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Brain & Development|May 13, 2018
Distinctive facies, macrocephaly, and developmental delay are signs of a PTEN mutation in childhoodKohji Kato, Seiji Mizuno, Mie Inaba, et al.Brain & Development|May 19, 2018
Robot-assisted training using Hybrid Assistive Limb® for cerebral palsyMayumi Matsuda, Nobuaki Iwasaki, Yuki Mataki, et al.Brain & Development|May 3, 2018
Early prognostic factors for acute encephalopathy with reduced subcortical diffusionTetsuhiro Fukuyama, Shouko Yamauchi, Shunsuke Amagasa, et al.Brain & Development|June 11, 2019
Transition from Leigh syndrome to MELAS syndrome in a patient with heteroplasmic MT-ND3 m.10158T>CAtsuko Kori, Ikumi Hori, Tatsushi Tanaka, et al.Brain & Development|January 1, 1986
The syndrome of the absence of a septum pellucidum with porencephalyN Shimozawa, K Ohno, S Takashima, et al.Brain & Development|January 1, 1985
The cephalization index: a screening device for brain maturity and vulnerability in normal and intrauterine growth retarded newbornsS Harel, A Tomer, Y Barak, et al.Brain & Development|October 16, 2012
Radiation hazards in children - lessons from Chernobyl, Three Mile Island and FukushimaShinji FushikiBrain & Development|October 20, 2012
Clinical and cytogenetic features of a Potocki-Lupski syndrome with the shortest 0.25Mb microduplication in 17p11.2 including RAI1Cha Gon Lee, Sang-Jin Park, Shin-Young Yim, et al.Brain & Development|August 28, 2012
Regional cerebral blood flow and abnormal eating behavior in Prader-Willi syndromeKaeko Ogura, Toshikatsu Fujii, Nobuhito Abe, et al.Brain & Development|January 1, 1987
Cerebral lesions in early prematurity: EEG prognostic value in the neonatal periodM F Radvanyi-Bouvet, O de Bethmann, M Monset-Couchard, et al.Pageof 478