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10 in total

1. Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion.

Authors: Tayfun Ozcelik; Nurten Akarsu; Elif Uz; Safak Caglayan; Suleyman Gulsuner; Onur Emre Onat; Meliha Tan; Uner Tan
Journal: Proc Natl Acad Sci U S A Date: 2008-06-10 Impact factor: 11.205

2. Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification.

Authors: Kym M Boycott; Shauna Flavelle; Alexandre Bureau; Hannah C Glass; T Mary Fujiwara; Elaine Wirrell; Krista Davey; Albert E Chudley; James N Scott; D Ross McLeod; Jillian S Parboosingh
Journal: Am J Hum Genet Date: 2005-07-22 Impact factor: 11.025

3. Genetic aspects of congenital cerebellar ataxia.

Authors: D Kumar
Journal: Indian J Pediatr Date: 1986 Nov-Dec Impact factor: 1.967

4. Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy.

Authors: Luis E Kolb; Zulfikar Arlier; Cengiz Yalcinkaya; Ali K Ozturk; Jennifer A Moliterno; Ozdem Erturk; Fatih Bayrakli; Baris Korkmaz; Michael L DiLuna; Katsuhito Yasuno; Kaya Bilguvar; Tayfun Ozcelik; Beyhan Tuysuz; Matthew W State; Murat Gunel
Journal: Neurogenetics Date: 2010-01-15 Impact factor: 2.660

5. A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

Authors: D P McHale; S Mitchell; S Bundey; L Moynihan; D A Campbell; C G Woods; N J Lench; R F Mueller; A F Markham
Journal: Am J Hum Genet Date: 1999-02 Impact factor: 11.025

6. Vascular endothelial growth factors A and C are induced in the SVZ following neonatal hypoxia-ischemia and exert different effects on neonatal glial progenitors.

Authors: Jennifer M Bain; Lisamarie Moore; Zhihua Ren; Sophia Simonishvili; Steven W Levison
Journal: Transl Stroke Res Date: 2013-04 Impact factor: 6.829

7. Mutations in VLDLR as a cause for autosomal recessive cerebellar ataxia with mental retardation (dysequilibrium syndrome).

Authors: Kym M Boycott; Carsten Bonnemann; Joachim Herz; Stephanie Neuert; Chandree Beaulieu; James N Scott; Anuradha Venkatasubramanian; Jillian S Parboosingh
Journal: J Child Neurol Date: 2009-03-30 Impact factor: 1.987

Review 8. Two families with quadrupedalism, mental retardation, no speech, and infantile hypotonia (Uner Tan Syndrome Type-II); a novel theory for the evolutionary emergence of human bipedalism.

Authors: Uner Tan
Journal: Front Neurosci Date: 2014-04-22 Impact factor: 4.677

9. Assessment of oral and dental health status in children with cerebral palsy: An exploratory study.

Authors: Nabila A Sedky
Journal: Int J Health Sci (Qassim) Date: 2018 Jan-Feb

10. Cerebral palsy in a total population of 4-11 year olds in southern Sweden. Prevalence and distribution according to different CP classification systems.

Authors: Lena Westbom; Gunnar Hagglund; Eva Nordmark
Journal: BMC Pediatr Date: 2007-12-05 Impact factor: 2.125

10 in total