2001
Composite nodular lymphocyte-predominance Hodgkin disease and gamma-heavy-chain disease: a case report and review of the literature.
Hudnall S, Alperin J, Petersen J. Composite nodular lymphocyte-predominance Hodgkin disease and gamma-heavy-chain disease: a case report and review of the literature. Archives Of Pathology & Laboratory Medicine 2001, 125: 803-7. PMID: 11371236, DOI: 10.5858/2001-125-0803-cnlphd.Peer-Reviewed Original ResearchConceptsNodular lymphocyte predominance Hodgkin's diseaseLymphocyte predominance Hodgkin's diseaseHodgkin's diseaseChain diseaseAutoimmune hemolytic anemiaB-cell natureB-cell lymphoproliferative processesComplete remissionGraves' diseaseLymph nodesCase reportLymphoproliferative processMonoclonal gammopathyHemolytic anemiaBone marrowUnique caseDiseaseClonal relationshipFurther treatment
2000
T‐gamma gene rearrangement and CMV mononucleosis
Mathew P, Hudnall S, Elghetany M, Payne D. T‐gamma gene rearrangement and CMV mononucleosis. American Journal Of Hematology 2000, 66: 64-66. PMID: 11426498, DOI: 10.1002/1096-8652(200101)66:1<64::aid-ajh1013>3.0.co;2-v.Peer-Reviewed Original ResearchMeSH KeywordsAntibodies, ViralBlood CellsBone Marrow CellsClone CellsCytomegalovirusCytomegalovirus InfectionsDiagnosis, DifferentialFemaleGene Rearrangement, gamma-Chain T-Cell Antigen ReceptorHumansImmunoglobulin MImmunophenotypingInfectious MononucleosisLymphoproliferative DisordersMiddle AgedT-Lymphocyte SubsetsViremiaConceptsT gamma gene rearrangementCMV infectionLymphoproliferative diseaseAcute CMV infectionGene rearrangementsAtypical lymphocytosisCMV mononucleosisCMV viremiaNight sweatsIgM serologyClinical featuresLymphoid aggregatesBlood countPeripheral bloodHemolytic anemiaImmune responseBone marrowWeight lossCytomegalovirusInfectionDiseaseMononucleosisViremiaSplenomegalyLymphocytosis
1999
Methylenetetrahydrofolate reductase (MTHFR): The incidence of mutations C677T and A1298C in the Ashkenazi Jewish population
Rady P, Tyring S, Hudnall S, Vargas T, Kellner L, Nitowsky H, Matalon R. Methylenetetrahydrofolate reductase (MTHFR): The incidence of mutations C677T and A1298C in the Ashkenazi Jewish population. American Journal Of Medical Genetics 1999, 86: 380-384. PMID: 10494095, DOI: 10.1002/(sici)1096-8628(19991008)86:4<380::aid-ajmg13>3.0.co;2-9.Peer-Reviewed Original ResearchConceptsMutation C677TC677TMethylenetetrahydrofolate reductaseVascular diseaseA1298C mutationA1298C allelesAshkenazi Jewish populationSpina bifidaRisk mutationsC677T alleleC677T mutationAshkenazi JewsHealthy individualsT alleleMTHFR geneJewish individualsA1298CHealthy Jewish individualsDNA samplesCommon mutationsFurther studiesT mutationDiseaseJewish populationBifida