Genes, brainstem development, and eye movements

Neurology

Volumn 59, Issue 3, 2002, Pages 304-305

  Engle, Elizabeth C ^a   Leigh, R John ^b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABDUCENS NUCLEUS; AUTOSOMAL RECESSIVE DISORDER; BRAIN DEVELOPMENT; CRANIAL NERVE PARALYSIS; DUANE RETRACTION SYNDROME; EDITORIAL; EYE MOVEMENT CONTROL; GAZE PARALYSIS; HUMAN; MOEBIUS SYNDROME; MYOFIBROSIS; OCULOMOTOR NUCLEUS; PRIORITY JOURNAL; PTOSIS;

EID: 0037072259     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.59.3.304     Document Type: Editorial

References (20)

1. Neurobiology of eye movements, from molecules to behavior
2. Medial rectus subgroups of the oculomotor nucleus and their abducens internuclear input in monkey
3. Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles
4. CFEOM3: A new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3
5. A gene for isolated congenital ptosis maps to a 3 cM region within 1p32-p34.1
6. Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12
7. CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX
8. A novel X-linked dominant condition: X-linked congenital isolated ptosis
9. Congenital fibrosis of the extraocular muscles type 2 (CFEOM2), an inherited exotropic strabismus fixus, maps to distal 11q13
10. Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2
11. Development of noradrenergic neurons in the zebrafish hindbrain requires BMP, FGF8, and the homeodomain protein soulless/Phox2a
12. Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis
13. Bilateral Duane's retraction syndrome: Clinical-pathological case report
14. Unilateral Duane's retraction syndrome (type 1)
15. Localization of a gene for Duane retraction syndrome to chromosome 2q31
16. A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia: Implications for the mapping of the BOR gene
17. Brain stem hypoplasia in familial congenital horizontal gaze paralysis (FCGP) and kyphoscoliosis
18. Familial horizontal gaze palsy with progressive scoliosis (HGPS) maps to chromosome 11q23-25
19. Etiology of idiopathic scoliosis: Current trends in research