A proposal for a molecular genetic classification of the malformations of the nervous system;Propuesta para una clasificación genética molecular de las malformaciones del sistema nervioso

Revista de Neurologia

Volumn 33, Issue 1, 2001, Pages 68-75

  Sarnat, H B ^a  

^a SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

Author keywords

Classification; Malformations; Molecular genetics; Nervous system

Indexed keywords

CELL ADHESION MOLECULE; DOUBLECORTIN; FILAMIN; REELIN;

AGYRIA; CELL MIGRATION; DISEASE CLASSIFICATION; GANGLIONEUROMA; GENE DELETION; GENE SEQUENCE; HOLOPROSENCEPHALY; HUMAN; HUMAN CELL; HUMAN TISSUE; MOLECULAR GENETICS; NERVOUS SYSTEM MALFORMATION; NEURAL TUBE; NEUROBLAST; NEURULATION; ONTOGENY; PATHOLOGICAL ANATOMY; REVIEW;

EID: 0034807536     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.3301.2000534     Document Type: Review

References (41)

1. Towards a greater understanding of the pathogenesis of holoprosencephaly
2. Holoprosencephaly: Molecular study of a California population
3. Genetics of ventral forebrain development and holoprosencephaly
4. Gene table. Central nervous system malformations: Locations of known human mutations
5. Familial schizencephaly associated with EMX2 mutation
6. Mutation analysis of the EMX2 gene in Kallmann's syndrome
7. The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
8. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal pathfinding molecules
9. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
10. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
11. Immunohistochemical expression of doublecortin in the human cerebrum: Comparison of normal development and neuronal migration disorders
12. The new neuroembryology. How to construct a neural tube
13. Molecular genetic classification for central nervous system malformations
14. Control of anteroposterior and dorsoventral domains of Nkx-6.1 gene expression relative to other Nkx genes during vertebrate CNS development
15. Vertebrate embryonic cells will become nerve cells unless told otherwise
16. Transient notch activation initiates an irreversible switch from neurogenesis to gliogenesis by neural crest stem cells
17. Control of neural crest cell fate by the Wnt signalling pathway
18. The midbrain-hindbrain phenotype of Wnt-1-/Wnt-1- mice results from stepwise deletion of engrailed-expressing cells by 9.5 days postcoitum
19. Absence of the midbrain and upper pons with cerebellar hypoplasia in two infants: Putative defective expression of the EN2 gene
20. Interactions of Wnt-1 and Wnt-3a are essential for neural tube patterning
21. Cooperation of Pax2 and Pax5 in midbrain and cerebellum development
22. Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system
23. A brain with two hypophyses in median cleft face syndrome
24. Monstrous, crablike hypertrophy of the cerebellar vermis and its relationship with Lhermitte-Duclos disease
25. On finding striated muscle in the brain
26. Light microscopic demonstration of myoid fibres in the nervous system
27. Quergestreifte muskelfasser in der Pars infundibularis des Affenhypophyse
28. Striated muscle in the pineal gland of swine
29. The occurrence of striated muscle within the cerebellum of the albino rat
30. Medullomyoblastomas: A histological, immunocytochemical, ultrastructural and molecular genetic study
31. Molecular cloning of a human neuro D from a neuroblastoma cell line specifically expressed in the fetal brain and adult cerebellum
32. Dysembryoplastic neuroepithelial tumors: A surgically curable tumor of young patients with intractable partial seizures
33. Dysembryoplastic neuroepithelial tumors nonspecific histological forms: A study of 40 cases
34. Dysembryoplastic neuroepithelial tumor (DNT): An ultrastructural study of six cases
35. Tumores neuroepiteliales disembrioplásicos
36. Conservation of neurogenic genes and mechanisms
37. Ectopic or heterotopic? An appeal for semantic precision in describing developmental disorders of the nervous system
38. Semantic precision for central nervous system malformations
39. Neurenteric cysts of the spinal cord resembling multiple sclerosis