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Acta Paediatrica (Oslo, Norway : 1992)|April 1, 1996
Truncated XPA protein detected in atypical group A xeroderma pigmentosumT Mimaki, M Nitta, M Saijo, et al.Neurology|August 1, 1997
Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophinN Tachi, K Ohya, S Chiba, et al.Pediatric Neurology|November 27, 1998
Phenotypic variability in a family with a mitochondrial DNA T8993C mutationY Suzuki, T Wada, T Sakai, et al.Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1995
Clinical features of retinal detachment in the elderlyH Tanihara, S Okinami, H Minami, et al.No to Hattatsu = Brain and Development|September 1, 1992
[Ataxic cerebral palsy and brain imaging]S Imamura, N Tachi, A Tsuzuki, et al.Acta Paediatrica Japonica : Overseas Edition|February 1, 1991
Benign familial neonatal convulsions: clinical features of the propositus and comparison with the previously reported casesS Wakai, N Tachi, S Chiba, et al.Acta Neurologica Scandinavica|May 1, 1992
Allelic heterogeneity in group A xeroderma pigmentosumT Mimaki, K Tanaka, Y Okada, et al.Brain & Development|January 1, 1996
Muscle pathology in Marinesco-Sjogren syndrome: a unique ultrastructural featureK Sasaki, K Suga, S Tsugawa, et al.Neuroscience Letters|February 9, 1996
A new mutation of the Po gene in patients with Charcot-Marie-Tooth disease type 1B: screening of the Po gene by heteroduplex analysisN Tachi, N Kozuka, K Ohya, et al.Cellular and Molecular Life Sciences : CMLS|October 19, 2005
Structural analysis of leucine-rich-repeat variants in proteins associated with human diseasesN Matsushima, N Tachi, Y Kuroki, et al.Pageof 10