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  Najwi瘯szy - 95784 hase (47892 polskich, 47892 angielskich)

Archiwum hase

self-serving bias | fibrates  | broad QRS complex tachycardia  | reperfusion therapy  | ACE inhibitors (angiotensin-converting enzyme inhibitors) | polyunsaturated fatty acids omega-3  | residual risk  | intensive glucose-lowering treatment  | reccurent urinary tract infection  | nephrologist  | tubulo-interstitial nephropathy  | sympathetic overactivity  | diabetic kidney disease  | multifactorial therapy  | markers of kidney injury  | malnutrition-inflammation-atherosclerosis {MIA} syndrome  | induction therapy  | consolidation therapy  | secondary glomerulonephritis Przew Lek 2009; 5: 51-54 | hyperphosphatemia  | Severe combined immunodeficiency (SCID) with low T-and B-cell numbers | Severe combined immunodeficiency (SCID) with low or normal B-cell number | Immunodeficiency following hereditary defective response to Epstein-Barr virus | Immunodeficiency with thymic alymphoplasia | thymic alymphoplasia | Immunodeficiency with thymic aplasia | thymic aplasia | X-linked lymphoproliferative immunodeficiency | Immunodeficiency with increased immunoglobulin | Immunodeficiency with thymic hypoplasia | Immunodeficiency associated with other major defects | Immunodeficiency with short-limbed stature | Immunodeficiency with thrombocytopenia and eczema | Immunodeficiency with predominantly antibody defects | Di George's syndrome | Immunodeficiency associated with hyperimmunoglobulin E (IgE) syndrome | Immunodeficiency with pharyngeal pouch syndrome | pharyngeal pouch syndrome | Sulfite oxidase deficiency | sulfite oxidase | 5-alpha Reductase deficiency (with male pseudohermaphroditism) | Pyridoxine deficiency | Dietary zinc deficiency | 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 |
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