Literature DB >> 16157712

A novel mutation in a patient with pantothenate kinase-associated neurodegeneration.

Danish Saleheen, Aisha Nazir, Shaheen Khanum, Shajjia Razi Haider, Philippe Frossard.   

Abstract

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Year:  2005        PMID： 16157712      PMCID： PMC1197146          DOI： 10.1503/cmaj.1050096

Source DB:  PubMed          Journal:  CMAJ        ISSN： 0820-3946            Impact factor:   8.262


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  4 in total

1.  The "eye of the tiger" sign.

Authors:  Danish Saleheen; Philippe Frossard; Mahammed Zeeshan Ozair; Mohammad Ali Kazmi; Hamza Khalid; Bhojo Khealani
Journal:  CMAJ       Date:  2005-01-04       Impact factor: 8.262

2.  A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome.

Authors:  B Zhou; S K Westaway; B Levinson; M A Johnson; J Gitschier; S J Hayflick
Journal:  Nat Genet       Date:  2001-08       Impact factor: 38.330

Review 3.  Iron in the Hallervorden-Spatz syndrome.

Authors:  A H Koeppen; A C Dickson
Journal:  Pediatr Neurol       Date:  2001-08       Impact factor: 3.372

4.  Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.

Authors:  Susan J Hayflick; Shawn K Westaway; Barbara Levinson; Bing Zhou; Monique A Johnson; Katherine H L Ching; Jane Gitschier
Journal:  N Engl J Med       Date:  2003-01-02       Impact factor: 91.245
  4 in total
  1 in total

1.  Characteristics of TIA and its management in a tertiary care hospital in Pakistan.

Authors:  Ayeesha Kamal; Farhad Khimani; Rushna Raza; Sahar Zafar; Salman Bandeali; Sayeedullah Jan
Journal:  BMC Res Notes       Date:  2008-08-29
  1 in total

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