High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia

Alain Aurias, Bernard Dutrillaux, D Buriot, +1

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

ChromatinGenome InstabilityChromosome DynamicsCytogeneticsGenetic Disorder +10

The cell cycle of lymphocytes in Fanconi anemia

Bernard Dutrillaux, Alain Aurias, Anne‐Marie Dutrillaux, +2

Human Genetics

Cell DivisionHematologyImmunologyBlood CellCell Cycle +4

Lactoferrin deficiency as a consequence of a lack of specific granules in neutrophils from a patient with recurrent infections. Detection by immunoperoxidase staining for lactoferrin and cytochemical electron microscopy.

J Breton-Gorius, D Y Mason, D Buriot, +2

PubMed

Evidence that abnormal platelet functions in human Chédiak-Higashi syndrome are the result of a lack of dense bodies.

Francine Rendu, J Breton-Gorius, Marius Lebret, +5

PubMed

Immunoglobulins in ataxia-telangiectasia: Evidence for IgG4 and IgA2 subclass deficiencies

Liliane Rivat‐Peran, D Buriot, Jean‐Philippe Salier, +3

Clinical Immunology and Immunopathology

Primary ImmunodeficiencyImmunogeneticsAutoimmune DiseaseImmunodeficienciesImmunology +9

Possible toxicity of levamisole in children with rheumatoid arthritis

A M Prieur, D Buriot, J. M. Lefur, +1

The Journal of Pediatrics

Rheumatoid DisorderRheumatologyMedicineRheumatic DiseasesChildhood Arthritis +5

Antibody‐induced von willebrand syndrome: Inhibition of VIII VWF and VIII AGN with sparing of VIII AHF by the autoanti body

C. Gazengel, C. Jacques, J. Nedellec, +3

American Journal of Hematology

ImmunohematologyImmunodeficienciesImmunologyPathologyViii Ahf +22

[Chronic neutropenia and Crohn's disease in childhood. Report of 2 cases ].

Vannier Jp, F Arnaud‐Battandier, C Ricour, +4

PubMed

Autoimmune DiseaseGood Clinical ToleranceGastroenterologyPediatricsPathology +8

[Acute leukemia in 3 children with chronic juvenile arthritis treated with chlorambucil].

D Buriot, Prieur Am, Y Lebranchu, +2

PubMed

Hematological MalignancyRheumatologyRheumatoid DisorderChronic Juvenile ArthritisAcute Leukaemia +12

FULMINANT MENINGOCOCCEMIA IN A CHILD WITH HEREDITARY DEFICIENCY OF THE SEVENTH COMPONENT OF COMPLEMENT AND PROTEINURIA

C Loirat, D Buriot, A Peltier, +4

Acta Paediatrica