Literature DB >> 16118898

Sinus histiocytosis with massive lymphadenopathy in three brothers.

Erol Kismet1, Vedat Köseoglu, Abdullah Avni Atay, Salih Deveci, Erkan Demirkaya, Kemal Tuncer.   

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Year:  2005        PMID： 16118898     DOI： 10.1111/j.1442-200x.2005.02096.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  11 in total

1.  Mutation in the SLC29A3 Gene in an Egyptian Patient with H Syndrome: A Case Report and Review of Literature.

Authors:  Hala T El-Bassyouni; Manal M Thomas; Angie M S Tosson
Journal:  J Pediatr Genet       Date:  2019-09-30

2.  Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.

Authors:  Neil V Morgan; Mark R Morris; Hakan Cangul; Diane Gleeson; Anna Straatman-Iwanowska; Nicholas Davies; Stephen Keenan; Shanaz Pasha; Fatimah Rahman; Dean Gentle; Maaike P G Vreeswijk; Peter Devilee; Margaret A Knowles; Serdar Ceylaner; Richard C Trembath; Carlos Dalence; Erol Kismet; Vedat Köseoğlu; Hans-Christoph Rossbach; Paul Gissen; David Tannahill; Eamonn R Maher
Journal:  PLoS Genet       Date:  2010-02-05       Impact factor: 5.917

3.  Isolated Intraocular Rosai-Dorfman Disease.

Authors:  Franz Fogt; Thomas Rüediger; Albert J Augustin; Dale M Frank; Andreas Rosenwald; Axel Wellmann; Vivian Lee
Journal:  Ocul Oncol Pathol       Date:  2019-04-10

4.  H syndrome: 5 new cases from the United States with novel features and responses to therapy.

Authors:  Jessica L Bloom; Clara Lin; Lisa Imundo; Stephen Guthery; Shelly Stepenaskie; Csaba Galambos; Amy Lowichik; John F Bohnsack
Journal:  Pediatr Rheumatol Online J       Date:  2017-10-17       Impact factor: 3.054

Review 5.  A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature.

Authors:  Sadaf Noavar; Samira Behroozi; Taraneh Tatarcheh; Farshid Parvini; Majid Foroutan; Hossein Fahimi
Journal:  BMC Med Genet       Date:  2019-08-29       Impact factor: 2.103

Review 6.  Hereditary Hearing Impairment with Cutaneous Abnormalities.

Authors:  Tung-Lin Lee; Pei-Hsuan Lin; Pei-Lung Chen; Jin-Bon Hong; Chen-Chi Wu
Journal:  Genes (Basel)       Date:  2020-12-30       Impact factor: 4.096

7.  Phenotypic intrafamilial variability including H syndrome and Rosai-Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene.

Authors:  Hamza Chouk; Mohamed Ben Rejeb; Lobna Boussofara; Haїfa Elmabrouk; Najet Ghariani; Badreddine Sriha; Ali Saad; Dorra H'Mida; Mohamed Denguezli
Journal:  Hum Genomics       Date:  2021-10-17       Impact factor: 4.639

Review 8.  Review of the current literature on H syndrome treatment.

Authors:  Kimia Saleh Anaraki; Sepehr Khosravi; Elham Behrangi; Afsaneh Sadeghzadeh-Bazargan; Azadeh Goodarzi
Journal:  J Family Med Prim Care       Date:  2022-03-10

9.  NRAS Mutations May Be Involved in the Pathogenesis of Cutaneous Rosai Dorfman Disease: A Pilot Study.

Authors:  Kuan-Jou Wu; Shu-Hao Li; Jia-Bin Liao; Chien-Chun Chiou; Chieh-Shan Wu; Chien-Chin Chen
Journal:  Biology (Basel)       Date:  2021-05-02

Review 10.  Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature.

Authors:  Francesco di Dio; Ilaria Mariotti; Elena Coccolini; Patrizia Bruzzi; Barbara Predieri; Lorenzo Iughetti
Journal:  BMC Pediatr       Date:  2016-05-03       Impact factor: 2.125
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