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Items: 1 to 20 of 30

1.

Structural and Diffusion MRI Analyses With Histological Observations in Patients With Lissencephaly.

Vasung L, Rezayev A, Yun HJ, Song JW, van der Kouwe A, Stewart N, Palani A, Shiohama T, Chouinard-Decorte F, Levman J, Takahashi E.

Front Cell Dev Biol. 2019 Jul 11;7:124. doi: 10.3389/fcell.2019.00124. eCollection 2019.

2.

Low-prevalence mosaicism of chromosome 18q distal deletion identified by exome-based copy number profiling in a child with cerebral hypomyelination.

Shiohama T, Nakashima M, Ikehara H, Kato M, Saitsu H.

Congenit Anom (Kyoto). 2019 Jul 21. doi: 10.1111/cga.12351. [Epub ahead of print] No abstract available.

PMID:
31328296
3.

Structural magnetic resonance imaging demonstrates abnormal cortical thickness in Down syndrome: Newborns to young adults.

Levman J, MacDonald A, Baumer N, MacDonald P, Stewart N, Lim A, Cogger L, Shiohama T, Takahashi E.

Neuroimage Clin. 2019;23:101874. doi: 10.1016/j.nicl.2019.101874. Epub 2019 May 28.

4.

The left lateral occipital cortex exhibits decreased thickness in children with sensorineural hearing loss.

Shiohama T, McDavid J, Levman J, Takahashi E.

Int J Dev Neurosci. 2019 Aug;76:34-40. doi: 10.1016/j.ijdevneu.2019.05.009. Epub 2019 Jun 4.

PMID:
31173823
5.

Quantitative brain morphological analysis in CHARGE syndrome.

Shiohama T, McDavid J, Levman J, Takahashi E.

Neuroimage Clin. 2019;23:101866. doi: 10.1016/j.nicl.2019.101866. Epub 2019 May 21.

6.

MicroRNAs profiling in fibroblasts derived from patients with Gorlin syndrome.

Shiohama T, Fujii K, Miyashita T, Takatani T, Ikehara H, Uchikawa H, Motojima T, Uchida T, Shimojo N.

J Hum Genet. 2019 Aug;64(8):757-765. doi: 10.1038/s10038-019-0607-3. Epub 2019 May 14.

PMID:
31089267
7.

Structural Magnetic Resonance Imaging-Based Brain Morphology Study in Infants and Toddlers With Down Syndrome: The Effect of Comorbidities.

Shiohama T, Levman J, Baumer N, Takahashi E.

Pediatr Neurol. 2019 Nov;100:67-73. doi: 10.1016/j.pediatrneurol.2019.03.015. Epub 2019 Mar 22.

PMID:
31036426
8.

Ex vivo fetal brain MRI: Recent advances, challenges, and future directions.

Vasung L, Charvet CJ, Shiohama T, Gagoski B, Levman J, Takahashi E.

Neuroimage. 2019 Jul 15;195:23-37. doi: 10.1016/j.neuroimage.2019.03.034. Epub 2019 Mar 21. Review. No abstract available.

9.

Surface- and voxel-based brain morphologic study in Rett and Rett-like syndrome with MECP2 mutation.

Shiohama T, Levman J, Takahashi E.

Int J Dev Neurosci. 2019 Apr;73:83-88. doi: 10.1016/j.ijdevneu.2019.01.005. Epub 2019 Jan 25.

PMID:
30690146
10.

A novel CUL7 mutation in a Japanese patient with 3M syndrome.

Takatani T, Shiohama T, Takatani R, Shimojo N.

Hum Genome Var. 2018 Oct 23;5:30. doi: 10.1038/s41439-018-0029-3. eCollection 2018.

11.

Facial nerve palsy associated with atomoxetine-induced hypertension.

Kobayashi H, Fujii K, Kobayashi M, Saito N, Okunushi K, Ebata R, Shiohama T, Sawada D, Shimojo N.

Brain Dev. 2019 Mar;41(3):310-312. doi: 10.1016/j.braindev.2018.09.009. Epub 2018 Oct 9.

PMID:
30314873
12.

Bilateral spinal anterior horn lesions in acute motor axonal neuropathy.

Sawada D, Fujii K, Misawa S, Shiohama T, Fukuhara T, Fujita M, Kuwabara S, Shimojo N.

Brain Dev. 2018 Oct;40(9):830-832. doi: 10.1016/j.braindev.2018.05.009. Epub 2018 May 28.

PMID:
29853225
13.

Acute myelitis associated with human herpesvirus 7 infection.

Fukuhara T, Fujii K, Ogawa T, Shiohama T, Shimojo N.

Pediatr Int. 2018 Feb;60(2):198-199. doi: 10.1111/ped.13459. Epub 2018 Jan 23. No abstract available.

PMID:
29359421
14.

l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case report.

Shiohama T, Ohashi H, Shimizu K, Fujii K, Oba D, Takatani T, Kato M, Shimojo N.

Brain Dev. 2018 Apr;40(4):353-356. doi: 10.1016/j.braindev.2017.12.008. Epub 2017 Dec 27.

PMID:
29289388
15.

An Acquired Form of Dandy-Walker Malformation with Enveloping Hemosiderin Deposits.

Shiohama T, Ando R, Fujii K, Mukai H, Naruke Y, Sugita K, Kato E, Shimojo N.

Case Rep Pediatr. 2017;2017:3861608. doi: 10.1155/2017/3861608. Epub 2017 Oct 25.

16.

Progressive subglottic stenosis in a child with Pallister-Killian syndrome.

Shiohama T, Fujii K, Shimizu K, Ohashi H, Takatani T, Okamoto N, Nishimura G, Kato M, Shimojo N.

Congenit Anom (Kyoto). 2018 May;58(3):102-104. doi: 10.1111/cga.12240. Epub 2017 Aug 29.

PMID:
28745802
17.

Brain morphology in children with nevoid basal cell carcinoma syndrome.

Shiohama T, Fujii K, Miyashita T, Mizuochi H, Uchikawa H, Shimojo N.

Am J Med Genet A. 2017 Apr;173(4):946-952. doi: 10.1002/ajmg.a.38115.

PMID:
28328116
18.

Coronary ostium occlusion by coronary cusp displacement in Williams syndrome.

Shiohama T, Fujii K, Ebata R, Funabashi N, Matsumiya G, Saito YK, Takechi F, Yonemori Y, Nakatani Y, Shimojo N.

Pediatr Int. 2016 Jun;58(6):487-490. doi: 10.1111/ped.12828. Epub 2015 Dec 29.

PMID:
26711184
19.

Focal Coxsackie virus B5 encephalitis with synchronous seizure cluster and eruption: Infantile case.

Shiohama T, Omata T, Muta K, Kodama K, Fujii K, Shimojo N.

Pediatr Int. 2016 May;58(5):415-417. doi: 10.1111/ped.12827. Epub 2015 Dec 29.

PMID:
26711006
20.

[A 9-month-old boy manifesting generalized hypotonia and tented mouth].

Shiohama T.

No To Hattatsu. 2015 Sep;47(5):341-2. Japanese. No abstract available.

PMID:
26502649

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