Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?
- Author
- KATO, M1 ; TAKIZAWA, N2 ; YAMADA, S2 ; ITO, A1 ; HONMA, T1 ; HASHIMOTO, M3 ; SAITO, E3 ; OHTA, T3 ; CHIKAOKA, H4 ; HAYASAKA, K1
[1] Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan
[2] Department of Pediatrics, National Sanatorium Ishikawa Hospital, Kaga, Ishikawa, Japan
[3] Department of Pediatrics and Neonatal Medicine, Yamagata Saisei Hospital, Yamagata, Japan
[4] Chikaoka Pediatric Clinic, Yamagata, Japan - Source
Annals of neurology. 1999, Vol 46, Num 4, pp 660-663 ; ref : 13 ref
- Publisher
- Willey-Liss, Hoboken
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Association morbide Cervelet Enfant Etude cas Exploration Forme clinique Hypoplasie Imagerie RMN Lissencéphalie Pachygyrie Encéphale pathologie Homme Imagerie médicale Malformation Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Concomitant disease Cerebellum Child Case study Exploration Clinical form Hypoplasia Nuclear magnetic resonance imaging Lissencephaly Cerebral disorder Human Medical imagery Malformation Central nervous system disease Nervous system diseases
- Keyword (es)
- Asociación morbosa Cerebelo Niño Estudio caso Exploración Forma clínica Hipoplasia Imageria RMN Lisencefalia Encéfalo patología Hombre Imageneria medical Malformación Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17D Malformations of the nervous system
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 1961064
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
Access to the document
Install on your browser
DOI
10.1002/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q 
https://dx.doi.org/10.1002/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q
"O:13:\"PanistOpenUrl\":36:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000idc\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:55:\"10.1002\/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:9:\"\u0000*\u0000jtitle\";s:19:\"Annals of neurology\";s:9:\"\u0000*\u0000stitle\";s:11:\"Ann. neurol\";s:7:\"\u0000*\u0000date\";s:4:\"1999\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:1:\"4\";s:8:\"\u0000*\u0000spage\";s:3:\"660\";s:8:\"\u0000*\u0000epage\";s:3:\"663\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0364-5134\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:4:\"KATO\";s:10:\"\u0000*\u0000aufirst\";s:1:\"M\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:9:{i:0;s:11:\"TAKIZAWA, N\";i:1;s:9:\"YAMADA, S\";i:2;s:6:\"ITO, A\";i:3;s:8:\"HONMA, T\";i:4;s:12:\"HASHIMOTO, M\";i:5;s:8:\"SAITO, E\";i:6;s:7:\"OHTA, T\";i:7;s:11:\"CHIKAOKA, H\";i:8;s:11:\"HAYASAKA, K\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"ANNED3\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:8:\"\u0000*\u0000place\";s:7:\"Hoboken\";s:6:\"\u0000*\u0000pub\";s:11:\"Willey-Liss\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Panist access
"O:12:\"IstexOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:55:\"10.1002\/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:9:\"\u0000*\u0000jtitle\";s:19:\"Annals of neurology\";s:9:\"\u0000*\u0000stitle\";s:11:\"Ann. neurol\";s:7:\"\u0000*\u0000date\";s:4:\"1999\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:1:\"4\";s:8:\"\u0000*\u0000spage\";s:3:\"660\";s:8:\"\u0000*\u0000epage\";s:3:\"663\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0364-5134\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:4:\"KATO\";s:10:\"\u0000*\u0000aufirst\";s:1:\"M\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:9:{i:0;s:11:\"TAKIZAWA, N\";i:1;s:9:\"YAMADA, S\";i:2;s:6:\"ITO, A\";i:3;s:8:\"HONMA, T\";i:4;s:12:\"HASHIMOTO, M\";i:5;s:8:\"SAITO, E\";i:6;s:7:\"OHTA, T\";i:7;s:11:\"CHIKAOKA, H\";i:8;s:11:\"HAYASAKA, K\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"ANNED3\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:8:\"\u0000*\u0000place\";s:7:\"Hoboken\";s:6:\"\u0000*\u0000pub\";s:11:\"Willey-Liss\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Istex access
"O:16:\"UnpaywallOpenUrl\":35:{s:8:\"\u0000*\u0000email\";s:27:\"assistance-portail@inist.fr\";s:6:\"\u0000*\u0000fmt\";N;s:6:\"\u0000*\u0000doi\";s:55:\"10.1002\/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q\";s:6:\"\u0000*\u0000pii\";N;s:7:\"\u0000*\u0000pmid\";N;s:9:\"\u0000*\u0000atitle\";N;s:9:\"\u0000*\u0000jtitle\";N;s:9:\"\u0000*\u0000stitle\";N;s:7:\"\u0000*\u0000date\";N;s:9:\"\u0000*\u0000volume\";N;s:8:\"\u0000*\u0000issue\";N;s:8:\"\u0000*\u0000spage\";N;s:8:\"\u0000*\u0000epage\";N;s:8:\"\u0000*\u0000pages\";N;s:7:\"\u0000*\u0000issn\";N;s:8:\"\u0000*\u0000eissn\";N;s:9:\"\u0000*\u0000aulast\";N;s:10:\"\u0000*\u0000aufirst\";N;s:9:\"\u0000*\u0000auinit\";N;s:10:\"\u0000*\u0000auinitm\";N;s:5:\"\u0000*\u0000au\";N;s:9:\"\u0000*\u0000aucorp\";N;s:7:\"\u0000*\u0000isbn\";N;s:8:\"\u0000*\u0000coden\";N;s:8:\"\u0000*\u0000genre\";N;s:7:\"\u0000*\u0000part\";N;s:9:\"\u0000*\u0000btitle\";N;s:8:\"\u0000*\u0000title\";N;s:8:\"\u0000*\u0000place\";N;s:6:\"\u0000*\u0000pub\";N;s:10:\"\u0000*\u0000edition\";N;s:9:\"\u0000*\u0000tpages\";N;s:9:\"\u0000*\u0000series\";N;s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";N;}"
Unpaywall access
"O:16:\"EuropePMCOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:55:\"10.1002\/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:9:\"\u0000*\u0000jtitle\";s:19:\"Annals of neurology\";s:9:\"\u0000*\u0000stitle\";s:11:\"Ann. neurol\";s:7:\"\u0000*\u0000date\";s:4:\"1999\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:1:\"4\";s:8:\"\u0000*\u0000spage\";s:3:\"660\";s:8:\"\u0000*\u0000epage\";s:3:\"663\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0364-5134\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:4:\"KATO\";s:10:\"\u0000*\u0000aufirst\";s:1:\"M\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:9:{i:0;s:11:\"TAKIZAWA, N\";i:1;s:9:\"YAMADA, S\";i:2;s:6:\"ITO, A\";i:3;s:8:\"HONMA, T\";i:4;s:12:\"HASHIMOTO, M\";i:5;s:8:\"SAITO, E\";i:6;s:7:\"OHTA, T\";i:7;s:11:\"CHIKAOKA, H\";i:8;s:11:\"HAYASAKA, K\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"ANNED3\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:8:\"\u0000*\u0000place\";s:7:\"Hoboken\";s:6:\"\u0000*\u0000pub\";s:11:\"Willey-Liss\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Europe PubMed Central access
"O:11:\"BaseOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:55:\"10.1002\/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:9:\"\u0000*\u0000jtitle\";s:19:\"Annals of neurology\";s:9:\"\u0000*\u0000stitle\";s:11:\"Ann. neurol\";s:7:\"\u0000*\u0000date\";s:4:\"1999\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:1:\"4\";s:8:\"\u0000*\u0000spage\";s:3:\"660\";s:8:\"\u0000*\u0000epage\";s:3:\"663\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0364-5134\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:4:\"KATO\";s:10:\"\u0000*\u0000aufirst\";s:1:\"M\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:9:{i:0;s:11:\"TAKIZAWA, N\";i:1;s:9:\"YAMADA, S\";i:2;s:6:\"ITO, A\";i:3;s:8:\"HONMA, T\";i:4;s:12:\"HASHIMOTO, M\";i:5;s:8:\"SAITO, E\";i:6;s:7:\"OHTA, T\";i:7;s:11:\"CHIKAOKA, H\";i:8;s:11:\"HAYASAKA, K\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"ANNED3\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:8:\"\u0000*\u0000place\";s:7:\"Hoboken\";s:6:\"\u0000*\u0000pub\";s:11:\"Willey-Liss\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Base Search access
"O:12:\"ArXivOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:55:\"10.1002\/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:9:\"\u0000*\u0000jtitle\";s:19:\"Annals of neurology\";s:9:\"\u0000*\u0000stitle\";s:11:\"Ann. neurol\";s:7:\"\u0000*\u0000date\";s:4:\"1999\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:1:\"4\";s:8:\"\u0000*\u0000spage\";s:3:\"660\";s:8:\"\u0000*\u0000epage\";s:3:\"663\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0364-5134\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:4:\"KATO\";s:10:\"\u0000*\u0000aufirst\";s:1:\"M\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:9:{i:0;s:11:\"TAKIZAWA, N\";i:1;s:9:\"YAMADA, S\";i:2;s:6:\"ITO, A\";i:3;s:8:\"HONMA, T\";i:4;s:12:\"HASHIMOTO, M\";i:5;s:8:\"SAITO, E\";i:6;s:7:\"OHTA, T\";i:7;s:11:\"CHIKAOKA, H\";i:8;s:11:\"HAYASAKA, K\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"ANNED3\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:110:\"Diffuse pachygyria with cerebellar hypoplasia : A milder form of microlissencephaly or a new genetic syndrome?\";s:8:\"\u0000*\u0000place\";s:7:\"Hoboken\";s:6:\"\u0000*\u0000pub\";s:11:\"Willey-Liss\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
arXiv access
