The diverse neurological features of Niemann-Pick disease type C: a report of two cases
Identifieur interne :
002E32 ( PascalFrancis/Curation );
précédent :
002E31;
suivant :
002E33
The diverse neurological features of Niemann-Pick disease type C: a report of two cases
Auteurs : R. J. Coleman ;
S. A. Robb ;
B. D. Lake ;
E. M. Brett ;
A. E. HardingSource :
-
Movement disorders [ 0885-3185 ] ; 1988.
RBID : Pascal:90-0140310
Descripteurs français
- Pascal (Inist)
- Sphingolipidose héréditaire Niemann Pick,
Lipide,
Ataxie,
Maladie héréditaire,
Métabolisme pathologie,
Système nerveux pathologie,
Cervelet,
Symptomatologie,
Enfant,
Etude cas,
Parkinson syndrome.
- Wicri :
English descriptors
| pA |
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|---|
| A03 | | 1 | | @0 Mov. disord. |
|---|
| A05 | | | | @2 3 |
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| A06 | | | | @2 4 |
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| A08 | 01 | 1 | ENG | @1 The diverse neurological features of Niemann-Pick disease type C: a report of two cases |
|---|
| A11 | 01 | 1 | | @1 COLEMAN (R. J.) |
|---|
| A11 | 02 | 1 | | @1 ROBB (S. A.) |
|---|
| A11 | 03 | 1 | | @1 LAKE (B. D.) |
|---|
| A11 | 04 | 1 | | @1 BRETT (E. M.) |
|---|
| A11 | 05 | 1 | | @1 HARDING (A. E.) |
|---|
| A14 | 01 | | | @1 Inst. neurology @2 London WC1N 3BG @3 GBR @Z A11011000 |
|---|
| A20 | | | | @1 295-299 |
|---|
| A21 | | | | @1 1988 |
|---|
| A23 | 01 | | | @0 ENG |
|---|
| A43 | 01 | | | @1 CNRS @2 20953 |
|---|
| A44 | | | | @0 0000 |
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| A45 | | | | @0 12 ref. |
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| A47 | 01 | 1 | | @0 90-0140310 |
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| A60 | | | | @1 P |
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| A61 | | | | @0 A |
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| A64 | | 1 | | @0 Movement disorders |
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| A66 | 01 | | | @0 USA |
|---|
| C02 | 01 | X | | @0 002B22D02 |
|---|
| C03 | 01 | X | FRE | @0 Sphingolipidose héréditaire Niemann Pick |
|---|
| C03 | 02 | X | FRE | @0 Lipide |
|---|
| C03 | 03 | X | FRE | @0 Ataxie |
|---|
| C03 | 04 | X | FRE | @0 Maladie héréditaire |
|---|
| C03 | 05 | X | FRE | @0 Métabolisme pathologie |
|---|
| C03 | 06 | X | FRE | @0 Système nerveux pathologie |
|---|
| C03 | 07 | X | FRE | @0 Cervelet |
|---|
| C03 | 08 | X | FRE | @0 Symptomatologie |
|---|
| C03 | 09 | X | FRE | @0 Enfant |
|---|
| C03 | 10 | X | FRE | @0 Etude cas |
|---|
| C03 | 11 | X | FRE | @0 Parkinson syndrome @4 INC |
|---|
| C03 | 01 | X | ENG | @0 Niemann Pick disease |
|---|
| C03 | 02 | X | ENG | @0 Lipids |
|---|
| C03 | 03 | X | ENG | @0 Ataxia |
|---|
| C03 | 04 | X | ENG | @0 Genetic disease |
|---|
| C03 | 05 | X | ENG | @0 Metabolic diseases |
|---|
| C03 | 06 | X | ENG | @0 Nervous system diseases |
|---|
| C03 | 07 | X | ENG | @0 Cerebellum |
|---|
| C03 | 08 | X | ENG | @0 Symptomatology |
|---|
| C03 | 09 | X | ENG | @0 Child |
|---|
| C03 | 10 | X | ENG | @0 Case study |
|---|
| C03 | 01 | X | SPA | @0 Esfingolipidosis hereditaria Niemann Pick |
|---|
| C03 | 02 | X | SPA | @0 Lípido |
|---|
| C03 | 03 | X | SPA | @0 Ataxia |
|---|
| C03 | 04 | X | SPA | @0 Enfermedad hereditaria |
|---|
| C03 | 05 | X | SPA | @0 Metabolismo patología |
|---|
| C03 | 06 | X | SPA | @0 Sistema nervioso patología |
|---|
| C03 | 07 | X | SPA | @0 Cerebelo |
|---|
| C03 | 08 | X | SPA | @0 Sintomatología |
|---|
| C03 | 09 | X | SPA | @0 Niño |
|---|
| C03 | 10 | X | SPA | @0 Estudio caso |
|---|
| C07 | 01 | X | FRE | @0 Homme |
|---|
| C07 | 02 | X | ENG | @0 Human |
|---|
| C07 | 03 | X | SPA | @0 Hombre |
|---|
| N21 | | | | @1 848 |
|---|
| N82 | | | | @1 NBS |
|---|
|
|---|
Links toward previous steps (curation, corpus...)
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Links to Exploration step
Pascal:90-0140310
Le document en format XML
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</author><author><name sortKey="Lake, B D" sort="Lake, B D" uniqKey="Lake B" first="B. D." last="Lake">B. D. Lake</name>
</author><author><name sortKey="Brett, E M" sort="Brett, E M" uniqKey="Brett E" first="E. M." last="Brett">E. M. Brett</name>
</author><author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
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