• A 34-year-old Japanese patient exhibiting NBAS deficiency with a novel mutation and extended phenotypic variation
• A case of benign Pelger-Huet anomaly
• A case report on reversible Pelger-Huet anomaly depending on serum free fraction of valproic acid
• A chance diagnosis of Pelger-Huet anomaly in a 49-year-old woman hospitalized for an acute episode of Crohn disease
• A family with congenital Pelger-Huet anomaly
• A homozygous variant in the Lamin B receptor gene LBR results in a non-lethal skeletal dysplasia without Pelger-Huet anomaly
• A new case of Greenberg dysplasia and literature review suggest that Greenberg dysplasia, dappled diaphyseal dysplasia, and Astley-Kendall dysplasia are allelic disorders
• A novel case of Greenberg dysplasia and genotype-phenotype correlation analysis for LBR pathogenic variants: An instructive example of one gene-multiple phenotypes
• A novel compound heterozygous mutation in NBAS gene causes SOPH syndrome and liver function damage
• Acquired Pelger-Huet anomaly in a patient treated with valganciclovir
• Acquired Pelger-Huet anomaly in two patients with chronic lymphocytic leukemia treated with venetoclax
• Acquired Pelger-Huet anomaly/abnormal chromatin clumping of granulocytes after allogeneic hematopoietic stem cell transplantation for acute myeloid leukaemia: medication or relapse?
• Acquired pseudo-Pelger-Huet anomaly under maintenance therapy with rituximab in follicular lymphoma
• Acute Liver Failure Meets SOPH Syndrome: A Case Report on an Intermediate Phenotype
• Alterations in nuclear structure promote lupus autoimmunity in a mouse model
• An anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia secondary to lamin B receptor (LBR) gene mutations: further definition of the phenotypic heterogeneity of LBR-bone dysplasias
• Analysis of LBR gene mutation in a pedigree affected with Pelger-Hut anomaly
• Analysis of LBR gene mutation in a pedigree affected with Pelger-Huёt anomaly
• Antenatal diagnostic dilemma in a pseudodominant pedigree with lamin-B receptor (LBR)-related regressive spondylometaphyseal dysplasia
• Appearance of pseudo-Pelger Huet anomaly after accidental exposure to ionizing radiation in vivo
• Atypical "accelerated" chronic lymphocytic leukemia with abnormal lymphocyte chromatin clumping, bone involvement, and exceptional response to Imbruvica
• Autosomal recessive hyposegmentation of granulocytes in Australian Shepherd Dogs indicates a role for LMBR1L in myeloid leukocytes
• Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huet anomaly
• Blended Phenotype of Pelger-Huet Anomaly with Osteochondroma and Autosomal Recessive Deafness with Enlarged Vestibular Aqueduct
• Case of acquired or pseudo-Pelger-Huet anomaly
• Characterization of a complex phenotype (fever-dependent recurrent acute liver failure and osteogenesis imperfecta) due to NBAS and P4HB variants
• Characterization of a novel non-canonical splice site variant (c.886-5T>A) in NBAS and description of the associated phenotype
• Chronic myelogenous leukaemia with a p53 mutation demonstrated neutrophilic granulocytes with nuclear hypolobation (pseudo-Pelger-Huet anomaly) and hypogranulation in the peripheral blood smear
• Classification and clinical findings of myelodysplastic syndromes
• Comparison of hematologic abnormalities between hospitalized coronavirus disease 2019 positive and negative patients with correlation to disease severity and outcome
• Compound heterozygous variants in NBAS as a cause of atypical osteogenesis imperfecta
• Coronavirus disease 2019 (COVID-19): Focus on peripheral blood cell morphology
• Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients
• Deletion of LBR N-terminal domains recapitulates Pelger-Huet anomaly phenotypes in mouse without disrupting X chromosome inactivation
• Detection of Perlger-Huet anomaly based on augmented fast marching method and speeded up robust features
• Dysplastic Changes of Peripheral Blood Cells in COVID-19 Infection
• Extracts Prepared from a Canadian Toxic Plant Induce Light-Dependent Perinuclear Vacuoles in Human Cells
• Familial case of hereditary Pelger-Huet anomaly
• Familial Pelger-Huet Anomaly
• Fly clock, my clock, and lamin B receptor
• Foveal hypoplasia in short stature with optic atrophy and Pelger-Huet anomaly syndrome with neuroblastoma-amplified sequence (NBAS) gene mutation
• Genetic analysis of a fetus with Rhizomelic skeletal dysplasia
• Genetic architecture of band neutrophil fraction in Iceland
• Hemophagocytic lymphohistiocytosis and pelger-huet anomaly associated with colchicine intoxication
• High diagnostic yield of clinically unidentifiable syndromic growth disorders by targeted exome sequencing
• Human Genetics of Ventricular Septal Defect
• Hyposplenic changes and pseudo-Pelger-Huet anomaly following allogeneic stem cell transplantation
• Idiopathic dysplasia of undetermined/uncertain significance (IDUS) initially presenting erythroblastosis and hyperferritinemia
• Image analysis of neutrophil nuclear morphology: Learning about phenotypic range and its reliable analysis from patients with pelger-Huet-anomaly and treated with colchicine
• Impact of genetic and non-genetic factors on phenotypic diversity in NBAS-associated disease
• Inter-observer variance and the need for standardization in the morphological classification of myelodysplastic syndrome
• Lamin B receptor recognizes specific modifications of histone H4 in heterochromatin formation
• Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypes
• Lamin B Receptor: Interplay between Structure, Function and Localization
• Lamin B1 deletion in myeloid neoplasms causes nuclear anomaly and altered hematopoietic stem cell function
• Like son, like father
• Liver transplantation for the treatment of acute liver failure in 3 cases with NBAS gene deficiency and literature review
• Lymphocyte nuclei of nodal marginal zone lymphoma mimicking granulocytic morphology with Pelger-Huet-like features
• MDS/AML with del5q: An acquired "laminopathy"?
• NBAS disease: 14 new patients, a recurrent mutation, and genotype-phenotype correlation among 24 Chinese patients
• NBAS mutations cause a multisystem disorder involving bone, connective tissue, liver, immune system, and retina
• Necrobiotic xanthogranuloma (without paraproteinemia) in a patient with Pelger-Huet anomaly
• Novel neuroblastoma amplified sequence (<em>NBAS</em>) mutations in a Japanese boy with fever-triggered recurrent acute liver failure
• Nuclear envelope composition determines the ability of neutrophil-type cells to passage through micron-scale constrictions
• Occurrence of neutrophil dysplasia in the course of severe nephrotic syndrome in a 12-year-old boy on immunosuppressive therapy: Answers
• Pelger-huet anomaly and a mild skeletal phenotype secondary to mutations in LBR
• Pelger-Huet anomaly and Greenberg skeletal dysplasia: LBR-associated diseases of cholesterol metabolism
• Pelger-Huet anomaly and T-cell lymphoma
• Pelger-Huet anomaly in a cat
• Peripheral Blood Examination Findings in SARS-CoV-2 Infection
• Peripheral Blood Smear Findings of COVID-19 Patients Provide İnformation about the Severity of the Disease and the Duration of Hospital Stay
• Persistent pseudo-Pelger-Huet anomaly
• Population frequency and age of mutation G5741→A in gene NBAS which is a cause of SOPH syndrome in Sakha (Yakutia) Republic
• Prenatal diagnosis of recurrent moderate skeletal dysplasias in lamin B receptors
• Presumed pseudo-Pelger-Huet anomaly and basophilia secondary to chronic lymphocytic leukemia in a dog
• Protean Regulation of Leukocyte Function by Nuclear Lamins
• Pseudo Pelger-Huet anomalies as potential biomarkers for acute exposure radiation dose in rhesus macaques (Macaca mulatta)
• Pseudo Pelger-Huët anomalies as potential biomarkers for acute exposure radiation dose in rhesus macaques <em>(Macaca mulatta)</em>
• Pseudo-Pelger-Huet anomaly and granulocytic dysplasia associated with human granulocytic anaplasmosis
• Pseudo-Pelger-Huet anomaly in a 58-year-old woman treated with mycophenolate mofetil for flare of systemic lupus erythematosus
• Pseudo-Pelger-Huet anomaly in a patient on tacrolimus
• Pseudo-Pelger-Huet neutrophil morphology due to sodium valproate toxicity
• Pseudo-Pelger-Hut Nuclear Anomaly in Systemic Lupus Erythematosus
• Pseudo-Pelger-Huёt Nuclear Anomaly in Systemic Lupus Erythematosus
• Pyoderma gangrenosum associated with pseudo-Pelger-Huet anomaly in a patient with idiopathic myelofibrosis
• Rare diseases recognizable from blood smears
• Resolution of recurrent pediatric acute liver failure with liver transplantation in a patient with NBAS mutation
• Septic shock caused by Capnocytophaga canimorsus in a patient with heterozygous Pelger-Huet anomaly
• Severe generalized muscular atrophia, nerve optic atrophia, ear problem and disability with Pelger-Huet anomaly
• Severe SOPH syndrome due to a novel NBAS mutation in a 27-year-old woman-Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades
• Short stature, optic nerve atrophy and Pelger-Huet anomaly syndrome with antibody immunodeficiency and aplastic anemia: a case report and literature review
• SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy
• SOPH Syndrome with Growth Hormone Deficiency, Normal Bone Age, and Novel Compound Heterozygous Mutations in NBAS
• Stodtmeister Cells (Polymorphs with Pelger-Huet Anomaly) Showing "Faggots" in Mixed Phenotypic Acute Leukemia (T/Myeloid)
• The Lamin B receptor is essential for cholesterol synthesis and perturbed by disease-causing mutations
• The Pseudo-Pelger huet Cell as a Retrospective Dosimeter: Analysis of a Radium Dial Painter Cohort
• The Pseudo-Pelger HuEt Cell-A New Permanent Radiation Biomarker
• Transient Deformation of Neutrophils in Kawasaki Disease
• Vimentin regulates nuclear segmentation in neutrophils
• Young Woman with Unexplained Neutropenia and Neutrophils with Bilobed Nuclei: Marrow Findings