Literature DB >> 15729534

Diffuse cortical atrophy in a patient with Turner syndrome and Leber hereditary optic neuropathy.

Pierre Blaise, Arnaud Fumal, Nicolas Janin, Alain Verloes, Gustave Moonen, Cécile Andris.   

Abstract

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Year:  2005        PMID： 15729534     DOI： 10.1007/s00415-005-0615-4

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  10 in total

1.  Brain development in Turner syndrome: a magnetic resonance imaging study.

Authors:  Wendy E Brown; Shelli R Kesler; Stephan Eliez; Ilana S Warsofsky; Michael Haberecht; Anil Patwardhan; Judith L Ross; E Kirk Neely; She Min Zeng; Jerome Yankowitz; Allan L Reiss
Journal:  Psychiatry Res       Date:  2002-12-30       Impact factor: 3.222

2.  No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriers.

Authors:  R J Oostra; S Kemp; P A Bolhuis; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

3.  The cerebral cortex is damaged in chronic alcoholics.

Authors:  J J Kril; G M Halliday; M D Svoboda; H Cartwright
Journal:  Neuroscience       Date:  1997-08       Impact factor: 3.590

4.  White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.

Authors:  D Lev; M Yanoov-Sharav; N Watemberg; E Leshinsky-Silver; T Lerman-Sagie
Journal:  Eur J Paediatr Neurol       Date:  2002       Impact factor: 3.140

Review 5.  Turner's syndrome.

Authors:  M B Ranke; P Saenger
Journal:  Lancet       Date:  2001-07-28       Impact factor: 79.321

Review 6.  Leber hereditary optic neuropathy.

Authors:  P Yu-Wai-Man; D M Turnbull; P F Chinnery
Journal:  J Med Genet       Date:  2002-03       Impact factor: 6.318

7.  Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy.

Authors:  H Y Handoko; P J Wirapati; H A Sudoyo; M Sitepu; S Marzuki
Journal:  J Med Genet       Date:  1998-08       Impact factor: 6.318

8.  X-chromosome effects on female brain: a magnetic resonance imaging study of Turner's syndrome.

Authors:  D G Murphy; C DeCarli; E Daly; J V Haxby; G Allen; B J White; A R McIntosh; C M Powell; B Horwitz; S I Rapoport
Journal:  Lancet       Date:  1993-11-13       Impact factor: 79.321

9.  Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy.

Authors:  E K Nikoskelainen; R J Marttila; K Huoponen; V Juvonen; T Lamminen; P Sonninen; M L Savontaus
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-08       Impact factor: 10.154

10.  X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant.

Authors:  E Pegoraro; V Carelli; M Zeviani; P Cortelli; P Montagna; P Barboni; C Angelini; E P Hoffman
Journal:  Am J Med Genet       Date:  1996-02-02
  10 in total
  1 in total

1.  Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance.

Authors:  Kelly L Jones; Erin A McNamara; Mauro Longoni; Danny E Miller; Mersedeh Rohanizadegan; Laura A Newman; Frances Hayes; Lynne L Levitsky; Betty L Herrington; Angela E Lin
Journal:  Am J Med Genet A       Date:  2018-08-06       Impact factor: 2.802
  1 in total

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