Literature DB >> 6022522

Chediak-Higashi syndrome with severe cutaneous involvement. Occurrence in two brothers 14 and 15 years of age.

P E Weary, A S Bender.   

Abstract

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Mesh：

Year:  1967        PMID： 6022522

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN： 0003-9926


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  8 in total

1.  Chédiak-Higashi syndrome neutrophils are characterized by the absence of both normal azurophilic granules.

Authors:  B C West
Journal:  Am J Pathol       Date:  1986-01       Impact factor: 4.307

2.  Parkinsonism and Other Movement Disorders Associated with Chediak-Higashi Syndrome: Case Report and Systematic Literature Review.

Authors:  Bettina Balint; Kailash P Bhatia
Journal:  Mov Disord Clin Pract       Date:  2015-01-14

3.  Periodontitis in Chédiak-Higashi Syndrome: An Altered Immunoinflammatory Response.

Authors:  V Thumbigere Math; P Rebouças; P A Giovani; R M Puppin-Rontani; R Casarin; L Martins; L Wang; K Krzewski; W J Introne; M J Somerman; F H Nociti; K R Kantovitz
Journal:  JDR Clin Trans Res       Date:  2017-08-03

4.  Peripheral neuropathy in the Chediak-Higashi syndrome.

Authors:  V P Misra; R H King; A E Harding; J R Muddle; P K Thomas
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

5.  Defective granulocyte chemotaxis in the Chediak-Higashi syndrome.

Authors:  R A Clark; H R Kimball
Journal:  J Clin Invest       Date:  1971-12       Impact factor: 14.808

6.  Silvery Hair with Speckled Dyspigmentation: Chediak-Higashi Syndrome in Three Indian Siblings.

Authors:  Chekuri Raghuveer; Sambasiviah Chidambara Murthy; Mallur N Mithuna; Tamraparni Suresh
Journal:  Int J Trichology       Date:  2015 Jul-Sep

7.  The neuropsychological phenotype of Chediak-Higashi disease.

Authors:  Talia N Shirazi; Joseph Snow; Lillian Ham; Greta B Raglan; Edythe A Wiggs; Angela C Summers; Camilo Toro; Wendy J Introne
Journal:  Orphanet J Rare Dis       Date:  2019-05-06       Impact factor: 4.123

8.  Atypical Chédiak-Higashi syndrome with attenuated phenotype: three adult siblings homozygous for a novel LYST deletion and with neurodegenerative disease.

Authors:  James D Weisfeld-Adams; Lakshmi Mehta; Janet C Rucker; Francine R Dembitzer; Arnold Szporn; Fred D Lublin; Wendy J Introne; Vikas Bhambhani; Michael C Chicka; Catherine Cho
Journal:  Orphanet J Rare Dis       Date:  2013-03-22       Impact factor: 4.123
  8 in total

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