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Tsurusaki, Y
84  results:
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1

Comprehensive simulation training for E-CPR improves the 1-..:

Inamori, T ; Unoki, T ; Tsurusaki, Y...
European Heart Journal.  44 (2023)  Supplement_2 - p. , 2023
Link: https://doi.org/10.1093/..
 
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2

Combined use of VA-ECMO and Impella (ECPELLA) improves shor..:

Unoki, T ; Nakayama, T ; Tsurusaki, Y...
European Heart Journal.  44 (2023)  Supplement_2 - p. , 2023
Link: https://doi.org/10.1093/..
 
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3

Impact of age and body mass index (BMI) on the short-term p..:

Nakayama, T ; Unoki, T ; Tsurusaki, Y...
European Heart Journal.  44 (2023)  Supplement_2 - p. , 2023
Link: https://doi.org/10.1093/..
 
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4

Molecular genetic analysis of 30 families with Joubert synd..:

Suzuki, T. ; Miyake, N. ; Tsurusaki, Y....
Clinical Genetics.  90 (2016)  6 - p. 526-535 , 2016
Link: https://doi.org/10.1111/..
 
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5

Different X-linkedKDM5Cmutations in affected male siblings:..:

Fujita, A. ; Waga, C. ; Hachiya, Y....
Clinical Genetics.  90 (2016)  3 - p. 276-281 , 2016
Link: https://doi.org/10.1111/..
 
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6

Delineation of clinical features in Wiedemann–Steiner syndr..:

Miyake, N. ; Tsurusaki, Y. ; Koshimizu, E....
Clinical Genetics.  89 (2015)  1 - p. 115-119 , 2015
Link: https://doi.org/10.1111/..
 
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7

Atypical giant axonal neuropathy arising from a homozygous ..:

Miyatake, S. ; Tada, H. ; Moriya, S....
Clinical Genetics.  87 (2014)  4 - p. 395-397 , 2014
Link: https://doi.org/10.1111/..
 
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8

Mutations in COG2 encoding a subunit of the conserved oligo..:

Kodera, H. ; Ando, N. ; Yuasa, I....
Clinical Genetics.  87 (2014)  5 - p. 455-460 , 2014
Link: https://doi.org/10.1111/..
 
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9

De novo EEF1A2mutations in patients with characteristic fac..:

Nakajima, J. ; Okamoto, N. ; Tohyama, J....
Clinical Genetics.  87 (2014)  4 - p. 356-361 , 2014
Link: https://doi.org/10.1111/..
 
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10

AKT3 and PIK3R2 mutations in two patients with megalencepha..:

Nakamura, K. ; Kato, M. ; Tohyama, J....
Clinical Genetics.  85 (2013)  4 - p. 396-398 , 2013
Link: https://doi.org/10.1111/..
 
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11

Whole exome sequencing revealed biallelic IFT122 mutations ..:

Tsurusaki, Y. ; Yonezawa, R. ; Furuya, M....
Clinical Genetics.  85 (2013)  6 - p. 592-594 , 2013
Link: https://doi.org/10.1111/..
 
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12

Coffin–Siris syndrome is a SWI/SNF complex disorder:

Tsurusaki, Y. ; Okamoto, N. ; Ohashi, H....
Clinical Genetics.  85 (2013)  6 - p. 548-554 , 2013
Link: https://doi.org/10.1111/..
 
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13

Exome sequencing in a family with an X‐linked lethal malfor..:

Tsurusaki, Y ; Kosho, T ; Hatasaki, K...
Clinical Genetics.  83 (2012)  2 - p. 135-144 , 2012
Link: https://doi.org/10.1111/..
 
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14

Homozygous c.14576G>A variant ofRNF213predicts early-onset ..:

Miyatake, S. ; Miyake, N. ; Touho, H....
Neurology.  78 (2012)  11 - p. 803-810 , 2012
Link: https://doi.org/10.1212/..
 
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15

A novel homozygous mutation of DARS2 may cause a severe LBS..:

Miyake, N ; Yamashita, S ; Kurosawa, K...
Clinical Genetics.  80 (2011)  3 - p. 293-296 , 2011
Link: https://doi.org/10.1111/..
 
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