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Pyridoxine-dependent seizures: report of a case with atypical clinical features and abnormal MRI scans.
J Child Neurol. 1992 Jan;7(1):24-8. doi: 10.1177/088307389200700104.
J Child Neurol. 1992.
PMID: 1552147
Type 3 GM1 gangliosidosis: clinical and neuroradiological findings in an 11-year-old girl.
Tanaka R, Momoi T, Yoshida A, Okumura M, Yamakura S, Takasaki Y, Kiyomasu T, Yamanaka C.
Tanaka R, et al. Among authors: yamakura s.
J Neurol. 1995 May;242(5):299-303. doi: 10.1007/BF00878872.
J Neurol. 1995.
PMID: 7643138
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Elevation of serum creatine phosphokinase during growth hormone treatment in patients with multiple pituitary hormone deficiency.
Momoi T, Yamanaka C, Tanaka R, Yoshida A, Okumura M, Yamakura S, Takasaki Y, Sasaki H, Kawai M.
Momoi T, et al. Among authors: yamakura s.
Eur J Pediatr. 1995 Nov;154(11):886-9. doi: 10.1007/BF01957498.
Eur J Pediatr. 1995.
PMID: 8582399
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Rotavirus encephalitis: detection of the virus genomic RNA in the cerebrospinal fluid of a child.
Yoshida A, Kawamitu T, Tanaka R, Okumura M, Yamakura S, Takasaki Y, Hiramatsu H, Momoi T, Iizuka M, Nakagomi O.
Yoshida A, et al. Among authors: yamakura s.
Pediatr Infect Dis J. 1995 Oct;14(10):914-6.
Pediatr Infect Dis J. 1995.
PMID: 8584327
Review.
No abstract available.
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Arima syndrome caused by CEP290 specific variant and accompanied with pathological cilium; clinical comparison with Joubert syndrome and its related diseases.
Itoh M, Ide S, Iwasaki Y, Saito T, Narita K, Dai H, Yamakura S, Furue T, Kitayama H, Maeda K, Takahashi E, Matsui K, Goto YI, Takeda S, Arima M.
Itoh M, et al. Among authors: yamakura s.
Brain Dev. 2018 Apr;40(4):259-267. doi: 10.1016/j.braindev.2017.11.002. Epub 2017 Dec 6.
Brain Dev. 2018.
PMID: 29217415
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[Case of infantile autism with pediatric Wernicke's encephalopathy due to severe eating disorder].
Watanabe S, Yamakura S, Hirano K, Okumura Y, Aiba H.
Watanabe S, et al. Among authors: yamakura s.
No To Hattatsu. 2009 Jan;41(1):43-6.
No To Hattatsu. 2009.
PMID: 19172816
Japanese.
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