Hatakeyama, Noriaki Kubo, Nobutada Tachi, Hitoshi Kanno, Hisaichi Fujii, Hiroyuki Tsutsumi

INTERNATIONAL JOURNAL OF HEMATOLOGY 86(4) 325-328 2007年11月査読有り
New mutation of the PTCH gene in Nevoid basal-cell carcinoma syndrome with West syndrome

Nobutada Tachi, Katstmori Fujii, Mitsugu Kimura, Kouhei Seki, Masahisa Hirakai, Toshiyuki Miyashita

PEDIATRIC NEUROLOGY 37(5) 363-365 2007年11月査読有り
Structural analysis of leucine-rich-repeat variants in proteins associated with human diseases

N Matsushima, N Tachi, Y Kuroki, P Enkhbayar, M Osaki, M Kamiya, R Kretsinger

CELLULAR AND MOLECULAR LIFE SCIENCES 62(23) 2771-2791 2005年12月査読有り
Clinicopathological and virological analyses of familial human T-lymphotropic virus type I-associated polyneuropathy

H Sawa, T Nagashima, K Nagashima, T Shinohara, T Chuma, Y Mano, N Tachi, WW Hall

JOURNAL OF NEUROVIROLOGY 11(2) 199-207 2005年4月査読有り
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin

MC Moreira, C Barbot, N Tachi, N Kozuka, E Uchida, T Gibson, P Mendonca, M Costa, J Barros, T Yanagisawa …

NATURE GENETICS 29(2) 189-193 2001年10月査読有り
Homozygosity mapping of portuguese and Japanese forms of ataxia-oculomotor apraxia to 9p13, and evidence for genetic heterogeneity

MD Moreira, C Barbot, N Tachi, N Kozuka, P Mendonca, J Barros, P Coutinho, J Sequeiros, M Koenig

AMERICAN JOURNAL OF HUMAN GENETICS 68(2) 501-508 2001年2月査読有り
Charcot-Marie-Tooth disease type 1A duplication by PCR analysis

N Tachi, N Kozuka, K Ohya, S Chiba

PEDIATRIC NEUROLOGY 20(5) 360-363 1999年5月査読有り
Long-term effects of zonisamide in the treatment of epilepsy in children with intellectual disability

K Iinuma, T Minami, K Cho, N Kajii, N Tachi

JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42 68-73 1998年12月査読有り
Phenotypic variability in a family with a mitochondrial DNA T8993C mutation

Y Suzuki, T Wada, T Sakai, Y Ishikawa, R Minami, N Tachi, S Saitoh

PEDIATRIC NEUROLOGY 19(4) 283-286 1998年10月査読有り
A small direct tandem duplication of the myelin protein zero gene in a patient with Dejerine-Sottas disease phenotype

N Tachi, N Kozuka, K Ohya, S Chiba, S Yamashita

JOURNAL OF THE NEUROLOGICAL SCIENCES 156(2) 167-171 1998年4月査読有り
Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination

J Lopes, N Ravise, A Vandenberghe, F Palau, Ionasescu, V, M Mayer, N Levy, N Wood, N Tachi, P Bouche …

HUMAN MOLECULAR GENETICS 7(1) 141-148 1998年1月査読有り
A child case of haemophagocytic syndrome associated with cryptococcal meningoencephalitis

K Numata, H Tsutsumi, S Wakai, N Tachi, S Chiba

JOURNAL OF INFECTION 36(1) 118-119 1998年1月査読有り

もっとみる

MISC

A new mutation of IGHMBP2 gene in spinal muscular atrophy with respiratory distress type 1.

Pediatr Neurol 32 288-90 2005年
Non-radioactive PCR southern method for analysis of CTG repeat in myotonic dystrophy

Naoki Kozuka, Nobutada Tachi, Kazuhiro Ohya, Eiji Uchida, Shin Kikuchi, Yasuhito Sengoku

No To Hattatsu 35(5) 380-387 2003年
Expression of peripheral myelin protein zero in sural nerve of patients with Charcot-Marie-Tooth disease 1B.

Pediatr Neurol 24 33-5 2001年
A double mutation in a patient with X-linked myotubular myopathy.

Pediatr Neurol 24 297-9 2001年
Fukuyama muscular dystrophy associated with lack of C-terminal domain of dystrophin.

Pediatr Neurol 24 373-8 2001年
Hereditary cerebellar ataxia with peripheral neuropathy and mental retardation.

Eur Neurol 43 82-7 2000年
Expression of the myotonic dystrophy locus-associated homeodomain protein in congenital myotonic dystrophy.

J Child Neurol 14 471-3 1999年

所属学協会

共同研究・競争的資金等の研究課題

科研費等

舘延忠