Page 2498 - Williams Hematology ( PDFDrive )
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 2468  Index                                                                                            Index         2469



                       detection methods, 1711            consolidation therapy, 1752–1753  Myosin light-chain kinase, 1833t
                       DIS3, 233t, 1737                   continuous therapy, 1753         Myristoylated alanine-rich C-kinase substrate
                       drug resistance and, 1711          cyclin-dependent kinase inhibitors, 218  (MARCKS), 667, 668f
                       early events, 1710                 hematopoietic cell transplantation,
                       EGR1, 234t                            364–366, 365f, 1750, 1755–1756  N
                       FAM46C, 1737                       histone deacetylase inhibitors, 240, 1754  N -formyl FH , 584
                                                                                            5
                                                                                                     4
                       FGFR3, 233t                        immunomodulatory drugs, 1754     N -methyl FH –homocysteine
                                                                                            5
                                                                                                     4
                       heterogeneity, 1760                maintenance therapy, 1751–1752, 1752t   methyltransferase, 585, 587f,
                       IGH, 188                           monoclonal antibodies, 345, 345f, 346t,   589–590
                                                                                            5
                       KRAS (K-RAS), 188, 233t, 1709, 1737,   1754–1755                    N -methyl FH –homocysteine
                                                                                                     4
                         1759, 1760                       of osteonecrosis of the jaw, 1757       methyltransferase deficiency, 608
                       late events, 1710–1711             of peripheral neuropathy, 1757   N370S, 1122, 1123, 1123t
                       LRRK2, 233t                        proteasome inhibitors, 342–343,    N803, 487
                       MAF, 233t                             1749–1750                     NAD+, in glucose metabolism, 693
                       MYC, 1711                          in relapsed or refractory disease,    NADH, in glucose metabolism, 692
                       NRAS (N-RAS), 188, 233t, 1709, 1759   1753–1755, 1753t              NADH diaphorase. See Cytochrome b 5
                       p53, 1710                          response criteria, 1758, 1758t   NADH-methemoglobin reductase, 692t
                       PRDM1, 234t                        in transplant-eligible patients, 1748t,   NADP
                       prognosis and, 1759–1760              1750–1751                      in folate metabolism, 584
                       RAS, 1710, 1735f, 1736t, 1737      in transplant-ineligible patients, 1751,   in glucose metabolism, 694
                       RB/RB1, 234t, 1710                    1752t                         NADPH
                       somatic, 1736–1737                 of venous thromboembolism,        in folate metabolism, 584, 585
                       TP53, 1735f                           1756–1757                      in glucose metabolism, 694
                       TP53, 233t, 1737               Myeloma stem cell, 1713–1714          in neurodegenerative disorders, 1840
                     marrow microenvironment, 1712–1713,   Myelomastocytic leukemia (MML), 978  NADPH diaphorase, 692t, 701t, 790, 793
                         1737, 1738f                  Myelomonocytic leukemia. See Acute   NADPH oxidase
                     myeloma stem cell, 1713–1714, 1734      myelomonocytic leukemia;       in atherothrombosis, 2283
                     occupation, 1709, 1734                  Chronic myelomonocytic leukemia   in chronic granulomatous disease,
                     plasma cell differentiation, 1710, 1710f  (CMML)                             1027–1029, 1028f
                     preclinical models, 1739–1740, 1739f  Myeloperoxidase (MPO), 107, 1011, 1012t,   in inflammatory response, 286
                     radiation, 1709                         1068f                          neutrophil granules and, 927
                     stages, 1734–1735, 1734f         Myeloperoxidase (MPO) deficiency, 1020t,   respiratory burst and, 1068f
                    Gaucher disease and, 1125                1033                          Nadroparin, 2274t
                    IgM, 1760                         Myelophthisic anemia, 657. See also Marrow,   Nails, examination of, 8
                    initial evaluation, 1747, 1747t          infiltration                  NAIT (neonatal alloimmune
                    laboratory features, 1740t        Myeloproliferative disease, atypical, 1473  thrombocytopenia). See
                     blood, 1740–1741                 Myeloproliferative leukemia virus (MPLV),   Newborns/infants, alloimmune
                     imaging, 1715, 1748–1749, 1748f, 1749f  1822                                 thrombocytopenia in
                     immunoglobulins, 1714, 1741      Myelosuppression, for polycythemia vera,   Nalidixic acid, maternal ingestion of, effect
                     lactate dehydrogenase levels, 1716      1298–1299, 1298t                     on fetus and newborn, 112, 112t
                     marrow, 31–32, 1715, 1741–1744, 1742f,   MYH9 (Myh9), 1818, 1842      NAMPT (nicotinamide
                         1743f, 1744f                 MYH9-related thrombocytopenia               phosphoribosyltransferase), 200
                     β -microglobulin, 1715–1716             syndromes, 1996, 1999f, 2061  Nantucket fever, 819
                      2
                     serum, 1714                      MYL9, 2058, 2060                     NAP-1 (neutrophil-activating peptide 1).
                     urine, 1714                      Myocardial infarction (MI), 2294–2297       See Interleukin (IL)-8
                    larval, 1726                        clinical features, 2295            NAP-2 (neutrophil-activating peptide 2),
                    minimal residual disease assessment,   diagnosis, 2294–2295                   1856
                         1716–1717                      factor VIII levels and, 2226–2227  NAPc2 (nematode anticoagulant protein c2),
                    monocytosis and, 1097               genetic factors, 1850, 1853, 2288         2214
                    plasmablastic, 1742                 in hemophilia, 2130                Naproxen
                    prognosis, 1712, 1759–1760          laboratory features, 2295           antiplatelet effects, 404, 2075
                    smoldering, 1708–1709, 1726, 1734f, 1761  monocytosis and, 1097         maternal ingestion of, effect on fetus and
                    staging, 1747–1748, 1747t, 1748t    therapy, 1855, 2076, 2295–2297, 2313      newborn, 112
                    treatment                         Myoglobin, 618                       Nasopharynx, history of disorders of, 5
                     of bone pain, 1756               Myosin, 1833t, 1842                  Natural killer (NK) cell antigens, 1142,
                     of complications, 1756–1757      Myosin II, 1833t                            1142t








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