Geometry.Net - the online learning center
Home  - Health_Conditions - Kearns Sayre Syndrome
e99.com Bookstore
  
Images 
Newsgroups
Page 6     101-102 of 102    Back | 1  | 2  | 3  | 4  | 5  | 6 
A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z  

         Kearns Sayre Syndrome:     more detail
  1. The Official Parent's Sourcebook on Kearns-Sayre Syndrome: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09-16
  2. Mitochondrial Diseases: Mitochondrial Disease, Leber's Hereditary Optic Neuropathy, Kearns-Sayre Syndrome
  3. Disorders of Ocular Muscles, Binocular Movement, Accommodation and Refraction: Myopia, Kearns-Sayre Syndrome, Sixth Nerve Palsy, Duane Syndrome
  4. Maladie Mitochondriale: Neuropathie Optique de Leber, Syndrome Melas, Syndrome Narp, Syndrome de Kearns-Sayre (French Edition)

101. Spontaneous Kearns-Sayre/Chronic External Ophthalmoplegia Plus Syndrome Associat
Spontaneous kearnssayre/Chronic External Ophthalmoplegia Plus syndrome Associated with a Mitochondrial DNA Deletion A Slip-Replication Model and Metabolic
http://www.pnas.org/cgi/content/abstract/86/20/7952
This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted ... Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Add to My File Cabinet ... Cited by other online articles PubMed PubMed Citation Articles by Shoffner, J. M. Articles by Wallace, D. C. October 15, 1989
Spontaneous Kearns-Sayre/Chronic External Ophthalmoplegia Plus Syndrome Associated with a Mitochondrial DNA Deletion: A Slip-Replication Model and Metabolic Therapy John M. Shoffner, Marie T. Lott, Alexander S. Voljavec, Shawke A. Soueidan, Donal A. Costigan, and Douglas C. Wallace
This article has been cited by other articles in HighWire Press -hosted journals:
A. M. Remes, K. Majamaa-Voltti, M. Karppa, J. S. Moilanen, S. Uimonen, H. Helander, H. Rusanen, P. I. Salmela, M. Sorri, I. E. Hassinen, and K. Majamaa
Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population
Neurology, March 22, 2005; 64(6): 976 - 981.

102. Detection Of "Deleted" Mitochondrial Genomes In Cytochrome-c Oxidase-Deficient M
Detection of Deleted Mitochondrial Genomes in Cytochromec Oxidase-Deficient Muscle Fibers of a Patient with kearns-sayre syndrome
http://www.pnas.org/cgi/content/abstract/86/23/9509
This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted ... Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Add to My File Cabinet ... Cited by other online articles PubMed PubMed Citation Articles by Mita, S. Articles by Bonilla, E. December 1, 1989
Detection of "Deleted" Mitochondrial Genomes in Cytochrome-c Oxidase-Deficient Muscle Fibers of a Patient with Kearns-Sayre Syndrome Shuji Mita, Beny Schmidt, Eric A. Schon, Salvatore DiMauro, and Eduardo Bonilla
This article has been cited by other articles in HighWire Press -hosted journals:
M. Zeviani and S. Di Donato
Mitochondrial disorders
Brain, October 1, 2004; 127(10): 2153 - 2172.
[Abstract]
[Full Text] [PDF]
M. R. Rose
Mitochondrial Myopathies: Genetic Mechanisms
Arch Neurol, January 1, 1998; 55(1): 17 - 24.
[Abstract]
[Full Text] [PDF] H. A. COLLER, N. D. BODYAK, and K. KHRAPKO Frequent Intracellular Clonal Expansions of Somatic mtDNA Mutations: Significance and Mechanisms Ann. N.Y. Acad. Sci., April 1, 2002; 959(1): 434 - 447.

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z  

Page 6     101-102 of 102    Back | 1  | 2  | 3  | 4  | 5  | 6 

free hit counter