Sudo A - Search Results

1

Germline mosaicism of a novel mutation in lysosome-associated membrane protein-2 deficiency (Danon disease).

Takahashi M, Yamamoto A, Takano K, Sudo A, Wada T, Goto Y, Nishino I, Saitoh S. Takahashi M, et al. Among authors: sudo a. Ann Neurol. 2002 Jul;52(1):122-5. doi: 10.1002/ana.10235. Ann Neurol. 2002. PMID: 12112061

2

Cerebellar and brainstem involvement in familial juvenile nephronophthisis type I.

Takano K, Nakamoto T, Okajima M, Sudo A, Uetake K, Saitoh S. Takano K, et al. Among authors: sudo a. Pediatr Neurol. 2003 Feb;28(2):142-4. doi: 10.1016/s0887-8994(02)00619-7. Pediatr Neurol. 2003. PMID: 12699867

3

Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome.

Saitoh S, Wada T, Okajima M, Takano K, Sudo A, Niikawa N. Saitoh S, et al. Among authors: sudo a. Brain Dev. 2005 Aug;27(5):389-91. doi: 10.1016/j.braindev.2003.12.013. Brain Dev. 2005. PMID: 16023557

4

Germline mosaicism of a novel UBE3A mutation in Angelman syndrome.

Hosoki K, Takano K, Sudo A, Tanaka S, Saitoh S. Hosoki K, et al. Among authors: sudo a. Am J Med Genet A. 2005 Oct 1;138A(2):187-9. doi: 10.1002/ajmg.a.30926. Am J Med Genet A. 2005. PMID: 16100729 No abstract available.

5

An infantile-juvenile form of Alexander disease caused by a R79H mutation in GFAP.

Asahina N, Okamoto T, Sudo A, Kanazawa N, Tsujino S, Saitoh S. Asahina N, et al. Among authors: sudo a. Brain Dev. 2006 Mar;28(2):131-3. doi: 10.1016/j.braindev.2005.05.004. Epub 2005 Sep 15. Brain Dev. 2006. PMID: 16168593 Free article.

6

[Sibling cases of severe infantile form of nemaline myopathy with ACTA1-gene mutation].

Sudo A, Hayashi Y, Sano H, Kawamura N, Nishino I, Nonaka I. Sudo A, et al. No To Hattatsu. 2013 Nov;45(6):452-6. No To Hattatsu. 2013. PMID: 24313005 Japanese.

7

High uptake on 11C-methionine positron emission tomographic scan of basal ganglia germinoma with cerebral hemiatrophy.

Sudo A, Shiga T, Okajima M, Takano K, Terae S, Sawamura Y, Ohnishi A, Nagashima K, Saitoh S. Sudo A, et al. AJNR Am J Neuroradiol. 2003 Oct;24(9):1909-11. AJNR Am J Neuroradiol. 2003. PMID: 14561627 Free PMC article.

8

Possible involvement of the tip of temporal lobe in Landau-Kleffner syndrome.

Shiraishi H, Takano K, Shiga T, Okajima M, Sudo A, Asahina N, Kohsaka S, Fukuhara M, Saitoh S. Shiraishi H, et al. Among authors: sudo a. Brain Dev. 2007 Sep;29(8):529-33. doi: 10.1016/j.braindev.2007.01.011. Epub 2007 Mar 26. Brain Dev. 2007. PMID: 17383838

9

Barth syndrome diagnosed in the subclinical stage of heart failure based on the presence of lipid storage myopathy and isolated noncompaction of the ventricular myocardium.

Takeda A, Sudo A, Yamada M, Yamazawa H, Izumi G, Nishino I, Ariga T. Takeda A, et al. Among authors: sudo a. Eur J Pediatr. 2011 Nov;170(11):1481-4. doi: 10.1007/s00431-011-1576-5. Epub 2011 Sep 20. Eur J Pediatr. 2011. PMID: 21932011

10

Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition.

Sudo A, Takeichi N, Hosoki K, Saitoh S. Sudo A, et al. J Laryngol Otol. 2011 Dec;125(12):1282-5. doi: 10.1017/S0022215111002453. Epub 2011 Sep 14. J Laryngol Otol. 2011. PMID: 21914246

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