Literature DB >> 13840590

Reticular dysgenesia.

O de VAAL, V SEYNHAEVE.   

Abstract

Entities:  

Keywords:  LEUKOCYTES; RETICULOENDOTHELIAL SYSTEM/abnormalities

Mesh：

Year:  1959        PMID： 13840590     DOI： 10.1016/s0140-6736(59)90105-9

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  28 in total

Review 1.  Primary T-lymphocyte immunodeficiencies.

Authors:  A Fischer
Journal:  Clin Rev Allergy Immunol       Date:  2001-02       Impact factor: 8.667

2.  The Immunological System of the Child: Part II: Immunological Deficiency States.

Authors:  C A Janeway
Journal:  Arch Dis Child       Date:  1966-08       Impact factor: 3.791

3.  Thymic function and disease processes.

Authors: 
Journal:  Br Med J       Date:  1967-08-19

Review 4.  Application of marrow grafts in human disease.

Authors:  G W Santos
Journal:  Am J Pathol       Date:  1971-12       Impact factor: 4.307

Review 5.  Genetic insights into congenital neutropenia.

Authors:  Christoph Klein; Karl Welte
Journal:  Clin Rev Allergy Immunol       Date:  2010-02       Impact factor: 8.667

6.  Pathomorphologic findings in severe combined immunodeficiency and reticular dysgenesia.

Authors:  B Heymer; D Niethammer; R Haas; H Meister; O Haferkamp
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1976-05-03

7.  [Incomplete, combined hereditary immunodeficiency with generalized tuberculosis after BCG-vaccination from bacille Calmette Guérin (author's transl)].

Authors:  T Radaszkiewicz; M Eibl; R Jarisch; D Lachmann
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1975

8.  Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2.

Authors:  Ulrich Pannicke; Manfred Hönig; Isabell Hess; Claudia Friesen; Karlheinz Holzmann; Eva-Maria Rump; Thomas F Barth; Markus T Rojewski; Ansgar Schulz; Thomas Boehm; Wilhelm Friedrich; Klaus Schwarz
Journal:  Nat Genet       Date:  2008-11-30       Impact factor: 38.330

9.  Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.

Authors:  Chantal Lagresle-Peyrou; Emmanuelle M Six; Capucine Picard; Frédéric Rieux-Laucat; Vincent Michel; Andrea Ditadi; Corinne Demerens-de Chappedelaine; Estelle Morillon; Françoise Valensi; Karen L Simon-Stoos; James C Mullikin; Lenora M Noroski; Céline Besse; Nicolas M Wulffraat; Alina Ferster; Manuel M Abecasis; Fabien Calvo; Christine Petit; Fabio Candotti; Laurent Abel; Alain Fischer; Marina Cavazzana-Calvo
Journal:  Nat Genet       Date:  2008-11-30       Impact factor: 38.330

Review 10.  The inherited bone marrow failure syndromes.

Authors:  S Deborah Chirnomas; Gary M Kupfer
Journal:  Pediatr Clin North Am       Date:  2013-12       Impact factor: 3.278
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