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Pelger-Huet Anomaly

Known as: Pelger Huët Nuclear Anomaly, Pelger Huet Anomaly, anomaly huet pelger 
Autosomal dominant anomaly characterized by abnormal ovoid shape GRANULOCYTE nuclei and their clumping chromatin. Mutations in the LAMIN B receptor… 
National Institutes of Health

Papers overview

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Highly Cited
2003
Highly Cited
2003
May-Hegglin anomaly (MHA), Fechtner syndrome (FTNS), Sebastian syndrome (SBS), and Epstein syndrome (EPS) are a group of rare… 
Highly Cited
1996
Highly Cited
1996
Autosomal dominant iridogoniodysgenesis anomaly (IGDA) is characterized by iris hypoplasia and goniodysgenesis with frequent… 
1993
1993
A flow-cytometric method with fluorescence-labeled monoclonal antibodies (MABs) against the low density lipoprotein (LDL… 
Highly Cited
1989
Highly Cited
1989
In this study, we investigated whether an interleukin 2 (IL-2) secretion defect by peripheral blood mononuclear cells (PBMCs… 
Highly Cited
1987
Highly Cited
1987
Peripheral lymphocytes stimulated with phytohemagglutinin (PHA-blasts) were examined for their responsiveness to exogenous… 
1980
1980
Polymorphonuclear leukocytes (PMNL) from two individuals with congenital Pelger-Huet anomaly (PHA) were examined to determine… 
Highly Cited
1977
Highly Cited
1977
Acid α‐naphthyl acetate esterase (ANAE) activity is charecteristic of resting human T lymphocytes. The expression of the ANAE… 
1973
1973
Serial measurements were made of the morphological blast transformation response of lymphocytes to phytohemagglutinin (PHA) in… 
1972
1972
All five members of one generation in an Icelandic family were affected by acute myeloid leukaemia or preleukaemia. Two sibs died… 
Highly Cited
1959
Highly Cited
1959
THE abnormality of granulocytic leukocytes manifested by poor segmentation and condensation of nuclear chromatin was first…