Izumi T - Search Results

1

Manifestation of neurofibromatosis 1 in a patient with X-linked adrenoleukodystrophy.

Yamada H, Izumi T. Yamada H, et al. Among authors: izumi t. Pediatr Neurol. 2009 Sep;41(3):211-4. doi: 10.1016/j.pediatrneurol.2009.03.015. Pediatr Neurol. 2009. PMID: 19664540

2

Acute necrotizing encephalopathy associated with hemophagocytic syndrome.

Akiyoshi K, Hamada Y, Yamada H, Kojo M, Izumi T. Akiyoshi K, et al. Among authors: izumi t. Pediatr Neurol. 2006 Apr;34(4):315-8. doi: 10.1016/j.pediatrneurol.2005.08.030. Pediatr Neurol. 2006. PMID: 16638510

3

A relapse of systemic type juvenile idiopathic arthritis after a rubella vaccination in a patient during a long-term remission period.

Korematsu S, Miyahara H, Kawano T, Yamada H, Akiyoshi K, Sato K, Maeda T, Suenobu S, Izumi T. Korematsu S, et al. Among authors: izumi t. Vaccine. 2009 Aug 13;27(37):5041-2. doi: 10.1016/j.vaccine.2009.06.052. Epub 2009 Jul 2. Vaccine. 2009. PMID: 19576941

4

The ominous sequence in patients with tuberous sclerosis complex.

Yamada H, Akiyoshi K, Izumi T. Yamada H, et al. Among authors: izumi t. Brain Dev. 2014 Mar;36(3):254-8. doi: 10.1016/j.braindev.2013.04.002. Epub 2013 May 3. Brain Dev. 2014. PMID: 23647917

5

Clinical presentation of patients with neurofibromatosis type 1 in infancy and childhood: genetic traits and gender effects.

Suenobu S, Akiyoshi K, Maeda T, Korematsu S, Izumi T. Suenobu S, et al. Among authors: izumi t. J Child Neurol. 2008 Nov;23(11):1282-7. doi: 10.1177/0883073808318539. J Child Neurol. 2008. PMID: 18984837

6

Novel mutation of early, perinatal-onset, myopathic-type very-long-chain acyl-CoA dehydrogenase deficiency.

Korematsu S, Kosugi Y, Kumamoto T, Yamaguchi S, Izumi T. Korematsu S, et al. Among authors: izumi t. Pediatr Neurol. 2009 Aug;41(2):151-3. doi: 10.1016/j.pediatrneurol.2009.02.020. Pediatr Neurol. 2009. PMID: 19589468

7

PLEDs in an infant with congenital protein C deficiency: a case report.

Sekiguchi K, Akiyoshi K, Okazaki N, Yamada H, Suzuki M, Maeda T, Suenobu S, Izumi T, Kang D. Sekiguchi K, et al. Among authors: izumi t. Clin Neurophysiol. 2010 May;121(5):800-1. doi: 10.1016/j.clinph.2009.12.031. Epub 2010 Jan 22. Clin Neurophysiol. 2010. PMID: 20097123 No abstract available.

8

A new cholesterol biosynthesis and absorption disorder associated with epilepsy, hypogonadism, and cerebro-cerebello-bulbar degeneration.

Korematsu S, Uchiyama S, Honda A, Izumi T. Korematsu S, et al. Among authors: izumi t. Pediatr Neurol. 2014 Jun;50(6):601-4. doi: 10.1016/j.pediatrneurol.2014.01.050. Epub 2014 Feb 10. Pediatr Neurol. 2014. PMID: 24726258

9

Progressive dysautonomia in two patients with xeroderma pigmentosum group A.

Kobayashi O, Miyahara H, Abe N, Goto C, Okanari K, Akiyoshi K, Korematsu S, Izumi T. Kobayashi O, et al. Among authors: izumi t. Pediatr Neurol. 2014 Jun;50(6):619-21. doi: 10.1016/j.pediatrneurol.2014.01.026. Epub 2014 Jan 16. Pediatr Neurol. 2014. PMID: 24679606

10

Hemimegalencephaly in a patient with coexisting trisomy 21 and hypomelanosis of Ito.

Okanari K, Miyahara H, Itoh M, Takahashi A, Aizaki K, Nakagawa E, Otsuki T, Izumi T. Okanari K, et al. Among authors: izumi t. J Child Neurol. 2014 Mar;29(3):415-20. doi: 10.1177/0883073812469297. Epub 2012 Dec 23. J Child Neurol. 2014. PMID: 23266943

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