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Understanding Cystic Fibrosis (Understanding Health and Sickness Series)

معرفی کتاب «Understanding Cystic Fibrosis (Understanding Health and Sickness Series)» نوشتهٔ Ph.D. Karen Hopkin، منتشرشده توسط نشر University Press of Mississippi در سال 1998. این کتاب در فرمت pdf، زبان انگلیسی ارائه شده است.

Cystic fibrosis (CF) is the most common genetic disorder in the white population. Since the discovery of the CF gene in 1989, scientists have learned a great deal about the biology of this disease, which strikes one child in every 3.300 births. With the gene pinpointed, scientists are now working on ways to replace it and are developing better tests for early diagnosis. Understanding Cystic Fibrosis charts the progress that has been made in identifying the mutations that cause CF and in understanding how these genetic errors cause a disease whose symptoms can range from mild respiratory distress to life-threatening lung infections. This book features a review of current available treatments; research that can lead to therapies and perhaps a cure; advice and resources for families and patients; how to work best with health-care providers and HMOs; the history and diagnosis of CF; who gets CF and why; how CF affects the lungs, intestines, and other organs; and a list of organizations, support groups, and resources. Локальный диск......Page 0 cover......Page 1 page_i......Page 2 page_ii......Page 3 page_iii......Page 4 page_iv......Page 5 page_v......Page 6 page_vii......Page 7 page_viii......Page 8 page_ix......Page 9 page_x......Page 10 page_3......Page 11 page_4......Page 12 page_5......Page 13 page_6......Page 14 page_7......Page 15 page_8......Page 16 page_9......Page 17 page_10......Page 18 page_10-0......Page 19 page_12......Page 20 page_13......Page 21 page_14......Page 22 page_15......Page 23 page_16......Page 24 page_17......Page 25 page_18......Page 26 page_19......Page 27 page_20......Page 28 page_21......Page 29 page_22......Page 30 page_23......Page 31 page_24......Page 32 page_25......Page 33 page_26......Page 34 page_27......Page 35 page_28......Page 36 page_29......Page 37 page_30......Page 38 page_31......Page 39 page_32......Page 40 page_33......Page 41 page_34......Page 42 page_35......Page 43 page_36......Page 45 page_37......Page 46 page_38......Page 47 page_39......Page 48 page_40......Page 49 page_41......Page 50 page_42......Page 51 page_43......Page 52 page_44......Page 53 page_45......Page 54 page_46......Page 55 page_47......Page 56 page_48......Page 57 page_49......Page 58 page_50......Page 59 page_51......Page 60 page_52......Page 61 page_53......Page 62 page_54......Page 63 page_55......Page 64 page_56......Page 65 page_57......Page 66 page_58......Page 67 page_59......Page 68 page_60......Page 69 page_61......Page 70 page_62......Page 71 page_63......Page 72 page_64......Page 73 page_65......Page 74 page_66......Page 75 page_67......Page 76 page_68......Page 77 page_69......Page 78 page_70......Page 79 page_71......Page 80 page_72......Page 81 page_73......Page 82 page_74......Page 83 page_75......Page 84 page_76......Page 85 page_77......Page 86 page_78......Page 87 page_79......Page 88 page_80......Page 89 page_81......Page 90 page_82......Page 91 page_83......Page 92 page_84......Page 93 page_85......Page 94 page_86......Page 95 page_87......Page 96 page_88......Page 97 page_89......Page 98 page_90......Page 99 page_91......Page 100 page_92......Page 101 page_93......Page 102 page_94......Page 103 page_95......Page 104 page_96......Page 105 page_97......Page 106 page_98......Page 107 page_99......Page 108 page_100......Page 109 page_101......Page 111 page_102......Page 113 page_103......Page 115 page_104......Page 117 page_105......Page 119 page_106......Page 121 page_107......Page 123 page_108......Page 125 page_109......Page 127 page_110......Page 129 page_111......Page 131 page_112......Page 133 page_113......Page 135 page_114......Page 137 page_115......Page 139 page_116......Page 141 page_117......Page 142 page_118......Page 143 page_119......Page 144 page_120......Page 145 page_121......Page 147 page_122......Page 149 page_123......Page 151 page_124......Page 153 page_125......Page 155 page_126......Page 158 page_127......Page 161 page_128......Page 164 page_129......Page 167 page_130......Page 170 page_131......Page 173 page_132......Page 176 page_133......Page 179 Локальный диск -1 cover 1 page_i 2 page_ii 3 page_iii 4 page_iv 5 page_v 6 page_vii 7 page_viii 8 page_ix 9 page_x 10 page_3 11 page_4 12 page_5 13 page_6 14 page_7 15 page_8 16 page_9 17 page_10 18 page_10-0 19 page_12 20 page_13 21 page_14 22 page_15 23 page_16 24 page_17 25 page_18 26 page_19 27 page_20 28 page_21 29 page_22 30 page_23 31 page_24 32 page_25 33 page_26 34 page_27 35 page_28 36 page_29 37 page_30 38 page_31 39 page_32 40 page_33 41 page_34 42 page_35 43 page_36 45 page_37 46 page_38 47 page_39 48 page_40 49 page_41 50 page_42 51 page_43 52 page_44 53 page_45 54 page_46 55 page_47 56 page_48 57 page_49 58 page_50 59 page_51 60 page_52 61 page_53 62 page_54 63 page_55 64 page_56 65 page_57 66 page_58 67 page_59 68 page_60 69 page_61 70 page_62 71 page_63 72 page_64 73 page_65 74 page_66 75 page_67 76 page_68 77 page_69 78 page_70 79 page_71 80 page_72 81 page_73 82 page_74 83 page_75 84 page_76 85 page_77 86 page_78 87 page_79 88 page_80 89 page_81 90 page_82 91 page_83 92 page_84 93 page_85 94 page_86 95 page_87 96 page_88 97 page_89 98 page_90 99 page_91 100 page_92 101 page_93 102 page_94 103 page_95 104 page_96 105 page_97 106 page_98 107 page_99 108 page_100 109 page_101 111 page_102 113 page_103 115 page_104 117 page_105 119 page_106 121 page_107 123 page_108 125 page_109 127 page_110 129 page_111 131 page_112 133 page_113 135 page_114 137 page_115 139 page_116 141 page_117 142 page_118 143 page_119 144 page_120 145 page_121 147 page_122 149 page_123 151 page_124 153 page_125 155 page_126 158 page_127 161 page_128 164 page_129 167 page_130 170 page_131 173 page_132 176 page_133 179 "Cystic Fibrosis (CF) is the most common genetic disorder in the white population."--BOOK JACKET. "Understanding Cystic Fibrosis charts the progress that has been made in identifying the mutations that cause CF and in understanding how these genetic errors cause a disease whose symptoms can range from mild respiratory distress to life-threatening lung infections."--Jacket
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