Yoshihisa Higuchi - Search Results

Year	Number of Results
2004	1
2005	3
2006	1
2007	1
2008	1
2011	1
2013	1
2016	1
2017	1
2022	1
2024	1

1

Inflammatory changes in infantile-onset LMNA-associated myopathy.

Komaki H, Hayashi YK, Tsuburaya R, Sugie K, Kato M, Nagai T, Imataka G, Suzuki S, Saitoh S, Asahina N, Honke K, Higuchi Y, Sakuma H, Saito Y, Nakagawa E, Sugai K, Sasaki M, Nonaka I, Nishino I. Komaki H, et al. Among authors: higuchi y. Neuromuscul Disord. 2011 Aug;21(8):563-8. doi: 10.1016/j.nmd.2011.04.010. Epub 2011 May 31. Neuromuscul Disord. 2011. PMID: 21632249

2

Descending Necrotizing Mediastinitis Caused by Streptococcus pyogenes in a Child with Primary Epstein-Barr Virus Infection.

Yoshimura M, Daifu T, Suehiro M, Shoji T, Higuchi Y. Yoshimura M, et al. Among authors: higuchi y. Pediatr Rep. 2022 Dec 27;15(1):16-19. doi: 10.3390/pediatric15010003. Pediatr Rep. 2022. PMID: 36649003 Free PMC article.

3

Epilepsy in children with trisomy 18.

Kumada T, Maihara T, Higuchi Y, Nishida Y, Taniguchi Y, Fujii T. Kumada T, et al. Among authors: higuchi y. Am J Med Genet A. 2013 Apr;161A(4):696-701. doi: 10.1002/ajmg.a.35763. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23494888

4

Familial acute necrotizing encephalopathy without RANBP2 mutation: Poor outcome.

Nishimura N, Higuchi Y, Kimura N, Nozaki F, Kumada T, Hoshino A, Saitoh M, Mizuguchi M. Nishimura N, et al. Among authors: higuchi y. Pediatr Int. 2016 Nov;58(11):1215-1218. doi: 10.1111/ped.13119. Pediatr Int. 2016. PMID: 27882739

5

Seizure-genotype relationship in Fukuyama-type congenital muscular dystrophy.

Yoshioka M, Higuchi Y, Fujii T, Aiba H, Toda T. Yoshioka M, et al. Among authors: higuchi y. Brain Dev. 2008 Jan;30(1):59-67. doi: 10.1016/j.braindev.2007.05.012. Epub 2007 Jun 26. Brain Dev. 2008. PMID: 17597323

6

[Non-invasive positive pressure ventilation during the management of severe spinal muscular atrophy type I].

Inoue K, Kimura N, Higuchi Y, Nakamoto M, Imai T, Nishio H. Inoue K, et al. Among authors: higuchi y. No To Hattatsu. 2017 Mar;49(2):141-4. No To Hattatsu. 2017. PMID: 30113157 Japanese.

7

Juvenile xanthogranuloma manifesting with LCH-associated neurodegenerative disease-like radiological findings.

Daifu T, Umeda K, Yokoyama A, Yoshida T, Saida S, Kato I, Hiramatsu H, Kudo K, Higuchi Y, Takita J. Daifu T, et al. Among authors: higuchi y. Pediatr Blood Cancer. 2024 Apr 28:e31043. doi: 10.1002/pbc.31043. Online ahead of print. Pediatr Blood Cancer. 2024. PMID: 38679849

8

Dystonia in a 13-year-old boy with secondary progressive multiple sclerosis.

Shiraishi K, Higuchi Y, Ozawa K. Shiraishi K, et al. Among authors: higuchi y. Brain Dev. 2004 Dec;26(8):539-41. doi: 10.1016/j.braindev.2004.02.014. Brain Dev. 2004. PMID: 15533657

9

Long-term prognosis of epilepsies and related seizure disorders in Fukuyama-type congenital muscular dystrophy.

Yoshioka M, Higuchi Y. Yoshioka M, et al. Among authors: higuchi y. J Child Neurol. 2005 Apr;20(4):385-91. doi: 10.1177/08830738050200041901. J Child Neurol. 2005. PMID: 15921243

10

A family of Emery-Dreifuss muscular dystrophy with extreme difference in severity.

Higuchi Y, Hongou M, Ozawa K, Kokawa H, Masaki M. Higuchi Y, et al. Pediatr Neurol. 2005 May;32(5):358-60. doi: 10.1016/j.pediatrneurol.2004.12.011. Pediatr Neurol. 2005. PMID: 15866440

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