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Kumakura, Akira
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1

Three-Year Longitudinal Motor Function and Disability Level..:

Chong, Pin Fee ; Kira, Ryutaro ; Torisu, Hiroyuki...
Pediatric Neurology.  116 (2021)  - p. 14-19 , 2021
Link: https://doi.org/10.1016/..
 
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2

Thermolabile polymorphism of carnitine palmitoyltransferase..:

Shibata, Akiko ; Kasai, Mariko ; Hoshino, Ai...
Brain and Development.  41 (2019)  10 - p. 862-869 , 2019
Link: https://doi.org/10.1016/..
 
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3

Identification of a rare homozygous SZT2 variant due to uni..:

Imaizumi, Taichi ; Kumakura, Akira ; Yamamoto-Shimojima, Keiko.
Intractable & Rare Diseases Research.  7 (2018)  4 - p. 245-250 , 2018
Link: https://doi.org/10.5582/..
 
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4

Two mild cases of Dravet syndrome with truncating mutation ..:

Takaori, Toru ; Kumakura, Akira ; Ishii, Atsushi..
Brain and Development.  39 (2017)  1 - p. 72-74 , 2017
Link: https://doi.org/10.1016/..
 
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5

Herpes zoster meningitis in immunocompetent children: Two c..:

Itoh, Naohiro ; Motokura, Kouji ; Kumakura, Akira..
Pediatrics International.  59 (2017)  10 - p. 1116-1118 , 2017
Link: https://doi.org/10.1111/..
 
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6

Severe Hemolytic Jaundice in a Neonate with a Novel COL4A1 ..:

Tomotaki, Seiichi ; Mizumoto, Hiroshi ; Hamabata, Takayuki...
Pediatrics & Neonatology.  57 (2016)  6 - p. 522-525 , 2016
Link: https://doi.org/10.1016/..
 
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7

Comorbid Epilepsy and Developmental Disorders in Congenital..:

Miyazaki, Aya ; Sakaguchi, Heima ; Aiba, Takeshi...
JACC: Clinical Electrophysiology.  2 (2016)  3 - p. 266-276 , 2016
Link: https://doi.org/10.1016/..
 
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8

A haploinsufficiency of FOXG1 identified in a boy with cong..:

Kumakura, Akira ; Takahashi, Satoru ; Okajima, Kazuki.
Brain and Development.  36 (2014)  8 - p. 725-729 , 2014
Link: https://doi.org/10.1016/..
 
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9

ADORA2Apolymorphism predisposes children to encephalopathy ..:

Shinohara, Mayu ; Saitoh, Makiko ; Nishizawa, Daisuke...
Neurology.  80 (2013)  17 - p. 1571-1576 , 2013
Link: https://doi.org/10.1212/..
 
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10

Phenotypic Spectrum ofCOL4A1Mutations: Porencephaly to Schi..:

Yoneda, Yuriko ; Haginoya, Kazuhiro ; Kato, Mitsuhiro...
Annals of Neurology.  73 (2012)  1 - p. 48-57 , 2012
Link: https://doi.org/10.1002/..
 
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11

Mild case of d‐bifunctional protein deficiency associated w..:

Mizumoto, Hiroshi ; Akashi, Ryoko ; Hikita, Norikatsu...
Pediatrics International.  54 (2012)  2 - p. 303-304 , 2012
Link: https://doi.org/10.1111/..
 
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12

Pandemic Influenza A-Associated Acute Necrotizing Encephalo..:

Kumakura, Akira ; Iida, Chihiro ; Saito, Makiko..
Pediatric Neurology.  45 (2011)  5 - p. 344-346 , 2011
Link: https://doi.org/10.1016/..
 
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13

Novel de novo splice-site mutation of SCN1A in a patient wi..:

Kumakura, Akira ; Ito, Masatoshi ; Hata, Daisuke...
Brain and Development.  31 (2009)  2 - p. 179-182 , 2009
Link: https://doi.org/10.1016/..
 
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14

Diffusion-Weighted Imaging in Preclinical Leigh Syndrome:

Kumakura, Akira ; Asada, Junko ; Okumura, Ryosuke..
Pediatric Neurology.  41 (2009)  4 - p. 309-311 , 2009
Link: https://doi.org/10.1016/..
 
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15

Letters to the Editor:

Hata, Atsuko ; Fujita, Masaaki ; Morishima, Tatsuya..
Journal of Paediatrics and Child Health.  44 (2008)  10 - p. 607-609 , 2008
Link: https://doi.org/10.1111/..
 
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