Copyright © Philip M. Parker, INSEAD. Terms of Use.
| Domain | Definition |
Health | A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. (references) |
Source: compiled by the editor from various references; see credits. | |
| Domain | Title |
Books | |
Source: compiled by the editor from various references; see credits. | |
Hexadecimal (or equivalents, 770AD-1900s) (references)53 50 49 4E 4F 43 45 52 45 42 45 4C 4C 41 52 44 45 47 45 4E 45 52 41 54 49 4F 4E 53 |
| Leonardo da Vinci (1452-1519; backwards) (references)
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Binary Code (1918-1938, probably earlier) (references)01010011 01010000 01001001 01001110 01001111 01000011 01000101 01010010 01000101 01000010 01000101 01001100 01001100 01000001 01010010 00100000 01000100 01000101 01000111 01000101 01001110 01000101 01010010 01000001 01010100 01001001 01001111 01001110 01010011 |
HTML Code (1990) (references)S P I N O C E R E B E L L A R   D E G E N E R A T I O N S |
ISO 10646 (1991-1993) (references)0053 0050 0049 004E 004F 0043 0045 0052 0045 0042 0045 004C 004C 0041 0052 0044 0045 0047 0045 004E 0045 0052 0041 0054 0049 004F 004E 0053 |
Encryption (beginner's substitution cypher): (references)535043484937395239363946463552238394139483952355443494853 |
| 1. Usage: Commercial 2. Orthography 3. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.
