Archiwum hase³
Dietary calcium deficiency | Potassium (K) deficiency | Antibody deficiency with near-normal immunoglobulins | Antibody deficiency with hyperimmunoglobulinaemia | Purine nucleoside phosphorylase (PNP) deficiency | Ariboflavinosis | Sucrase deficiency | group therapy | transference | countertransference | creativity | hypnotherapy | seropositive | psychoneuroimmunology | projective identification | psychotherapy termination | epistemology | complex sleep-related behaviors | therapeutic encounter | discussion groups | body empathy | psychotherapist embodiment | unresolved mourning | family context | family therapy | individual therapy | mental disturbances | subliminal perception | acculturation | professional self | possible self | cognitive behavioral therapy {CBT} | psychodynamic therapy | assimilative integration | psychometry | psychiatric scales | separation anxiety disorder | Dietary selenium deficiency | Sodium (Na) deficiency | Sulfatase deficiency | Thiamine deficiency | Attention deficit with hyperactivity | Vanadium deficiency | Vitamin A deficiency | Vitamin A deficiency with xerophthalmic scars of cornea | Vitamin A deficiency with night blindness | Vitamin A deficiency with keratomalacia | Vitamin A deficiency with corneal ulceration | Vitamin A deficiency with corneal ulceration and xerosis | Vitamin A deficiency with Bitot`s spot and conjunctival xerosis | Bitot`s spot | Vitamin A deficiency with corneal xerosis | Biotin deficiency | Deficiency of vitamin K | Vitamin K deficiency of newborn | Lack of growth | Iron deficiency | Deficiency of vitamin C | Deficiency of vitamin E | Vitamin B6 deficiency | Vitamin B12 deficiency | Vitamin A deficiency with conjunctival xerosis | Orthostatic hypotension | Postural hypotension | Chronic hypotension | Idiopathic hypotension | Hypotension due to drugs | Hypofunction of labyrinth | Postprocedural ovarian failure | Testicular hypofunction | Postprocedural testicular hypofunction | Adrenocortical insufficiency | Hypofunction of pituitary gland | Postprocedural hypopituitarism | Idiopathic hypoparathyroidism | Transitory neonatal hypoparathyroidism | Postprocedural hypoparathyroidism | Pseudohypoparathyroidism | Postirradiation hypothyroidism | Postsurgical hypothyroidism | Postinfectious hypothyroidism | Postprocedural hypothyroidism | Subclinical iodine-deficiency hypothyroidism | Congenital hypothyroidism without goitre | Congenital iodine-deficiency hypothyroidism | Acquired iodine-deficiency hypothyroidism | Hypothyroidism due to medicaments and other exogenous substances | Primary atelectasis of newborn | Pulmonary dysmaturity | Underfeeding of newborn | Silent myocardial ischaemia | Acute smali intestine ischaemia | Traumatic ischaemia of muscle | Cerebral ischaemia, arteriosclerotic | Neonatal cerebral ischaemia | Chronic cerebral ischaemia | Ischaemia of kidney | Transient carotid artery syndrome | Familial hypoplastic anaemia | Idiopathic aplastic anaemia | Fanconi's aplastic anaemia | Drug-induced aplastic anaemia | Aplastic anaemia, panmyelophthisis | Blackfan-Diamond aplastic anaemia syndrome | Cooley's anaemia | Dyshaematopoietic anaemia, congenital | Anaemia haemolytic nonspherocytic (hereditary), type I | planned pregnancy | unplanned pregnancy | maternal hypoglycemia | infant of the diabetic mother | Anaesthesia of skin | Ovarian hypofunction | Hypoaesthesia of skin | Maternal hypotension syndrome | niacin deficiency | Riboflavin deficiency | Hereditary sideroblastic anaemia | Hereditary haemolytic anaemia, Hb-C disease | Hereditary haemolytic anaemia, Hb-D disease | Hereditary haemolytic anaemia, unstable haemoglobin haemolytic disease | Hereditary haemolytic anaemia, hereditary elliptocytosis | Hereditary haemolytic anaemia, congenital elliptocytosis | Congenital Heinz body anaemia | Hereditary haemolytic anaemia, abnormal haemoglobin | Hereditary haemolytic anaemia, ovalocytosis (congenital) (familial) | Hereditary haemolytic anaemia, spherocytosis | Hereditary haemolytic anaemia, stomatocytosis | Hereditary haemolytic anaemia, Chauffard-Minkowski syndrome | Hereditary haemolytic anaemia, spherocytic haemolytic icterus | Hereditary haemolytic anaemia, acholuric (familial) jaundice | Acquired drug-induced autoimmune haemolytic anaemia | Acquired autoimmune haemolytic anaemia warm type | Acquired haemolytic anaemia, march haemoglobinuria | march haemoglobinuria | Acquired haemolytic anaemia, paroxysmal cold haemoglobinuria | Acquired haemolytic anaemia, paroxysmal nocturnal haemoglobinuria | paroxysmal nocturnal haemoglobinuria | Acquired haemolytic anaemia, haemoglobinuria from exertion | Acquired haemolytic anaemia, cold agglutinin haemoglobinuria | cold agglutinin | Acquired mechanical haemolytic anaemia | Acquired microangiopathic haemolytic anaemia | Acquired drug-induced nonautoimmune haemolytic anaemia | Acquired drug-induced enzyme deficiency anaemia | Acquired chronic cold haemagglutinin disease | cold haemagglutinin disease | Acquired idiopathic haemolytic anaemia, chronic | Acquired haemolytic anaemia, toxic | Acquired haemolytic anaemia: warm type (secondary) (symptomatic) | Acquired haemolytic anaemia: cold type (secondary) (symptomatic) | Acquired haemolytic anaemia, haemolytic-uraemic syndrome | Acquired haemolytic anaemia, Marchiafava-Micheli syndrome | Hypoplastic anaemia | Leukoerythroblastic anaemia | Refractory anaemia without sideroblasts | Refractory anaemia with excess of blasts | Refractory anaemia with excess of blasts with transformation | Refractory anaemia with sideroblasts | Acute posthaemorrhagic anaemia | Simple chronic anaemia | Infantile pseudoleukaemia | Sickle-cell anaemia | mycophenolate mofetil | neonatal lupus erythematosus | third-degree heart block | complete heart block | third-degree atrioventricular (AV) block | serological negativization | alopecia mucinosa | grumose degeneration {GD} | Neurogenic bladder | senile purpura | simethicone | tangle associated neuritic clusters {TANCs} | mitomycin C {MMC} | estimated GFR {EGFR}{eGFR} | hypnotherapy | group psychotherapy | Grand mal seizures on awakening {GMA} | Finger tapping | International Headache Society | lumbar puncture {LP} | familial hemiplegic migraine {FHM} | American Council for Headache Education {ACHE} | Migraine Disability Assessment Score {MIDAS} | acute promyelocytic leukemia {APL} | partial tandem duplication {PTD} | stem cell transplant {SCT} | Randomized Evaluation of Mechanical Assistance in the Treatment of Heart Failure {REMATCH} | pagetoid reticulosis {PR} | Woringer-Kolopp disease | follicular mucinosis | cutaneous anaplastic large cell lympohma {C-ALCL} | athritis mutilans | Psoriatic arthritis (PsA) | Visual Analogue Score {VAS} | Digestive Disease | Mebeverine | alverine citrate |
Poprzednia 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 239 240 241 242 243 Nastêpna
