Kobayashi Y - Search Results

1

Successful treatment with liposteroid followed by reduced intensity stem cell transplantation in an infant with perforin deficiency presenting with hemophagocytic lymphohistiocytosis.

Kobayashi Y, Salih HM, Kajiume T, Nakamura K, Miyagawa S, Sato T, Nishimura S, Kobayashi M. Kobayashi Y, et al. Among authors: kobayashi m. J Pediatr Hematol Oncol. 2007 Mar;29(3):178-82. doi: 10.1097/MPH.0b013e3180335030. J Pediatr Hematol Oncol. 2007. PMID: 17356398

2

A case of frontal lobe epilepsy in which amplitude-integrated EEG combined with conventional EEG was useful for evaluating clusters of seizures.

Ishikawa N, Kobayashi Y, Kobayashi M. Ishikawa N, et al. Among authors: kobayashi y, kobayashi m. Epilepsy Behav. 2010 Aug;18(4):485-7. doi: 10.1016/j.yebeh.2010.05.018. Epub 2010 Jun 26. Epilepsy Behav. 2010. PMID: 20580620

3

Acute severe encephalopathy related to human herpesvirus-6 infection in a patient with carnitine palmitoyltransferase 2 deficiency carrying thermolabile variants.

Kobayashi Y, Ishikawa N, Tsumura M, Fujii Y, Okada S, Shigematsu Y, Kobayashi M. Kobayashi Y, et al. Among authors: kobayashi m. Brain Dev. 2013 May;35(5):449-53. doi: 10.1016/j.braindev.2012.06.013. Epub 2012 Jul 31. Brain Dev. 2013. PMID: 22854105

4

Paroxysmal periodic dystonic postures in an infant with 18q23 deletion syndrome.

Ishikawa N, Kobayashi Y, Fujii Y, Kobayashi M. Ishikawa N, et al. Among authors: kobayashi y, kobayashi m. Neuropediatrics. 2013 Jun;44(3):163-6. doi: 10.1055/s-0032-1329613. Epub 2012 Nov 1. Neuropediatrics. 2013. PMID: 23117893

5

Identification of the integrin β3 L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis.

Kobayashi Y, Matsui H, Kanai A, Tsumura M, Okada S, Miki M, Nakamura K, Kunishima S, Inaba T, Kobayashi M. Kobayashi Y, et al. Among authors: kobayashi m. Br J Haematol. 2013 Feb;160(4):521-9. doi: 10.1111/bjh.12160. Epub 2012 Dec 17. Br J Haematol. 2013. PMID: 23253071 Free article.

6

Management of advanced-stage neuroblastoma in a patient with 21-hydroxalase deficiency.

Utsunomiya AN, Okada S, Hara K, Miki M, Mizoguchi Y, Kobayashi Y, Miyagawa S, Jinno K, Nakamura K, Sato T, Kobayashi M. Utsunomiya AN, et al. Among authors: kobayashi y, kobayashi m. Pediatr Int. 2013 Aug;55(4):e96-9. doi: 10.1111/ped.12093. Pediatr Int. 2013. PMID: 23910817

7

Compound heterozygosity in GPR56 with bilateral frontoparietal polymicrogyria.

Fujii Y, Ishikawa N, Kobayashi Y, Kobayashi M, Kato M. Fujii Y, et al. Among authors: kobayashi y, kobayashi m. Brain Dev. 2014 Jun;36(6):528-31. doi: 10.1016/j.braindev.2013.07.015. Epub 2013 Aug 24. Brain Dev. 2014. PMID: 23981349

8

Ictal electroencephalography and electromyography features in symptomatic infantile epileptic encephalopathy with late-onset spasms.

Ishikawa N, Kobayashi Y, Fujii Y, Tajima G, Kobayashi M. Ishikawa N, et al. Among authors: kobayashi y, kobayashi m. Neuropediatrics. 2014 Feb;45(1):36-41. doi: 10.1055/s-0033-1357479. Epub 2013 Oct 13. Neuropediatrics. 2014. PMID: 24122274

9

A case of trisomy 18 with exacerbation of seizures triggered by administration of valproic acid.

Kobayashi Y, Ishikawa N, Fujii Y, Nakamura K, Kobayashi M. Kobayashi Y, et al. Among authors: kobayashi m. Am J Med Genet A. 2014 Jan;164A(1):285-6. doi: 10.1002/ajmg.a.36205. Epub 2013 Nov 15. Am J Med Genet A. 2014. PMID: 24243702 No abstract available.

10

A pediatric case of peripheral polyneuropathy with IgM anti-GM1 antibody associated with A group a beta-hemolytic Streptococcus infection.

Ishikawa N, Kobayashi Y, Fujii Y, Samukawa M, Kusunoki S, Kobayashi M. Ishikawa N, et al. Among authors: kobayashi y, kobayashi m. Pediatr Neurol. 2014 Sep;51(3):441-3. doi: 10.1016/j.pediatrneurol.2014.03.019. Epub 2014 Mar 27. Pediatr Neurol. 2014. PMID: 25160552

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