Sato H - Search Results

1

Multiple craniosynostosis and facial dysmorphisms with homozygous IL11RA variant caused by maternal uniparental isodisomy of chromosome 9.

Nishimura N, Murakami H, Hayashi T, Sato H, Kurosawa K. Nishimura N, et al. Among authors: sato h. Congenit Anom (Kyoto). 2020 Sep;60(5):153-155. doi: 10.1111/cga.12371. Epub 2020 Apr 16. Congenit Anom (Kyoto). 2020. PMID: 32277509 No abstract available.

2

Neuroendoscopic fenestration for intracranial unilocular cysts and isolated lateral ventricles: four pediatric cases.

Shinohara N, Hirokawa D, Fukuyama R, Hayashi T, Sato H. Shinohara N, et al. Among authors: sato h. Childs Nerv Syst. 2022 Sep;38(9):1803-1807. doi: 10.1007/s00381-022-05451-5. Epub 2022 Jan 27. Childs Nerv Syst. 2022. PMID: 35083514

3

Moyamoya Syndrome in a Patient with Williams Syndrome: A Case Report.

Akimoto T, Suenaga J, Hayashi T, Hirokawa D, Ito S, Sato H, Yamamoto T. Akimoto T, et al. Among authors: sato h. Pediatr Neurosurg. 2022;57(5):365-370. doi: 10.1159/000525229. Epub 2022 May 31. Pediatr Neurosurg. 2022. PMID: 35640559 Free article.

4

Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations.

Ito S, Sekido K, Kanno H, Sato H, Tanaka M, Yamaguchi K, Yamamoto I. Ito S, et al. Among authors: sato h. J Neurosurg. 2005 Jan;102(1 Suppl):23-30. doi: 10.3171/ped.2005.102.1.0023. J Neurosurg. 2005. PMID: 16206730

5

Hypofractionated radiotherapy in children with diffuse intrinsic pontine glioma.

Hayashi A, Ito E, Omura M, Aida N, Tanaka M, Tanaka Y, Sato H, Miyagawa N, Yokosuka T, Iwasaki F, Hamanoue S, Goto H. Hayashi A, et al. Among authors: sato h. Pediatr Int. 2020 Jan;62(1):47-51. doi: 10.1111/ped.14070. Pediatr Int. 2020. PMID: 31785177 Free PMC article.

6

Long-term urological outcomes of spinal lipoma after prophylactic untethering in infancy: real-world outcomes by lipoma anatomy.

Hayashi C, Kumano Y, Hirokawa D, Sato H, Yamazaki Y. Hayashi C, et al. Among authors: sato h. Spinal Cord. 2020 Apr;58(4):490-495. doi: 10.1038/s41393-019-0385-y. Epub 2019 Nov 26. Spinal Cord. 2020. PMID: 31772345

7

A new phenotype of amniotic band syndrome with occipital encephalocele-like morphology: a case report.

Yazawa O, Hirokawa D, Okamoto K, Tanaka M, Shibasaki J, Sato H. Yazawa O, et al. Among authors: sato h. Childs Nerv Syst. 2022 Jul;38(7):1405-1408. doi: 10.1007/s00381-021-05406-2. Epub 2021 Nov 5. Childs Nerv Syst. 2022. PMID: 34739550

8

Myelomeningocele associated with split cord malformation type I -three case reports-.

Higashida T, Sasano M, Sato H, Sekido K, Ito S. Higashida T, et al. Among authors: sato h. Neurol Med Chir (Tokyo). 2010;50(5):426-30. doi: 10.2176/nmc.50.426. Neurol Med Chir (Tokyo). 2010. PMID: 20505305 Free article.

9

Prevalence of obesity, hyperlipemia and insulin resistance in children with suprasellar brain tumors.

Adachi M, Tsuchiya T, Muroya K, Asakura Y, Sekido K, Sato H. Adachi M, et al. Among authors: sato h. Clin Pediatr Endocrinol. 2007;16(1):1-9. doi: 10.1297/cpe.16.1. Epub 2007 Dec 7. Clin Pediatr Endocrinol. 2007. PMID: 24790338 Free PMC article.

10

Concurrent Ewing sarcoma family of tumors and fibrous dysplasia: possible diagnostic pitfall.

Kato K, Hayashi T, Tabuchi K, Okuzumi N, Kigasawa H, Abe Y, Toyoda Y, Aida N, Sekido K, Sato H, Tanaka M, Tanaka Y. Kato K, et al. Among authors: sato h. J Pediatr Hematol Oncol. 2007 Jan;29(1):15-8. doi: 10.1097/MPH.0b013e31803076bb. J Pediatr Hematol Oncol. 2007. PMID: 17230061

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