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Nagano Prefectural Hospital Organization
Homepage:
pref-nagano-hosp.jp
Alternate name:
長野県立病院機構
Child institutions:
Nagano Prefectural Suzaka Hospital,
Nagano Children's Hospital
ROR:
03cqxaf95
OpenAlex ID:
I4405284341
Works
26
Awards
8
Calculation of child and adult standard liver volume for liver transplantation
1995
·
Koichi Urata
, Seiji Kawasaki
, et al.
·
Hepatology
·
981
PDF
Germline mutations in HRAS proto-oncogene cause Costello syndrome
2005
·
Yoko Aoki
, Tetsuya Niihori
, et al.
·
Nature Genetics
·
687
Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome
2012
·
Yoshinori Tsurusaki
, Nobuhiko Okamoto
, et al.
·
Nature Genetics
·
534
Guidelines for the Evaluation of Valvular Regurgitation After Percutaneous Valve Repair or Replacement
2019
·
William A. Zoghbi
, Federico M. Asch
, et al.
·
Journal of the American Society of Echocardiography
·
467
Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations
2004
·
Ken Inoue
, Mehrdad Khajavi
, et al.
·
Nature Genetics
·
437
Mutations in the integrin α7 gene cause congenital myopathy
1998
·
Yukiko K. Hayashi
, Fan-Li Chou
, et al.
·
Nature Genetics
·
372
Normal values and clinical relevance of left atrial myocardial function analysed by speckle-tracking echocardiography: multicentre study
2014
·
D. A. Morris
, M. Takeuchi
, et al.
·
European Heart Journal - Cardiovascular Imaging
·
282
Consensus statement for the diagnosis and treatment of drug-induced lung injuries
2013
·
Keishi Kubo
, Arata Azuma
, et al.
·
Respiratory Investigation
·
280
PDF
Developmental perspective of sensory organization on postural control
1995
·
Shin-ichi Hirabayashi
, Yuuji Iwasaki
·
Brain and Development
·
278
Normal Range of Left Ventricular 2-Dimensional Strain: Japanese Ultrasound Speckle Tracking of the Left Ventricle (JUSTICE) Study
2012
·
Kiyohiro Takigiku
, Masaaki Takeuchi
, et al.
·
Circulation Journal
·
267
PDF
ZNF384 -related fusion genes define a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with a characteristic immunotype
2016
·
Shinsuke Hirabayashi
, Kentaro Ohki
, et al.
·
Haematologica
·
240
PDF
Bacterial interference among nasal inhabitants: eradication of Staphylococcus aureus from nasal cavities by artificial implantation of Corynebacterium sp.
2000
·
Y. Uehara
, H. Nakama
, et al.
·
Journal of Hospital Infection
·
234
Neonatal management of trisomy 18: Clinical details of 24 patients receiving intensive treatment
2006
·
Tomoki Kosho
, Tomohiko Nakamura
, et al.
·
American Journal of Medical Genetics Part A
·
202
Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity
2006
·
Yanlin Xing
, Fukiko Ichida
, et al.
·
Molecular Genetics and Metabolism
·
189
JCS 2017 Guideline on Prevention and Treatment of Infective Endocarditis
2019
·
Satoshi Nakatani
, Takahiro Ohara
, et al.
·
Circulation Journal
·
186
Molecular analysis of congenital central hypoventilation syndrome
2003
·
Ayako Sasaki
, Masayo Kanai
, et al.
·
Human Genetics
·
185
Phenotypic Spectrum of COL4A1 Mutations: Porencephaly to Schizencephaly
2012
·
Yuriko Yoneda
, Kazuhiro Haginoya
, et al.
·
Annals of Neurology
·
183
Phenotypic spectrum of CHARGE syndrome with CHD7 mutations
2006
·
Michihiko Aramaki
, Toru Udaka
, et al.
·
The Journal of Pediatrics
·
175
Age-Related Normal Range of Left Ventricular Strain and Torsion Using Three-Dimensional Speckle-Tracking Echocardiography
2013
·
Kyoko Kaku
, Masaaki Takeuchi
, et al.
·
Journal of the American Society of Echocardiography
·
173
Esophageal atresia: Prognostic classification revisited
2009
·
Tatsuya Okamoto
, Shigeru Takamizawa
, et al.
·
Surgery
·
173
Guidelines for obstetrical practice in Japan: Japan Society of Obstetrics and Gynecology and Japan Association of Obstetricians and Gynecologists 2020 edition
2022
·
Atsuo Itakura
, Shoji Satoh
, et al.
·
Journal of obstetrics and gynaecology research
·
147
Mental Health of Adolescents Exposed to the War in Ukraine
2024
·
Ryunosuke Goto
, Irina Pinchuk
, et al.
·
Archives of Pediatrics and Adolescent Medicine
·
140
Molecular and clinical analysis ofRAF1in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation
2010
·
Tomoko Kobayashi
, Yoko Aoki
, et al.
·
Human Mutation
·
136
Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia
2005
·
Tetsuya Niihori
, Yoko Aoki
, et al.
·
Journal of Human Genetics
·
136
Fifty microdeletions among 112 cases of Sotos syndrome: Low copy repeats possibly mediate the common deletion
2003
·
Naohiro Kurotaki
, Naoki Harada
, et al.
·
Human Mutation
·
136
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Works count:
26
Works count with child institutions:
1,276
Citation count:
857
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